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201. Comparison of Chief Complaints and Patient-Reported Symptoms of Treatment-Naive Lung Cancer Patients Before Surgery

Author: Feng Y, Dai W, Wang Y, Liao J, Wei X, Xie S, Xu W, Li Q, Liu F, and Shi Q
Subjects: lung cancer, chief complaint, surgery, symptom, patient-reported outcomes, Medicine (General), R5-920
Abstract: Yaqian Feng,1 Wei Dai,1 Yaqin Wang,1 Jia Liao,1 Xing Wei,1 Shaohua Xie,1 Wei Xu,2 Qiang Li,1 Fang Liu,3 Qiuling Shi4 1Department of Thoracic Surgery, Sichuan Cancer Hospital & Institute, School of Medicine, University of Electronic Science and Technology of China, Chengdu, 610041, People’s Republic of China; 2School of Public Health and Management, Chongqing Medical University, Chongqing, People’s Republic of China; 3Traditional Chinese Medicine Department of Oncology, Sichuan Cancer Hospital & Institute, School of Medicine, University of Electronic Science and Technology of China, Chengdu, 610041, People’s Republic of China; 4Center for Cancer Prevention Research, Sichuan Cancer Hospital & Institute, School of Medicine, University of Electronic Science and Technology of China, Chengdu, 610041, People’s Republic of ChinaCorrespondence: Qiuling Shi; Fang LiuSichuan Cancer Hospital & Institute, Sichuan Cancer Center, School of Medicine, University of Electronic Science and Technology of China, No. 55, Section 4, South Renmin Road, Chengdu, 610041, People’s Republic of ChinaEmail qshi@cqmu.edu.cn; 1937239721@qq.comBackground: Lung cancer patients without chief complaints have been increasingly identified by physical examination. This study aimed to profile and compare chief complaints with patient-reported symptoms of lung cancer patients before surgery.Methods: Data were extracted from a multicenter, prospective longitudinal study (CN-PRO-Lung 1) in China from November 2017 to January 2020. A comparison between chief complaints and patient-reported symptoms was analyzed using the Chi-squared test.Results: A total of 201 (50.8%) lung cancer patients without chief complaints were found by physical examination at admission, and 195 (49.2%) patients had chief complaints. The top 5 chief complaints were coughing (38.1%), expectoration (25.5%), chest pain (13.6%), hemoptysis (10.6%), and shortness of breath (5.3%). There were significantly more patients with chief complaints of coughing (38.1% vs 15.0%, P < 0.001) and pain (20.5% vs 6.9%, P< 0.001) than those with the same symptoms rated ≥ 4 via MD Anderson Symptom Inventory‒Lung Cancer (MDASI-LC). There were less patients with chief complaints of fatigue (1.8% vs 10.9%, P< 0.001), nausea (0.3% vs 2.5%, P=0.006), and vomiting (0.3% vs 1.8%, p=0.032) than those with the same symptoms rated ≥ 4 via MDASI-LC. In patients without chief complaints, the five most common moderate to severe patient-reported symptoms were disturbed sleep (19.5%), distress (13.5%), dry mouth (13%), sadness (12%), and difficulty remembering (11.1%).Conclusion: Symptoms of lung cancer patients not included in the chief complaint could be identified via a patient-reported outcome instrument, suggesting the necessity of implementing the patient-reported outcome assessment before lung cancer surgery for better patient care.Keywords: lung cancer, chief complaint, surgery, symptom, patient-reported outcomes
Published: 2021

202. Long Non-Coding RNA XIST Promotes Wilms Tumor Progression Through the miR-194-5p/YAP Axis

Author: He X, Luo X, Dong J, Deng X, Liu F, and Wei G
Subjects: lncrna, xist, wilms tumor, yap, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
Abstract: Xingyue He,1 Xin Luo,2 Junjun Dong,1 Xing Deng,1 Feng Liu,1,2 Guanghui Wei1,2 1Department of Urology, Children’s Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing, People’s Republic of China; 2Chongqing Key Laboratory of Children Urogenital Development and Tissue Engineering; Chongqing Key Laboratory of Pediatrics, Chongqing, People’s Republic of ChinaCorrespondence: Feng Liu; Guanghui WeiDepartment of Urology, Children’s Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, 136, Zhongshan 2nd Road, Yuzhong District, Chongqing, 400014, People’s Republic of ChinaTel +8613983693965; +8613883617398Email liuu_ff@163.com; u806806@cqmu.edu.cnPurpose: Although the long non-coding RNA (lncRNA) X inactive-specific transcript (XIST) has been reported to have an anti-tumor effect in multiple malignant tumors, its role in Wilms tumor (WT) progression has not been characterized. Thus, we investigated the underlying mechanism by which XIST regulates WT progression.Patients and Methods: We performed microarray analysis and real-time quantitative PCR (RT-qPCR) to detect the expression levels of XIST lncRNA, microRNA-194-5p (miR-194-5p), and YAP (yes-associated protein in Hippo pathway) in tumor and matched adjacent normal tissues and blood collected from 49 WT patients. We also conducted bioinformatics analyses to identify differentially expressed genes. We measured the effects of XIST overexpression and knockdown on cell proliferation, apoptosis, migration, and invasion, and its association with the miR-194-5p/YAP pathway in the rhabdoid G401cell line using flow cytometry, transwell assays, immunohistochemistry, Western blot analysis, and the dual luciferase reporter gene assay.Results: We found that XIST lncRNA levels were increased in blood and tissue samples of WT patients, and this upregulation was significantly correlated with TNM staging and shorter survival time. Notably, we found that XIST upregulation correlated with miR-194-5p downregulation and YAP upregulation in WT tissues, suggesting that XIST regulates the miR-194-5p/YAP pathway. Conversely, XIST downregulation inhibited WT cell proliferation, migration, and invasion and induced apoptosis. Our study revealed the oncogenic role of the lncRNA XIST in WT and demonstrated its role as a competitive endogenous RNA that regulates the miR-194-5p/YAP pathway.Conclusion: Our study demonstrates XIST’s potential as a clinical prognostic biomarker and therapeutic target for WT.Keywords: lncRNA, XIST, Wilms tumor, YAP
Published: 2021

203. Maxing Shigan Decoction Mitigates Mycoplasma pneumonia-Induced Pyroptosis in A549 Cells via the NLRP3 Inflammasome

Author: Liu F, Liu TT, Sun M, Zhou JM, Xue F, Chen SH, Chen J, and Zhang L
Subjects: mycoplasma pneumoniae, pyroptosis, maxing shigan decoction, nlrp3 inflammasome, Infectious and parasitic diseases, RC109-216
Abstract: Fang Liu,1,2,* TianTian Liu,2,* Min Sun,2 JingMin Zhou,2 Feng Xue,2 ShuangHui Chen,2 Jia Chen,3 Lei Zhang1 1Department of Pediatrics, Pudong New Area People’s Hospital, Shanghai, 201200, People’s Republic of China; 2Department of Pediatrics, East Hospital Affiliated to Tongji University, Shanghai, 200123, People’s Republic of China; 3Department of Traditional Chinese Medicine, Shanghai Children’s Medical Center, Shanghai, 200127, People’s Republic of China*These authors contributed equally to this workCorrespondence: Lei Zhang; Jia Chen Email cnhff3098@126.com; 304453596@qq.comBackground: Mycoplasma pneumoniae is a predominant cause of community-acquired respiratory infections. We recently discovered the clinical efficacy of Maxing shigan decoction (MXSG) in M. pneumoniae infection and designed a study to explore the mechanism of action.Methods: Serum IL-1β, IL-18, and TNF-α, and transcript expression of the NLR Family, Pyrin Domain Containing Protein 3 (NLRP3) were measured in the peripheral blood mononuclear cells (PBMCs) of 30 children with M. pneumoniae infection and 30 healthy donors. An in vitro model of M. pneumoniae infection in A549 cell culture was used to explore the curative effects and mechanisms of MXSG. Pyroptosis was measured by flow cytometry with activated caspase-1 and propidium iodide staining. IL-1β, IL-18, and TNF-α, and NLRP3 transcript expression were measured by qRT-PCR. Protein expression of NLRP3, Caspase-1, pro-caspase-1, IL-1β, pro-IL-1β, and GSDMD-N was determined by Western blotting. Experimental confirmation was performed in NLRP3-overexpressing A549 cells and in the presence of an NLRP3 inhibitor, INF39.Results: M. pneumoniae infection-induced IL-1β, IL-18, TNF-α, and mRNA expression of NLRP3 in PBMCs and promoted pyroptosis in A549 cells. It also induced IL-1β, IL-18, TNF-α, and up-regulated NLRP3, ro-IL-1β, Caspase-1, Pro-Caspase-1, and GSDMD-N in culture. Similar to the NLRP3 inhibitor INF39, MXSG (0.1, 0.2, and 0.4 mg/mL) suppressed pyroptosis induced by M. pneumoniae infection and decreased IL-1β (P < 0.001), IL-18, TNF-α in culture. MXSG down-regulated NLRP3, pro-IL-1β, Caspase-1, pro-Caspase-1, and GSDMD-N in infected cultures and mitigated NLRP3 overexpression-induced pyroptosis.Conclusion: MXSG mitigates M. pneumoniae-induced pyroptosis in A549 cells via the NLRP3 inflammasome.Keywords: Mycoplasma pneumoniae, pyroptosis, Maxing shigan decoction, NLRP3 inflammasome
Published: 2021

204. The Prognostic Value of Baseline Distant Metastasis in Icotinib-Treated Patients with EGFR-Mutated Stage IV Non-Small Cell Lung Cancer

Author: Wang L, Shi T, Feng L, Fan Z, Xu X, Zhou X, Zhang X, Han J, Jing L, Liu J, Shan Y, Liu F, Zuo J, and Wang Y
Subjects: metastasis, non-small cell lung cancer, egfr mutations, icotinib, prognostic value, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
Abstract: Long Wang,1,* Tiantian Shi,1,* Li Feng,1 Zhisong Fan,1 Xiaoli Xu,2 Xinliang Zhou,1 Xue Zhang,1 Jing Han,1 Li Jing,1 Jiayin Liu,1 Yujie Shan,1 Fengling Liu,1 Jing Zuo,1 Yudong Wang1 1Department of Medical Oncology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, 050011, People’s Republic of China; 2Department of Medical Records, The Fourth Hospital of Hebei Medical University, Shijiazhuang, 050011, People’s Republic of China*These authors contributed equally to this workCorrespondence: Yudong Wang Email 15931166600@126.comPurpose: Several studies have revealed the prognostic value distant metastasis in non-small-cell lung cancer (NSCLC) patients receiving first-line epidermal growth factor receptor (EGFR) inhibitors. However, the question of whether the specific metastatic site could predict survival outcomes remain elusive. This study evaluated the prognostic value of specific metastatic site at diagnosis in first-line icotinib-treated patients with EGFR-mutated advanced NSCLC.Methods: A total of 216 patients with EGFR-mutated stage IV NSCLC who received first-line icotinib treatment were retrospectively enrolled. The associations between the presence of distant metastasis to certain organs at diagnosis and survival outcomes were analyzed.Patients and methods: The presence of distant metastases was not associated with progression-free survival. Patients with liver metastasis showed a significantly shorter OS than those without liver metastasis (14.6m vs 33.0m, p=0.024). Patients with brain metastasis showed a marginally shorter OS than those without brain metastasis (26.5m vs 33.8m, p=0.051). Patients with lung metastasis showed a significantly longer OS than those without lung metastasis (36.0m vs 28.6m, p=0.038). Multivariable Cox regression analysis showed the presence of liver metastasis (HR [hazard ratio]: 2.265, 95% CI [confidence interval]: 1.239– 4.139, p=0.008) and brain metastasis (HR: 1.493, 95% CI: 1.012– 2.202, p=0.043) were independent predictors for unfavorable OS, while lung metastasis (HR: 0.669, 95% CI: 0.460– 0.971, p=0.034) was an independent predictor for favorable OS.Conclusion: The presence of liver and brain metastasis predicted unfavorable OS, while the presence of lung metastasis predicted favorable OS in first-line icotinib-treated patients with EGFR-mutated stage IV NSCLC.Keywords: metastasis, non-small cell lung cancer, EGFR mutations, icotinib, prognostic value
Published: 2021

205. Effectiveness of a WeChat Combined Continuous Flash Glucose Monitoring System on Glycemic Control in Juvenile Type 1 Diabetes Mellitus Management: Randomized Controlled Trial

Author: Xu Y, Xu L, Zhao W, Li Q, Li M, Lu W, Zeng H, Yan J, Yang D, Wu W, Weng J, Pan J, and Liu F
Subjects: wechat, type 1 diabetes, self-management；glycated hemoglobin a1c, Specialties of internal medicine, RC581-951
Abstract: Yuejie Xu,1,* Lei Xu,1,* Weijing Zhao,1 Qing Li,1 Ming Li,1 Wei Lu,1 Hui Zeng,1 Jinhua Yan,2 Daizhi Yang,2 Wei Wu,3 Jianping Weng,2 Jiemin Pan,1 Fang Liu1 1Department of Endocrinology and Metabolism, Shanghai Jiao Tong University Affiliated Sixth People’s Hospital, Shanghai Clinical Center for Diabetes, Shanghai Key Clinical Center for Metabolic Disease, Shanghai Diabetes Institute, Shanghai Key Laboratory of Diabetes Mellitus, Shanghai, 200233, People’s Republic of China; 2Department of Endocrinology and Metabolic Disease, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, 510630, People’s Republic of China; 3Department of Pediatrics, Tongji Hospital, Wuhan Tongji Medical University, Wuhan, Hubei, 430030, People’s Republic of China*These authors contributed equally to this workCorrespondence: Jiemin Pan; Fang LiuDepartment of Endocrinology and Metabolism, Shanghai Jiao Tong University Affiliated Sixth People’s Hospital, Shanghai Clinical Center for Diabetes, Shanghai Key Clinical Center for Metabolic Disease, Shanghai Diabetes Institute, Shanghai Key Laboratory of Diabetes Mellitus, 600 Yishan Road, Xuhui District, Shanghai, 200233, People’s Republic of ChinaTel +86-18930173803Email lilypjm@hotmail.com; f-liu@sjtu.edu.cnPurpose: Smartphones have received increasing attention and achieved positive outcomes in diabetes intervention. The widespread use of WeChat in China provides an opportunity for self-management practices in patients with diabetes. Nevertheless, how to combine the strengths of the WeChat platform with traditional medical strategy remains to be explored. This study aimed to evaluate the efficacy of a novel flash glucose monitoring device combined with the WeChat platform in juvenile type 1 diabetes management.Patients and Methods: A total of 60 juvenile patients with type 1 diabetes were randomly assigned into three groups: a blood glucose self-monitoring group (group A), a flash glucose monitoring (group B), and a flash glucose monitoring combined WeChat-interactive management group (group C). The intergroup differences in demographics, biochemical indicators, and questionnaire scores of the Diabetes Monitoring and Treatment Satisfaction Questionnaire and Diabetes Specific Quality of Life assessment were compared at the baseline and after 6 months.Results: After the 6-month intervention, groups B and C showed significantly lower glycated hemoglobin A1c (HbA1c) levels compared to those observed at baseline (both P < 0.05), with the largest decrease observed in group C (group B vs group C, P =0.04). Hypoglycemic episodes per month decreased from baseline in groups B and C (both P < 0.05) and were more significant in group C (P < 0.001). In addition, the DMTSQ scores increased in the 6th month in all groups (all P < 0.05), and the largest rise in scores was found in group C, followed by groups B and A. The DQOL scores in groups B and C decreased significantly from the baseline (both P < 0.05), with no change in group A.Conclusion: Flash glucose monitoring combined with the WeChat-interactive system may help achieve sustained glycemic control and higher satisfaction in patients with juvenile type 1 diabetes.Trial Registration: This study was registered at chictr.org.cn, number ChiCTR1900025495. Registered 29 August 2019.Keywords: WeChat, type 1 diabetes, self-management, glycated hemoglobin A1c
Published: 2021

206. Self-Monitoring and Self-Delivery of Self-Assembled Fluorescent Nanoparticles in Cancer Therapy

Author: Liu H, Yuan M, Liu Y, Guo Y, Xiao H, Guo L, and Liu F
Subjects: carrier-free, irinotecan hydrochloride, curcumin, multifunctional nanoparticles, Medicine (General), R5-920
Abstract: Hongmei Liu,1,2 Minghao Yuan,1,2 Yushi Liu,1,2 Yiping Guo,3 Haijun Xiao,4 Li Guo,1,2 Fei Liu1,2 1School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, 611137, People’s Republic of China; 2State Key Laboratory of Characteristic Chinese Medicine Resources in Southwest China, Chengdu, 611137, People’s Republic of China; 3Quantitative and Systems Biology Program, University of California, Merced, CA, 95343, USA; 4Centre of Polymer Systems, Tomas Bata University in Zlin, Zlin, 76001, Czech RepublicCorrespondence: Li GuoChengdu University of Traditional Chinese Medicine, Chengdu, 611137, People’s Republic of ChinaTel +86 28-61800237Email guoli@cdutcm.edu.cnPurpose: Due to the shortcomings of nanocarriers, the development of carrier-free nanodelivery systems has attracted more and more attention in cancer treatment. However, there are few studies on carrier-free nanosystems that can simultaneously achieve monitoring functions. Here a multifunctional carrier-free nanosystem loaded with curcumin and irinotecan hydrochloride was established for the treatment and monitoring of gastric cancer.Methods: In this study, an irinotecan hydrochloride-curcumin nanosystem in the early stage (the system is named SICN) was prepared. Based on the fluorescence of curcumin, flow cytometry, laser confocal microscopy, and zebrafish fluorescence imaging were used to study the monitoring function of SICN in vivo and in vitro. In addition, HGC-27 human gastric cancer cells were used to study SICN cytotoxicity.Results: Flow cytometry and zebrafish fluorescence imaging monitoring results showed that the uptake of SICN was significantly higher than free curcumin, and the excretion rate was lower. SICN had higher accumulation and retention in cells and zebrafish. Laser confocal microscopy monitoring results showed that SICN was internalized into HGC-27 cells through multiple pathways, including macropinocytosis, caveolin, and clathrin-mediated and clathrin -independent endocytosis, and distributed intracellularly throughout the whole cytoplasm, including lysosomes and Golgi apparatus. In vitro cell experiments showed that SICN nanoparticles were more toxic than single components, and HGC-27 cells had more absorption and higher toxicity to nanoparticles under slightly acidic conditions.Conclusion: SICN is a promising carrier-free nanoparticle, and the combination of two single-component therapies can exert a synergistic antitumor effect. When exposed to a tumor acidic environment, SICN showed stronger cytotoxicity due to charge conversion. More importantly, the nanoparticles’ self-monitoring function has been developed, opening up new ideas for combined tumor therapy.Keywords: carrier-free, irinotecan hydrochloride, curcumin, multifunctional nanoparticles
Published: 2021

207. Heterogeneity of Helicobacter pylori Strains Isolated from Patients with Gastric Disorders in Guiyang, China

Author: Mi M, Wu F, Zhu J, Liu F, Cui G, Wen X, Hu Y, Deng Z, Wu X, Zhang Z, Qi T, and Chen Z
Subjects: helicobacter pylori, heterogeneity, antibiotic resistance, caga typing, Infectious and parasitic diseases, RC109-216
Abstract: Mengheng Mi,1,2,* Fangcao Wu1 12 2,* Jian Zhu3 3, Fang Liu1 12 2, Guzhen Cui1 14 4, Xueqing Wen1 12 2, Yue Hu5 5, Zhaohui Deng3 3, Xiaojuan Wu1 12 2, Zhengrong Zhang1 14 4, Tingna Qi1 14 4, Zhenghong Chen1 12 2 1Key Laboratory of Microbiology and Parasitology of Education Department of Guizhou, School of Basic Medical Science, Guizhou Medical University/Joint Laboratory of Helicobacter Pylori and Intestinal Microecology of Affiliated Hospital of Guizhou Medical University, Guiyang, People’s Republic of China; 2Key Laboratory of Environmental Pollution Monitoring and Disease Control, Ministry of Education, Guizhou Medical University, Guiyang, People’s Republic of China; 3Department of Gastroenterology, Guiyang Hospital of Guizhou Aviation Industry Group, Guiyang, People’s Republic of China; 4Key Laboratory of Endemic and Ethnic Diseases (Guizhou Medical University), Ministry of Education, Guiyang, People’s Republic of China; 5Department of Gastroenterology, Affiliated Hospital of Guizhou Medical University, Guiyang, People’s Republic of China*These authors contributed equally to this workCorrespondence: Zhenghong ChenDepartment of Microbiology, School of Basic Medical Science, Guizhou Medical University, Guiyang, People’s Republic of ChinaTel + 86-13985006815Fax + 86-85188174015Email chenzhenghong@gmc.edu.cnPurpose: Chronic Helicobacter pylori infection causes peptic ulcers in a subpopulation of individuals and is a risk factor for the development of gastric cancer. Multiple infections and heteroresistant H. pylori contribute to poor treatment efficacy. Here, we investigated the extent of genetic diversity among H. pylori strains within a given host and its influence on the results of antibiotic (metronidazole, levofloxacin, clarithromycin, amoxicillin, and tetracycline) susceptibility testing.Materials and Methods: Gastric mucosa biopsy samples were obtained from patients with gastric disorders, including 48 H. pylori positive patients, who were never previously treated for H. pylori infection. Five potential H. pylori colonies isolated from each sample were subcultured for enrichment. Enriched H. pylori colonies were identified through Gram staining and assays for urease, oxidase, and catalase. For each H. pylori monoclonal colony, the antibiotic susceptibility was assessed, genomic DNA was sequenced, and the cytotoxin-associated gene A (cagA) genotype was verified. Co-infection with multiple H. pylori strains was determined using random amplified polymorphic DNA (RAPD)-polymerase chain reaction (PCR).Results: Thirteen gastric mucosa biopsy samples were positive for H. pylori. Five monoclonal strains isolated from each of these 13 patients were identified as H. pylori. RAPD-PCR indicated that intra-patient monoclonal strains of H. pylori in 10 of the 13 samples exhibited heterogeneity. Among the 13 patients, intra-patient monoclonal strains isolated from 4 patients had identical cagA genotype, whereas intra-patient monoclonal strains isolated from the other 9 patients harbored more than one cagA genotype. The antibiotic susceptibility of five intra-patient monoclonal strains from seven patients was inconsistent.Conclusion: The existence of heterogeneous H. pylori strains with resistance to different drugs and virulence were common within the gastric mucosa of an individual patient.Keywords: Helicobacter pylori, heterogeneity, antibiotic resistance, cagA typing
Published: 2021

208. Bitter Taste Receptor as a Therapeutic Target in Orthopaedic Disorders

Author: Cheng W, Yao M, and Liu F
Subjects: tas2r, calcium signaling, osteoblasts, drug target, bone inflammation, Therapeutics. Pharmacology, RM1-950
Abstract: Weyland Cheng,1,2 Manye Yao,1 Fangna Liu1 1Department of Orthopaedic Surgery, Children’s Hospital Affiliated to Zhengzhou University, Henan Children’s Hospital, Zhengzhou Children’s Hospital, Zhengzhou, Henan, People’s Republic of China; 2Henan Provincial Key Laboratory of Children’s Genetics and Metabolic Diseases, Children’s Hospital Affiliated to Zhengzhou University, Henan Children’s Hospital, Zhengzhou Children’s Hospital, Zhengzhou, Henan, People’s Republic of ChinaCorrespondence: Weyland Cheng Tel +86 18502758200Email wey_c@hotmail.comAbstract: Non-gustatory, extraoral bitter taste receptors (T2Rs) are G-protein coupled receptors that are expressed throughout the body and have various functional responses when stimulated by bitter agonists. Presently, T2Rs have been found to be expressed in osteoclasts and osteocytes where osteoclasts were capable of detecting bacterial quorum-sensing molecules through the T2R38 isoform. In the innate immune system, stimulating T2Rs induces anti-inflammatory and anti-pathogenic effects through the phospholipase C/inositol triphosphate pathway, which leads to intracellular calcium release from the endoplasmic reticulum. The immune cells with functional responses to T2R activation also play a role in bone inflammation and orthopaedic disorders. Furthermore, increasing intracellular calcium levels in bone cells through T2R activation can potentially influence bone formation and resorption. With recent studies finding T2R expression in bone cells, we examine the potential of targeting this receptor to treat bone inflammation and to promote bone anabolism.Keywords: TAS2R, calcium signaling, osteoblasts, drug target, bone inflammation
Published: 2021

209. CC Chemokine Receptors in Lung Adenocarcinoma: The Inflammation-Related Prognostic Biomarkers and Immunotherapeutic Targets

Author: Liu F and Wu H
Subjects: cc chemokine receptors, lung adenocarcinoma, prognostic biomarker, immunotherapeutic target, bioinformatics analysis, Pathology, RB1-214, Therapeutics. Pharmacology, RM1-950
Abstract: Fangteng Liu,1,2 Hengyu Wu1 1Department of Breast Surgery, The Third Hospital of Nanchang, Nanchang, Jiangxi, 330009, People’s Republic of China; 2Faculty of Medicine, University of Munich, Munich, 80336, GermanyCorrespondence: Hengyu Wu Tel +86-15270280590Email why_wuhengyu0590@163.comBackground: Lung adenocarcinoma (LUAD) is the most common type of lung cancer with a high incidence and increased mortality. CC chemokine receptors were participating in the modulation of the tumor microenvironment and involved in carcinogenesis and tumor development. However, the potential mechanistic values of CC chemokine receptors as clinical biomarkers and therapeutic targets in LUAD have not been fully clarified.Methodology: ONCOMINE, UALCAN, GEPIA, Kaplan–Meier Plotter, SurvExpress, MethSurv, SurvivalMeth, cBioPortal, String, GeneMANIA, DAVID, Metascape, TRRUST, LinkedOmics, and Timer were applied in this work.Results: The transcriptional levels of CCR1/10 in LUAD tissues were significantly reduced while the transcriptional levels of CCR3/6/7/8 were significantly elevated, and the expression of CCR1 was the highest in LUAD among these CC chemokine receptors. A significant correlation was found between the expression of CCR2/4/6/7 and the pathological stage of LUAD patients. There were significant associations between CCR2/3/4/5/6/10 expression levels and OS in LUAD, and LUAD patients with high transcriptional levels of CCR3/4 had inferior first-progression survival. In addition, the prognostic values of CC chemokine receptors signature in LUAD were explored in three independent cohorts, the high-risk group displayed unfavorable OS compared with the low-risk group, and the LUAD cases in the high-risk group also suffered inferior RFS than that in the low-risk group. And for the prognostic value of the DNA methylation of CC chemokine receptors, we found 1 CpG of CCR2, 2 CpGs of CCR3, 1 CpG of CCR4, 3 CpGs of CCR6, 3 CpGs of CCR7, 1 CpG of CCR8, and 3 CpGs of CCR9 were significantly associated with prognosis in LUAD patients. However, the DNA methylation signature analysis showed there was no statistically significant association between the high- and low-risk group. For potential mechanism, the neighbor gene networks, interaction analyses, functional enrichment analyses of CC chemokine receptors in LUAD were performed, the transcription factor targets, kinase targets, and miRNA targets of CC chemokine receptors were also identified in LUAD. We also found significant correlations among CC chemokine receptors expression and the infiltration of immune cells, the tumor infiltration levels among LUAD with different somatic copy number alterations of these chemokine receptors were also assessed. Moreover, the Cox proportional hazard model showed that CCR1/2/10, B_cell, CD4_Tcell were significantly related to the clinical outcome of LUAD patients.Conclusion: CC chemokine receptors might serve as immunotherapeutic targets and prognostic biomarkers in LUAD.Keywords: CC chemokine receptors, lung adenocarcinoma, prognostic biomarker, immunotherapeutic target, bioinformatics analysis
Published: 2021

210. Comprehensive Analysis of LncRNA-mRNA Expression Profiles and the ceRNA Network Associated with Pyroptosis in LPS-Induced Acute Lung Injury

Author: Luo D, Liu F, Zhang J, Shao Q, Tao W, Xiao R, Dai W, Ding C, and Qian K
Subjects: acute lung injury, alveolar macrophage, cerna network long noncoding rnas, pyroptosis, rna sequencing., Pathology, RB1-214, Therapeutics. Pharmacology, RM1-950
Abstract: Deqiang Luo,1,2 Fen Liu,1 Jianguo Zhang,1 Qiang Shao,1 Wenqiang Tao,1 Rui Xiao,1 Wei Dai,2 Chengzhi Ding,1 Kejian Qian1 1Department of Intensive Care Unit, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, 330000, People’s Republic of China; 2Department of Intensive Care Unit, The Fifth People’s Hospital of Shangrao City, Shangrao, 334000, People’s Republic of ChinaCorrespondence: Kejian QianDepartment of Intensive Care Unit, The First Affiliated Hospital of Nanchang University, No. 17 Yongwaizheng Street, Dong Lake District, Nanchang, Jiangxi Province, 330000, People’s Republic of ChinaEmail ndyfyicu@email.ncu.edu.cnPurpose: To explore the molecular mechanism and search for candidate lncRNA and mRNA associated with pyroptosis in the gene expression profile of LPS-induced acute lung injury (ALI).Methods: We investigated lncRNA and mRNA expression in lipopolysaccharide (LPS)-induced ALI at an early stage. RNA sequencing (RNA-Seq) was carried out to analyze lncRNA and mRNA expression profiles between the LPS-induced and control groups. We used bioinformatics analysis to predict target genes of early differential lncRNAs among obtained the differential mRNAs.Results: A total of 78 lncRNAs and 248 mRNAs were upregulated at 2 hours and downregulated at 9 hours, and 21 lncRNAs and 107 mRNAs were downregulated at 2 and upregulated at 9 hours in early ALI models. We predicted 7 cis-and trans-regulated target genes of the top 20 lncRNAs. Gene Ontology (GO) analysis indicated that the target genes for the screened lncRNAs were most enriched in three-terms: regulation of protein serine/threonine kinase activity, pertussis, and cellular response to LPS. Additionally, target genes of lncRNAs were the top three enriched in pertussis, osteoclast differentiation, and cAMP signaling pathways with Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis. We also identified vital mRNAs and lncRNAs. Protein-protein interaction (PPI) network analysis suggested that Tnf, Jun, and Atf3 were the top three key genes. Hub lncRNA4344 (NONRATT004344.2) and cis-regulated target mRNA (NLRP3) were validated in vitro. Finally, luciferase assay results confirmed that lncRNA4344 sponged miR‐138-5p to promote pyroptosis in inflammatory responses to LPS‐induced acute lung injury by targeting NLRP3.Conclusion: Based on analysis of lncRNA and mRNA expression profiles by RNA-Seq and experimental verification, this study is the first to reveal that lncRNA4344 sponged miR‐138-5p to promote pyroptosis in inflammatory responses of LPS‐induced acute lung injury by targeting NLRP3. These newly identified lncRNA, miRNA, and mRNA might be novel potential targets for early treatment and prevention in early ALI.Keywords: acute lung injury, alveolar macrophage, ceRNA network long noncoding RNAs, pyroptosis, RNA sequencing
Published: 2021

211. Diagnostic Performance of a Blood Urea Nitrogen to Creatinine Ratio-based Nomogram for Predicting In-hospital Mortality in COVID-19 Patients

Author: Liu Q, Wang Y, Zhao X, Wang L, Liu F, Wang T, Ye D, and Lv Y
Subjects: blood urea nitrogen, creatinine, coronavirus, covid-19, Public aspects of medicine, RA1-1270
Abstract: Qingquan Liu,1,* Yiru Wang,1,* Xuecheng Zhao,2 Lixuan Wang,2 Feng Liu,3 Tao Wang,4 Dawei Ye,5 Yongman Lv1,2 1Department of Nephrology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, People’s Republic of China; 2Department of Health Management Centre, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, People’s Republic of China; 3Department of Urology, Shaoyang Central Hospital, Shaoyang 422000, People’s Republic of China; 4Department of Respiratory and Critical Care Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, People’s Republic of China; 5Department of Internal Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, People’s Republic of China*These authors contributed equally to this workCorrespondence: Yongman Lv; Dawei YeTongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, No. 1095 Jiefang Avenue, Wuhan 430030, People’s Republic of ChinaTel +86-2783662848; +86-2783663409Fax + 86-2783662848Email lvyongman@126.com; dy0711@gmail.comBackground: The novel coronavirus disease (COVID-19) is leading to high morbidity and mortality. This aim of this study was to test whether blood urea nitrogen-to-creatinine ratio (BCR) is a predictor for mortality in patients with COVID-19.Methods: Ranges of “normal” BCR values were calculated from 9165 healthy subjects, and 337 and 79 COVID-19 patients were randomly assigned to the training cohort and the validation cohort, respectively. Prognostic factor of death incidence was selected by LASSO regression analyses. The prognostic ability of BCR range was assessed by logistic regression analysis. A nomogram for predicting in-hospital mortality based on BCR was developed. The performance of the nomogram was evaluated with respect to its calibration, discrimination, and clinical usefulness.Results: Among 337 COVID-19 patients, 13.4% and 11.3% were classified into higher and lower than normal range group, respectively. Kaplan–Meier curves for all-cause mortality showed that patients with higher BCR group had worse prognosis (P< 0.0001). BCR above the normal range was independently associated with death in COVID-19 patients (OR: 7.54; 95%CI: 1.55– 36.66; P=0.012). The nomogram had good discrimination in the training cohort (C-index 0.838; 0.795– 0.880) and the validation cohort (C-index 0.929; 0.869– 0.989), and good calibration. Using maximum Youden index, the cutoff values of 59.8 points, the sensitivity and specificity were 75.4% and 81%. Decision curve and clinical impact curve analysis demonstrated that the nomogram was clinically useful.Conclusion: BCR was a useful prognostic factor for COVID-19 patients. Development of an individualized BCR-based prediction nomogram can effectively predict the risk of mortality and help clinicians to make individual treatment early.Keywords: blood urea nitrogen, creatinine, coronavirus, COVID-19
Published: 2021

212. Fixed Cutaneous Sporotrichosis Due to Sporothrix globosa

Author: Liu F, Liu Y, Yuan N, Zhang X, Cao M, Dong J, and Zhang J
Subjects: fixed cutaneous sporotrichosis, sporothrix globosa, Dermatology, RL1-803
Abstract: Fang Liu,1 Yingmei Liu,2 Na Yuan,1 Xiuying Zhang,1 Mei Cao,1 Jie Dong,1 Jinqing Zhang1 1Department of Dermatology, Beijing Chaoyang Hospital, Capital Medical University, Beijing 100020, People’s Republic of China; 2Laboratory of Clinical Microbiology and Infectious Diseases, Department of Pulmonary and Critical Care Medicine, China-Japan Friendship Hospital, Beijing 100029, People’s Republic of ChinaCorrespondence: Fang LiuDepartment of Dermatology, Beijing Chaoyang Hospital, Capital Medical University, 8 Gongti South Road, Beijing 100020, People’s Republic of ChinaTel +86-18611369216Email roseliufang@qq.comPurpose: This report describes a case of a skin sporotrichosis infection and the steps taken to identify an effective antifungal treatment.Patients and Methods: A 50-year-old woman from Jilin province, China, presented complaining of a small mass that had been on her right upper eyelid for two years. A skin biopsy was taken and submitted for bacterial and mycological assessment. Bacterial culture from the lesion was negative, but a fungal culture was positive. In vitro susceptibility test was performed to assess its susceptibility to antifungal drugs.Results: The skin biopsy showed infectious granuloma. Fungal culture was identified as Sporothrix globosa based on both the morphological features and confirmation by the molecular method; it was resistant to many kinds of antifungal drugs, including amphotericin B, voriconazole, fluconazole, and caspofungin. However, it was relatively sensitive to itraconazole. The patient was prescribed 0.2 g itraconazole to be taken twice per day. One month later, she had almost completely recovered from her symptoms. The treatment lasted for 3 months and her liver function and renal function were normal at the endpoint.Conclusion: Itraconazole was an effective treatment in this case of a multidrug-resistant sporotrichosis caused by S. globosa.Keywords: fixed cutaneous sporotrichosis, Sporothrix globosa
Published: 2021

213. Identification of Prognostic Biomarkers and Molecular Targets Among JAK Family in Breast Cancer

Author: Liu F and Wu H
Subjects: janus kinase, breast cancer, prognosis, immunity, biomarker, target, Pathology, RB1-214, Therapeutics. Pharmacology, RM1-950
Abstract: Fangteng Liu,1,2 Hengyu Wu1 1Department of Breast Surgery, The Third Hospital of Nanchang, Nanchang 330009, Jiangxi, People’s Republic of China; 2Faculty of Medicine, University of Munich, Munich 80336, GermanyCorrespondence: Hengyu Wu Tel +86-15270280590Email why_wuhengyu0590@163.comBackground: Janus kinases (JAKs) are a family of non-receptor tyrosine kinases involved in multiple malignancies. However, clinical values of JAKs as prognostic markers and potential mechanism as molecular targets in breast invasive carcinoma (BC) are not completely clarified.Methodology: TIMER, UALCAN and GEPIA were used to assess the expression and methylation levels of JAKs in BC. Kaplan–Meier Plotter, bc-GenExMiner, SurvExpress, TRGAted, MethSurv, and SurvivalMeth were used to assess the multilevel prognostic significance of JAKs in breast cancer patients. And cBioPortal, TIMER, STRING, GeneMANIA, NetworkAnalysis, LinkedOmics, DAVID 6.8, and Metascape were applied for multilayer networks and functional enrichment analyses. Correlations between immune cell infiltrates/their gene markers and JAKs were evaluated by TIMER.Results: We first explored the expression and methylation level of JAKs in breast cancer and found significantly reduced JAK1 and JAK2 expression at mRNA and protein levels, significantly higher JAK3 protein expression, and significantly increased TYK2 expression at mRNA level but decreased at protein level. In addition, hypermethylation of JAK3 and TYK2 and hypomethylation of JAK1 were found in tumor samples. In terms of prognostic values of JAKs in BC patients, low transcriptional levels of JAK1, JAK2, JAK3, and TYK2 indicated worse OS/DMFS/PPS/RFS/DFS, inferior DFS, worse RFS, and shorter OS/DMFS/RFS, respectively. The mRNA signature analysis showed that high-risk group had unfavorable OS/RFS/MFS. Low JAK2 protein level indicated unfavorable DSS/PFS in BC patients. Five CpGs of JAK1, four CpGs of JAK2, 20 CpGs of JAK3, and 13 CpGs of TYK2 were significantly associated with prognosis in BC patients. The DNA methylation signature analysis also suggested worse prognosis in the high-risk group. For potential biological roles of JAKs, interaction analyses, functional enrichment analyses for biological process, cellular component, molecular function, and KEGG pathway analyses of JAKs and their neighbor genes in BC were conducted. Kinase targets, gene–miRNA interactions, and transcription factor–gene interactions of JAKs were also identified. Furthermore, JAKs were found to be significantly related to immune infiltrates as well as the expression levels of multiple immune markers in BC.Conclusion: JAKs showed multilevel prognostic value and important biological roles in BC. They might serve as promising prognostic markers and possible targets in breast cancer.Keywords: Janus kinase, breast cancer, prognosis, immunity, biomarker, target
Published: 2021

214. Downregulation of lncRNA EPB41L4A-AS1 Mediates Activation of MYD88-Dependent NF-κB Pathway in Diabetes-Related Inflammation

Author: Wang Z, Liao W, Liu F, Yang T, Xie W, Liao M, Gu D, and Zhang Y
Subjects: inflammation, diabetes, epb41l4a-as1, nf-κb, myd88, Specialties of internal medicine, RC581-951
Abstract: Ziqing Wang,1,2 Weijie Liao,2,3 Fuhai Liu,2,4 Tingpeng Yang,2 Weidong Xie,2,3 Meijian Liao,3,4 Dayong Gu,5 Yaou Zhang2,3 1School of Chemistry, Tsinghua University, Beijing 100084, People’s Republic of China; 2State Key Laboratory of Chemical Oncogenomics, Tsinghua Shenzhen International Graduate School, Shenzhen 518055, People’s Republic of China; 3Key Laboratory in Healthy Science and Technology, Division of Life Science, Tsinghua Shenzhen International Graduate School, Shenzhen 518055, People’s Republic of China; 4Department of Pathology, Xuzhou Medical University, Xuzhou 221104, People’s Republic of China; 5Department of Laboratory Medicine, Shenzhen Second People’s Hospital, The First Affiliated Hospital of Shenzhen University, Shenzhen 518035, People’s Republic of ChinaCorrespondence: Yaou ZhangState Key Laboratory of Chemical Oncogenomics, Tsinghua Shenzhen International Graduate School, Shenzhen 518055, People’s Republic of ChinaTel +86-755-2603-6884Email zhangyo@sz.tsinghua.edu.cnDayong GuDepartment of Laboratory Medicine, Shenzhen Second People’s Hospital, The First Affiliated Hospital of Shenzhen University, Shenzhen 518035, People’s Republic of ChinaTel +86-13602601597Email wanhood@163.comPurpose: Long non-coding RNAs (lncRNAs) have been shown to be involved in many human diseases. In this study, we aimed to reveal the role and molecular mechanism of lncRNA EPB41L4A-AS1 in type 2 diabetic mellitus (T2DM)-related inflammation.Methods: To explore the relationships between the expression of EPB41L4A-AS1 and inflammatory factors in the blood of T2DM patients, we analyzed peripheral blood mononuclear cell (PBMC) expression microarrays of T2DM patients and expression microarrays of PBMC treated with lipopolysaccharide (LPS) from the GEO database. The relationship between EPB41L4A-AS1 and phospho-p65 was explored by Western blotting (WB) and immunofluorescence. The interactions between EPB41L4A-AS1 and myeloid differentiation factor 88 (MYD88) were also verified through quantitative real-time PCR, WB, and chromatin immunoprecipitation. Glycolysis and mitochondrial stress were detected by Seahorse.Results: EPB41L4A-AS1 showed very low expression, which was significantly negatively correlated with levels of inflammatory factors in PBMCs of T2DM patients and PBMCs treated with LPS. These results were verified by cell experiments on PBMC and THP-1 cells. Knockdown of EPB41L4A-AS1 led to the phosphorylation and nuclear translocation of p65 and thus activated the NF-κB signaling pathway; it also reduced the enrichment of H3K9me3 in the MYD88 promoter and increased expression of MYD88. Overall, EPB41L4A-AS1 knockdown promoted the level of glycolysis and ultimately enhanced the inflammatory response.Conclusion: EPB41L4A-AS1 knockdown activated the NF-κB signaling pathway through a MYD88-dependent regulatory mechanism, promoted glycolysis, and ultimately enhanced the inflammatory response. These results demonstrate that EPB41L4A-AS1 is closely associated with inflammation in T2DM, and that low expression of EPB41L4A-AS1 may be used as an indicator of chronic inflammation and possible diabetic vascular complications in T2DM patients.Keywords: inflammation, diabetes, EPB41L4A-AS1, NF-κB, MYD88
Published: 2021

215. Study of the rare decay $J/\psi \to \mu^+\mu^-\mu^+\mu^-$

Author: LHCb collaboration, Aaij, R., Abdelmotteleb, A. S. W., Beteta, C. Abellan, Abudinén, F., Ackernley, T., Adefisoye, A. A., Adeva, B., Adinolfi, M., Adlarson, P., Agapopoulou, C., Aidala, C. A., Ajaltouni, Z., Akar, S., Akiba, K., Albicocco, P., Albrecht, J., Alessio, F., Alexander, M., Aliouche, Z., Cartelle, P. Alvarez, Amalric, R., Amato, S., Amey, J. L., Amhis, Y., An, L., Anderlini, L., Andersson, M., Andreianov, A., Andreola, P., Andreotti, M., Andreou, D., Anelli, A., Ao, D., Archilli, F., Argenton, M., Cuendis, S. Arguedas, Artamonov, A., Artuso, M., Aslanides, E., Da Silva, R. Ataíde, Atzeni, M., Audurier, B., Bacher, D., Perea, I. Bachiller, Bachmann, S., Bachmayer, M., Back, J. J., Rodriguez, P. Baladron, Balagura, V., Baldini, W., Balzani, L., Bao, H., Leite, J. Baptista de Souza, Pretel, C. Barbero, Barbetti, M., Barbosa, I. R., Barlow, R. J., Barnyakov, M., Barsuk, S., Barter, W., Bartolini, M., Bartz, J., Basels, J. M., Bashir, S., Bassi, G., Batsukh, B., Battista, P. B., Bay, A., Beck, A., Becker, M., Bedeschi, F., Bediaga, I. B., Behling, N. B., Belin, S., Bellee, V., Belous, K., Belov, I., Belyaev, I., Benane, G., Bencivenni, G., Ben-Haim, E., Berezhnoy, A., Bernet, R., Andres, S. Bernet, Bertolin, A., Betancourt, C., Betti, F., Bex, J., Bezshyiko, Ia., Bhom, J., Bieker, M. S., Biesuz, N. V., Billoir, P., Biolchini, A., Birch, M., Bishop, F. C. R., Bitadze, A., Bizzeti, A., Blake, T., Blanc, F., Blank, J. E., Blusk, S., Bocharnikov, V., Boelhauve, J. A., Garcia, O. Boente, Boettcher, T., Bohare, A., Boldyrev, A., Bolognani, C. S., Bolzonella, R., Bondar, N., Borgato, F., Borghi, S., Borsato, M., Borsuk, J. T., Bouchiba, S. A., Bovill, M., Bowcock, T. J. V., Boyer, A., Bozzi, C., Rodriguez, A. Brea, Breer, N., Brodzicka, J., Gonzalo, A. Brossa, Brown, J., Brundu, D., Buchanan, E., Buonaura, A., Buonincontri, L., Burke, A. T., Burr, C., Butkevich, A., Butter, J. S., Buytaert, J., Byczynski, W., Cadeddu, S., Cai, H., Caillet, A. C., Calabrese, R., Ramirez, S. Calderon, Calefice, L., Cali, S., Calvi, M., Gomez, M. Calvo, Magalhaes, P. Camargo, Bouzas, J. I. Cambon, Campana, P., Perez, D. H. Campora, Quezada, A. F. Campoverde, Capelli, S., Capriotti, L., Caravaca-Mora, R., Carbone, A., Salgado, L. Carcedo, Cardinale, R., Cardini, A., Carniti, P., Carus, L., Vidal, A. Casais, Caspary, R., Casse, G., Godinez, J. Castro, Cattaneo, M., Cavallero, G., Cavallini, V., Celani, S., Cervenkov, D., Cesare, S., Chadwick, A. J., Chahrour, I., Chang, X., Charles, M., Charpentier, Ph., Chatzianagnostou, E., Barajas, C. A. Chavez, Chefdeville, M., Chen, C., Chen, S., Chen, Z., Chernov, A., Chernyshenko, S., Chiotopoulos, X., Chobanova, V., Cholak, S., Chrzaszcz, M., Chubykin, A., Chulikov, V., Ciambrone, P., Vidal, X. Cid, Ciezarek, G., Cifra, P., Clarke, P. E. L., Clemencic, M., Cliff, H. V., Closier, J., Toapaxi, C. Cocha, Coco, V., Cogan, J., Cogneras, E., Cojocariu, L., Collins, P., Colombo, T., Colonna, M. C., Comerma-Montells, A., Congedo, L., Contu, A., Cooke, N., Corredoira, I., Correia, A., Corti, G., Meldrum, J. J. Cottee, Couturier, B., Craik, D. C., Torres, M. Cruz, Rivera, E. Curras, Currie, R., Da Silva, C. L., Dadabaev, S., Dai, L., Dai, X., Dall'Occo, E., Dalseno, J., D'Ambrosio, C., Daniel, J., Danilina, A., d'Argent, P., Davidson, A., Davies, J. E., Davis, A., Francisco, O. De Aguiar, De Angelis, C., De Benedetti, F., de Boer, J., De Bruyn, K., De Capua, S., De Cian, M., Da Graca, U. De Freitas Carneiro, De Lucia, E., De Miranda, J. M., De Paula, L., De Serio, M., De Simone, P., De Vellis, F., de Vries, J. A., Debernardis, F., Decamp, D., Dedu, V., Del Buono, L., Delaney, B., Dembinski, H. -P., Deng, J., Denysenko, V., Deschamps, O., Dettori, F., Dey, B., Di Nezza, P., Diachkov, I., Didenko, S., Ding, S., Dittmann, L., Dobishuk, V., Docheva, A. D., Dong, C., Donohoe, A. M., Dordei, F., Reis, A. C. dos, Dowling, A. D., Duan, W., Duda, P., Dudek, M. W., Dufour, L., Duk, V., Durante, P., Duras, M. M., Durham, J. M., Durmus, O. D., Dziurda, A., Dzyuba, A., Easo, S., Eckstein, E., Egede, U., Egorychev, A., Egorychev, V., Eisenhardt, S., Ejopu, E., Eklund, L., Elashri, M., Ellbracht, J., Ely, S., Ene, A., Epple, E., Eschle, J., Esen, S., Evans, T., Fabiano, F., Falcao, L. N., Fan, Y., Fang, B., Fantini, L., Faria, M., Farmer, K., Fazzini, D., Felkowski, L., Feng, M., Feo, M., Casani, A. Fernandez, Gomez, M. Fernandez, Fernez, A. D., Ferrari, F., Rodrigues, F. Ferreira, Ferrillo, M., Ferro-Luzzi, M., Filippov, S., Fini, R. A., Fiorini, M., Fischer, K. L., Fitzgerald, D. S., Fitzpatrick, C., Fleuret, F., Fontana, M., Foreman, L. F., Forty, R., Foulds-Holt, D., Sevilla, M. Franco, Frank, M., Franzoso, E., Frau, G., Frei, C., Friday, D. A., Fu, J., Fuehring, Q., Fujii, Y., Fulghesu, T., Gabriel, E., Galati, G., Galati, M. D., Torreira, A. Gallas, Galli, D., Gambetta, S., Gandelman, M., Gandini, P., Ganie, B., Gao, H., Gao, R., Gao, Y., Garau, M., Martin, L. M. Garcia, Moreno, P. Garcia, Pardiñas, J. García, Garg, K. G., Garrido, L., Gaspar, C., Geertsema, R. E., Gerken, L. L., Gersabeck, E., Gersabeck, M., Gershon, T., Ghorbanimoghaddam, Z., Giambastiani, L., Giasemis, F. I., Gibson, V., Giemza, H. K., Gilman, A. L., Giovannetti, M., Gioventù, A., Girardey, L., Gironell, P. Gironella, Giugliano, C., Giza, M. A., Gkougkousis, E. L., Glaser, F. C., Gligorov, V. V., Göbel, C., Golobardes, E., Golubkov, D., Golutvin, A., Gomes, A., Fernandez, S. Gomez, Abrantes, F. Goncalves, Goncerz, M., Gong, G., Gooding, J. A., Gorelov, I. V., Gotti, C., Grabowski, J. P., Cardoso, L. A. Granado, Graugés, E., Graverini, E., Grazette, L., Graziani, G., Grecu, A. T., Greeven, L. M., Grieser, N. A., Grillo, L., Gromov, S., Gu, C., Guarise, M., Guittiere, M., Guliaeva, V., Günther, P. A., Guseinov, A. -K., Gushchin, E., Guz, Y., Gys, T., Habermann, K., Hadavizadeh, T., Hadjivasiliou, C., Haefeli, G., Haen, C., Haimberger, J., Hajheidari, M., Hallett, G. H., Halvorsen, M. M., Hamilton, P. M., Hammerich, J., Han, Q., Han, X., Hansmann-Menzemer, S., Hao, L., Harnew, N., Hartmann, M., Hashmi, S., He, J., Hemmer, F., Henderson, C., Henderson, R. D. L., Hennequin, A. M., Hennessy, K., Henry, L., Herd, J., Gascon, P. Herrero, Heuel, J., Hicheur, A., Mendizabal, G. Hijano, Hill, D., Hollitt, S. E., Horswill, J., Hou, R., Hou, Y., Howarth, N., Hu, J., Hu, W., Hu, X., Huang, W., Hulsbergen, W., Hunter, R. J., Hushchyn, M., Hutchcroft, D., Ilin, D., Ilten, P., Inglessi, A., Iniukhin, A., Ishteev, A., Ivshin, K., Jacobsson, R., Jage, H., Elles, S. J. Jaimes, Jakobsen, S., Jans, E., Jashal, B. K., Jawahery, A., Jevtic, V., Jiang, E., Jiang, X., Jiang, Y., Jiang, Y. J., John, M., Rajan, A. John Rubesh, Johnson, D., Jones, C. R., Jones, T. P., Joshi, S., Jost, B., Castella, J. Juan, Jurik, N., Juszczak, I., Kaminaris, D., Kandybei, S., Kane, M., Kang, Y., Kar, C., Karacson, M., Karpenkov, D., Kauniskangas, A., Kautz, J. W., Keizer, F., Kenzie, M., Ketel, T., Khanji, B., Kharisova, A., Kholodenko, S., Khreich, G., Kirn, T., Kirsebom, V. S., Kitouni, O., Klaver, S., Kleijne, N., Klimaszewski, K., Kmiec, M. R., Koliiev, S., Kolk, L., Konoplyannikov, A., Kopciewicz, P., Koppenburg, P., Korolev, M., Kostiuk, I., Kot, O., Kotriakhova, S., Kozachuk, A., Kravchenko, P., Kravchuk, L., Kreps, M., Krokovny, P., Krupa, W., Krzemien, W., Kshyvanskyi, O. K., Kubat, J., Kubis, S., Kucharczyk, M., Kudryavtsev, V., Kulikova, E., Kupsc, A., Kutsenko, B. K., Lacarrere, D., Gonzalez, P. Laguarta, Lai, A., Lampis, A., Lancierini, D., Gomez, C. Landesa, Lane, J. J., Lane, R., Langenbruch, C., Langer, J., Lantwin, O., Latham, T., Lazzari, F., Lazzeroni, C., Gac, R. Le, Lee, H., Lefèvre, R., Leflat, A., Legotin, S., Lehuraux, M., Cid, E. Lemos, Leroy, O., Lesiak, T., Leverington, B., Li, A., Li, C., Li, H., Li, K., Li, L., Li, P., Li, P. -R., Li, Q., Li, S., Li, T., Li, Y., Lian, Z., Liang, X., Libralon, S., Lin, C., Lin, T., Lindner, R., Lisovskyi, V., Litvinov, R., Liu, F. L., Liu, G., Liu, K., Liu, S., Liu, W., Liu, Y., Liu, Y. L., Salvia, A. Lobo, Loi, A., Castro, J. Lomba, Long, T., Lopes, J. H., Huertas, A. Lopez, Soliño, S. López, Lucarelli, C., Lucchesi, D., Martinez, M. Lucio, Lukashenko, V., Luo, Y., Lupato, A., Luppi, E., Lynch, K., Lyu, X. -R., Ma, G. M., Ma, R., Maccolini, S., Machefert, F., Maciuc, F., Mack, B., Mackay, I., Mackey, L. M., Mohan, L. R. Madhan, Madurai, M. J., Maevskiy, A., Magdalinski, D., Maisuzenko, D., Majewski, M. W., Malczewski, J. J., Malde, S., Malentacca, L., Malinin, A., Maltsev, T., Manca, G., Mancinelli, G., Mancuso, C., Escalero, R. Manera, Manuzzi, D., Marangotto, D., Marchand, J. F., Marchevski, R., Marconi, U., Mariani, S., Benito, C. Marin, Marks, J., Marshall, A. M., Martel, L., Martelli, G., Martellotti, G., Martinazzoli, L., Martinelli, M., Santos, D. Martinez, Vidal, F. Martinez, Massafferri, A., Matev, R., Mathad, A., Matiunin, V., Matteuzzi, C., Mattioli, K. R., Mauri, A., Maurice, E., Mauricio, J., Mayencourt, P., de Cos, J. Mazorra, Mazurek, M., McCann, M., Mcconnell, L., McGrath, T. H., McHugh, N. T., McNab, A., McNulty, R., Meadows, B., Meier, G., Melnychuk, D., Meng, F. M., Merk, M., Merli, A., Garcia, L. Meyer, Miao, D., Miao, H., Mikhasenko, M., Milanes, D. A., Minotti, A., Minucci, E., Miralles, T., Mitreska, B., Mitzel, D. S., Modak, A., Mohammed, R. A., Moise, R. D., Mokhnenko, S., Mombächer, T., Monk, M., Monteil, S., Gomez, A. Morcillo, Morello, G., Morello, M. J., Morgenthaler, M. P., Morris, A. B., Morris, A. G., Mountain, R., Mu, H., Mu, Z. M., Muhammad, E., Muheim, F., Mulder, M., Müller, K., Muñoz-Rojas, F., Murta, R., Naik, P., Nakada, T., Nandakumar, R., Nanut, T., Nasteva, I., Needham, M., Neri, N., Neubert, S., Neufeld, N., Neustroev, P., Nicolini, J., Nicotra, D., Niel, E. M., Nikitin, N., Nogarolli, P., Nogga, P., Nolte, N. S., Normand, C., Fernandez, J. Novoa, Nowak, G., Nunez, C., Nur, H. N., Oblakowska-Mucha, A., Obraztsov, V., Oeser, T., Okamura, S., Okhotnikov, A., Okhrimenko, O., Oldeman, R., Oliva, F., Olocco, M., Onderwater, C. J. G., O'Neil, R. H., Osthues, D., Goicochea, J. M. Otalora, Owen, P., Oyanguren, A., Ozcelik, O., Padee, A., Padeken, K. O., Pagare, B., Pais, P. R., Pajero, T., Palano, A., Palutan, M., Panshin, G., Paolucci, L., Papanestis, A., Pappagallo, M., Pappalardo, L. L., Pappenheimer, C., Parkes, C., Passalacqua, B., Passaleva, G., Passaro, D., Pastore, A., Patel, M., Patoc, J., Patrignani, C., Paul, A., Pawley, C. J., Pellegrino, A., Peng, J., Altarelli, M. Pepe, Perazzini, S., Pereima, D., Da Costa, H. Pereira, Castro, A. Pereiro, Perret, P., Perro, A., Petridis, K., Petrolini, A., Pfaller, J. P., Pham, H., Pica, L., Piccini, M., Pietrzyk, B., Pietrzyk, G., Pinci, D., Pisani, F., Pizzichemi, M., Placinta, V., Casasus, M. Plo, Poeschl, T., Polci, F., Lener, M. Poli, Poluektov, A., Polukhina, N., Polyakov, I., Polycarpo, E., Ponce, S., Popov, D., Poslavskii, S., Prasanth, K., Prouve, C., Pugatch, V., Punzi, G., Qasim, S., Qian, Q. Q., Qian, W., Qin, N., Qu, S., Quagliani, R., Trejo, R. I. Rabadan, Rademacker, J. H., Rama, M., García, M. Ramírez, De Oliveira, V. Ramos, Pernas, M. Ramos, Rangel, M. S., Ratnikov, F., Raven, G., De Miguel, M. Rebollo, Redi, F., Reich, J., Reiss, F., Ren, Z., Resmi, P. K., Ribatti, R., Ricart, G. R., Riccardi, D., Ricciardi, S., Richardson, K., Richardson-Slipper, M., Rinnert, K., Robbe, P., Robertson, G., Rodrigues, E., Fernandez, E. Rodriguez, Lopez, J. A. Rodriguez, Rodriguez, E. Rodriguez, Roensch, J., Rogachev, A., Rogovskiy, A., Rolf, D. L., Roloff, P., Romanovskiy, V., Lamas, M. Romero, Vidal, A. Romero, Romolini, G., Ronchetti, F., Rong, T., Rotondo, M., Roy, S. R., Rudolph, M. S., Diaz, M. Ruiz, Fernandez, R. A. Ruiz, Vidal, J. Ruiz, Ryzhikov, A., Ryzka, J., Saavedra-Arias, J. J., Silva, J. J. Saborido, Sadek, R., Sagidova, N., Sahoo, D., Sahoo, N., Saitta, B., Salomoni, M., Gras, C. Sanchez, Sanderswood, I., Santacesaria, R., Rios, C. Santamarina, Santimaria, M., Santoro, L., Santovetti, E., Saputi, A., Saranin, D., Sarnatskiy, A., Sarpis, G., Sarpis, M., Satriano, C., Satta, A., Saur, M., Savrina, D., Sazak, H., Smead, L. G. Scantlebury, Scarabotto, A., Schael, S., Scherl, S., Schiller, M., Schindler, H., Schmelling, M., Schmidt, B., Schmitt, S., Schmitz, H., Schneider, O., Schopper, A., Schulte, N., Schulte, S., Schune, M. H., Schwemmer, R., Schwering, G., Sciascia, B., Sciuccati, A., Sellam, S., Semennikov, A., Senger, T., Soares, M. Senghi, Sergi, A., Serra, N., Sestini, L., Seuthe, A., Shang, Y., Shangase, D. M., Shapkin, M., Sharma, R. S., Shchemerov, I., Shchutska, L., Shears, T., Shekhtman, L., Shen, Z., Sheng, S., Shevchenko, V., Shi, B., Shi, Q., Shimizu, Y., Shmanin, E., Shorkin, R., Shupperd, J. D., Coutinho, R. Silva, Simi, G., Simone, S., Skidmore, N., Skwarnicki, T., Slater, M. W., Smallwood, J. C., Smith, E., Smith, K., Smith, M., Snoch, A., Lavra, L. Soares, Sokoloff, M. D., Soler, F. J. P., Solomin, A., Solovev, A., Solovyev, I., Song, R., Song, Y., Song, Y. S., De Almeida, F. L. Souza, De Paula, B. Souza, Norella, E. Spadaro, Spedicato, E., Speer, J. G., Spiridenkov, E., Spradlin, P., Sriskaran, V., Stagni, F., Stahl, M., Stahl, S., Stanislaus, S., Stein, E. N., Steinkamp, O., Stenyakin, O., Stevens, H., Strekalina, D., Su, Y., Suljik, F., Sun, J., Sun, L., Sun, Y., Sundfeld, D., Sutcliffe, W., Swallow, P. N., Swystun, F., Szabelski, A., Szumlak, T., Tan, Y., Tat, M. D., Terentev, A., Terzuoli, F., Teubert, F., Thomas, E., Thompson, D. J. D., Tilquin, H., Tisserand, V., T'Jampens, S., Tobin, M., Tomassetti, L., Tonani, G., Tong, X., Machado, D. Torres, Toscano, L., Tou, D. Y., Trippl, C., Tuci, G., Tuning, N., Uecker, L. H., Ukleja, A., Unverzagt, D. J., Ursov, E., Usachov, A., Ustyuzhanin, A., Uwer, U., Vagnoni, V., Valenti, G., Canudas, N. Valls, Van Hecke, H., van Herwijnen, E., Van Hulse, C. B., Van Laak, R., van Veghel, M., Vasquez, G., Gomez, R. Vazquez, Regueiro, P. Vazquez, Sierra, C. Vázquez, Vecchi, S., Velthuis, J. J., Veltri, M., Venkateswaran, A., Vesterinen, M., Benet, D. Vico, Diaz, M. Vieites, Vilasis-Cardona, X., Figueras, E. Vilella, Villa, A., Vincent, P., Volle, F. C., Bruch, D. vom, Voropaev, N., Vos, K., Vouters, G., Vrahas, C., Wagner, J., Walsh, J., Walton, E. J., Wan, G., Wang, C., Wang, G., Wang, J., Wang, M., Wang, N. W., Wang, R., Wang, X., Wang, X. W., Wang, Y., Wang, Z., Ward, J. A., Waterlaat, M., Watson, N. K., Websdale, D., Wei, Y., Wendel, J., Westhenry, B. D. C., White, C., Whitehead, M., Whiter, E., Wiederhold, A. R., Wiedner, D., Wilkinson, G., Wilkinson, M. K., Williams, M., Williams, M. R. J., Williams, R., Williams, Z., Wilson, F. F., Wislicki, W., Witek, M., Witola, L., Wong, C. P., Wormser, G., Wotton, S. A., Wu, H., Wu, J., Wu, Y., Wu, Z., Wyllie, K., Xian, S., Xiang, Z., Xie, Y., Xu, A., Xu, J., Xu, L., Xu, M., Xu, Z., Yang, D., Yang, K., Yang, S., Yang, X., Yang, Y., Yang, Z., Yeroshenko, V., Yeung, H., Yin, H., Yu, C. Y., Yu, J., Yuan, X., Yuan, Y, Zaffaroni, E., Zavertyaev, M., Zdybal, M., Zeng, C., Zeng, M., Zhang, C., Zhang, D., Zhang, J., Zhang, L., Zhang, S., Zhang, Y., Zhang, Y. Z., Zhao, Y., Zharkova, A., Zhelezov, A., Zheng, S. Z., Zheng, X. Z., Zheng, Y., Zhou, T., Zhou, X., Zhou, Y., Zhovkovska, V., Zhu, L. Z., Zhu, X., Zhukov, V., Zhuo, J., Zou, Q., Zuliani, D., and Zunica, G.
Subjects: High Energy Physics - Experiment
Abstract: The rare electromagnetic $J/\psi \to \mu^+\mu^-\mu^+\mu^-$ decay is observed with a significance greatly exceeding the discovery threshold, using proton-proton collision data collected by the LHCb experiment during 2016-2018 at a center-of-mass energy of 13 TeV, corresponding to an integrated luminosity of $5.4\,\text{fb}^{-1}$. The rate of this decay is measured relative to that of the $J/\psi \to \mu^+\mu^-$ mode. Using the QED model for the four-muon decay in the efficiency estimation, its branching fraction is determined to be \begin{equation*} {\mathcal{B}}(J/\psi \to \mu^+\mu^-\mu^+\mu^-) = (1.13\pm0.10\pm0.05\pm0.01)\times 10^{-6}, \end{equation*} where the uncertainties are statistical, systematic and due to the uncertainty on the branching fraction of the $J/\psi \to \mu^+\mu^-$ decay., Comment: All figures and tables, along with machine-readable versions and any supplementary material and additional information, are available at https://lbfence.cern.ch/alcm/public/analysis/full-details/3453 (LHCb public pages)
Published: 2024

216. Observation of muonic Dalitz decays of $\chi_{b}$ mesons and precise spectroscopy of hidden-beauty states

Author: LHCb collaboration, Aaij, R., Abdelmotteleb, A. S. W., Beteta, C. Abellan, Abudinén, F., Ackernley, T., Adefisoye, A. A., Adeva, B., Adinolfi, M., Adlarson, P., Agapopoulou, C., Aidala, C. A., Ajaltouni, Z., Akar, S., Akiba, K., Albicocco, P., Albrecht, J., Alessio, F., Alexander, M., Aliouche, Z., Cartelle, P. Alvarez, Amalric, R., Amato, S., Amey, J. L., Amhis, Y., An, L., Anderlini, L., Andersson, M., Andreianov, A., Andreola, P., Andreotti, M., Andreou, D., Anelli, A., Ao, D., Archilli, F., Argenton, M., Cuendis, S. Arguedas, Artamonov, A., Artuso, M., Aslanides, E., Da Silva, R. Ataíde, Atzeni, M., Audurier, B., Bacher, D., Perea, I. Bachiller, Bachmann, S., Bachmayer, M., Back, J. J., Rodriguez, P. Baladron, Balagura, V., Baldini, W., Balzani, L., Bao, H., Leite, J. Baptista de Souza, Pretel, C. Barbero, Barbetti, M., Barbosa, I. R., Barlow, R. J., Barnyakov, M., Barsuk, S., Barter, W., Bartolini, M., Bartz, J., Basels, J. M., Bashir, S., Bassi, G., Batsukh, B., Battista, P. B., Bay, A., Beck, A., Becker, M., Bedeschi, F., Bediaga, I. B., Behling, N. B., Belin, S., Bellee, V., Belous, K., Belov, I., Belyaev, I., Benane, G., Bencivenni, G., Ben-Haim, E., Berezhnoy, A., Bernet, R., Andres, S. Bernet, Bertolin, A., Betancourt, C., Betti, F., Bex, J., Bezshyiko, Ia., Bhom, J., Bieker, M. S., Biesuz, N. V., Billoir, P., Biolchini, A., Birch, M., Bishop, F. C. R., Bitadze, A., Bizzeti, A., Blake, T., Blanc, F., Blank, J. E., Blusk, S., Bocharnikov, V., Boelhauve, J. A., Garcia, O. Boente, Boettcher, T., Bohare, A., Boldyrev, A., Bolognani, C. S., Bolzonella, R., Bondar, N., Bordelius, A., Borgato, F., Borghi, S., Borsato, M., Borsuk, J. T., Bouchiba, S. A., Bovill, M., Bowcock, T. J. V., Boyer, A., Bozzi, C., Rodriguez, A. Brea, Breer, N., Brodzicka, J., Gonzalo, A. Brossa, Brown, J., Brundu, D., Buchanan, E., Buonaura, A., Buonincontri, L., Burke, A. T., Burr, C., Butter, J. S., Buytaert, J., Byczynski, W., Cadeddu, S., Cai, H., Caillet, A. C., Calabrese, R., Ramirez, S. Calderon, Calefice, L., Cali, S., Calvi, M., Gomez, M. Calvo, Magalhaes, P. Camargo, Bouzas, J. I. Cambon, Campana, P., Perez, D. H. Campora, Quezada, A. F. Campoverde, Capelli, S., Capriotti, L., Caravaca-Mora, R., Carbone, A., Salgado, L. Carcedo, Cardinale, R., Cardini, A., Carniti, P., Carus, L., Vidal, A. Casais, Caspary, R., Casse, G., Godinez, J. Castro, Cattaneo, M., Cavallero, G., Cavallini, V., Celani, S., Cervenkov, D., Cesare, S., Chadwick, A. J., Chahrour, I., Charles, M., Charpentier, Ph., Chatzianagnostou, E., Chefdeville, M., Chen, C., Chen, S., Chen, Z., Chernov, A., Chernyshenko, S., Chiotopoulos, X., Chobanova, V., Cholak, S., Chrzaszcz, M., Chubykin, A., Chulikov, V., Ciambrone, P., Vidal, X. Cid, Ciezarek, G., Cifra, P., Clarke, P. E. L., Clemencic, M., Cliff, H. V., Closier, J., Toapaxi, C. Cocha, Coco, V., Cogan, J., Cogneras, E., Cojocariu, L., Collins, P., Colombo, T., Colonna, M. C., Comerma-Montells, A., Congedo, L., Contu, A., Cooke, N., Corredoira, I., Correia, A., Corti, G., Meldrum, J. J. Cottee, Couturier, B., Craik, D. C., Torres, M. Cruz, Rivera, E. Curras, Currie, R., Da Silva, C. L., Dadabaev, S., Dai, L., Dai, X., Dall'Occo, E., Dalseno, J., D'Ambrosio, C., Daniel, J., Danilina, A., d'Argent, P., Davidson, A., Davies, J. E., Davis, A., Francisco, O. De Aguiar, De Angelis, C., De Benedetti, F., de Boer, J., De Bruyn, K., De Capua, S., De Cian, M., Da Graca, U. De Freitas Carneiro, De Lucia, E., De Miranda, J. M., De Paula, L., De Serio, M., De Simone, P., De Vellis, F., de Vries, J. A., Debernardis, F., Decamp, D., Dedu, V., Dekkers, S., Del Buono, L., Delaney, B., Dembinski, H. -P., Deng, J., Denysenko, V., Deschamps, O., Dettori, F., Dey, B., Di Nezza, P., Diachkov, I., Didenko, S., Ding, S., Dittmann, L., Dobishuk, V., Docheva, A. D., Dong, C., Donohoe, A. M., Dordei, F., Reis, A. C. dos, Dowling, A. D., Duan, W., Duda, P., Dudek, M. W., Dufour, L., Duk, V., Durante, P., Duras, M. M., Durham, J. M., Durmus, O. D., Dziurda, A., Dzyuba, A., Easo, S., Eckstein, E., Egede, U., Egorychev, A., Egorychev, V., Eisenhardt, S., Ejopu, E., Eklund, L., Elashri, M., Ellbracht, J., Ely, S., Ene, A., Epple, E., Eschle, J., Esen, S., Evans, T., Fabiano, F., Falcao, L. N., Fan, Y., Fang, B., Fantini, L., Faria, M., Farmer, K., Fazzini, D., Felkowski, L., Feng, M., Feo, M., Casani, A. Fernandez, Gomez, M. Fernandez, Fernez, A. D., Ferrari, F., Rodrigues, F. Ferreira, Ferrillo, M., Ferro-Luzzi, M., Filippov, S., Fini, R. A., Fiorini, M., Firlej, M., Fischer, K. L., Fitzgerald, D. S., Fitzpatrick, C., Fiutowski, T., Fleuret, F., Fontana, M., Foreman, L. F., Forty, R., Foulds-Holt, D., Lima, V. Franco, Sevilla, M. Franco, Frank, M., Franzoso, E., Frau, G., Frei, C., Friday, D. A., Fu, J., Fuehring, Q., Fujii, Y., Fulghesu, T., Gabriel, E., Galati, G., Galati, M. D., Torreira, A. Gallas, Galli, D., Gambetta, S., Gandelman, M., Gandini, P., Ganie, B., Gao, H., Gao, R., Gao, T. Q., Gao, Y., Garau, M., Martin, L. M. Garcia, Moreno, P. Garcia, Pardiñas, J. García, Garg, K. G., Garrido, L., Gaspar, C., Geertsema, R. E., Gerken, L. L., Gersabeck, E., Gersabeck, M., Gershon, T., Ghizzo, S. G., Ghorbanimoghaddam, Z., Giambastiani, L., Giasemis, F. I., Gibson, V., Giemza, H. K., Gilman, A. L., Giovannetti, M., Gioventù, A., Girardey, L., Gironell, P. Gironella, Giugliano, C., Giza, M. A., Gkougkousis, E. L., Glaser, F. C., Gligorov, V. V., Göbel, C., Golobardes, E., Golubkov, D., Golutvin, A., Gomes, A., Fernandez, S. Gomez, Abrantes, F. Goncalves, Goncerz, M., Gong, G., Gooding, J. A., Gorelov, I. V., Gotti, C., Grabowski, J. P., Cardoso, L. A. Granado, Graugés, E., Graverini, E., Grazette, L., Graziani, G., Grecu, A. T., Greeven, L. M., Grieser, N. A., Grillo, L., Gromov, S., Gu, C., Guarise, M., Guerry, L., Guittiere, M., Guliaeva, V., Günther, P. A., Guseinov, A. -K., Gushchin, E., Guz, Y., Gys, T., Habermann, K., Hadavizadeh, T., Hadjivasiliou, C., Haefeli, G., Haen, C., Haimberger, J., Hajheidari, M., Hallett, G. H., Halvorsen, M. M., Hamilton, P. M., Hammerich, J., Han, Q., Han, X., Hansmann-Menzemer, S., Hao, L., Harnew, N., Hartmann, M., Hashmi, S., He, J., Hemmer, F., Henderson, C., Henderson, R. D. L., Hennequin, A. M., Hennessy, K., Henry, L., Herd, J., Gascon, P. Herrero, Heuel, J., Hicheur, A., Mendizabal, G. Hijano, Hill, D., Hollitt, S. E., Horswill, J., Hou, R., Hou, Y., Howarth, N., Hu, J., Hu, W., Hu, X., Huang, W., Hulsbergen, W., Hunter, R. J., Hushchyn, M., Hutchcroft, D., Idzik, M., Ilin, D., Ilten, P., Inglessi, A., Iniukhin, A., Ishteev, A., Ivshin, K., Jacobsson, R., Jage, H., Elles, S. J. Jaimes, Jakobsen, S., Jans, E., Jashal, B. K., Jawahery, A., Jevtic, V., Jiang, E., Jiang, X., Jiang, Y., Jiang, Y. J., John, M., Rajan, A. John Rubesh, Johnson, D., Jones, C. R., Jones, T. P., Joshi, S., Jost, B., Castella, J. Juan, Jurik, N., Juszczak, I., Kaminaris, D., Kandybei, S., Kane, M., Kang, Y., Kar, C., Karacson, M., Karpenkov, D., Kauniskangas, A., Kautz, J. W., Kazanecki, M. K., Keizer, F., Kenzie, M., Ketel, T., Khanji, B., Kharisova, A., Kholodenko, S., Khreich, G., Kirn, T., Kirsebom, V. S., Kitouni, O., Klaver, S., Kleijne, N., Klimaszewski, K., Kmiec, M. R., Koliiev, S., Kolk, L., Konoplyannikov, A., Kopciewicz, P., Koppenburg, P., Korolev, M., Kostiuk, I., Kot, O., Kotriakhova, S., Kozachuk, A., Kravchenko, P., Kravchuk, L., Kreps, M., Krokovny, P., Krupa, W., Krzemien, W., Kshyvanskyi, O. K., Kubis, S., Kucharczyk, M., Kudryavtsev, V., Kulikova, E., Kupsc, A., Kutsenko, B. K., Lacarrere, D., Gonzalez, P. Laguarta, Lai, A., Lampis, A., Lancierini, D., Gomez, C. Landesa, Lane, J. J., Lane, R., Lanfranchi, G., Langenbruch, C., Langer, J., Lantwin, O., Latham, T., Lazzari, F., Lazzeroni, C., Gac, R. Le, Lee, H., Lefèvre, R., Leflat, A., Legotin, S., Lehuraux, M., Cid, E. Lemos, Leroy, O., Lesiak, T., Lesser, E., Leverington, B., Li, A., Li, C., Li, H., Li, K., Li, L., Li, M., Li, P., Li, P. -R., Li, Q., Li, S., Li, T., Li, Y., Lian, Z., Liang, X., Libralon, S., Lin, C., Lin, T., Lindner, R., Lisovskyi, V., Litvinov, R., Liu, F. L., Liu, G., Liu, K., Liu, S., Liu, W., Liu, Y., Liu, Y. L., Salvia, A. Lobo, Loi, A., Castro, J. Lomba, Long, T., Lopes, J. H., Huertas, A. Lopez, Soliño, S. López, Lu, Q., Lucarelli, C., Lucchesi, D., Martinez, M. Lucio, Lukashenko, V., Luo, Y., Lupato, A., Luppi, E., Lynch, K., Lyu, X. -R., Ma, G. M., Ma, R., Maccolini, S., Machefert, F., Maciuc, F., Mack, B., Mackay, I., Mackey, L. M., Mohan, L. R. Madhan, Madurai, M. J., Maevskiy, A., Magdalinski, D., Maisuzenko, D., Majewski, M. W., Malczewski, J. J., Malde, S., Malentacca, L., Malinin, A., Maltsev, T., Manca, G., Mancinelli, G., Mancuso, C., Escalero, R. Manera, Manuzzi, D., Marangotto, D., Marchand, J. F., Marchevski, R., Marconi, U., Mariani, E., Mariani, S., Benito, C. Marin, Marks, J., Marshall, A. M., Martel, L., Martelli, G., Martellotti, G., Martinazzoli, L., Martinelli, M., Santos, D. Martinez, Vidal, F. Martinez, Massafferri, A., Matev, R., Mathad, A., Matiunin, V., Matteuzzi, C., Mattioli, K. R., Mauri, A., Maurice, E., Mauricio, J., Mayencourt, P., de Cos, J. Mazorra, Mazurek, M., McCann, M., Mcconnell, L., McGrath, T. H., McHugh, N. T., McNab, A., McNulty, R., Meadows, B., Meier, G., Melnychuk, D., Meng, F. M., Merk, M., Merli, A., Garcia, L. Meyer, Miao, D., Miao, H., Mikhasenko, M., Milanes, D. A., Minotti, A., Minucci, E., Miralles, T., Mitreska, B., Mitzel, D. S., Modak, A., Mohammed, R. A., Moise, R. D., Mokhnenko, S., Cardenas, E. F. Molina, Mombächer, T., Monk, M., Monteil, S., Gomez, A. Morcillo, Morello, G., Morello, M. J., Morgenthaler, M. P., Moron, J., Morris, A. B., Morris, A. G., Mountain, R., Mu, H., Mu, Z. M., Muhammad, E., Muheim, F., Mulder, M., Müller, K., Muñoz-Rojas, F., Murta, R., Naik, P., Nakada, T., Nandakumar, R., Nanut, T., Nasteva, I., Needham, M., Neri, N., Neubert, S., Neufeld, N., Neustroev, P., Nicolini, J., Nicotra, D., Niel, E. M., Nikitin, N., Nogarolli, P., Nogga, P., Normand, C., Fernandez, J. Novoa, Nowak, G., Nunez, C., Nur, H. N., Oblakowska-Mucha, A., Obraztsov, V., Oeser, T., Okamura, S., Okhotnikov, A., Okhrimenko, O., Oldeman, R., Oliva, F., Olocco, M., Onderwater, C. J. G., O'Neil, R. H., Osthues, D., Goicochea, J. M. Otalora, Owen, P., Oyanguren, A., Ozcelik, O., Paciolla, F., Padee, A., Padeken, K. O., Pagare, B., Pais, P. R., Pajero, T., Palano, A., Palutan, M., Panshin, G., Paolucci, L., Papanestis, A., Pappagallo, M., Pappalardo, L. L., Pappenheimer, C., Parkes, C., Passalacqua, B., Passaleva, G., Passaro, D., Pastore, A., Patel, M., Patoc, J., Patrignani, C., Paul, A., Pawley, C. J., Pellegrino, A., Peng, J., Altarelli, M. Pepe, Perazzini, S., Pereima, D., Da Costa, H. Pereira, Castro, A. Pereiro, Perret, P., Perro, A., Petridis, K., Petrolini, A., Pfaller, J. P., Pham, H., Pica, L., Piccini, M., Piccolo, L., Pietrzyk, B., Pietrzyk, G., Pinci, D., Pisani, F., Pizzichemi, M., Placinta, V., Casasus, M. Plo, Poeschl, T., Polci, F., Lener, M. Poli, Poluektov, A., Polukhina, N., Polyakov, I., Polycarpo, E., Ponce, S., Popov, D., Poslavskii, S., Prasanth, K., Prouve, C., Provenzano, D., Pugatch, V., Punzi, G., Qasim, S., Qian, Q. Q., Qian, W., Qin, N., Qu, S., Quagliani, R., Trejo, R. I. Rabadan, Rademacker, J. H., Rama, M., García, M. Ramírez, De Oliveira, V. Ramos, Pernas, M. Ramos, Rangel, M. S., Ratnikov, F., Raven, G., De Miguel, M. Rebollo, Redi, F., Reich, J., Reiss, F., Ren, Z., Resmi, P. K., Ribatti, R., Ricart, G. R., Riccardi, D., Ricciardi, S., Richardson, K., Richardson-Slipper, M., Rinnert, K., Robbe, P., Robertson, G., Rodrigues, E., Fernandez, E. Rodriguez, Lopez, J. A. Rodriguez, Rodriguez, E. Rodriguez, Roensch, J., Rogachev, A., Rogovskiy, A., Rolf, D. L., Roloff, P., Romanovskiy, V., Lamas, M. Romero, Vidal, A. Romero, Romolini, G., Ronchetti, F., Rong, T., Rotondo, M., Roy, S. R., Rudolph, M. S., Diaz, M. Ruiz, Fernandez, R. A. Ruiz, Vidal, J. Ruiz, Ryzhikov, A., Ryzka, J., Saavedra-Arias, J. J., Silva, J. J. Saborido, Sadek, R., Sagidova, N., Sahoo, D., Sahoo, N., Saitta, B., Salomoni, M., Sanderswood, I., Santacesaria, R., Rios, C. Santamarina, Santimaria, M., Santoro, L., Santovetti, E., Saputi, A., Saranin, D., Sarnatskiy, A., Sarpis, G., Sarpis, M., Satriano, C., Satta, A., Saur, M., Savrina, D., Sazak, H., Smead, L. G. Scantlebury, Scarabotto, A., Schael, S., Scherl, S., Schiller, M., Schindler, H., Schmelling, M., Schmidt, B., Schmitt, S., Schmitz, H., Schneider, O., Schopper, A., Schulte, N., Schulte, S., Schune, M. H., Schwemmer, R., Schwering, G., Sciascia, B., Sciuccati, A., Sellam, S., Semennikov, A., Senger, T., Soares, M. Senghi, Sergi, A., Serra, N., Sestini, L., Seuthe, A., Shang, Y., Shangase, D. M., Shapkin, M., Sharma, R. S., Shchemerov, I., Shchutska, L., Shears, T., Shekhtman, L., Shen, Z., Sheng, S., Shevchenko, V., Shi, B., Shi, Q., Shimizu, Y., Shmanin, E., Shorkin, R., Shupperd, J. D., Coutinho, R. Silva, Simi, G., Simone, S., Skidmore, N., Skwarnicki, T., Slater, M. W., Smallwood, J. C., Smith, E., Smith, K., Smith, M., Snoch, A., Lavra, L. Soares, Sokoloff, M. D., Soler, F. J. P., Solomin, A., Solovev, A., Solovyev, I., Song, R., Song, Y., Song, Y. S., De Almeida, F. L. Souza, De Paula, B. Souza, Norella, E. Spadaro, Spedicato, E., Speer, J. G., Spiridenkov, E., Spradlin, P., Sriskaran, V., Stagni, F., Stahl, M., Stahl, S., Stanislaus, S., Stein, E. N., Steinkamp, O., Stenyakin, O., Stevens, H., Strekalina, D., Su, Y., Suljik, F., Sun, J., Sun, L., Sun, Y., Sundfeld, D., Sutcliffe, W., Swallow, P. N., Swientek, K., Swystun, F., Szabelski, A., Szumlak, T., Tan, Y., Tat, M. D., Terentev, A., Terzuoli, F., Teubert, F., Thomas, E., Thompson, D. J. D., Tilquin, H., Tisserand, V., T'Jampens, S., Tobin, M., Tomassetti, L., Tonani, G., Tong, X., Machado, D. Torres, Toscano, L., Tou, D. Y., Trippl, C., Tuci, G., Tuning, N., Uecker, L. H., Ukleja, A., Unverzagt, D. J., Ursov, E., Usachov, A., Ustyuzhanin, A., Uwer, U., Vagnoni, V., Cadenas, V. Valcarce, Valenti, G., Canudas, N. Valls, Van Hecke, H., van Herwijnen, E., Van Hulse, C. B., Van Laak, R., van Veghel, M., Vasquez, G., Gomez, R. Vazquez, Regueiro, P. Vazquez, Sierra, C. Vázquez, Vecchi, S., Velthuis, J. J., Veltri, M., Venkateswaran, A., Verdoglia, M., Vesterinen, M., Benet, D. Vico, Villalba, P. V. Vidrier, Diaz, M. Vieites, Vilasis-Cardona, X., Figueras, E. Vilella, Villa, A., Vincent, P., Volle, F. C., Bruch, D. vom, Voropaev, N., Vos, K., Vouters, G., Vrahas, C., Wagner, J., Walsh, J., Walton, E. J., Wan, G., Wang, C., Wang, G., Wang, J., Wang, M., Wang, N. W., Wang, R., Wang, X., Wang, X. W., Wang, Y., Wang, Z., Ward, J. A., Waterlaat, M., Watson, N. K., Websdale, D., Wei, Y., Wendel, J., Westhenry, B. D. C., White, C., Whitehead, M., Whiter, E., Wiederhold, A. R., Wiedner, D., Wilkinson, G., Wilkinson, M. K., Williams, M., Williams, M. R. J., Williams, R., Williams, Z., Wilson, F. F., Wislicki, W., Witek, M., Witola, L., Wormser, G., Wotton, S. A., Wu, H., Wu, J., Wu, Y., Wu, Z., Wyllie, K., Xian, S., Xiang, Z., Xie, Y., Xu, A., Xu, J., Xu, L., Xu, M., Xu, Z., Yang, D., Yang, K., Yang, S., Yang, X., Yang, Y., Yang, Z., Yeroshenko, V., Yeung, H., Yin, H., Yu, C. Y., Yu, J., Yuan, X., Yuan, Y, Zaffaroni, E., Zavertyaev, M., Zdybal, M., Zenesini, F., Zeng, C., Zeng, M., Zhang, C., Zhang, D., Zhang, J., Zhang, L., Zhang, S., Zhang, Y., Zhang, Y. Z., Zhao, Y., Zharkova, A., Zhelezov, A., Zheng, S. Z., Zheng, X. Z., Zheng, Y., Zhou, T., Zhou, X., Zhou, Y., Zhovkovska, V., Zhu, L. Z., Zhu, X., Zhukov, V., Zhuo, J., Zou, Q., Zuliani, D., and Zunica, G.
Subjects: High Energy Physics - Experiment
Abstract: The decays of the $\chi_{b1}(1P)$, $\chi_{b2}(1P)$, $\chi_{b1}(2P)$ and $\chi_{b2}(2P)$ mesons into the $\Upsilon(1S)\mu^+\mu^-$ final state are observed with a high significance using proton-proton collision data collected with the LHCb detector and corresponding to an integrated luminosity of 9fb$^{-1}$. The newly observed decays together with the $\Upsilon(2S)\rightarrow \Upsilon(1S)\pi^+\pi^-$ and $\Upsilon(3S)\rightarrow \Upsilon(2S)\pi^+\pi^-$ decay modes are used for precision measurements of the mass and mass splittings for the hidden-beauty states., Comment: All figures and tables, along with any supplementary material and additional information, are available at https://lbfence.cern.ch/alcm/public/analysis/full-details/3633
Published: 2024
Full Text: View/download PDF

217. Measurement of $D^0-\overline{D}^0$ mixing and search for $CP$ violation with $D^0\rightarrow K^+\pi^-$ decays

Author: LHCb collaboration, Aaij, R., Abdelmotteleb, A. S. W., Beteta, C. Abellan, Abudinén, F., Ackernley, T., Adefisoye, A. A., Adeva, B., Adinolfi, M., Adlarson, P., Agapopoulou, C., Aidala, C. A., Ajaltouni, Z., Akar, S., Akiba, K., Albicocco, P., Albrecht, J., Alessio, F., Alexander, M., Aliouche, Z., Cartelle, P. Alvarez, Amalric, R., Amato, S., Amey, J. L., Amhis, Y., An, L., Anderlini, L., Andersson, M., Andreianov, A., Andreola, P., Andreotti, M., Andreou, D., Anelli, A., Ao, D., Archilli, F., Argenton, M., Cuendis, S. Arguedas, Artamonov, A., Artuso, M., Aslanides, E., Da Silva, R. Ataide, Atzeni, M., Audurier, B., Bacher, D., Perea, I. Bachiller, Bachmann, S., Bachmayer, M., Back, J. J., Rodriguez, P. Baladron, Balagura, V., Baldini, W., Bao, H., Leite, J. Baptista de Souza, Barbetti, M., Barbosa, I. R., Barlow, R. J., Barnyakov, M., Barsuk, S., Barter, W., Bartolini, M., Bartz, J., Basels, J. M., Bassi, G., Batsukh, B., Bay, A., Beck, A., Becker, M., Bedeschi, F., Bediaga, I. B., Belin, S., Bellee, V., Belous, K., Belov, I., Belyaev, I., Benane, G., Bencivenni, G., Ben-Haim, E., Berezhnoy, A., Bernet, R., Andres, S. Bernet, Bertolin, A., Betancourt, C., Betti, F., Bex, J., Bezshyiko, Ia., Bhom, J., Bieker, M. S., Biesuz, N. V., Billoir, P., Biolchini, A., Birch, M., Bishop, F. C. R., Bitadze, A., Bizzeti, A., Blake, T., Blanc, F., Blank, J. E., Blusk, S., Bocharnikov, V., Boelhauve, J. A., Garcia, O. Boente, Boettcher, T., Bohare, A., Boldyrev, A., Bolognani, C. S., Bolzonella, R., Bondar, N., Borgato, F., Borghi, S., Borsato, M., Borsuk, J. T., Bouchiba, S. A., Bowcock, T. J. V., Boyer, A., Bozzi, C., Rodriguez, A. Brea, Breer, N., Brodzicka, J., Gonzalo, A. Brossa, Brown, J., Brundu, D., Buchanan, E., Buonaura, A., Buonincontri, L., Burke, A. T., Burr, C., Butkevich, A., Butter, J. S., Buytaert, J., Byczynski, W., Cadeddu, S., Cai, H., Calabrese, R., Ramirez, S. Calderon, Calefice, L., Cali, S., Calvi, M., Gomez, M. Calvo, Magalhaes, P. Camargo, Bouzas, J. I. Cambon, Campana, P., Perez, D. H. Campora, Quezada, A. F. Campoverde, Capelli, S., Capriotti, L., Caravaca-Mora, R., Carbone, A., Salgado, L. Carcedo, Cardinale, R., Cardini, A., Carniti, P., Carus, L., Vidal, A. Casais, Caspary, R., Casse, G., Godinez, J. Castro, Cattaneo, M., Cavallero, G., Cavallini, V., Celani, S., Cervenkov, D., Cesare, S., Chadwick, A. J., Chahrour, I., Charles, M., Charpentier, Ph., Chatzianagnostou, E., Barajas, C. A. Chavez, Chefdeville, M., Chen, C., Chen, S., Chen, Z., Chernov, A., Chernyshenko, S., Chobanova, V., Cholak, S., Chrzaszcz, M., Chubykin, A., Chulikov, V., Ciambrone, P., Vidal, X. Cid, Ciezarek, G., Cifra, P., Clarke, P. E. L., Clemencic, M., Cliff, H. V., Closier, J., Toapaxi, C. Cocha, Coco, V., Cogan, J., Cogneras, E., Cojocariu, L., Collins, P., Colombo, T., Comerma-Montells, A., Congedo, L., Contu, A., Cooke, N., Corredoira, I., Correia, A., Corti, G., Meldrum, J. J. Cottee, Couturier, B., Craik, D. C., Torres, M. Cruz, Rivera, E. Curras, Currie, R., Da Silva, C. L., Dadabaev, S., Dai, L., Dai, X., Dall'Occo, E., Dalseno, J., D'Ambrosio, C., Daniel, J., Danilina, A., d'Argent, P., Davidson, A., Davies, J. E., Davis, A., Francisco, O. De Aguiar, De Angelis, C., De Benedetti, F., de Boer, J., De Bruyn, K., De Capua, S., De Cian, M., Da Graca, U. De Freitas Carneiro, De Lucia, E., De Miranda, J. M., De Paula, L., De Serio, M., De Simone, P., De Vellis, F., de Vries, J. A., Debernardis, F., Decamp, D., Dedu, V., Del Buono, L., Delaney, B., Dembinski, H. -P., Deng, J., Denysenko, V., Deschamps, O., Dettori, F., Dey, B., Di Nezza, P., Diachkov, I., Didenko, S., Ding, S., Dittmann, L., Dobishuk, V., Docheva, A. D., Dong, C., Donohoe, A. M., Dordei, F., Reis, A. C. dos, Dowling, A. D., Duan, W., Duda, P., Dudek, M. W., Dufour, L., Duk, V., Durante, P., Duras, M. M., Durham, J. M., Durmus, O. D., Dziurda, A., Dzyuba, A., Easo, S., Eckstein, E., Egede, U., Egorychev, A., Egorychev, V., Eisenhardt, S., Ejopu, E., Eklund, L., Elashri, M., Ellbracht, J., Ely, S., Ene, A., Epple, E., Eschle, J., Esen, S., Evans, T., Fabiano, F., Falcao, L. N., Fan, Y., Fang, B., Fantini, L., Faria, M., Farmer, K., Fazzini, D., Felkowski, L., Feng, M., Feo, M., Gomez, M. Fernandez, Fernez, A. D., Ferrari, F., Rodrigues, F. Ferreira, Ferrillo, M., Ferro-Luzzi, M., Filippov, S., Fini, R. A., Fiorini, M., Fischer, K. M., Fitzgerald, D. S., Fitzpatrick, C., Fleuret, F., Fontana, M., Foreman, L. F., Forty, R., Foulds-Holt, D., Sevilla, M. Franco, Frank, M., Franzoso, E., Frau, G., Frei, C., Friday, D. A., Fu, J., Fuehring, Q., Fujii, Y., Fulghesu, T., Gabriel, E., Galati, G., Galati, M. D., Torreira, A. Gallas, Galli, D., Gambetta, S., Gandelman, M., Gandini, P., Ganie, B., Gao, H., Gao, R., Gao, Y., Garau, M., Martin, L. M. Garcia, Moreno, P. Garcia, Pardiñas, J. García, Garg, K. G., Garrido, L., Gaspar, C., Geertsema, R. E., Gerken, L. L., Gersabeck, E., Gersabeck, M., Gershon, T., Ghorbanimoghaddam, Z., Giambastiani, L., Giasemis, F. I., Gibson, V., Giemza, H. K., Gilman, A. L., Giovannetti, M., Gioventù, A., Gironell, P. Gironella, Giugliano, C., Giza, M. A., Gkougkousis, E. L., Glaser, F. C., Gligorov, V. V., Göbel, C., Golobardes, E., Golubkov, D., Golutvin, A., Gomes, A., Fernandez, S. Gomez, Abrantes, F. Goncalves, Goncerz, M., Gong, G., Gooding, J. A., Gorelov, I. V., Gotti, C., Grabowski, J. P., Cardoso, L. A. Granado, Graugés, E., Graverini, E., Grazette, L., Graziani, G., Grecu, A. T., Greeven, L. M., Grieser, N. A., Grillo, L., Gromov, S., Gu, C., Guarise, M., Guittiere, M., Guliaeva, V., Günther, P. A., Guseinov, A. -K., Gushchin, E., Guz, Y., Gys, T., Habermann, K., Hadavizadeh, T., Hadjivasiliou, C., Haefeli, G., Haen, C., Haimberger, J., Hajheidari, M., Halvorsen, M. M., Hamilton, P. M., Hammerich, J., Han, Q., Han, X., Hansmann-Menzemer, S., Hao, L., Harnew, N., Hartmann, M., He, J., Hemmer, F., Henderson, C., Henderson, R. D. L., Hennequin, A. M., Hennessy, K., Henry, L., Herd, J., Gascon, P. Herrero, Heuel, J., Hicheur, A., Mendizabal, G. Hijano, Hill, D., Hollitt, S. E., Horswill, J., Hou, R., Hou, Y., Howarth, N., Hu, J., Hu, W., Hu, X., Huang, W., Hulsbergen, W., Hunter, R. J., Hushchyn, M., Hutchcroft, D., Ilin, D., Ilten, P., Inglessi, A., Iniukhin, A., Ishteev, A., Ivshin, K., Jacobsson, R., Jage, H., Elles, S. J. Jaimes, Jakobsen, S., Jans, E., Jashal, B. K., Jawahery, A., Jevtic, V., Jiang, E., Jiang, X., Jiang, Y., Jiang, Y. J., John, M., Johnson, D., Jones, C. R., Jones, T. P., Joshi, S., Jost, B., Jurik, N., Juszczak, I., Kaminaris, D., Kandybei, S., Kang, Y., Kar, C., Karacson, M., Karpenkov, D., Kauniskangas, A., Kautz, J. W., Keizer, F., Kenzie, M., Ketel, T., Khanji, B., Kharisova, A., Kholodenko, S., Khreich, G., Kirn, T., Kirsebom, V. S., Kitouni, O., Klaver, S., Kleijne, N., Klimaszewski, K., Kmiec, M. R., Koliiev, S., Kolk, L., Konoplyannikov, A., Kopciewicz, P., Koppenburg, P., Korolev, M., Kostiuk, I., Kot, O., Kotriakhova, S., Kozachuk, A., Kravchenko, P., Kravchuk, L., Kreps, M., Krokovny, P., Krupa, W., Krzemien, W., Kshyvanskyi, O. K., Kubat, J., Kubis, S., Kucharczyk, M., Kudryavtsev, V., Kulikova, E., Kupsc, A., Kutsenko, B. K., Lacarrere, D., Lai, A., Lampis, A., Lancierini, D., Gomez, C. Landesa, Lane, J. J., Lane, R., Langenbruch, C., Langer, J., Lantwin, O., Latham, T., Lazzari, F., Lazzeroni, C., Gac, R. Le, Lefèvre, R., Leflat, A., Legotin, S., Lehuraux, M., Cid, E. Lemos, Leroy, O., Lesiak, T., Leverington, B., Li, A., Li, H., Li, K., Li, L., Li, P., Li, P. -R., Li, Q., Li, S., Li, T., Li, Y., Lian, Z., Liang, X., Libralon, S., Lin, C., Lin, T., Lindner, R., Lisovskyi, V., Litvinov, R., Liu, F. L., Liu, G., Liu, K., Liu, S., Liu, Y., Liu, Y. L., Salvia, A. Lobo, Loi, A., Castro, J. Lomba, Long, T., Lopes, J. H., Huertas, A. Lopez, Soliño, S. López, Lucarelli, C., Lucchesi, D., Martinez, M. Lucio, Lukashenko, V., Luo, Y., Lupato, A., Luppi, E., Lynch, K., Lyu, X. -R., Ma, G. M., Ma, R., Maccolini, S., Machefert, F., Maciuc, F., Mack, B., Mackay, I., Mackey, L. M., Mohan, L. R. Madhan, Madurai, M. M., Maevskiy, A., Magdalinski, D., Maisuzenko, D., Majewski, M. W., Malczewski, J. J., Malde, S., Malentacca, L., Malinin, A., Maltsev, T., Manca, G., Mancinelli, G., Mancuso, C., Escalero, R. Manera, Manuzzi, D., Marangotto, D., Marchand, J. F., Marchevski, R., Marconi, U., Mariani, S., Benito, C. Marin, Marks, J., Marshall, A. M., Martelli, G., Martellotti, G., Martinazzoli, L., Martinelli, M., Santos, D. Martinez, Vidal, F. Martinez, Massafferri, A., Matev, R., Mathad, A., Matiunin, V., Matteuzzi, C., Mattioli, K. R., Mauri, A., Maurice, E., Mauricio, J., Mayencourt, P., Mazurek, M., McCann, M., Mcconnell, L., McGrath, T. H., McHugh, N. T., McNab, A., McNulty, R., Meadows, B., Meier, G., Melnychuk, D., Meng, F. M., Merk, M., Merli, A., Garcia, L. Meyer, Miao, D., Miao, H., Mikhasenko, M., Milanes, D. A., Minotti, A., Minucci, E., Miralles, T., Mitreska, B., Mitzel, D. S., Modak, A., Mödden, A., Mohammed, R. A., Moise, R. D., Mokhnenko, S., Mombächer, T., Monk, M., Monteil, S., Gomez, A. Morcillo, Morello, G., Morello, M. J., Morgenthaler, M. P., Morris, A. B., Morris, A. G., Mountain, R., Mu, H., Mu, Z. M., Muhammad, E., Muheim, F., Mulder, M., Müller, K., Muñoz-Rojas, F., Murta, R., Naik, P., Nakada, T., Nandakumar, R., Nanut, T., Nasteva, I., Needham, M., Neri, N., Neubert, S., Neufeld, N., Neustroev, P., Nicolini, J., Nicotra, D., Niel, E. M., Nikitin, N., Nogarolli, P., Nogga, P., Nolte, N. S., Normand, C., Fernandez, J. Novoa, Nowak, G., Nunez, C., Nur, H. N., Oblakowska-Mucha, A., Obraztsov, V., Oeser, T., Okamura, S., Okhotnikov, A., Okhrimenko, O., Oldeman, R., Oliva, F., Olocco, M., Onderwater, C. J. G., O'Neil, R. H., Goicochea, J. M. Otalora, Owen, P., Oyanguren, A., Ozcelik, O., Padeken, K. O., Pagare, B., Pais, P. R., Pajero, T., Palano, A., Palutan, M., Panshin, G., Paolucci, L., Papanestis, A., Pappagallo, M., Pappalardo, L. L., Pappenheimer, C., Parkes, C., Passalacqua, B., Passaleva, G., Passaro, D., Pastore, A., Patel, M., Patoc, J., Patrignani, C., Paul, A., Pawley, C. J., Pellegrino, A., Peng, J., Altarelli, M. Pepe, Perazzini, S., Pereima, D., Da Costa, H. Pereira, Castro, A. Pereiro, Perret, P., Perro, A., Petridis, K., Petrolini, A., Pfaller, J. P., Pham, H., Pica, L., Piccini, M., Pietrzyk, B., Pietrzyk, G., Pinci, D., Pisani, F., Pizzichemi, M., Placinta, V., Casasus, M. Plo, Polci, F., Lener, M. Poli, Poluektov, A., Polukhina, N., Polyakov, I., Polycarpo, E., Ponce, S., Popov, D., Poslavskii, S., Prasanth, K., Prouve, C., Pugatch, V., Punzi, G., Qasim, S., Qian, Q. Q., Qian, W., Qin, N., Qu, S., Quagliani, R., Trejo, R. I. Rabadan, Rademacker, J. H., Rama, M., García, M. Ramírez, De Oliveira, V. Ramos, Pernas, M. Ramos, Rangel, M. S., Ratnikov, F., Raven, G., De Miguel, M. Rebollo, Redi, F., Reich, J., Reiss, F., Ren, Z., Resmi, P. K., Ribatti, R., Ricart, G. R., Riccardi, D., Ricciardi, S., Richardson, K., Richardson-Slipper, M., Rinnert, K., Robbe, P., Robertson, G., Rodrigues, E., Fernandez, E. Rodriguez, Lopez, J. A. Rodriguez, Rodriguez, E. Rodriguez, Rogovskiy, A., Rolf, D. L., Roloff, P., Romanovskiy, V., Lamas, M. Romero, Vidal, A. Romero, Romolini, G., Ronchetti, F., Rong, T., Rotondo, M., Roy, S. R., Rudolph, M. S., Diaz, M. Ruiz, Fernandez, R. A. Ruiz, Vidal, J. Ruiz, Ryzhikov, A., Ryzka, J., Saavedra-Arias, J. J., Silva, J. J. Saborido, Sadek, R., Sagidova, N., Sahoo, D., Sahoo, N., Saitta, B., Salomoni, M., Gras, C. Sanchez, Sanderswood, I., Santacesaria, R., Rios, C. Santamarina, Santimaria, M., Santoro, L., Santovetti, E., Saputi, A., Saranin, D., Sarnatskiy, A. S., Sarpis, G., Sarpis, M., Satriano, C., Satta, A., Saur, M., Savrina, D., Sazak, H., Smead, L. G. Scantlebury, Scarabotto, A., Schael, S., Scherl, S., Schiller, M., Schindler, H., Schmelling, M., Schmidt, B., Schmitt, S., Schmitz, H., Schneider, O., Schopper, A., Schulte, N., Schulte, S., Schune, M. H., Schwemmer, R., Schwering, G., Sciascia, B., Sciuccati, A., Sellam, S., Semennikov, A., Senger, T., Soares, M. Senghi, Sergi, A., Serra, N., Sestini, L., Seuthe, A., Shang, Y., Shangase, D. M., Shapkin, M., Sharma, R. S., Shchemerov, I., Shchutska, L., Shears, T., Shekhtman, L., Shen, Z., Sheng, S., Shevchenko, V., Shi, B., Shi, Q., Shimizu, Y., Shmanin, E., Shorkin, R., Shupperd, J. D., Coutinho, R. Silva, Simi, G., Simone, S., Skidmore, N., Skwarnicki, T., Slater, M. W., Smallwood, J. C., Smith, E., Smith, K., Smith, M., Snoch, A., Lavra, L. Soares, Sokoloff, M. D., Soler, F. J. P., Solomin, A., Solovev, A., Solovyev, I., Song, R., Song, Y., Song, Y. S., De Almeida, F. L. Souza, De Paula, B. Souza, Norella, E. Spadaro, Spedicato, E., Speer, J. G., Spiridenkov, E., Spradlin, P., Sriskaran, V., Stagni, F., Stahl, M., Stahl, S., Stanislaus, S., Stein, E. N., Steinkamp, O., Stenyakin, O., Stevens, H., Strekalina, D., Su, Y., Suljik, F., Sun, J., Sun, L., Sun, Y., Sundfeld, D., Sutcliffe, W., Swallow, P. N., Swystun, F., Szabelski, A., Szumlak, T., Tan, Y., Tat, M. D., Terentev, A., Terzuoli, F., Teubert, F., Thomas, E., Thompson, D. J. D., Tilquin, H., Tisserand, V., T'Jampens, S., Tobin, M., Tomassetti, L., Tonani, G., Tong, X., Machado, D. Torres, Toscano, L., Tou, D. Y., Trippl, C., Tuci, G., Tuning, N., Uecker, L. H., Ukleja, A., Unverzagt, D. J., Ursov, E., Usachov, A., Ustyuzhanin, A., Uwer, U., Vagnoni, V., Valenti, G., Canudas, N. Valls, Van Hecke, H., van Herwijnen, E., Van Hulse, C. B., Van Laak, R., van Veghel, M., Vasquez, G., Gomez, R. Vazquez, Regueiro, P. Vazquez, Sierra, C. Vázquez, Vecchi, S., Velthuis, J. J., Veltri, M., Venkateswaran, A., Vesterinen, M., Diaz, M. Vieites, Vilasis-Cardona, X., Figueras, E. Vilella, Villa, A., Vincent, P., Volle, F. C., Bruch, D. vom, Voropaev, N., Vos, K., Vouters, G., Vrahas, C., Wagner, J., Walsh, J., Walton, E. J., Wan, G., Wang, C., Wang, G., Wang, J., Wang, M., Wang, N. W., Wang, R., Wang, X., Wang, X. W., Wang, Y., Wang, Z., Ward, J. A., Waterlaat, M., Watson, N. K., Websdale, D., Wei, Y., Wendel, J., Westhenry, B. D. C., White, D. J., Whitehead, M., Wiederhold, A. R., Wiedner, D., Wilkinson, G., Wilkinson, M. K., Williams, M., Williams, M. R. J., Williams, R., Wilson, F. F., Wislicki, W., Witek, M., Witola, L., Wong, C. P., Wormser, G., Wotton, S. A., Wu, H., Wu, J., Wu, Y., Wu, Z., Wyllie, K., Xian, S., Xiang, Z., Xie, Y., Xu, A., Xu, J., Xu, L., Xu, M., Xu, Z., Yang, D., Yang, K., Yang, S., Yang, X., Yang, Y., Yang, Z., Yeroshenko, V., Yeung, H., Yin, H., Yu, C. Y., Yu, J., Yuan, X., Zaffaroni, E., Zavertyaev, M., Zdybal, M., Zeng, C., Zeng, M., Zhang, C., Zhang, D., Zhang, J., Zhang, L., Zhang, S., Zhang, Y., Zhang, Y. Z., Zhao, Y., Zharkova, A., Zhelezov, A., Zheng, S. Z., Zheng, X. Z., Zheng, Y., Zhou, T., Zhou, X., Zhou, Y., Zhovkovska, V., Zhu, L. Z., Zhu, X., Zhukov, V., Zhuo, J., Zou, Q., Zuliani, D., and Zunica, G.
Subjects: High Energy Physics - Experiment
Abstract: A measurement of the time-dependent ratio of the $D^0\rightarrow K^+\pi^-$ to $\overline{D}^0\rightarrow K^+\pi^-$ decay rates is reported. The analysis uses a sample of proton-proton collisions corresponding to an integrated luminosity of 6 fb$^-1$ recorded by the LHCb experiment from 2015 through 2018 at a center-of-mass energy of 13 TeV. The $D^0$ meson is required to originate from a $D^{*+}\rightarrow D^0\pi^+$ decay, such that its flavor at production is inferred from the charge of the accompanying pion. The measurement is performed simultaneously for the $K^+\pi^-$ and $K^-\pi^+$ final states, allowing both mixing and $CP$-violation parameters to be determined. The value of the ratio of the decay rates at production is determined to be $R_{K\pi} = (343.1 \pm 2.0) \times 10^{-5}$. The mixing parameters are measured to be $c_{K\pi} = (51.4 \pm 3.5) \times 10^{-4}$ and $c_{K\pi}^{\prime} = (13 \pm 4) \times 10^{-6}$, where $\sqrt{R_{K\pi}}c_{K\pi}$ is the linear coefficient of the expansion of the ratio as a function of decay time in units of the $D^0$ lifetime, and $c_{K\pi}^{\prime}$ is the quadratic coefficient, both averaged between the $K^+\pi^-$ and $K^-\pi^+$ final states. The precision is improved relative to the previous best measurement by approximately 60%. No evidence for $CP$ violation is found., Comment: All figures and tables, along with machine-readable versions and any supplementary material and additional information, are available at https://lhcbproject.web.cern.ch/Publications/LHCbProjectPublic/LHCb-PAPER-2024-008.html
Published: 2024

218. Observation of exotic $J/\psi\phi$ resonances in diffractive processes in proton-proton collisions

Author: LHCb collaboration, Aaij, R., Abdelmotteleb, A. S. W., Beteta, C. Abellan, Abudinén, F., Ackernley, T., Adefisoye, A. A., Adeva, B., Adinolfi, M., Adlarson, P., Agapopoulou, C., Aidala, C. A., Ajaltouni, Z., Akar, S., Akiba, K., Albicocco, P., Albrecht, J., Alessio, F., Alexander, M., Aliouche, Z., Cartelle, P. Alvarez, Amalric, R., Amato, S., Amey, J. L., Amhis, Y., An, L., Anderlini, L., Andersson, M., Andreianov, A., Andreola, P., Andreotti, M., Andreou, D., Anelli, A., Ao, D., Archilli, F., Argenton, M., Cuendis, S. Arguedas, Artamonov, A., Artuso, M., Aslanides, E., Atzeni, M., Audurier, B., Bacher, D., Perea, I. Bachiller, Bachmann, S., Bachmayer, M., Back, J. J., Rodriguez, P. Baladron, Balagura, V., Baldini, W., Leite, J. Baptista de Souza, Barbetti, M., Barbosa, I. R., Barlow, R. J., Barsuk, S., Barter, W., Bartolini, M., Bartz, J., Baryshnikov, F., Basels, J. M., Bassi, G., Batsukh, B., Battig, A., Bay, A., Beck, A., Becker, M., Bedeschi, F., Bediaga, I. B., Beiter, A., Belin, S., Bellee, V., Belous, K., Belov, I., Belyaev, I., Benane, G., Bencivenni, G., Ben-Haim, E., Berezhnoy, A., Bernet, R., Andres, S. Bernet, Bertella, C., Bertolin, A., Betancourt, C., Betti, F., Bex, J., Bezshyiko, Ia., Bhom, J., Bieker, M. S., Biesuz, N. V., Billoir, P., Biolchini, A., Birch, M., Bishop, F. C. R., Bitadze, A., Bizzeti, A., Blake, T., Blanc, F., Blank, J. E., Blusk, S., Bocharnikov, V., Boelhauve, J. A., Garcia, O. Boente, Boettcher, T., Bohare, A., Boldyrev, A., Bolognani, C. S., Bolzonella, R., Bondar, N., Borgato, F., Borghi, S., Borsato, M., Borsuk, J. T., Bouchiba, S. A., Bowcock, T. J. V., Boyer, A., Bozzi, C., Bradley, M. J., Rodriguez, A. Brea, Breer, N., Brodzicka, J., Gonzalo, A. Brossa, Brown, J., Brundu, D., Buchanan, E., Buonaura, A., Buonincontri, L., Burke, A. T., Burr, C., Bursche, A., Butkevich, A., Butter, J. S., Buytaert, J., Byczynski, W., Cadeddu, S., Cai, H., Calabrese, R., Calefice, L., Cali, S., Calvi, M., Gomez, M. Calvo, Bouzas, J. I. Cambon, Campana, P., Perez, D. H. Campora, Quezada, A. F. Campoverde, Capelli, S., Capriotti, L., Caravaca-Mora, R., Carbone, A., Salgado, L. Carcedo, Cardinale, R., Cardini, A., Carniti, P., Carus, L., Vidal, A. Casais, Caspary, R., Casse, G., Godinez, J. Castro, Cattaneo, M., Cavallero, G., Cavallini, V., Celani, S., Cerasoli, J., Cervenkov, D., Cesare, S., Chadwick, A. J., Chahrour, I., Charles, M., Charpentier, Ph., Barajas, C. A. Chavez, Chefdeville, M., Chen, C., Chen, S., Chen, Z., Chernov, A., Chernyshenko, S., Chobanova, V., Cholak, S., Chrzaszcz, M., Chubykin, A., Chulikov, V., Ciambrone, P., Vidal, X. Cid, Ciezarek, G., Cifra, P., Clarke, P. E. L., Clemencic, M., Cliff, H. V., Closier, J., Toapaxi, C. Cocha, Coco, V., Cogan, J., Cogneras, E., Cojocariu, L., Collins, P., Colombo, T., Comerma-Montells, A., Congedo, L., Contu, A., Cooke, N., Corredoira, I., Correia, A., Corti, G., Meldrum, J. J. Cottee, Couturier, B., Craik, D. C., Torres, M. Cruz, Rivera, E. Curras, Currie, R., Da Silva, C. L., Dadabaev, S., Dai, L., Dai, X., Dall'Occo, E., Dalseno, J., D'Ambrosio, C., Daniel, J., Danilina, A., d'Argent, P., Davidson, A., Davies, J. E., Davis, A., Francisco, O. De Aguiar, De Angelis, C., De Benedetti, F., de Boer, J., De Bruyn, K., De Capua, S., De Cian, M., Da Graca, U. De Freitas Carneiro, De Lucia, E., De Miranda, J. M., De Paula, L., De Serio, M., De Simone, D., De Simone, P., De Vellis, F., de Vries, J. A., Debernardis, F., Decamp, D., Dedu, V., Del Buono, L., Delaney, B., Dembinski, H. -P., Deng, J., Denysenko, V., Deschamps, O., Dettori, F., Dey, B., Di Nezza, P., Diachkov, I., Didenko, S., Ding, S., Dittmann, L., Dobishuk, V., Docheva, A. D., Dolmatov, A., Dong, C., Donohoe, A. M., Dordei, F., Reis, A. C. dos, Dowling, A. D., Downes, A. G., Duan, W., Duda, P., Dudek, M. W., Dufour, L., Duk, V., Durante, P., Duras, M. M., Durham, J. M., Durmus, O. D., Dziurda, A., Dzyuba, A., Easo, S., Eckstein, E., Egede, U., Egorychev, A., Egorychev, V., Eisenhardt, S., Ejopu, E., Ek-In, S., Eklund, L., Elashri, M., Ellbracht, J., Ely, S., Ene, A., Epple, E., Escher, S., Eschle, J., Esen, S., Evans, T., Fabiano, F., Falcao, L. N., Fan, Y., Fang, B., Fantini, L., Faria, M., Farmer, K., Fazzini, D., Felkowski, L., Feng, M., Feo, M., Gomez, M. Fernandez, Fernez, A. D., Ferrari, F., Rodrigues, F. Ferreira, Sole, S. Ferreres, Ferrillo, M., Ferro-Luzzi, M., Filippov, S., Fini, R. A., Fiorini, M., Fischer, K. M., Fitzgerald, D. S., Fitzpatrick, C., Fleuret, F., Fontana, M., Foreman, L. F., Forty, R., Foulds-Holt, D., Sevilla, M. Franco, Frank, M., Franzoso, E., Frau, G., Frei, C., Friday, D. A., Fu, J., Fuehring, Q., Fujii, Y., Fulghesu, T., Gabriel, E., Galati, G., Galati, M. D., Torreira, A. Gallas, Galli, D., Gambetta, S., Gandelman, M., Gandini, P., Gao, H., Gao, R., Gao, Y., Garau, M., Martin, L. M. Garcia, Moreno, P. Garcia, Pardiñas, J. García, Garg, K. G., Garrido, L., Gaspar, C., Geertsema, R. E., Gerken, L. L., Gersabeck, E., Gersabeck, M., Gershon, T., Ghorbanimoghaddam, Z., Giambastiani, L., Giasemis, F. I., Gibson, V., Giemza, H. K., Gilman, A. L., Giovannetti, M., Gioventù, A., Gironell, P. Gironella, Giugliano, C., Giza, M. A., Gkougkousis, E. L., Glaser, F. C., Gligorov, V. V., Göbel, C., Golobardes, E., Golubkov, D., Golutvin, A., Gomes, A., Fernandez, S. Gomez, Abrantes, F. Goncalves, Goncerz, M., Gong, G., Gooding, J. A., Gorelov, I. V., Gotti, C., Grabowski, J. P., Cardoso, L. A. Granado, Graugés, E., Graverini, E., Grazette, L., Graziani, G., Grecu, A. T., Greeven, L. M., Grieser, N. A., Grillo, L., Gromov, S., Gu, C., Guarise, M., Guittiere, M., Guliaeva, V., Günther, P. A., Guseinov, A. -K., Gushchin, E., Guz, Y., Gys, T., Habermann, K., Hadavizadeh, T., Hadjivasiliou, C., Haefeli, G., Haen, C., Haimberger, J., Hajheidari, M., Halvorsen, M. M., Hamilton, P. M., Hammerich, J., Han, Q., Han, X., Hansmann-Menzemer, S., Hao, L., Harnew, N., Harrison, T., Hartmann, M., He, J., Heijhoff, K., Hemmer, F., Henderson, C., Henderson, R. D. L., Hennequin, A. M., Hennessy, K., Henry, L., Herd, J., Gascon, P. Herrero, Heuel, J., Hicheur, A., Mendizabal, G. Hijano, Hill, D., Hollitt, S. E., Horswill, J., Hou, R., Hou, Y., Howarth, N., Hu, J., Hu, W., Hu, X., Huang, W., Hulsbergen, W., Hunter, R. J., Hushchyn, M., Hutchcroft, D., Ilin, D., Ilten, P., Inglessi, A., Iniukhin, A., Ishteev, A., Ivshin, K., Jacobsson, R., Jage, H., Elles, S. J. Jaimes, Jakobsen, S., Jans, E., Jashal, B. K., Jawahery, A., Jevtic, V., Jiang, E., Jiang, X., Jiang, Y., Jiang, Y. J., John, M., Johnson, D., Jones, C. R., Jones, T. P., Joshi, S., Jost, B., Jurik, N., Juszczak, I., Kaminaris, D., Kandybei, S., Kang, Y., Karacson, M., Karpenkov, D., Kauniskangas, A., Kautz, J. W., Keizer, F., Kenzie, M., Ketel, T., Khanji, B., Kharisova, A., Kholodenko, S., Khreich, G., Kirn, T., Kirsebom, V. S., Kitouni, O., Klaver, S., Kleijne, N., Klimaszewski, K., Kmiec, M. R., Koliiev, S., Kolk, L., Konoplyannikov, A., Kopciewicz, P., Koppenburg, P., Korolev, M., Kostiuk, I., Kot, O., Kotriakhova, S., Kozachuk, A., Kravchenko, P., Kravchuk, L., Kreps, M., Kretzschmar, S., Krokovny, P., Krupa, W., Krzemien, W., Kubat, J., Kubis, S., Kucewicz, W., Kucharczyk, M., Kudryavtsev, V., Kulikova, E., Kupsc, A., Kutsenko, B. K., Lacarrere, D., Lai, A., Lampis, A., Lancierini, D., Gomez, C. Landesa, Lane, J. J., Lane, R., Langenbruch, C., Langer, J., Lantwin, O., Latham, T., Lazzari, F., Lazzeroni, C., Gac, R. Le, Lefèvre, R., Leflat, A., Legotin, S., Lehuraux, M., Cid, E. Lemos, Leroy, O., Lesiak, T., Leverington, B., Li, A., Li, H., Li, K., Li, L., Li, P., Li, P. -R., Li, S., Li, T., Li, Y., Li, Z., Lian, Z., Liang, X., Libralon, S., Lin, C., Lin, T., Lindner, R., Lisovskyi, V., Litvinov, R., Liu, F. L., Liu, G., Liu, K., Liu, Q., Liu, S., Liu, Y., Liu, Y. L., Salvia, A. Lobo, Loi, A., Castro, J. Lomba, Long, T., Lopes, J. H., Huertas, A. Lopez, Soliño, S. López, Lovell, G. H., Lucarelli, C., Lucchesi, D., Luchuk, S., Martinez, M. Lucio, Lukashenko, V., Luo, Y., Lupato, A., Luppi, E., Lynch, K., Lyu, X. -R., Ma, G. M., Ma, R., Maccolini, S., Machefert, F., Maciuc, F., Mack, B., Mackay, I., Mackey, L. M., Mohan, L. R. Madhan, Madurai, M. M., Maevskiy, A., Magdalinski, D., Maisuzenko, D., Majewski, M. W., Malczewski, J. J., Malde, S., Malecki, B., Malentacca, L., Malinin, A., Maltsev, T., Manca, G., Mancinelli, G., Mancuso, C., Escalero, R. Manera, Manuzzi, D., Marangotto, D., Marchand, J. F., Marchevski, R., Marconi, U., Mariani, S., Benito, C. Marin, Marks, J., Marshall, A. M., Marshall, P. J., Martelli, G., Martellotti, G., Martinazzoli, L., Martinelli, M., Santos, D. Martinez, Vidal, F. Martinez, Massafferri, A., Materok, M., Matev, R., Mathad, A., Matiunin, V., Matteuzzi, C., Mattioli, K. R., Mauri, A., Maurice, E., Mauricio, J., Mayencourt, P., Mazurek, M., McCann, M., Mcconnell, L., McGrath, T. H., McHugh, N. T., McNab, A., McNulty, R., Meadows, B., Meier, G., Melnychuk, D., Merk, M., Merli, A., Garcia, L. Meyer, Miao, D., Miao, H., Mikhasenko, M., Milanes, D. A., Minotti, A., Minucci, E., Miralles, T., Mitreska, B., Mitzel, D. S., Modak, A., Mödden, A., Mohammed, R. A., Moise, R. D., Mokhnenko, S., Mombächer, T., Monk, M., Monteil, S., Gomez, A. Morcillo, Morello, G., Morello, M. J., Morgenthaler, M. P., Morris, A. B., Morris, A. G., Mountain, R., Mu, H., Mu, Z. M., Muhammad, E., Muheim, F., Mulder, M., Müller, K., Muñoz-Rojas, F., Murta, R., Naik, P., Nakada, T., Nandakumar, R., Nanut, T., Nasteva, I., Needham, M., Neri, N., Neubert, S., Neufeld, N., Neustroev, P., Nicolini, J., Nicotra, D., Niel, E. M., Nikitin, N., Nogga, P., Nolte, N. S., Normand, C., Fernandez, J. Novoa, Nowak, G., Nunez, C., Nur, H. N., Oblakowska-Mucha, A., Obraztsov, V., Oeser, T., Okamura, S., Okhotnikov, A., Oldeman, R., Oliva, F., Olocco, M., Onderwater, C. J. G., O'Neil, R. H., Goicochea, J. M. Otalora, Owen, P., Oyanguren, A., Ozcelik, O., Padeken, K. O., Pagare, B., Pais, P. R., Pajero, T., Palano, A., Palutan, M., Panshin, G., Paolucci, L., Papanestis, A., Pappagallo, M., Pappalardo, L. L., Pappenheimer, C., Parkes, C., Passalacqua, B., Passaleva, G., Passaro, D., Pastore, A., Patel, M., Patoc, J., Patrignani, C., Pawley, C. J., Pellegrino, A., Altarelli, M. Pepe, Perazzini, S., Pereima, D., Castro, A. Pereiro, Perret, P., Perro, A., Petridis, K., Petrolini, A., Petrucci, S., Pfaller, J. P., Pham, H., Pica, L., Piccini, M., Pietrzyk, B., Pietrzyk, G., Pinci, D., Pisani, F., Pizzichemi, M., Placinta, V., Casasus, M. Plo, Polci, F., Lener, M. Poli, Poluektov, A., Polukhina, N., Polyakov, I., Polycarpo, E., Ponce, S., Popov, D., Poslavskii, S., Prasanth, K., Prouve, C., Pugatch, V., Punzi, G., Qian, W., Qin, N., Qu, S., Quagliani, R., Raab, N. V., Trejo, R. I. Rabadan, Rademacker, J. H., Rama, M., García, M. Ramírez, Pernas, M. Ramos, Rangel, M. S., Ratnikov, F., Raven, G., De Miguel, M. Rebollo, Redi, F., Reich, J., Reiss, F., Ren, Z., Resmi, P. K., Ribatti, R., Ricart, G. R., Riccardi, D., Ricciardi, S., Richardson, K., Richardson-Slipper, M., Rinnert, K., Robbe, P., Robertson, G., Rodrigues, E., Fernandez, E. Rodriguez, Lopez, J. A. Rodriguez, Rodriguez, E. Rodriguez, Rogovskiy, A., Rolf, D. L., Roloff, P., Romanovskiy, V., Lamas, M. Romero, Vidal, A. Romero, Romolini, G., Ronchetti, F., Rotondo, M., Roy, S. R., Rudolph, M. S., Ruf, T., Diaz, M. Ruiz, Fernandez, R. A. Ruiz, Vidal, J. Ruiz, Ryzhikov, A., Ryzka, J., Saavedra-Arias, J. J., Silva, J. J. Saborido, Sadek, R., Sagidova, N., Sahoo, D., Sahoo, N., Saitta, B., Salomoni, M., Gras, C. Sanchez, Sanderswood, I., Santacesaria, R., Rios, C. Santamarina, Santimaria, M., Santoro, L., Santovetti, E., Saputi, A., Saranin, D., Sarpis, G., Sarpis, M., Sarti, A., Satriano, C., Satta, A., Saur, M., Savrina, D., Sazak, H., Smead, L. G. Scantlebury, Scarabotto, A., Schael, S., Scherl, S., Schertz, A. M., Schiller, M., Schindler, H., Schmelling, M., Schmidt, B., Schmitt, S., Schmitz, H., Schneider, O., Schopper, A., Schulte, N., Schulte, S., Schune, M. H., Schwemmer, R., Schwering, G., Sciascia, B., Sciuccati, A., Sellam, S., Semennikov, A., Senger, T., Soares, M. Senghi, Sergi, A., Serra, N., Sestini, L., Seuthe, A., Shang, Y., Shangase, D. M., Shapkin, M., Sharma, R. S., Shchemerov, I., Shchutska, L., Shears, T., Shekhtman, L., Shen, Z., Sheng, S., Shevchenko, V., Shi, B., Shields, E. B., Shimizu, Y., Shmanin, E., Shorkin, R., Shupperd, J. D., Coutinho, R. Silva, Simi, G., Simone, S., Skidmore, N., Skwarnicki, T., Slater, M. W., Smallwood, J. C., Smith, E., Smith, K., Smith, M., Snoch, A., Lavra, L. Soares, Sokoloff, M. D., Soler, F. J. P., Solomin, A., Solovev, A., Solovyev, I., Song, R., Song, Y., Song, Y. S., De Almeida, F. L. Souza, De Paula, B. Souza, Norella, E. Spadaro, Spedicato, E., Speer, J. G., Spiridenkov, E., Spradlin, P., Sriskaran, V., Stagni, F., Stahl, M., Stahl, S., Stanislaus, S., Stein, E. N., Steinkamp, O., Stenyakin, O., Stevens, H., Strekalina, D., Su, Y., Suljik, F., Sun, J., Sun, L., Sun, Y., Sutcliffe, W., Swallow, P. N., Swystun, F., Szabelski, A., Szumlak, T., Tan, Y., Taneja, S., Tat, M. D., Terentev, A., Terzuoli, F., Teubert, F., Thomas, E., Thompson, D. J. D., Tilquin, H., Tisserand, V., T'Jampens, S., Tobin, M., Tomassetti, L., Tonani, G., Tong, X., Machado, D. Torres, Toscano, L., Tou, D. Y., Trippl, C., Tuci, G., Tuning, N., Uecker, L. H., Ukleja, A., Unverzagt, D. J., Ursov, E., Usachov, A., Ustyuzhanin, A., Uwer, U., Vagnoni, V., Valassi, A., Valenti, G., Canudas, N. Valls, Van Hecke, H., van Herwijnen, E., Van Hulse, C. B., Van Laak, R., van Veghel, M., Gomez, R. Vazquez, Regueiro, P. Vazquez, Sierra, C. Vázquez, Vecchi, S., Velthuis, J. J., Veltri, M., Venkateswaran, A., Vesterinen, M., Diaz, M. Vieites, Vilasis-Cardona, X., Figueras, E. Vilella, Villa, A., Vincent, P., Volle, F. C., Bruch, D. vom, Vorobyev, V., Voropaev, N., Vos, K., Vouters, G., Vrahas, C., Wagner, J., Walsh, J., Walton, E. J., Wan, G., Wang, C., Wang, G., Wang, J., Wang, M., Wang, N. W., Wang, R., Wang, X., Wang, X. W., Wang, Y., Wang, Z., Ward, J. A., Waterlaat, M., Watson, N. K., Websdale, D., Wei, Y., Westhenry, B. D. C., White, D. J., Whitehead, M., Wiederhold, A. R., Wiedner, D., Wilkinson, G., Wilkinson, M. K., Williams, M., Williams, M. R. J., Williams, R., Wilson, F. F., Wislicki, W., Witek, M., Witola, L., Wong, C. P., Wormser, G., Wotton, S. A., Wu, H., Wu, J., Wu, Y., Wyllie, K., Xian, S., Xiang, Z., Xie, Y., Xu, A., Xu, J., Xu, L., Xu, M., Xu, Z., Yang, D., Yang, S., Yang, X., Yang, Y., Yang, Z., Yeroshenko, V., Yeung, H., Yin, H., Yu, C. Y., Yu, J., Yuan, X., Zaffaroni, E., Zavertyaev, M., Zdybal, M., Zeng, M., Zhang, C., Zhang, D., Zhang, J., Zhang, L., Zhang, S., Zhang, Y., Zhang, Y. Z., Zhao, Y., Zharkova, A., Zhelezov, A., Zheng, X. Z., Zheng, Y., Zhou, T., Zhou, X., Zhou, Y., Zhovkovska, V., Zhu, L. Z., Zhu, X., Zhukov, V., Zhuo, J., Zou, Q., Zuliani, D., and Zunica, G.
Subjects: High Energy Physics - Experiment
Abstract: The first study of $J/\psi\phi$ production in diffractive processes in proton-proton collisions is presented. The study is based on an LHCb dataset recorded at centre-of-mass energy of 13 TeV, corresponding to an integrated luminosity of 5 fb$^{-1}$. The data disfavour a nonresonant $J/\psi\phi$ production but are consistent with a resonant model including several resonant states observed previously only in $B^+ \to J/\psi\phi K^+$ decays. The $\chi_{c0}(4500)$ state is observed with a significance over $5\sigma$ and the $\chi_{c1}(4274)$ is confirmed with a significance of more than $4\sigma$., Comment: All figures and tables, along with any supplementary material and additional information, are available at: https://lhcbproject.web.cern.ch/Publications/LHCbProjectPublic/LHCb-PAPER-2023-043.html (LHCb public pages)
Published: 2024

219. Study of charmonium production via the decay to $p\bar{p}$ at $\sqrt{s} = 13 TeV$

Author: LHCb collaboration, Aaij, R., Abdelmotteleb, A. S. W., Beteta, C. Abellan, Abudinén, F., Ackernley, T., Adefisoye, A. A., Adeva, B., Adinolfi, M., Adlarson, P., Agapopoulou, C., Aidala, C. A., Ajaltouni, Z., Akar, S., Akiba, K., Albicocco, P., Albrecht, J., Alessio, F., Alexander, M., Aliouche, Z., Cartelle, P. Alvarez, Amalric, R., Amato, S., Amey, J. L., Amhis, Y., An, L., Anderlini, L., Andersson, M., Andreianov, A., Andreola, P., Andreotti, M., Andreou, D., Anelli, A., Ao, D., Archilli, F., Argenton, M., Cuendis, S. Arguedas, Artamonov, A., Artuso, M., Aslanides, E., Atzeni, M., Audurier, B., Bacher, D., Perea, I. Bachiller, Bachmann, S., Bachmayer, M., Back, J. J., Rodriguez, P. Baladron, Balagura, V., Baldini, W., Bao, H., Leite, J. Baptista de Souza, Barbetti, M., Barbosa, I. R., Barlow, R. J., Barnyakov, M., Barsuk, S., Barter, W., Bartolini, M., Bartz, J., Baryshnikov, F., Basels, J. M., Bassi, G., Batsukh, B., Bay, A., Beck, A., Becker, M., Bedeschi, F., Bediaga, I. B., Belin, S., Bellee, V., Belous, K., Belov, I., Belyaev, I., Benane, G., Bencivenni, G., Ben-Haim, E., Berezhnoy, A., Bernet, R., Andres, S. Bernet, Bertolin, A., Betancourt, C., Betti, F., Bex, J., Bezshyiko, Ia., Bhom, J., Bieker, M. S., Biesuz, N. V., Billoir, P., Biolchini, A., Birch, M., Bishop, F. C. R., Bitadze, A., Bizzeti, A., Blake, T., Blanc, F., Blank, J. E., Blusk, S., Bocharnikov, V., Boelhauve, J. A., Garcia, O. Boente, Boettcher, T., Bohare, A., Boldyrev, A., Bolognani, C. S., Bolzonella, R., Bondar, N., Borgato, F., Borghi, S., Borsato, M., Borsuk, J. T., Bouchiba, S. A., Bowcock, T. J. V., Boyer, A., Bozzi, C., Bradley, M. J., Rodriguez, A. Brea, Breer, N., Brodzicka, J., Gonzalo, A. Brossa, Brown, J., Brundu, D., Buchanan, E., Buonaura, A., Buonincontri, L., Burke, A. T., Burr, C., Butkevich, A., Butter, J. S., Buytaert, J., Byczynski, W., Cadeddu, S., Cai, H., Calabrese, R., Ramirez, S. Calderon, Calefice, L., Cali, S., Calvi, M., Gomez, M. Calvo, Magalhaes, P. Camargo, Bouzas, J. I. Cambon, Campana, P., Perez, D. H. Campora, Quezada, A. F. Campoverde, Capelli, S., Capriotti, L., Caravaca-Mora, R., Carbone, A., Salgado, L. Carcedo, Cardinale, R., Cardini, A., Carniti, P., Carus, L., Vidal, A. Casais, Caspary, R., Casse, G., Godinez, J. Castro, Cattaneo, M., Cavallero, G., Cavallini, V., Celani, S., Cervenkov, D., Cesare, S., Chadwick, A. J., Chahrour, I., Charles, M., Charpentier, Ph., Barajas, C. A. Chavez, Chefdeville, M., Chen, C., Chen, S., Chen, Z., Chernov, A., Chernyshenko, S., Chobanova, V., Cholak, S., Chrzaszcz, M., Chubykin, A., Chulikov, V., Ciambrone, P., Vidal, X. Cid, Ciezarek, G., Cifra, P., Clarke, P. E. L., Clemencic, M., Cliff, H. V., Closier, J., Toapaxi, C. Cocha, Coco, V., Cogan, J., Cogneras, E., Cojocariu, L., Collins, P., Colombo, T., Comerma-Montells, A., Congedo, L., Contu, A., Cooke, N., Corredoira, I., Correia, A., Corti, G., Meldrum, J. J. Cottee, Couturier, B., Craik, D. C., Torres, M. Cruz, Rivera, E. Curras, Currie, R., Da Silva, C. L., Dadabaev, S., Dai, L., Dai, X., Dall'Occo, E., Dalseno, J., D'Ambrosio, C., Daniel, J., Danilina, A., d'Argent, P., Davidson, A., Davies, J. E., Davis, A., Francisco, O. De Aguiar, De Angelis, C., De Benedetti, F., de Boer, J., De Bruyn, K., De Capua, S., De Cian, M., Da Graca, U. De Freitas Carneiro, De Lucia, E., De Miranda, J. M., De Paula, L., De Serio, M., De Simone, P., De Vellis, F., de Vries, J. A., Debernardis, F., Decamp, D., Dedu, V., Del Buono, L., Delaney, B., Dembinski, H. -P., Deng, J., Denysenko, V., Deschamps, O., Dettori, F., Dey, B., Di Nezza, P., Diachkov, I., Didenko, S., Ding, S., Dittmann, L., Dobishuk, V., Docheva, A. D., Dong, C., Donohoe, A. M., Dordei, F., Reis, A. C. dos, Dowling, A. D., Duan, W., Duda, P., Dudek, M. W., Dufour, L., Duk, V., Durante, P., Duras, M. M., Durham, J. M., Durmus, O. D., Dziurda, A., Dzyuba, A., Easo, S., Eckstein, E., Egede, U., Egorychev, A., Egorychev, V., Eisenhardt, S., Ejopu, E., Eklund, L., Elashri, M., Ellbracht, J., Ely, S., Ene, A., Epple, E., Eschle, J., Esen, S., Evans, T., Fabiano, F., Falcao, L. N., Fan, Y., Fang, B., Fantini, L., Faria, M., Farmer, K., Fazzini, D., Felkowski, L., Feng, M., Feo, M., Gomez, M. Fernandez, Fernez, A. D., Ferrari, F., Rodrigues, F. Ferreira, Ferrillo, M., Ferro-Luzzi, M., Filippov, S., Fini, R. A., Fiorini, M., Fischer, K. M., Fitzgerald, D. S., Fitzpatrick, C., Fleuret, F., Fontana, M., Foreman, L. F., Forty, R., Foulds-Holt, D., Sevilla, M. Franco, Frank, M., Franzoso, E., Frau, G., Frei, C., Friday, D. A., Fu, J., Fuehring, Q., Fujii, Y., Fulghesu, T., Gabriel, E., Galati, G., Galati, M. D., Torreira, A. Gallas, Galli, D., Gambetta, S., Gandelman, M., Gandini, P., Ganie, B., Gao, H., Gao, R., Gao, Y., Garau, M., Martin, L. M. Garcia, Moreno, P. Garcia, Pardiñas, J. García, Garg, K. G., Garrido, L., Gaspar, C., Geertsema, R. E., Gerken, L. L., Gersabeck, E., Gersabeck, M., Gershon, T., Ghorbanimoghaddam, Z., Giambastiani, L., Giasemis, F. I., Gibson, V., Giemza, H. K., Gilman, A. L., Giovannetti, M., Gioventù, A., Gironell, P. Gironella, Giugliano, C., Giza, M. A., Gkougkousis, E. L., Glaser, F. C., Gligorov, V. V., Göbel, C., Golobardes, E., Golubkov, D., Golutvin, A., Gomes, A., Fernandez, S. Gomez, Abrantes, F. Goncalves, Goncerz, M., Gong, G., Gooding, J. A., Gorelov, I. V., Gotti, C., Grabowski, J. P., Cardoso, L. A. Granado, Graugés, E., Graverini, E., Grazette, L., Graziani, G., Grecu, A. T., Greeven, L. M., Grieser, N. A., Grillo, L., Gromov, S., Gu, C., Guarise, M., Guittiere, M., Guliaeva, V., Günther, P. A., Guseinov, A. -K., Gushchin, E., Guz, Y., Gys, T., Habermann, K., Hadavizadeh, T., Hadjivasiliou, C., Haefeli, G., Haen, C., Haimberger, J., Hajheidari, M., Halvorsen, M. M., Hamilton, P. M., Hammerich, J., Han, Q., Han, X., Hansmann-Menzemer, S., Hao, L., Harnew, N., Hartmann, M., He, J., Hemmer, F., Henderson, C., Henderson, R. D. L., Hennequin, A. M., Hennessy, K., Henry, L., Herd, J., Gascon, P. Herrero, Heuel, J., Hicheur, A., Mendizabal, G. Hijano, Hill, D., Hollitt, S. E., Horswill, J., Hou, R., Hou, Y., Howarth, N., Hu, J., Hu, W., Hu, X., Huang, W., Hulsbergen, W., Hunter, R. J., Hushchyn, M., Hutchcroft, D., Ilin, D., Ilten, P., Inglessi, A., Iniukhin, A., Ishteev, A., Ivshin, K., Jacobsson, R., Jage, H., Elles, S. J. Jaimes, Jakobsen, S., Jans, E., Jashal, B. K., Jawahery, A., Jevtic, V., Jiang, E., Jiang, X., Jiang, Y., Jiang, Y. J., John, M., Johnson, D., Jones, C. R., Jones, T. P., Joshi, S., Jost, B., Jurik, N., Juszczak, I., Kaminaris, D., Kandybei, S., Kang, Y., Kar, C., Karacson, M., Karpenkov, D., Kauniskangas, A., Kautz, J. W., Keizer, F., Kenzie, M., Ketel, T., Khanji, B., Kharisova, A., Kholodenko, S., Khreich, G., Kirn, T., Kirsebom, V. S., Kitouni, O., Klaver, S., Kleijne, N., Klimaszewski, K., Kmiec, M. R., Koliiev, S., Kolk, L., Konoplyannikov, A., Kopciewicz, P., Koppenburg, P., Korolev, M., Kostiuk, I., Kot, O., Kotriakhova, S., Kozachuk, A., Kravchenko, P., Kravchuk, L., Kreps, M., Krokovny, P., Krupa, W., Krzemien, W., Kshyvanskyi, O. K., Kubat, J., Kubis, S., Kucharczyk, M., Kudryavtsev, V., Kulikova, E., Kupsc, A., Kutsenko, B. K., Lacarrere, D., Lai, A., Lampis, A., Lancierini, D., Gomez, C. Landesa, Lane, J. J., Lane, R., Langenbruch, C., Langer, J., Lantwin, O., Latham, T., Lazzari, F., Lazzeroni, C., Gac, R. Le, Lefèvre, R., Leflat, A., Legotin, S., Lehuraux, M., Cid, E. Lemos, Leroy, O., Lesiak, T., Leverington, B., Li, A., Li, H., Li, K., Li, L., Li, P., Li, P. -R., Li, Q., Li, S., Li, T., Li, Y., Lian, Z., Liang, X., Libralon, S., Lin, C., Lin, T., Lindner, R., Lisovskyi, V., Litvinov, R., Liu, F. L., Liu, G., Liu, K., Liu, S., Liu, Y., Liu, Y. L., Salvia, A. Lobo, Loi, A., Castro, J. Lomba, Long, T., Lopes, J. H., Huertas, A. Lopez, Soliño, S. López, Lucarelli, C., Lucchesi, D., Martinez, M. Lucio, Lukashenko, V., Luo, Y., Lupato, A., Luppi, E., Lynch, K., Lyu, X. -R., Ma, G. M., Ma, R., Maccolini, S., Machefert, F., Maciuc, F., Mack, B., Mackay, I., Mackey, L. M., Mohan, L. R. Madhan, Madurai, M. M., Maevskiy, A., Magdalinski, D., Maisuzenko, D., Majewski, M. W., Malczewski, J. J., Malde, S., Malentacca, L., Malinin, A., Maltsev, T., Manca, G., Mancinelli, G., Mancuso, C., Escalero, R. Manera, Manuzzi, D., Marangotto, D., Marchand, J. F., Marchevski, R., Marconi, U., Mariani, S., Benito, C. Marin, Marks, J., Marshall, A. M., Martelli, G., Martellotti, G., Martinazzoli, L., Martinelli, M., Santos, D. Martinez, Vidal, F. Martinez, Massafferri, A., Matev, R., Mathad, A., Matiunin, V., Matteuzzi, C., Mattioli, K. R., Mauri, A., Maurice, E., Mauricio, J., Mayencourt, P., Mazurek, M., McCann, M., Mcconnell, L., McGrath, T. H., McHugh, N. T., McNab, A., McNulty, R., Meadows, B., Meier, G., Melnychuk, D., Meng, F. M., Merk, M., Merli, A., Garcia, L. Meyer, Miao, D., Miao, H., Mikhasenko, M., Milanes, D. A., Minotti, A., Minucci, E., Miralles, T., Mitreska, B., Mitzel, D. S., Modak, A., Mödden, A., Mohammed, R. A., Moise, R. D., Mokhnenko, S., Mombächer, T., Monk, M., Monteil, S., Gomez, A. Morcillo, Morello, G., Morello, M. J., Morgenthaler, M. P., Morris, A. B., Morris, A. G., Mountain, R., Mu, H., Mu, Z. M., Muhammad, E., Muheim, F., Mulder, M., Müller, K., Muñoz-Rojas, F., Murta, R., Naik, P., Nakada, T., Nandakumar, R., Nanut, T., Nasteva, I., Needham, M., Neri, N., Neubert, S., Neufeld, N., Neustroev, P., Nicolini, J., Nicotra, D., Niel, E. M., Nikitin, N., Nogarolli, P., Nogga, P., Nolte, N. S., Normand, C., Fernandez, J. Novoa, Nowak, G., Nunez, C., Nur, H. N., Oblakowska-Mucha, A., Obraztsov, V., Oeser, T., Okamura, S., Okhotnikov, A., Okhrimenko, O., Oldeman, R., Oliva, F., Olocco, M., Onderwater, C. J. G., O'Neil, R. H., Goicochea, J. M. Otalora, Owen, P., Oyanguren, A., Ozcelik, O., Padeken, K. O., Pagare, B., Pais, P. R., Pajero, T., Palano, A., Palutan, M., Panshin, G., Paolucci, L., Papanestis, A., Pappagallo, M., Pappalardo, L. L., Pappenheimer, C., Parkes, C., Passalacqua, B., Passaleva, G., Passaro, D., Pastore, A., Patel, M., Patoc, J., Patrignani, C., Paul, A., Pawley, C. J., Pellegrino, A., Peng, J., Altarelli, M. Pepe, Perazzini, S., Pereima, D., Castro, A. Pereiro, Perret, P., Perro, A., Petridis, K., Petrolini, A., Pfaller, J. P., Pham, H., Pica, L., Piccini, M., Pietrzyk, B., Pietrzyk, G., Pinci, D., Pisani, F., Pizzichemi, M., Placinta, V., Casasus, M. Plo, Polci, F., Lener, M. Poli, Poluektov, A., Polukhina, N., Polyakov, I., Polycarpo, E., Ponce, S., Popov, D., Poslavskii, S., Prasanth, K., Prouve, C., Pugatch, V., Punzi, G., Qasim, S., Qian, W., Qin, N., Qu, S., Quagliani, R., Trejo, R. I. Rabadan, Rademacker, J. H., Rama, M., García, M. Ramírez, Pernas, M. Ramos, Rangel, M. S., Ratnikov, F., Raven, G., De Miguel, M. Rebollo, Redi, F., Reich, J., Reiss, F., Ren, Z., Resmi, P. K., Ribatti, R., Ricart, G. R., Riccardi, D., Ricciardi, S., Richardson, K., Richardson-Slipper, M., Rinnert, K., Robbe, P., Robertson, G., Rodrigues, E., Fernandez, E. Rodriguez, Lopez, J. A. Rodriguez, Rodriguez, E. Rodriguez, Rogovskiy, A., Rolf, D. L., Roloff, P., Romanovskiy, V., Lamas, M. Romero, Vidal, A. Romero, Romolini, G., Ronchetti, F., Rotondo, M., Roy, S. R., Rudolph, M. S., Ruf, T., Diaz, M. Ruiz, Fernandez, R. A. Ruiz, Vidal, J. Ruiz, Ryzhikov, A., Ryzka, J., Saavedra-Arias, J. J., Silva, J. J. Saborido, Sadek, R., Sagidova, N., Sahoo, D., Sahoo, N., Saitta, B., Salomoni, M., Gras, C. Sanchez, Sanderswood, I., Santacesaria, R., Rios, C. Santamarina, Santimaria, M., Santoro, L., Santovetti, E., Saputi, A., Saranin, D., Sarpis, G., Sarpis, M., Satriano, C., Satta, A., Saur, M., Savrina, D., Sazak, H., Smead, L. G. Scantlebury, Scarabotto, A., Schael, S., Scherl, S., Schiller, M., Schindler, H., Schmelling, M., Schmidt, B., Schmitt, S., Schmitz, H., Schneider, O., Schopper, A., Schulte, N., Schulte, S., Schune, M. H., Schwemmer, R., Schwering, G., Sciascia, B., Sciuccati, A., Sellam, S., Semennikov, A., Senger, T., Soares, M. Senghi, Sergi, A., Serra, N., Sestini, L., Seuthe, A., Shang, Y., Shangase, D. M., Shapkin, M., Sharma, R. S., Shchemerov, I., Shchutska, L., Shears, T., Shekhtman, L., Shen, Z., Sheng, S., Shevchenko, V., Shi, B., Shi, Q., Shields, E. B., Shimizu, Y., Shmanin, E., Shorkin, R., Shupperd, J. D., Coutinho, R. Silva, Simi, G., Simone, S., Skidmore, N., Skwarnicki, T., Slater, M. W., Smallwood, J. C., Smith, E., Smith, K., Smith, M., Snoch, A., Lavra, L. Soares, Sokoloff, M. D., Soler, F. J. P., Solomin, A., Solovev, A., Solovyev, I., Song, R., Song, Y., Song, Y. S., De Almeida, F. L. Souza, De Paula, B. Souza, Norella, E. Spadaro, Spedicato, E., Speer, J. G., Spiridenkov, E., Spradlin, P., Sriskaran, V., Stagni, F., Stahl, M., Stahl, S., Stanislaus, S., Stein, E. N., Steinkamp, O., Stenyakin, O., Stevens, H., Strekalina, D., Su, Y., Suljik, F., Sun, J., Sun, L., Sun, Y., Sundfeld, D., Sutcliffe, W., Swallow, P. N., Swystun, F., Szabelski, A., Szumlak, T., Tan, Y., Tat, M. D., Terentev, A., Terzuoli, F., Teubert, F., Thomas, E., Thompson, D. J. D., Tilquin, H., Tisserand, V., T'Jampens, S., Tobin, M., Tomassetti, L., Tonani, G., Tong, X., Machado, D. Torres, Toscano, L., Tou, D. Y., Trippl, C., Tuci, G., Tuning, N., Uecker, L. H., Ukleja, A., Unverzagt, D. J., Ursov, E., Usachov, A., Ustyuzhanin, A., Uwer, U., Vagnoni, V., Valassi, A., Valenti, G., Canudas, N. Valls, Van Hecke, H., van Herwijnen, E., Van Hulse, C. B., Van Laak, R., van Veghel, M., Vasquez, G., Gomez, R. Vazquez, Regueiro, P. Vazquez, Sierra, C. Vázquez, Vecchi, S., Velthuis, J. J., Veltri, M., Venkateswaran, A., Vesterinen, M., Diaz, M. Vieites, Vilasis-Cardona, X., Figueras, E. Vilella, Villa, A., Vincent, P., Volle, F. C., Bruch, D. vom, Voropaev, N., Vos, K., Vouters, G., Vrahas, C., Wagner, J., Walsh, J., Walton, E. J., Wan, G., Wang, C., Wang, G., Wang, J., Wang, M., Wang, N. W., Wang, R., Wang, X., Wang, X. W., Wang, Z., Ward, J. A., Waterlaat, M., Watson, N. K., Websdale, D., Wei, Y., Wendel, J., Westhenry, B. D. C., White, D. J., Whitehead, M., Wiederhold, A. R., Wiedner, D., Wilkinson, G., Wilkinson, M. K., Williams, M., Williams, M. R. J., Williams, R., Wilson, F. F., Wislicki, W., Witek, M., Witola, L., Wong, C. P., Wormser, G., Wotton, S. A., Wu, H., Wu, J., Wu, Y., Wu, Z., Wyllie, K., Xian, S., Xiang, Z., Xie, Y., Xu, A., Xu, J., Xu, L., Xu, M., Xu, Z., Yang, D., Yang, S., Yang, X., Yang, Y., Yang, Z., Yeroshenko, V., Yeung, H., Yin, H., Yu, C. Y., Yu, J., Yuan, X., Zaffaroni, E., Zavertyaev, M., Zdybal, M., Zeng, C., Zeng, M., Zhang, C., Zhang, D., Zhang, J., Zhang, L., Zhang, S., Zhang, Y., Zhang, Y. Z., Zhao, Y., Zharkova, A., Zhelezov, A., Zheng, X. Z., Zheng, Y., Zhou, T., Zhou, X., Zhou, Y., Zhovkovska, V., Zhu, L. Z., Zhu, X., Zhukov, V., Zhuo, J., Zou, Q., Zuliani, D., and Zunica, G.
Subjects: High Energy Physics - Experiment
Abstract: Charmonium production cross-section in proton-proton collisions is measured at the centre-of-mass energy $\sqrt{s}=13\,TeV$ using decays to $p\bar{p}$ final state. The study is performed using a data sample corresponding to an integrated luminosity of $2.2\,{fb}^{-1}$ collected in 2018 with the $LHCb$ detector. The production cross-section of the $\eta_c$ meson is measured in a rapidity range of $2.0 < y < 4.0$ and in a transverse momentum range of $5.0 < p_{T} < 20.0\,{GeV/\it{c}}$, which is extended compared with previous $LHCb$ analyses. The differential cross-section is measured in bins of $p_{T}$ and, for the first time, of $y$. Upper limits, at 90% and 95% confidence levels, on the $\eta_c(2S)$ and $h_c(1P)$ prompt production cross-sections are determined for the first time., Comment: All figures and tables, along with any supplementary material and additional information, are available at https://cern.ch/lhcbproject/Publications/p/LHCb-PAPER-2024-004.html (LHCb public pages)
Published: 2024

220. Amplitude analysis of $B^+ \to \psi(2S) K^+ \pi^+ \pi^-$ decays

Author: LHCb collaboration, Aaij, R., Abdelmotteleb, A. S. W., Beteta, C. Abellan, Abudinén, F., Ackernley, T., Adefisoye, A. A., Adeva, B., Adinolfi, M., Adlarson, P., Agapopoulou, C., Aidala, C. A., Ajaltouni, Z., Akar, S., Akiba, K., Albicocco, P., Albrecht, J., Alessio, F., Alexander, M., Aliouche, Z., Cartelle, P. Alvarez, Amalric, R., Amato, S., Amey, J. L., Amhis, Y., An, L., Anderlini, L., Andersson, M., Andreianov, A., Andreola, P., Andreotti, M., Andreou, D., Anelli, A., Ao, D., Archilli, F., Argenton, M., Cuendis, S. Arguedas, Artamonov, A., Artuso, M., Aslanides, E., Da Silva, R. Ataide, Atzeni, M., Audurier, B., Bacher, D., Perea, I. Bachiller, Bachmann, S., Bachmayer, M., Back, J. J., Rodriguez, P. Baladron, Balagura, V., Baldini, W., Balzani, L., Bao, H., Leite, J. Baptista de Souza, Pretel, C. Barbero, Barbetti, M., Barbosa, I. R., Barlow, R. J., Barnyakov, M., Barsuk, S., Barter, W., Bartolini, M., Bartz, J., Basels, J. M., Bashir, S., Bassi, G., Batsukh, B., Battista, P. B., Bay, A., Beck, A., Becker, M., Bedeschi, F., Bediaga, I. B., Behling, N. B., Belin, S., Bellee, V., Belous, K., Belov, I., Benane, G., Bencivenni, G., Ben-Haim, E., Berezhnoy, A., Bernet, R., Andres, S. Bernet, Bertolin, A., Betancourt, C., Betti, F., Bex, J., Bezshyiko, Ia., Bhom, J., Bieker, M. S., Biesuz, N. V., Billoir, P., Biolchini, A., Birch, M., Bishop, F. C. R., Bitadze, A., Bizzeti, A., Blake, T., Blanc, F., Blank, J. E., Blusk, S., Bocharnikov, V., Boelhauve, J. A., Garcia, O. Boente, Boettcher, T., Bohare, A., Boldyrev, A., Bolognani, C. S., Bolzonella, R., Bondar, N., Borgato, F., Borghi, S., Borsato, M., Borsuk, J. T., Bouchiba, S. A., Bovill, M., Bowcock, T. J. V., Boyer, A., Bozzi, C., Rodriguez, A. Brea, Breer, N., Brodzicka, J., Gonzalo, A. Brossa, Brown, J., Brundu, D., Buchanan, E., Buonaura, A., Buonincontri, L., Burke, A. T., Burr, C., Butkevich, A., Butter, J. S., Buytaert, J., Byczynski, W., Cadeddu, S., Cai, H., Caillet, A. C., Calabrese, R., Ramirez, S. Calderon, Calefice, L., Cali, S., Calvi, M., Gomez, M. Calvo, Magalhaes, P. Camargo, Bouzas, J. I. Cambon, Campana, P., Perez, D. H. Campora, Quezada, A. F. Campoverde, Capelli, S., Capriotti, L., Caravaca-Mora, R., Carbone, A., Salgado, L. Carcedo, Cardinale, R., Cardini, A., Carniti, P., Carus, L., Vidal, A. Casais, Caspary, R., Casse, G., Godinez, J. Castro, Cattaneo, M., Cavallero, G., Cavallini, V., Celani, S., Cervenkov, D., Cesare, S., Chadwick, A. J., Chahrour, I., Charles, M., Charpentier, Ph., Chatzianagnostou, E., Barajas, C. A. Chavez, Chefdeville, M., Chen, C., Chen, S., Chen, Z., Chernov, A., Chernyshenko, S., Chiotopoulos, X., Chobanova, V., Cholak, S., Chrzaszcz, M., Chubykin, A., Chulikov, V., Ciambrone, P., Vidal, X. Cid, Ciezarek, G., Cifra, P., Clarke, P. E. L., Clemencic, M., Cliff, H. V., Closier, J., Toapaxi, C. Cocha, Coco, V., Cogan, J., Cogneras, E., Cojocariu, L., Collins, P., Colombo, T., Colonna, M. C., Comerma-Montells, A., Congedo, L., Contu, A., Cooke, N., Corredoira, I., Correia, A., Corti, G., Meldrum, J. J. Cottee, Couturier, B., Craik, D. C., Torres, M. Cruz, Rivera, E. Curras, Currie, R., Da Silva, C. L., Dadabaev, S., Dai, L., Dai, X., Dall'Occo, E., Dalseno, J., D'Ambrosio, C., Daniel, J., Danilina, A., d'Argent, P., Davidson, A., Davies, J. E., Davis, A., Francisco, O. De Aguiar, De Angelis, C., De Benedetti, F., de Boer, J., De Bruyn, K., De Capua, S., De Cian, M., Da Graca, U. De Freitas Carneiro, De Lucia, E., De Miranda, J. M., De Paula, L., De Serio, M., De Simone, P., De Vellis, F., de Vries, J. A., Debernardis, F., Decamp, D., Dedu, V., Del Buono, L., Delaney, B., Dembinski, H. -P., Deng, J., Denysenko, V., Deschamps, O., Dettori, F., Dey, B., Di Nezza, P., Diachkov, I., Didenko, S., Ding, S., Dittmann, L., Dobishuk, V., Docheva, A. D., Dong, C., Donohoe, A. M., Dordei, F., Reis, A. C. dos, Dowling, A. D., Duan, W., Duda, P., Dudek, M. W., Dufour, L., Duk, V., Durante, P., Duras, M. M., Durham, J. M., Durmus, O. D., Dziurda, A., Dzyuba, A., Easo, S., Eckstein, E., Egede, U., Egorychev, A., Egorychev, V., Eisenhardt, S., Ejopu, E., Eklund, L., Elashri, M., Ellbracht, J., Ely, S., Ene, A., Epple, E., Eschle, J., Esen, S., Evans, T., Fabiano, F., Falcao, L. N., Fan, Y., Fang, B., Fantini, L., Faria, M., Farmer, K., Fazzini, D., Felkowski, L., Feng, M., Feo, M., Casani, A. Fernandez, Gomez, M. Fernandez, Fernez, A. D., Ferrari, F., Rodrigues, F. Ferreira, Ferrillo, M., Ferro-Luzzi, M., Filippov, S., Fini, R. A., Fiorini, M., Fischer, K. M., Fitzgerald, D. S., Fitzpatrick, C., Fleuret, F., Fontana, M., Foreman, L. F., Forty, R., Foulds-Holt, D., Sevilla, M. Franco, Frank, M., Franzoso, E., Frau, G., Frei, C., Friday, D. A., Fu, J., Fuehring, Q., Fujii, Y., Fulghesu, T., Gabriel, E., Galati, G., Galati, M. D., Torreira, A. Gallas, Galli, D., Gambetta, S., Gandelman, M., Gandini, P., Ganie, B., Gao, H., Gao, R., Gao, Y., Garau, M., Martin, L. M. Garcia, Moreno, P. Garcia, Pardiñas, J. García, Garg, K. G., Garrido, L., Gaspar, C., Geertsema, R. E., Gerken, L. L., Gersabeck, E., Gersabeck, M., Gershon, T., Ghorbanimoghaddam, Z., Giambastiani, L., Giasemis, F. I., Gibson, V., Giemza, H. K., Gilman, A. L., Giovannetti, M., Gioventù, A., Girardey, L., Gironell, P. Gironella, Giugliano, C., Giza, M. A., Gkougkousis, E. L., Glaser, F. C., Gligorov, V. V., Göbel, C., Golobardes, E., Golubkov, D., Golutvin, A., Gomes, A., Fernandez, S. Gomez, Abrantes, F. Goncalves, Goncerz, M., Gong, G., Gooding, J. A., Gorelov, I. V., Gotti, C., Grabowski, J. P., Cardoso, L. A. Granado, Graugés, E., Graverini, E., Grazette, L., Graziani, G., Grecu, A. T., Greeven, L. M., Grieser, N. A., Grillo, L., Gromov, S., Gu, C., Guarise, M., Guittiere, M., Guliaeva, V., Günther, P. A., Guseinov, A. -K., Gushchin, E., Guz, Y., Gys, T., Habermann, K., Hadavizadeh, T., Hadjivasiliou, C., Haefeli, G., Haen, C., Haimberger, J., Hajheidari, M., Hallett, G. H., Halvorsen, M. M., Hamilton, P. M., Hammerich, J., Han, Q., Han, X., Hansmann-Menzemer, S., Hao, L., Harnew, N., Hartmann, M., Hashmi, S., He, J., Hemmer, F., Henderson, C., Henderson, R. D. L., Hennequin, A. M., Hennessy, K., Henry, L., Herd, J., Gascon, P. Herrero, Heuel, J., Hicheur, A., Mendizabal, G. Hijano, Hill, D., Hollitt, S. E., Horswill, J., Hou, R., Hou, Y., Howarth, N., Hu, J., Hu, W., Hu, X., Huang, W., Hulsbergen, W., Hunter, R. J., Hushchyn, M., Hutchcroft, D., Ilin, D., Ilten, P., Inglessi, A., Iniukhin, A., Ishteev, A., Ivshin, K., Jacobsson, R., Jage, H., Elles, S. J. Jaimes, Jakobsen, S., Jans, E., Jashal, B. K., Jawahery, A., Jevtic, V., Jiang, E., Jiang, X., Jiang, Y., Jiang, Y. J., John, M., Rajan, A. John Rubesh, Johnson, D., Jones, C. R., Jones, T. P., Joshi, S., Jost, B., Castella, J. Juan, Jurik, N., Juszczak, I., Kaminaris, D., Kandybei, S., Kane, M., Kang, Y., Kar, C., Karacson, M., Karpenkov, D., Kauniskangas, A., Kautz, J. W., Keizer, F., Kenzie, M., Ketel, T., Khanji, B., Kharisova, A., Kholodenko, S., Khreich, G., Kirn, T., Kirsebom, V. S., Kitouni, O., Klaver, S., Kleijne, N., Klimaszewski, K., Kmiec, M. R., Koliiev, S., Kolk, L., Konoplyannikov, A., Kopciewicz, P., Koppenburg, P., Korolev, M., Kostiuk, I., Kot, O., Kotriakhova, S., Kozachuk, A., Kravchenko, P., Kravchuk, L., Kreps, M., Krokovny, P., Krupa, W., Krzemien, W., Kshyvanskyi, O. K., Kubat, J., Kubis, S., Kucharczyk, M., Kudryavtsev, V., Kulikova, E., Kupsc, A., Kutsenko, B. K., Lacarrere, D., Lai, A., Lampis, A., Lancierini, D., Gomez, C. Landesa, Lane, J. J., Lane, R., Langenbruch, C., Langer, J., Lantwin, O., Latham, T., Lazzari, F., Lazzeroni, C., Gac, R. Le, Lee, H., Lefèvre, R., Leflat, A., Legotin, S., Lehuraux, M., Cid, E. Lemos, Leroy, O., Lesiak, T., Leverington, B., Li, A., Li, C., Li, H., Li, K., Li, L., Li, P., Li, P. -R., Li, Q., Li, S., Li, T., Li, Y., Lian, Z., Liang, X., Libralon, S., Lin, C., Lin, T., Lindner, R., Lisovskyi, V., Litvinov, R., Liu, F. L., Liu, G., Liu, K., Liu, S., Liu, W., Liu, Y., Liu, Y. L., Salvia, A. Lobo, Loi, A., Castro, J. Lomba, Long, T., Lopes, J. H., Huertas, A. Lopez, Soliño, S. López, Lucarelli, C., Lucchesi, D., Martinez, M. Lucio, Lukashenko, V., Luo, Y., Lupato, A., Luppi, E., Lynch, K., Lyu, X. -R., Ma, G. M., Ma, R., Maccolini, S., Machefert, F., Maciuc, F., Mack, B., Mackay, I., Mackey, L. M., Mohan, L. R. Madhan, Madurai, M. M., Maevskiy, A., Magdalinski, D., Maisuzenko, D., Majewski, M. W., Malczewski, J. J., Malde, S., Malentacca, L., Malinin, A., Maltsev, T., Manca, G., Mancinelli, G., Mancuso, C., Escalero, R. Manera, Manuzzi, D., Marangotto, D., Marchand, J. F., Marchevski, R., Marconi, U., Mariani, S., Benito, C. Marin, Marks, J., Marshall, A. M., Martel, L., Martelli, G., Martellotti, G., Martinazzoli, L., Martinelli, M., Santos, D. Martinez, Vidal, F. Martinez, Massafferri, A., Matev, R., Mathad, A., Matiunin, V., Matteuzzi, C., Mattioli, K. R., Mauri, A., Maurice, E., Mauricio, J., Mayencourt, P., de Cos, J. Mazorra, Mazurek, M., McCann, M., Mcconnell, L., McGrath, T. H., McHugh, N. T., McNab, A., McNulty, R., Meadows, B., Meier, G., Melnychuk, D., Meng, F. M., Merk, M., Merli, A., Garcia, L. Meyer, Miao, D., Miao, H., Mikhasenko, M., Milanes, D. A., Minotti, A., Minucci, E., Miralles, T., Mitreska, B., Mitzel, D. S., Modak, A., Mohammed, R. A., Moise, R. D., Mokhnenko, S., Mombächer, T., Monk, M., Monteil, S., Gomez, A. Morcillo, Morello, G., Morello, M. J., Morgenthaler, M. P., Morris, A. B., Morris, A. G., Mountain, R., Mu, H., Mu, Z. M., Muhammad, E., Muheim, F., Mulder, M., Müller, K., Muñoz-Rojas, F., Murta, R., Naik, P., Nakada, T., Nandakumar, R., Nanut, T., Nasteva, I., Needham, M., Neri, N., Neubert, S., Neufeld, N., Neustroev, P., Nicolini, J., Nicotra, D., Niel, E. M., Nikitin, N., Nogarolli, P., Nogga, P., Nolte, N. S., Normand, C., Fernandez, J. Novoa, Nowak, G., Nunez, C., Nur, H. N., Oblakowska-Mucha, A., Obraztsov, V., Oeser, T., Okamura, S., Okhotnikov, A., Okhrimenko, O., Oldeman, R., Oliva, F., Olocco, M., Onderwater, C. J. G., O'Neil, R. H., Osthues, D., Goicochea, J. M. Otalora, Owen, P., Oyanguren, A., Ozcelik, O., Padee, A., Padeken, K. O., Pagare, B., Pais, P. R., Pajero, T., Palano, A., Palutan, M., Panshin, G., Paolucci, L., Papanestis, A., Pappagallo, M., Pappalardo, L. L., Pappenheimer, C., Parkes, C., Passalacqua, B., Passaleva, G., Passaro, D., Pastore, A., Patel, M., Patoc, J., Patrignani, C., Paul, A., Pawley, C. J., Pellegrino, A., Peng, J., Altarelli, M. Pepe, Perazzini, S., Pereima, D., Da Costa, H. Pereira, Castro, A. Pereiro, Perret, P., Perro, A., Petridis, K., Petrolini, A., Pfaller, J. P., Pham, H., Pica, L., Piccini, M., Pietrzyk, B., Pietrzyk, G., Pinci, D., Pisani, F., Pizzichemi, M., Placinta, V., Casasus, M. Plo, Poeschl, T., Polci, F., Lener, M. Poli, Poluektov, A., Polukhina, N., Polyakov, I., Polycarpo, E., Ponce, S., Popov, D., Poslavskii, S., Prasanth, K., Prouve, C., Pugatch, V., Punzi, G., Qasim, S., Qian, Q. Q., Qian, W., Qin, N., Qu, S., Quagliani, R., Trejo, R. I. Rabadan, Rademacker, J. H., Rama, M., García, M. Ramírez, De Oliveira, V. Ramos, Pernas, M. Ramos, Rangel, M. S., Ratnikov, F., Raven, G., De Miguel, M. Rebollo, Redi, F., Reich, J., Reiss, F., Ren, Z., Resmi, P. K., Ribatti, R., Ricart, G. R., Riccardi, D., Ricciardi, S., Richardson, K., Richardson-Slipper, M., Rinnert, K., Robbe, P., Robertson, G., Rodrigues, E., Fernandez, E. Rodriguez, Lopez, J. A. Rodriguez, Rodriguez, E. Rodriguez, Roensch, J., Rogovskiy, A., Rolf, D. L., Roloff, P., Romanovskiy, V., Lamas, M. Romero, Vidal, A. Romero, Romolini, G., Ronchetti, F., Rong, T., Rotondo, M., Roy, S. R., Rudolph, M. S., Diaz, M. Ruiz, Fernandez, R. A. Ruiz, Vidal, J. Ruiz, Ryzhikov, A., Ryzka, J., Saavedra-Arias, J. J., Silva, J. J. Saborido, Sadek, R., Sagidova, N., Sahoo, D., Sahoo, N., Saitta, B., Salomoni, M., Gras, C. Sanchez, Sanderswood, I., Santacesaria, R., Rios, C. Santamarina, Santimaria, M., Santoro, L., Santovetti, E., Saputi, A., Saranin, D., Sarnatskiy, A. S., Sarpis, G., Sarpis, M., Satriano, C., Satta, A., Saur, M., Savrina, D., Sazak, H., Smead, L. G. Scantlebury, Scarabotto, A., Schael, S., Scherl, S., Schiller, M., Schindler, H., Schmelling, M., Schmidt, B., Schmitt, S., Schmitz, H., Schneider, O., Schopper, A., Schulte, N., Schulte, S., Schune, M. H., Schwemmer, R., Schwering, G., Sciascia, B., Sciuccati, A., Sellam, S., Semennikov, A., Senger, T., Soares, M. Senghi, Sergi, A., Serra, N., Sestini, L., Seuthe, A., Shang, Y., Shangase, D. M., Shapkin, M., Sharma, R. S., Shchemerov, I., Shchutska, L., Shears, T., Shekhtman, L., Shen, Z., Sheng, S., Shevchenko, V., Shi, B., Shi, Q., Shimizu, Y., Shmanin, E., Shorkin, R., Shupperd, J. D., Coutinho, R. Silva, Simi, G., Simone, S., Skidmore, N., Skwarnicki, T., Slater, M. W., Smallwood, J. C., Smith, E., Smith, K., Smith, M., Snoch, A., Lavra, L. Soares, Sokoloff, M. D., Soler, F. J. P., Solomin, A., Solovev, A., Solovyev, I., Song, R., Song, Y., Song, Y. S., De Almeida, F. L. Souza, De Paula, B. Souza, Norella, E. Spadaro, Spedicato, E., Speer, J. G., Spiridenkov, E., Spradlin, P., Sriskaran, V., Stagni, F., Stahl, M., Stahl, S., Stanislaus, S., Stein, E. N., Steinkamp, O., Stenyakin, O., Stevens, H., Strekalina, D., Su, Y., Suljik, F., Sun, J., Sun, L., Sun, Y., Sundfeld, D., Sutcliffe, W., Swallow, P. N., Swystun, F., Szabelski, A., Szumlak, T., Tan, Y., Tat, M. D., Terentev, A., Terzuoli, F., Teubert, F., Thomas, E., Thompson, D. J. D., Tilquin, H., Tisserand, V., T'Jampens, S., Tobin, M., Tomassetti, L., Tonani, G., Tong, X., Machado, D. Torres, Toscano, L., Tou, D. Y., Trippl, C., Tuci, G., Tuning, N., Uecker, L. H., Ukleja, A., Unverzagt, D. J., Ursov, E., Usachov, A., Ustyuzhanin, A., Uwer, U., Vagnoni, V., Valenti, G., Canudas, N. Valls, Van Hecke, H., van Herwijnen, E., Van Hulse, C. B., Van Laak, R., van Veghel, M., Vasquez, G., Gomez, R. Vazquez, Regueiro, P. Vazquez, Sierra, C. Vázquez, Vecchi, S., Velthuis, J. J., Veltri, M., Venkateswaran, A., Vesterinen, M., Benet, D. Vico, Diaz, M. Vieites, Vilasis-Cardona, X., Figueras, E. Vilella, Villa, A., Vincent, P., Volle, F. C., Bruch, D. vom, Voropaev, N., Vos, K., Vouters, G., Vrahas, C., Wagner, J., Walsh, J., Walton, E. J., Wan, G., Wang, C., Wang, G., Wang, J., Wang, M., Wang, N. W., Wang, R., Wang, X., Wang, X. W., Wang, Y., Wang, Z., Ward, J. A., Waterlaat, M., Watson, N. K., Websdale, D., Wei, Y., Wendel, J., Westhenry, B. D. C., White, C., Whitehead, M., Whiter, E., Wiederhold, A. R., Wiedner, D., Wilkinson, G., Wilkinson, M. K., Williams, M., Williams, M. R. J., Williams, R., Williams, Z., Wilson, F. F., Wislicki, W., Witek, M., Witola, L., Wong, C. P., Wormser, G., Wotton, S. A., Wu, H., Wu, J., Wu, Y., Wu, Z., Wyllie, K., Xian, S., Xiang, Z., Xie, Y., Xu, A., Xu, J., Xu, L., Xu, M., Xu, Z., Yang, D., Yang, K., Yang, S., Yang, X., Yang, Y., Yang, Z., Yeroshenko, V., Yeung, H., Yin, H., Yu, C. Y., Yu, J., Yuan, X., Yuan, Y, Zaffaroni, E., Zavertyaev, M., Zdybal, M., Zeng, C., Zeng, M., Zhang, C., Zhang, D., Zhang, J., Zhang, L., Zhang, S., Zhang, Y., Zhang, Y. Z., Zhao, Y., Zharkova, A., Zhelezov, A., Zheng, S. Z., Zheng, X. Z., Zheng, Y., Zhou, T., Zhou, X., Zhou, Y., Zhovkovska, V., Zhu, L. Z., Zhu, X., Zhukov, V., Zhuo, J., Zou, Q., Zuliani, D., and Zunica, G.
Subjects: High Energy Physics - Experiment
Abstract: The first full amplitude analysis of $B^+ \to \psi(2S) K^+ \pi^+ \pi^-$ decays is performed using proton-proton collision data corresponding to an integrated luminosity of $9\,\text{fb}^{-1}$ recorded with the LHCb detector. The rich $K^+ \pi^+ \pi^-$ spectrum is studied and the branching fractions of the resonant substructure associated with the prominent $K_1(1270)^+$ contribution are measured. The data cannot be described by conventional strange and charmonium resonances only. An amplitude model with 53 components is developed comprising 11 hidden-charm exotic hadrons. New production mechanisms for charged charmonium-like states are observed. Significant resonant activity with spin-parity $J^P = 1^+$ in the $\psi(2S) \pi^+$ system is confirmed and a multi-pole structure is demonstrated. The spectral decomposition of the $\psi(2S) \pi^+ \pi^-$ invariant-mass structure, dominated by $X^0 \to \psi(2S) \rho(770)^0$ decays, broadly resembles the $J/\psi \phi$ spectrum observed in $B^+ \to J/\psi \phi K^+$ decays. Exotic $\psi(2S) K^+ \pi^-$ resonances are observed for the first time., Comment: All figures and tables, along with machine-readable versions and any supplementary material and additional information, are available at https://cern.ch/lhcbproject/Publications/p/LHCb-PAPER-2024-014.html (LHCb public pages)
Published: 2024

221. Search for the rare decay of charmed baryon $\Lambda_c^+$ into $p \mu^+ \mu^-$ final state

Author: LHCb collaboration, Aaij, R., Abdelmotteleb, A. S. W., Beteta, C. Abellan, Abudinén, F., Ackernley, T., Adefisoye, A. A., Adeva, B., Adinolfi, M., Adlarson, P., Agapopoulou, C., Aidala, C. A., Ajaltouni, Z., Akar, S., Akiba, K., Albicocco, P., Albrecht, J., Alessio, F., Alexander, M., Aliouche, Z., Cartelle, P. Alvarez, Amalric, R., Amato, S., Amey, J. L., Amhis, Y., An, L., Anderlini, L., Andersson, M., Andreianov, A., Andreola, P., Andreotti, M., Andreou, D., Anelli, A., Ao, D., Archilli, F., Argenton, M., Cuendis, S. Arguedas, Artamonov, A., Artuso, M., Aslanides, E., Atzeni, M., Audurier, B., Bacher, D., Perea, I. Bachiller, Bachmann, S., Bachmayer, M., Back, J. J., Rodriguez, P. Baladron, Balagura, V., Baldini, W., Bao, H., Leite, J. Baptista de Souza, Barbetti, M., Barbosa, I. R., Barlow, R. J., Barnyakov, M., Barsuk, S., Barter, W., Bartolini, M., Bartz, J., Baryshnikov, F., Basels, J. M., Bassi, G., Batsukh, B., Bay, A., Beck, A., Becker, M., Bedeschi, F., Bediaga, I. B., Belin, S., Bellee, V., Belous, K., Belov, I., Belyaev, I., Benane, G., Bencivenni, G., Ben-Haim, E., Berezhnoy, A., Bernet, R., Andres, S. Bernet, Bertolin, A., Betancourt, C., Betti, F., Bex, J., Bezshyiko, Ia., Bhom, J., Bieker, M. S., Biesuz, N. V., Billoir, P., Biolchini, A., Birch, M., Bishop, F. C. R., Bitadze, A., Bizzeti, A., Blake, T., Blanc, F., Blank, J. E., Blusk, S., Bocharnikov, V., Boelhauve, J. A., Garcia, O. Boente, Boettcher, T., Bohare, A., Boldyrev, A., Bolognani, C. S., Bolzonella, R., Bondar, N., Borgato, F., Borghi, S., Borsato, M., Borsuk, J. T., Bouchiba, S. A., Bowcock, T. J. V., Boyer, A., Bozzi, C., Bradley, M. J., Rodriguez, A. Brea, Breer, N., Brodzicka, J., Gonzalo, A. Brossa, Brown, J., Brundu, D., Buchanan, E., Buonaura, A., Buonincontri, L., Burke, A. T., Burr, C., Butkevich, A., Butter, J. S., Buytaert, J., Byczynski, W., Cadeddu, S., Cai, H., Calabrese, R., Ramirez, S. Calderon, Calefice, L., Cali, S., Calvi, M., Gomez, M. Calvo, Magalhaes, P. Camargo, Bouzas, J. I. Cambon, Campana, P., Perez, D. H. Campora, Quezada, A. F. Campoverde, Capelli, S., Capriotti, L., Caravaca-Mora, R., Carbone, A., Salgado, L. Carcedo, Cardinale, R., Cardini, A., Carniti, P., Carus, L., Vidal, A. Casais, Caspary, R., Casse, G., Godinez, J. Castro, Cattaneo, M., Cavallero, G., Cavallini, V., Celani, S., Cervenkov, D., Cesare, S., Chadwick, A. J., Chahrour, I., Charles, M., Charpentier, Ph., Barajas, C. A. Chavez, Chefdeville, M., Chen, C., Chen, S., Chen, Z., Chernov, A., Chernyshenko, S., Chobanova, V., Cholak, S., Chrzaszcz, M., Chubykin, A., Chulikov, V., Ciambrone, P., Vidal, X. Cid, Ciezarek, G., Cifra, P., Clarke, P. E. L., Clemencic, M., Cliff, H. V., Closier, J., Toapaxi, C. Cocha, Coco, V., Cogan, J., Cogneras, E., Cojocariu, L., Collins, P., Colombo, T., Comerma-Montells, A., Congedo, L., Contu, A., Cooke, N., Corredoira, I., Correia, A., Corti, G., Meldrum, J. J. Cottee, Couturier, B., Craik, D. C., Torres, M. Cruz, Rivera, E. Curras, Currie, R., Da Silva, C. L., Dadabaev, S., Dai, L., Dai, X., Dall'Occo, E., Dalseno, J., D'Ambrosio, C., Daniel, J., Danilina, A., d'Argent, P., Davidson, A., Davies, J. E., Davis, A., Francisco, O. De Aguiar, De Angelis, C., De Benedetti, F., de Boer, J., De Bruyn, K., De Capua, S., De Cian, M., Da Graca, U. De Freitas Carneiro, De Lucia, E., De Miranda, J. M., De Paula, L., De Serio, M., De Simone, P., De Vellis, F., de Vries, J. A., Debernardis, F., Decamp, D., Dedu, V., Del Buono, L., Delaney, B., Dembinski, H. -P., Deng, J., Denysenko, V., Deschamps, O., Dettori, F., Dey, B., Di Nezza, P., Diachkov, I., Didenko, S., Ding, S., Dittmann, L., Dobishuk, V., Docheva, A. D., Dong, C., Donohoe, A. M., Dordei, F., Reis, A. C. dos, Dowling, A. D., Duan, W., Duda, P., Dudek, M. W., Dufour, L., Duk, V., Durante, P., Duras, M. M., Durham, J. M., Durmus, O. D., Dziurda, A., Dzyuba, A., Easo, S., Eckstein, E., Egede, U., Egorychev, A., Egorychev, V., Eisenhardt, S., Ejopu, E., Eklund, L., Elashri, M., Ellbracht, J., Ely, S., Ene, A., Epple, E., Eschle, J., Esen, S., Evans, T., Fabiano, F., Falcao, L. N., Fan, Y., Fang, B., Fantini, L., Faria, M., Farmer, K., Fazzini, D., Felkowski, L., Feng, M., Feo, M., Gomez, M. Fernandez, Fernez, A. D., Ferrari, F., Rodrigues, F. Ferreira, Ferrillo, M., Ferro-Luzzi, M., Filippov, S., Fini, R. A., Fiorini, M., Fischer, K. L., Fitzgerald, D. S., Fitzpatrick, C., Fleuret, F., Fontana, M., Foreman, L. F., Forty, R., Foulds-Holt, D., Sevilla, M. Franco, Frank, M., Franzoso, E., Frau, G., Frei, C., Friday, D. A., Fu, J., Fuehring, Q., Fujii, Y., Fulghesu, T., Gabriel, E., Galati, G., Galati, M. D., Torreira, A. Gallas, Galli, D., Gambetta, S., Gandelman, M., Gandini, P., Ganie, B., Gao, H., Gao, R., Gao, Y., Garau, M., Martin, L. M. Garcia, Moreno, P. Garcia, Pardiñas, J. García, Garg, K. G., Garrido, L., Gaspar, C., Geertsema, R. E., Gerken, L. L., Gersabeck, E., Gersabeck, M., Gershon, T., Ghorbanimoghaddam, Z., Giambastiani, L., Giasemis, F. I., Gibson, V., Giemza, H. K., Gilman, A. L., Giovannetti, M., Gioventù, A., Gironell, P. Gironella, Giugliano, C., Giza, M. A., Gkougkousis, E. L., Glaser, F. C., Gligorov, V. V., Göbel, C., Golobardes, E., Golubkov, D., Golutvin, A., Gomes, A., Fernandez, S. Gomez, Abrantes, F. Goncalves, Goncerz, M., Gong, G., Gooding, J. A., Gorelov, I. V., Gotti, C., Grabowski, J. P., Cardoso, L. A. Granado, Graugés, E., Graverini, E., Grazette, L., Graziani, G., Grecu, A. T., Greeven, L. M., Grieser, N. A., Grillo, L., Gromov, S., Gu, C., Guarise, M., Guittiere, M., Guliaeva, V., Günther, P. A., Guseinov, A. -K., Gushchin, E., Guz, Y., Gys, T., Habermann, K., Hadavizadeh, T., Hadjivasiliou, C., Haefeli, G., Haen, C., Haimberger, J., Hajheidari, M., Halvorsen, M. M., Hamilton, P. M., Hammerich, J., Han, Q., Han, X., Hansmann-Menzemer, S., Hao, L., Harnew, N., Hartmann, M., He, J., Hemmer, F., Henderson, C., Henderson, R. D. L., Hennequin, A. M., Hennessy, K., Henry, L., Herd, J., Gascon, P. Herrero, Heuel, J., Hicheur, A., Mendizabal, G. Hijano, Hill, D., Hollitt, S. E., Horswill, J., Hou, R., Hou, Y., Howarth, N., Hu, J., Hu, W., Hu, X., Huang, W., Hulsbergen, W., Hunter, R. J., Hushchyn, M., Hutchcroft, D., Ilin, D., Ilten, P., Inglessi, A., Iniukhin, A., Ishteev, A., Ivshin, K., Jacobsson, R., Jage, H., Elles, S. J. Jaimes, Jakobsen, S., Jans, E., Jashal, B. K., Jawahery, A., Jevtic, V., Jiang, E., Jiang, X., Jiang, Y., Jiang, Y. J., John, M., Johnson, D., Jones, C. R., Jones, T. P., Joshi, S., Jost, B., Jurik, N., Juszczak, I., Kaminaris, D., Kandybei, S., Kang, Y., Kar, C., Karacson, M., Karpenkov, D., Kauniskangas, A., Kautz, J. W., Keizer, F., Kenzie, M., Ketel, T., Khanji, B., Kharisova, A., Kholodenko, S., Khreich, G., Kirn, T., Kirsebom, V. S., Kitouni, O., Klaver, S., Kleijne, N., Klimaszewski, K., Kmiec, M. R., Koliiev, S., Kolk, L., Konoplyannikov, A., Kopciewicz, P., Koppenburg, P., Korolev, M., Kostiuk, I., Kot, O., Kotriakhova, S., Kozachuk, A., Kravchenko, P., Kravchuk, L., Kreps, M., Krokovny, P., Krupa, W., Krzemien, W., Kshyvanskyi, O. K., Kubat, J., Kubis, S., Kucharczyk, M., Kudryavtsev, V., Kulikova, E., Kupsc, A., Kutsenko, B. K., Lacarrere, D., Lai, A., Lampis, A., Lancierini, D., Gomez, C. Landesa, Lane, J. J., Lane, R., Langenbruch, C., Langer, J., Lantwin, O., Latham, T., Lazzari, F., Lazzeroni, C., Gac, R. Le, Lefèvre, R., Leflat, A., Legotin, S., Lehuraux, M., Cid, E. Lemos, Leroy, O., Lesiak, T., Leverington, B., Li, A., Li, H., Li, K., Li, L., Li, P., Li, P. -R., Li, Q., Li, S., Li, T., Li, Y., Lian, Z., Liang, X., Libralon, S., Lin, C., Lin, T., Lindner, R., Lisovskyi, V., Litvinov, R., Liu, F. L., Liu, G., Liu, K., Liu, S., Liu, Y., Liu, Y. L., Salvia, A. Lobo, Loi, A., Castro, J. Lomba, Long, T., Lopes, J. H., Huertas, A. Lopez, Soliño, S. López, Lucarelli, C., Lucchesi, D., Martinez, M. Lucio, Lukashenko, V., Luo, Y., Lupato, A., Luppi, E., Lynch, K., Lyu, X. -R., Ma, G. M., Ma, R., Maccolini, S., Machefert, F., Maciuc, F., Mack, B., Mackay, I., Mackey, L. M., Mohan, L. R. Madhan, Madurai, M. J., Maevskiy, A., Magdalinski, D., Maisuzenko, D., Majewski, M. W., Malczewski, J. J., Malde, S., Malentacca, L., Malinin, A., Maltsev, T., Manca, G., Mancinelli, G., Mancuso, C., Escalero, R. Manera, Manuzzi, D., Marangotto, D., Marchand, J. F., Marchevski, R., Marconi, U., Mariani, S., Benito, C. Marin, Marks, J., Marshall, A. M., Martelli, G., Martellotti, G., Martinazzoli, L., Martinelli, M., Santos, D. Martinez, Vidal, F. Martinez, Massafferri, A., Matev, R., Mathad, A., Matiunin, V., Matteuzzi, C., Mattioli, K. R., Mauri, A., Maurice, E., Mauricio, J., Mayencourt, P., Mazurek, M., McCann, M., Mcconnell, L., McGrath, T. H., McHugh, N. T., McNab, A., McNulty, R., Meadows, B., Meier, G., Melnychuk, D., Meng, F. M., Merk, M., Merli, A., Garcia, L. Meyer, Miao, D., Miao, H., Mikhasenko, M., Milanes, D. A., Minotti, A., Minucci, E., Miralles, T., Mitreska, B., Mitzel, D. S., Modak, A., Mödden, A., Mohammed, R. A., Moise, R. D., Mokhnenko, S., Mombächer, T., Monk, M., Monteil, S., Gomez, A. Morcillo, Morello, G., Morello, M. J., Morgenthaler, M. P., Morris, A. B., Morris, A. G., Mountain, R., Mu, H., Mu, Z. M., Muhammad, E., Muheim, F., Mulder, M., Müller, K., Muñoz-Rojas, F., Murta, R., Naik, P., Nakada, T., Nandakumar, R., Nanut, T., Nasteva, I., Needham, M., Neri, N., Neubert, S., Neufeld, N., Neustroev, P., Nicolini, J., Nicotra, D., Niel, E. M., Nikitin, N., Nogarolli, P., Nogga, P., Nolte, N. S., Normand, C., Fernandez, J. Novoa, Nowak, G., Nunez, C., Nur, H. N., Oblakowska-Mucha, A., Obraztsov, V., Oeser, T., Okamura, S., Okhotnikov, A., Okhrimenko, O., Oldeman, R., Oliva, F., Olocco, M., Onderwater, C. J. G., O'Neil, R. H., Goicochea, J. M. Otalora, Owen, P., Oyanguren, A., Ozcelik, O., Padeken, K. O., Pagare, B., Pais, P. R., Pajero, T., Palano, A., Palutan, M., Panshin, G., Paolucci, L., Papanestis, A., Pappagallo, M., Pappalardo, L. L., Pappenheimer, C., Parkes, C., Passalacqua, B., Passaleva, G., Passaro, D., Pastore, A., Patel, M., Patoc, J., Patrignani, C., Paul, A., Pawley, C. J., Pellegrino, A., Peng, J., Altarelli, M. Pepe, Perazzini, S., Pereima, D., Da Costa, H. Pereira, Castro, A. Pereiro, Perret, P., Perro, A., Petridis, K., Petrolini, A., Pfaller, J. P., Pham, H., Pica, L., Piccini, M., Pietrzyk, B., Pietrzyk, G., Pinci, D., Pisani, F., Pizzichemi, M., Placinta, V., Casasus, M. Plo, Polci, F., Lener, M. Poli, Poluektov, A., Polukhina, N., Polyakov, I., Polycarpo, E., Ponce, S., Popov, D., Poslavskii, S., Prasanth, K., Prouve, C., Pugatch, V., Punzi, G., Qasim, S., Qian, W., Qin, N., Qu, S., Quagliani, R., Trejo, R. I. Rabadan, Rademacker, J. H., Rama, M., García, M. Ramírez, De Oliveira, V. Ramos, Pernas, M. Ramos, Rangel, M. S., Ratnikov, F., Raven, G., De Miguel, M. Rebollo, Redi, F., Reich, J., Reiss, F., Ren, Z., Resmi, P. K., Ribatti, R., Ricart, G. R., Riccardi, D., Ricciardi, S., Richardson, K., Richardson-Slipper, M., Rinnert, K., Robbe, P., Robertson, G., Rodrigues, E., Fernandez, E. Rodriguez, Lopez, J. A. Rodriguez, Rodriguez, E. Rodriguez, Rogovskiy, A., Rolf, D. L., Roloff, P., Romanovskiy, V., Lamas, M. Romero, Vidal, A. Romero, Romolini, G., Ronchetti, F., Rotondo, M., Roy, S. R., Rudolph, M. S., Ruf, T., Diaz, M. Ruiz, Fernandez, R. A. Ruiz, Vidal, J. Ruiz, Ryzhikov, A., Ryzka, J., Saavedra-Arias, J. J., Silva, J. J. Saborido, Sadek, R., Sagidova, N., Sahoo, D., Sahoo, N., Saitta, B., Salomoni, M., Gras, C. Sanchez, Sanderswood, I., Santacesaria, R., Rios, C. Santamarina, Santimaria, M., Santoro, L., Santovetti, E., Saputi, A., Saranin, D., Sarpis, G., Sarpis, M., Satriano, C., Satta, A., Saur, M., Savrina, D., Sazak, H., Smead, L. G. Scantlebury, Scarabotto, A., Schael, S., Scherl, S., Schiller, M., Schindler, H., Schmelling, M., Schmidt, B., Schmitt, S., Schmitz, H., Schneider, O., Schopper, A., Schulte, N., Schulte, S., Schune, M. H., Schwemmer, R., Schwering, G., Sciascia, B., Sciuccati, A., Sellam, S., Semennikov, A., Senger, T., Soares, M. Senghi, Sergi, A., Serra, N., Sestini, L., Seuthe, A., Shang, Y., Shangase, D. M., Shapkin, M., Sharma, R. S., Shchemerov, I., Shchutska, L., Shears, T., Shekhtman, L., Shen, Z., Sheng, S., Shevchenko, V., Shi, B., Shi, Q., Shields, E. B., Shimizu, Y., Shmanin, E., Shorkin, R., Shupperd, J. D., Coutinho, R. Silva, Simi, G., Simone, S., Skidmore, N., Skwarnicki, T., Slater, M. W., Smallwood, J. C., Smith, E., Smith, K., Smith, M., Snoch, A., Lavra, L. Soares, Sokoloff, M. D., Soler, F. J. P., Solomin, A., Solovev, A., Solovyev, I., Song, R., Song, Y., Song, Y. S., De Almeida, F. L. Souza, De Paula, B. Souza, Norella, E. Spadaro, Spedicato, E., Speer, J. G., Spiridenkov, E., Spradlin, P., Sriskaran, V., Stagni, F., Stahl, M., Stahl, S., Stanislaus, S., Stein, E. N., Steinkamp, O., Stenyakin, O., Stevens, H., Strekalina, D., Su, Y., Suljik, F., Sun, J., Sun, L., Sun, Y., Sundfeld, D., Sutcliffe, W., Swallow, P. N., Swystun, F., Szabelski, A., Szumlak, T., Tan, Y., Tat, M. D., Terentev, A., Terzuoli, F., Teubert, F., Thomas, E., Thompson, D. J. D., Tilquin, H., Tisserand, V., T'Jampens, S., Tobin, M., Tomassetti, L., Tonani, G., Tong, X., Machado, D. Torres, Toscano, L., Tou, D. Y., Trippl, C., Tuci, G., Tuning, N., Uecker, L. H., Ukleja, A., Unverzagt, D. J., Ursov, E., Usachov, A., Ustyuzhanin, A., Uwer, U., Vagnoni, V., Valassi, A., Valenti, G., Canudas, N. Valls, Van Hecke, H., van Herwijnen, E., Van Hulse, C. B., Van Laak, R., van Veghel, M., Vasquez, G., Gomez, R. Vazquez, Regueiro, P. Vazquez, Sierra, C. Vázquez, Vecchi, S., Velthuis, J. J., Veltri, M., Venkateswaran, A., Vesterinen, M., Diaz, M. Vieites, Vilasis-Cardona, X., Figueras, E. Vilella, Villa, A., Vincent, P., Volle, F. C., Bruch, D. vom, Voropaev, N., Vos, K., Vouters, G., Vrahas, C., Wagner, J., Walsh, J., Walton, E. J., Wan, G., Wang, C., Wang, G., Wang, J., Wang, M., Wang, N. W., Wang, R., Wang, X., Wang, X. W., Wang, Z., Ward, J. A., Waterlaat, M., Watson, N. K., Websdale, D., Wei, Y., Wendel, J., Westhenry, B. D. C., White, D. J., Whitehead, M., Wiederhold, A. R., Wiedner, D., Wilkinson, G., Wilkinson, M. K., Williams, M., Williams, M. R. J., Williams, R., Wilson, F. F., Wislicki, W., Witek, M., Witola, L., Wong, C. P., Wormser, G., Wotton, S. A., Wu, H., Wu, J., Wu, Y., Wu, Z., Wyllie, K., Xian, S., Xiang, Z., Xie, Y., Xu, A., Xu, J., Xu, L., Xu, M., Xu, Z., Yang, D., Yang, K., Yang, S., Yang, X., Yang, Y., Yang, Z., Yeroshenko, V., Yeung, H., Yin, H., Yu, C. Y., Yu, J., Yuan, X., Zaffaroni, E., Zavertyaev, M., Zdybal, M., Zeng, C., Zeng, M., Zhang, C., Zhang, D., Zhang, J., Zhang, L., Zhang, S., Zhang, Y., Zhang, Y. Z., Zhao, Y., Zharkova, A., Zhelezov, A., Zheng, X. Z., Zheng, Y., Zhou, T., Zhou, X., Zhou, Y., Zhovkovska, V., Zhu, L. Z., Zhu, X., Zhukov, V., Zhuo, J., Zou, Q., Zuliani, D., and Zunica, G.
Subjects: High Energy Physics - Experiment
Abstract: A search for the nonresonant $\Lambda_c^+ \to p \mu^+ \mu^-$ decay is performed using proton-proton collision data recorded at a centre-of-mass energy of 13 TeV by the LHCb experiment, corresponding to an integrated luminosity of 5.4 fb$^{-1}$. No evidence for the decay is found in the dimuon invariant-mass regions where the expected contributions of resonances is subdominant. The upper limit on the branching fraction of the $\Lambda_c^+ \to p \mu^+ \mu^-$ decay is determined to be $2.9~(3.2) \times 10^{-8}$ at 90% (95%) confidence level. The branching fractions in the dimuon invariant-mass regions dominated by the $\eta$, $\rho$ and $\omega$ resonances are also determined., Comment: All figures and tables, along with any supplementary material and additional information, are available at https://cern.ch/lhcbproject/Publications/p/LHCb-PAPER-2024-005.html (LHCb public pages)
Published: 2024
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222. Observation of the Electromagnetic Dalitz Transition $h_c \rightarrow e^+e^-\eta_c$

Author: BESIII Collaboration, Ablikim, M., Achasov, M. N., Adlarson, P., Ahmed, S., Albrecht, M., Aliberti, R., Amoroso, A., An, M. R., An, Q., Bai, X. H., Bai, Y., Bakina, O., Ferroli, R. Baldini, Balossino, I., Ban, Y., Begzsuren, K., Berger, N., Bertani, M., Bettoni, D., Bianchi, F., Bloms, J., Bortone, A., Boyko, I., Briere, R. A., Cai, H., Cai, X., Calcaterra, A., Cao, G. F., Cao, N., Cetin, S. A., Chang, J. F., Chang, W. L., Chelkov, G., Chen, D. Y., Chen, G., Chen, H. S., Chen, M. L., Chen, S. J., Chen, X. R., Chen, Y. B., Chen, Z. J, Cheng, W. S., Cibinetto, G., Cossio, F., Cui, X. F., Dai, H. L., Dai, X. C., Dbeyssi, A., de Boer, R. E., Dedovich, D., Deng, Z. Y., Denig, A., Denysenko, I., Destefanis, M., De Mori, F., Ding, Y., Dong, C., Dong, J., Dong, L. Y., Dong, M. Y., Dong, X., Du, S. X., Fan, Y. L., Fang, J., Fang, S. S., Fang, Y., Farinelli, R., Fava, L., Feldbauer, F., Felici, G., Feng, C. Q., Feng, J. H., Fritsch, M., Fu, C. D., Gao, Y., Gao, Y. G., Garzia, I., Ge, P. T., Geng, C., Gersabeck, E. M., Gilman, A, Goetzen, K., Gong, L., Gong, W. X., Gradl, W., Greco, M., Gu, L. M., Gu, M. H., Gu, S., Gu, Y. T., Guan, C. Y, Guo, A. Q., Guo, L. B., Guo, R. P., Guo, Y. P., Guskov, A., Han, T. T., Han, W. Y., Hao, X. Q., Harris, F. A., Hüsken, N, He, K. L., Heinsius, F. H., Heinz, C. H., Held, T., Heng, Y. K., Herold, C., Himmelreich, M., Holtmann, T., Hou, Y. R., Hou, Z. L., Hu, H. M., Hu, J. F., Hu, T., Hu, Y., Huang, G. S., Huang, L. Q., Huang, X. T., Huang, Y. P., Huang, Z., Hussain, T., Andersson, W. Ikegami, Imoehl, W., Irshad, M., Jaeger, S., Janchiv, S., Ji, Q., Ji, Q. P., Ji, X. B., Ji, X. L., Ji, Y. Y., Jiang, H. B., Jiang, X. S., Jiao, J. B., Jiao, Z., Jin, S., Jin, Y., Johansson, T., Kalantar-Nayestanaki, N., Kang, X. S., Kappert, R., Kavatsyuk, M., Ke, B. C., Keshk, I. K., Khoukaz, A., Kiese, P., Kiuchi, R., Kliemt, R., Koch, L., Kolcu, O. B., Kopf, B., Kuemmel, M., Kuessner, M., Kupsc, A., Kurth, M. G., Kühn, W., Lane, J. J., Lange, J. S., Larin, P., Lavania, A., Lavezzi, L., Lei, Z. H., Leithoff, H., Lellmann, M., Lenz, T., Li, C., Li, C. H., Li, Cheng, Li, D. M., Li, F., Li, G., Li, H., Li, H. B., Li, H. J., Li, J. L., Li, J. Q., Li, J. S., Li, Ke, Li, L. K., Li, Lei, Li, P. R., Li, S. Y., Li, W. D., Li, W. G., Li, X. H., Li, X. L., Li, Xiaoyu, Li, Z. Y., Liang, H., Liang, Y. F., Liang, Y. T., Liao, G. R., Liao, L. Z., Libby, J., Lin, C. X., Liu, B. J., Liu, C. X., Liu, D., Liu, F. H., Liu, Fang, Liu, Feng, Liu, H. B., Liu, H. M., Liu, Huanhuan, Liu, Huihui, Liu, J. B., Liu, J. L., Liu, J. Y., Liu, K., Liu, K. Y., Liu, Ke, Liu, L., Liu, M. H., Liu, P. L., Liu, Q., Liu, S. B., Liu, Shuai, Liu, T., Liu, W. M., Liu, X., Liu, Y., Liu, Y. B., Liu, Z. A., Liu, Z. Q., Lou, X. C., Lu, F. X., Lu, H. J., Lu, J. D., Lu, J. G., Lu, X. L., Lu, Y., Lu, Y. P., Luo, C. L., Luo, M. X., Luo, P. W., Luo, T., Luo, X. L., Lusso, S., Lyu, X. R., Ma, F. C., Ma, H. L., Ma, L. L., Ma, M. M., Ma, Q. M., Ma, R. Q., Ma, R. T., Ma, X. X., Ma, X. Y., Maas, F. E., Maggiora, M., Maldaner, S., Malde, S., Malik, Q. A., Mangoni, A., Mao, Y. J., Mao, Z. P., Marcello, S., Meng, Z. X., Messchendorp, J. G., Mezzadri, G., Min, T. J., Mitchell, R. E., Mo, X. H., Mo, Y. J., Muchnoi, N. Yu., Muramatsu, H., Nakhoul, S., Nefedov, Y., Nerling, F., Nikolaev, I. B., Ning, Z., Nisar, S., Olsen, S. L., Ouyang, Q., Pacetti, S., Pan, X., Pan, Y., Pathak, A., Patteri, P., Pelizaeus, M., Peng, H. P., Peters, K., Pettersson, J., Ping, J. L., Ping, R. G., Poling, R., Prasad, V., Qi, H., Qi, H. R., Qi, K. H., Qi, M., Qi, T. Y., Qian, S., Qian, W. B., Qian, Z., Qiao, C. F., Qin, L. Q., Qin, X. P., Qin, X. S., Qin, Z. H., Qiu, J. F., Qu, S. Q., Rashid, K. H., Ravindran, K., Redmer, C. F., Rivetti, A., Rodin, V., Rolo, M., Rong, G., Rosner, Ch., Rump, M., Sang, H. S., Sarantsev, A., Schelhaas, Y., Schnier, C., Schoenning, K., Scodeggio, M., Shan, D. C., Shan, W., Shan, X. Y., Shangguan, J. F., Shao, M., Shen, C. P., Shen, P. X., Shen, X. Y., Shi, H. C., Shi, R. S., Shi, X., Shi, X. D, Song, J. J., Song, W. M., Song, Y. X., Sosio, S., Spataro, S., Su, K. X., Su, P. P., Sui, F. F., Sun, G. X., Sun, H. K., Sun, J. F., Sun, L., Sun, S. S., Sun, T., Sun, W. Y., Sun, X, Sun, Y. J., Sun, Y. K., Sun, Y. Z., Sun, Z. T., Tan, Y. H., Tan, Y. X., Tang, C. J., Tang, G. Y., Tang, J., Teng, J. X., Thoren, V., Tian, Y. T., Uman, I., Wang, B., Wang, C. W., Wang, D. Y., Wang, H. J., Wang, H. P., Wang, K., Wang, L. L., Wang, M., Wang, M. Z., Wang, Meng, Wang, W., Wang, W. H., Wang, W. P., Wang, X., Wang, X. F., Wang, X. L., Wang, Y., Wang, Y. D., Wang, Y. F., Wang, Y. Q., Wang, Y. Y., Wang, Z., Wang, Z. Y., Wang, Ziyi, Wang, Zongyuan, Wei, D. H., Weidenkaff, P., Weidner, F., Wen, S. P., White, D. J., Wiedner, U., Wilkinson, G., Wolke, M., Wollenberg, L., Wu, J. F., Wu, L. H., Wu, L. J., Wu, X., Wu, Z., Xia, L., Xiao, H., Xiao, S. Y., Xiao, Z. J., Xie, X. H., Xie, Y. G., Xie, Y. H., Xing, T. Y., Xu, G. F., Xu, Q. J., Xu, W., Xu, X. P., Xu, Y. C., Yan, F., Yan, L., Yan, W. B., Yan, W. C., Yan, Xu, Yang, H. J., Yang, H. X., Yang, L., Yang, S. L., Yang, Y. X., Yang, Yifan, Yang, Zhi, Ye, M., Ye, M. H., Yin, J. H., You, Z. Y., Yu, B. X., Yu, C. X., Yu, G., Yu, J. S., Yu, T., Yuan, C. Z., Yuan, L., Yuan, X. Q., Yuan, Y., Yuan, Z. Y., Yue, C. X., Yuncu, A., Zafar, A. A., Zeng, Y., Zhang, B. X., Zhang, Guangyi, Zhang, H., Zhang, H. H., Zhang, H. Y., Zhang, J. J., Zhang, J. L., Zhang, J. Q., Zhang, J. W., Zhang, J. Y., Zhang, J. Z., Zhang, Jianyu, Zhang, Jiawei, Zhang, L. M., Zhang, L. Q., Zhang, Lei, Zhang, S., Zhang, S. F., Zhang, Shulei, Zhang, X. D., Zhang, X. Y., Zhang, Y., Zhang, Y. H., Zhang, Y. T., Zhang, Yan, Zhang, Yao, Zhang, Yi, Zhang, Z. H., Zhang, Z. Y., Zhao, G., Zhao, J., Zhao, J. Y., Zhao, J. Z., Zhao, Lei, Zhao, Ling, Zhao, M. G., Zhao, Q., Zhao, S. J., Zhao, Y. B., Zhao, Y. X., Zhao, Z. G., Zhemchugov, A., Zheng, B., Zheng, J. P., Zheng, W. J., Zheng, Y., Zheng, Y. H., Zhong, B., Zhong, C., Zhou, L. P., Zhou, Q., Zhou, X., Zhou, X. K., Zhou, X. R., Zhou, X. Y., Zhu, A. N., Zhu, J., Zhu, K., Zhu, K. J., Zhu, S. H., Zhu, T. J., Zhu, W. J., Zhu, Y. C., Zhu, Z. A., Zou, B. S., and Zou, J. H.
Subjects: High Energy Physics - Experiment
Abstract: Using $(27.12\pm 0.14)\times10^8$ $\psi(3686)$ decays and data samples of $e^+e^-$ collisions with $\sqrt{s}$ from 4.130 to 4.780~GeV collected with the BESIII detector, we report the first observation of the electromagnetic Dalitz transition $h_c\to e^+e^-\eta_c$ with a statistical significance of $5.4\sigma$. We measure the ratio of the branching fractions $\frac{\mathcal{B}(h_c\rightarrow e^+e^-\eta_c)}{\mathcal{B}(h_c\rightarrow \gamma \eta_c)}$ separately for the $h_c$ samples produced via $\psi(3686)\to\pi^0h_c$ and $e^+e^-\to\pi^+\pi^-h_c$. The average ratio is determined to be $(0.59\pm0.10(\text{stat.})\pm0.04(\text{syst.}))\%$, where the uncertainty includes both statistical and systematic components.
Published: 2024

223. Probing the nature of the $\chi_{c1}(3872)$ state using radiative decays

Author: LHCb collaboration, Aaij, R., Abdelmotteleb, A. S. W., Beteta, C. Abellan, Abudinén, F., Ackernley, T., Adefisoye, A. A., Adeva, B., Adinolfi, M., Adlarson, P., Agapopoulou, C., Aidala, C. A., Ajaltouni, Z., Akar, S., Akiba, K., Albicocco, P., Albrecht, J., Alessio, F., Alexander, M., Aliouche, Z., Cartelle, P. Alvarez, Amalric, R., Amato, S., Amey, J. L., Amhis, Y., An, L., Anderlini, L., Andersson, M., Andreianov, A., Andreola, P., Andreotti, M., Andreou, D., Anelli, A., Ao, D., Archilli, F., Argenton, M., Cuendis, S. Arguedas, Artamonov, A., Artuso, M., Aslanides, E., Da Silva, R. Ataide, Atzeni, M., Audurier, B., Bacher, D., Perea, I. Bachiller, Bachmann, S., Bachmayer, M., Back, J. J., Rodriguez, P. Baladron, Balagura, V., Baldini, W., Balzani, L., Bao, H., Leite, J. Baptista de Souza, Pretel, C. Barbero, Barbetti, M., Barbosa, I. R., Barlow, R. J., Barnyakov, M., Barsuk, S., Barter, W., Bartolini, M., Bartz, J., Basels, J. M., Bashir, S., Bassi, G., Batsukh, B., Battista, P. B., Bay, A., Beck, A., Becker, M., Bedeschi, F., Bediaga, I. B., Behling, N. B., Belin, S., Bellee, V., Belous, K., Belov, I., Belyaev, I., Benane, G., Bencivenni, G., Ben-Haim, E., Berezhnoy, A., Bernet, R., Andres, S. Bernet, Bertolin, A., Betancourt, C., Betti, F., Bex, J., Bezshyiko, Ia., Bhom, J., Bieker, M. S., Biesuz, N. V., Billoir, P., Biolchini, A., Birch, M., Bishop, F. C. R., Bitadze, A., Bizzeti, A., Blake, T., Blanc, F., Blank, J. E., Blusk, S., Bocharnikov, V., Boelhauve, J. A., Garcia, O. Boente, Boettcher, T., Bohare, A., Boldyrev, A., Bolognani, C. S., Bolzonella, R., Bondar, N., Borgato, F., Borghi, S., Borsato, M., Borsuk, J. T., Bouchiba, S. A., Bovill, M., Bowcock, T. J. V., Boyer, A., Bozzi, C., Rodriguez, A. Brea, Breer, N., Brodzicka, J., Gonzalo, A. Brossa, Brown, J., Brundu, D., Buchanan, E., Buonaura, A., Buonincontri, L., Burke, A. T., Burr, C., Butkevich, A., Butter, J. S., Buytaert, J., Byczynski, W., Cadeddu, S., Cai, H., Caillet, A. C., Calabrese, R., Ramirez, S. Calderon, Calefice, L., Cali, S., Calvi, M., Gomez, M. Calvo, Magalhaes, P. Camargo, Bouzas, J. I. Cambon, Campana, P., Perez, D. H. Campora, Quezada, A. F. Campoverde, Capelli, S., Capriotti, L., Caravaca-Mora, R., Carbone, A., Salgado, L. Carcedo, Cardinale, R., Cardini, A., Carniti, P., Carus, L., Vidal, A. Casais, Caspary, R., Casse, G., Godinez, J. Castro, Cattaneo, M., Cavallero, G., Cavallini, V., Celani, S., Cervenkov, D., Cesare, S., Chadwick, A. J., Chahrour, I., Charles, M., Charpentier, Ph., Chatzianagnostou, E., Barajas, C. A. Chavez, Chefdeville, M., Chen, C., Chen, S., Chen, Z., Chernov, A., Chernyshenko, S., Chiotopoulos, X., Chobanova, V., Cholak, S., Chrzaszcz, M., Chubykin, A., Chulikov, V., Ciambrone, P., Vidal, X. Cid, Ciezarek, G., Cifra, P., Clarke, P. E. L., Clemencic, M., Cliff, H. V., Closier, J., Toapaxi, C. Cocha, Coco, V., Cogan, J., Cogneras, E., Cojocariu, L., Collins, P., Colombo, T., Colonna, M. C., Comerma-Montells, A., Congedo, L., Contu, A., Cooke, N., Corredoira, I., Correia, A., Corti, G., Meldrum, J. J. Cottee, Couturier, B., Craik, D. C., Torres, M. Cruz, Rivera, E. Curras, Currie, R., Da Silva, C. L., Dadabaev, S., Dai, L., Dai, X., Dall'Occo, E., Dalseno, J., D'Ambrosio, C., Daniel, J., Danilina, A., d'Argent, P., Davidson, A., Davies, J. E., Davis, A., Francisco, O. De Aguiar, De Angelis, C., De Benedetti, F., de Boer, J., De Bruyn, K., De Capua, S., De Cian, M., Da Graca, U. De Freitas Carneiro, De Lucia, E., De Miranda, J. M., De Paula, L., De Serio, M., De Simone, P., De Vellis, F., de Vries, J. A., Debernardis, F., Decamp, D., Dedu, V., Del Buono, L., Delaney, B., Dembinski, H. -P., Deng, J., Denysenko, V., Deschamps, O., Dettori, F., Dey, B., Di Nezza, P., Diachkov, I., Didenko, S., Ding, S., Dittmann, L., Dobishuk, V., Docheva, A. D., Dong, C., Donohoe, A. M., Dordei, F., Reis, A. C. dos, Dowling, A. D., Duan, W., Duda, P., Dudek, M. W., Dufour, L., Duk, V., Durante, P., Duras, M. M., Durham, J. M., Durmus, O. D., Dziurda, A., Dzyuba, A., Easo, S., Eckstein, E., Egede, U., Egorychev, A., Egorychev, V., Eisenhardt, S., Ejopu, E., Eklund, L., Elashri, M., Ellbracht, J., Ely, S., Ene, A., Epple, E., Eschle, J., Esen, S., Evans, T., Fabiano, F., Falcao, L. N., Fan, Y., Fang, B., Fantini, L., Faria, M., Farmer, K., Fazzini, D., Felkowski, L., Feng, M., Feo, M., Casani, A. Fernandez, Gomez, M. Fernandez, Fernez, A. D., Ferrari, F., Rodrigues, F. Ferreira, Ferrillo, M., Ferro-Luzzi, M., Filippov, S., Fini, R. A., Fiorini, M., Fischer, K. M., Fitzgerald, D. S., Fitzpatrick, C., Fleuret, F., Fontana, M., Foreman, L. F., Forty, R., Foulds-Holt, D., Sevilla, M. Franco, Frank, M., Franzoso, E., Frau, G., Frei, C., Friday, D. A., Fu, J., Fuehring, Q., Fujii, Y., Fulghesu, T., Gabriel, E., Galati, G., Galati, M. D., Torreira, A. Gallas, Galli, D., Gambetta, S., Gandelman, M., Gandini, P., Ganie, B., Gao, H., Gao, R., Gao, Y., Garau, M., Martin, L. M. Garcia, Moreno, P. Garcia, Pardiñas, J. García, Garg, K. G., Garrido, L., Gaspar, C., Geertsema, R. E., Gerken, L. L., Gersabeck, E., Gersabeck, M., Gershon, T., Ghorbanimoghaddam, Z., Giambastiani, L., Giasemis, F. I., Gibson, V., Giemza, H. K., Gilman, A. L., Giovannetti, M., Gioventù, A., Girardey, L., Gironell, P. Gironella, Giugliano, C., Giza, M. A., Gkougkousis, E. L., Glaser, F. C., Gligorov, V. V., Göbel, C., Golobardes, E., Golubkov, D., Golutvin, A., Gomes, A., Fernandez, S. Gomez, Abrantes, F. Goncalves, Goncerz, M., Gong, G., Gooding, J. A., Gorelov, I. V., Gotti, C., Grabowski, J. P., Cardoso, L. A. Granado, Graugés, E., Graverini, E., Grazette, L., Graziani, G., Grecu, A. T., Greeven, L. M., Grieser, N. A., Grillo, L., Gromov, S., Gu, C., Guarise, M., Guittiere, M., Guliaeva, V., Günther, P. A., Guseinov, A. -K., Gushchin, E., Guz, Y., Gys, T., Habermann, K., Hadavizadeh, T., Hadjivasiliou, C., Haefeli, G., Haen, C., Haimberger, J., Hajheidari, M., Hallett, G. H., Halvorsen, M. M., Hamilton, P. M., Hammerich, J., Han, Q., Han, X., Hansmann-Menzemer, S., Hao, L., Harnew, N., Hartmann, M., Hashmi, S., He, J., Hemmer, F., Henderson, C., Henderson, R. D. L., Hennequin, A. M., Hennessy, K., Henry, L., Herd, J., Gascon, P. Herrero, Heuel, J., Hicheur, A., Mendizabal, G. Hijano, Hill, D., Hollitt, S. E., Horswill, J., Hou, R., Hou, Y., Howarth, N., Hu, J., Hu, W., Hu, X., Huang, W., Hulsbergen, W., Hunter, R. J., Hushchyn, M., Hutchcroft, D., Ilin, D., Ilten, P., Inglessi, A., Iniukhin, A., Ishteev, A., Ivshin, K., Jacobsson, R., Jage, H., Elles, S. J. Jaimes, Jakobsen, S., Jans, E., Jashal, B. K., Jawahery, A., Jevtic, V., Jiang, E., Jiang, X., Jiang, Y., Jiang, Y. J., John, M., Rajan, A. John Rubesh, Johnson, D., Jones, C. R., Jones, T. P., Joshi, S., Jost, B., Castella, J. Juan, Jurik, N., Juszczak, I., Kaminaris, D., Kandybei, S., Kane, M., Kang, Y., Kar, C., Karacson, M., Karpenkov, D., Kauniskangas, A., Kautz, J. W., Keizer, F., Kenzie, M., Ketel, T., Khanji, B., Kharisova, A., Kholodenko, S., Khreich, G., Kirn, T., Kirsebom, V. S., Kitouni, O., Klaver, S., Kleijne, N., Klimaszewski, K., Kmiec, M. R., Koliiev, S., Kolk, L., Konoplyannikov, A., Kopciewicz, P., Koppenburg, P., Korolev, M., Kostiuk, I., Kot, O., Kotriakhova, S., Kozachuk, A., Kravchenko, P., Kravchuk, L., Kreps, M., Krokovny, P., Krupa, W., Krzemien, W., Kshyvanskyi, O. K., Kubat, J., Kubis, S., Kucharczyk, M., Kudryavtsev, V., Kulikova, E., Kupsc, A., Kutsenko, B. K., Lacarrere, D., Gonzalez, P. Laguarta, Lai, A., Lampis, A., Lancierini, D., Gomez, C. Landesa, Lane, J. J., Lane, R., Langenbruch, C., Langer, J., Lantwin, O., Latham, T., Lazzari, F., Lazzeroni, C., Gac, R. Le, Lee, H., Lefèvre, R., Leflat, A., Legotin, S., Lehuraux, M., Cid, E. Lemos, Leroy, O., Lesiak, T., Leverington, B., Li, A., Li, C., Li, H., Li, K., Li, L., Li, P., Li, P. -R., Li, Q., Li, S., Li, T., Li, Y., Lian, Z., Liang, X., Libralon, S., Lin, C., Lin, T., Lindner, R., Lisovskyi, V., Litvinov, R., Liu, F. L., Liu, G., Liu, K., Liu, S., Liu, W., Liu, Y., Liu, Y. L., Salvia, A. Lobo, Loi, A., Castro, J. Lomba, Long, T., Lopes, J. H., Huertas, A. Lopez, Soliño, S. López, Lucarelli, C., Lucchesi, D., Martinez, M. Lucio, Lukashenko, V., Luo, Y., Lupato, A., Luppi, E., Lynch, K., Lyu, X. -R., Ma, G. M., Ma, R., Maccolini, S., Machefert, F., Maciuc, F., Mack, B., Mackay, I., Mackey, L. M., Mohan, L. R. Madhan, Madurai, M. M., Maevskiy, A., Magdalinski, D., Maisuzenko, D., Majewski, M. W., Malczewski, J. J., Malde, S., Malentacca, L., Malinin, A., Maltsev, T., Manca, G., Mancinelli, G., Mancuso, C., Escalero, R. Manera, Manuzzi, D., Marangotto, D., Marchand, J. F., Marchevski, R., Marconi, U., Mariani, S., Benito, C. Marin, Marks, J., Marshall, A. M., Martel, L., Martelli, G., Martellotti, G., Martinazzoli, L., Martinelli, M., Santos, D. Martinez, Vidal, F. Martinez, Massafferri, A., Matev, R., Mathad, A., Matiunin, V., Matteuzzi, C., Mattioli, K. R., Mauri, A., Maurice, E., Mauricio, J., Mayencourt, P., de Cos, J. Mazorra, Mazurek, M., McCann, M., Mcconnell, L., McGrath, T. H., McHugh, N. T., McNab, A., McNulty, R., Meadows, B., Meier, G., Melnychuk, D., Meng, F. M., Merk, M., Merli, A., Garcia, L. Meyer, Miao, D., Miao, H., Mikhasenko, M., Milanes, D. A., Minotti, A., Minucci, E., Miralles, T., Mitreska, B., Mitzel, D. S., Modak, A., Mohammed, R. A., Moise, R. D., Mokhnenko, S., Mombächer, T., Monk, M., Monteil, S., Gomez, A. Morcillo, Morello, G., Morello, M. J., Morgenthaler, M. P., Morris, A. B., Morris, A. G., Mountain, R., Mu, H., Mu, Z. M., Muhammad, E., Muheim, F., Mulder, M., Müller, K., Muñoz-Rojas, F., Murta, R., Naik, P., Nakada, T., Nandakumar, R., Nanut, T., Nasteva, I., Needham, M., Neri, N., Neubert, S., Neufeld, N., Neustroev, P., Nicolini, J., Nicotra, D., Niel, E. M., Nikitin, N., Nogarolli, P., Nogga, P., Nolte, N. S., Normand, C., Fernandez, J. Novoa, Nowak, G., Nunez, C., Nur, H. N., Oblakowska-Mucha, A., Obraztsov, V., Oeser, T., Okamura, S., Okhotnikov, A., Okhrimenko, O., Oldeman, R., Oliva, F., Olocco, M., Onderwater, C. J. G., O'Neil, R. H., Osthues, D., Goicochea, J. M. Otalora, Owen, P., Oyanguren, A., Ozcelik, O., Padee, A., Padeken, K. O., Pagare, B., Pais, P. R., Pajero, T., Palano, A., Palutan, M., Panshin, G., Paolucci, L., Papanestis, A., Pappagallo, M., Pappalardo, L. L., Pappenheimer, C., Parkes, C., Passalacqua, B., Passaleva, G., Passaro, D., Pastore, A., Patel, M., Patoc, J., Patrignani, C., Paul, A., Pawley, C. J., Pellegrino, A., Peng, J., Altarelli, M. Pepe, Perazzini, S., Pereima, D., Da Costa, H. Pereira, Castro, A. Pereiro, Perret, P., Perro, A., Petridis, K., Petrolini, A., Pfaller, J. P., Pham, H., Pica, L., Piccini, M., Pietrzyk, B., Pietrzyk, G., Pinci, D., Pisani, F., Pizzichemi, M., Placinta, V., Casasus, M. Plo, Poeschl, T., Polci, F., Lener, M. Poli, Poluektov, A., Polukhina, N., Polyakov, I., Polycarpo, E., Ponce, S., Popov, D., Poslavskii, S., Prasanth, K., Prouve, C., Pugatch, V., Punzi, G., Qasim, S., Qian, Q. Q., Qian, W., Qin, N., Qu, S., Quagliani, R., Trejo, R. I. Rabadan, Rademacker, J. H., Rama, M., García, M. Ramírez, De Oliveira, V. Ramos, Pernas, M. Ramos, Rangel, M. S., Ratnikov, F., Raven, G., De Miguel, M. Rebollo, Redi, F., Reich, J., Reiss, F., Ren, Z., Resmi, P. K., Ribatti, R., Ricart, G. R., Riccardi, D., Ricciardi, S., Richardson, K., Richardson-Slipper, M., Rinnert, K., Robbe, P., Robertson, G., Rodrigues, E., Fernandez, E. Rodriguez, Lopez, J. A. Rodriguez, Rodriguez, E. Rodriguez, Roensch, J., Rogachev, A., Rogovskiy, A., Rolf, D. L., Roloff, P., Romanovskiy, V., Lamas, M. Romero, Vidal, A. Romero, Romolini, G., Ronchetti, F., Rong, T., Rotondo, M., Roy, S. R., Rudolph, M. S., Diaz, M. Ruiz, Fernandez, R. A. Ruiz, Vidal, J. Ruiz, Ryzhikov, A., Ryzka, J., Saavedra-Arias, J. J., Silva, J. J. Saborido, Sadek, R., Sagidova, N., Sahoo, D., Sahoo, N., Saitta, B., Salomoni, M., Gras, C. Sanchez, Sanderswood, I., Santacesaria, R., Rios, C. Santamarina, Santimaria, M., Santoro, L., Santovetti, E., Saputi, A., Saranin, D., Sarnatskiy, A. S., Sarpis, G., Sarpis, M., Satriano, C., Satta, A., Saur, M., Savrina, D., Sazak, H., Smead, L. G. Scantlebury, Scarabotto, A., Schael, S., Scherl, S., Schiller, M., Schindler, H., Schmelling, M., Schmidt, B., Schmitt, S., Schmitz, H., Schneider, O., Schopper, A., Schulte, N., Schulte, S., Schune, M. H., Schwemmer, R., Schwering, G., Sciascia, B., Sciuccati, A., Sellam, S., Semennikov, A., Senger, T., Soares, M. Senghi, Sergi, A., Serra, N., Sestini, L., Seuthe, A., Shang, Y., Shangase, D. M., Shapkin, M., Sharma, R. S., Shchemerov, I., Shchutska, L., Shears, T., Shekhtman, L., Shen, Z., Sheng, S., Shevchenko, V., Shi, B., Shi, Q., Shimizu, Y., Shmanin, E., Shorkin, R., Shupperd, J. D., Coutinho, R. Silva, Simi, G., Simone, S., Skidmore, N., Skwarnicki, T., Slater, M. W., Smallwood, J. C., Smith, E., Smith, K., Smith, M., Snoch, A., Lavra, L. Soares, Sokoloff, M. D., Soler, F. J. P., Solomin, A., Solovev, A., Solovyev, I., Song, R., Song, Y., Song, Y. S., De Almeida, F. L. Souza, De Paula, B. Souza, Norella, E. Spadaro, Spedicato, E., Speer, J. G., Spiridenkov, E., Spradlin, P., Sriskaran, V., Stagni, F., Stahl, M., Stahl, S., Stanislaus, S., Stein, E. N., Steinkamp, O., Stenyakin, O., Stevens, H., Strekalina, D., Su, Y., Suljik, F., Sun, J., Sun, L., Sun, Y., Lima, D. S. Sundfeld, Sutcliffe, W., Swallow, P. N., Swystun, F., Szabelski, A., Szumlak, T., Tan, Y., Tat, M. D., Terentev, A., Terzuoli, F., Teubert, F., Thomas, E., Thompson, D. J. D., Tilquin, H., Tisserand, V., T'Jampens, S., Tobin, M., Tomassetti, L., Tonani, G., Tong, X., Machado, D. Torres, Toscano, L., Tou, D. Y., Trippl, C., Tuci, G., Tuning, N., Uecker, L. H., Ukleja, A., Unverzagt, D. J., Ursov, E., Usachov, A., Ustyuzhanin, A., Uwer, U., Vagnoni, V., Valenti, G., Canudas, N. Valls, Van Hecke, H., van Herwijnen, E., Van Hulse, C. B., Van Laak, R., van Veghel, M., Vasquez, G., Gomez, R. Vazquez, Regueiro, P. Vazquez, Sierra, C. Vázquez, Vecchi, S., Velthuis, J. J., Veltri, M., Venkateswaran, A., Vesterinen, M., Benet, D. Vico, Diaz, M. Vieites, Vilasis-Cardona, X., Figueras, E. Vilella, Villa, A., Vincent, P., Volle, F. C., Bruch, D. vom, Voropaev, N., Vos, K., Vouters, G., Vrahas, C., Wagner, J., Walsh, J., Walton, E. J., Wan, G., Wang, C., Wang, G., Wang, J., Wang, M., Wang, N. W., Wang, R., Wang, X., Wang, X. W., Wang, Y., Wang, Z., Ward, J. A., Waterlaat, M., Watson, N. K., Websdale, D., Wei, Y., Wendel, J., Westhenry, B. D. C., White, C., Whitehead, M., Whiter, E., Wiederhold, A. R., Wiedner, D., Wilkinson, G., Wilkinson, M. K., Williams, M., Williams, M. R. J., Williams, R., Williams, Z., Wilson, F. F., Wislicki, W., Witek, M., Witola, L., Wong, C. P., Wormser, G., Wotton, S. A., Wu, H., Wu, J., Wu, Y., Wyllie, K., Xian, S., Xiang, Z., Xie, Y., Xu, A., Xu, J., Xu, L., Xu, M., Xu, Z., Yang, D., Yang, K., Yang, S., Yang, X., Yang, Y., Yang, Z., Yeroshenko, V., Yeung, H., Yin, H., Yu, C. Y., Yu, J., Yuan, X., Yuan, Y, Zaffaroni, E., Zavertyaev, M., Zdybal, M., Zeng, C., Zeng, M., Zhang, C., Zhang, D., Zhang, J., Zhang, L., Zhang, S., Zhang, Y., Zhang, Y. Z., Zhao, Y., Zharkova, A., Zhelezov, A., Zheng, S. Z., Zheng, X. Z., Zheng, Y., Zhou, T., Zhou, X., Zhou, Y., Zhovkovska, V., Zhu, L. Z., Zhu, X., Zhukov, V., Zhuo, J., Zou, Q., Zuliani, D., and Zunica, G.
Subjects: High Energy Physics - Experiment
Abstract: The radiative decays $\chi_{c1}(3872)\rightarrow\psi(2S)\gamma$ and $\chi_{c1}(3872)\rightarrow J/\psi\gamma$ are used to probe the~nature of the~$\chi_{c1}(3872)$ state using proton-proton collision data collected with the LHCb detector, corresponding to an~integrated luminosity of~9fb$^{-1}$. Using the~$B^+\rightarrow \chi_{c1}(3872)K^+$decay, the $\chi_{c1}(3872)\rightarrow \psi(2S)\gamma$ process is observed for the first time and the ratio of its partial width to that of the $\chi_{c1}(3872)\rightarrow J/\psi\gamma$ decay is measured to be $$ \frac{\Gamma_{\chi_{c1}(3872)\rightarrow \psi(2S)\gamma}} {\Gamma_{\chi_{c1}(3872)\rightarrow J/\psi\gamma}} = 1.67 \pm 0.21 \pm 0.12 \pm0.04 , $$ where the first uncertainty is statistical, the second systematic and the third is due to the uncertainties on the branching fractions of the $\psi(2S)$ and $J/\psi$ mesons. The measured ratio makes the interpretation of the $\chi_{c1}(3872)$ state as a~pure $D^0\bar{D}^{*0}+\bar{D}^0D^{*0}$ molecule questionable and strongly indicates a sizeable compact charmonium or tetraquark component within the $\chi_{c1}(3872)$ state., Comment: 31 pages, 2 figures. All figures and tables, along with any supplementary material and additional information, are available at https://cern.ch/lhcbproject/Publications/p/LHCb-PAPER-2024-015.html (LHCb public pages)
Published: 2024

224. Precision measurement of the $\Xi^-_b$ baryon lifetime

Author: LHCb collaboration, Aaij, R., Abdelmotteleb, A. S. W., Beteta, C. Abellan, Abudinén, F., Ackernley, T., Adefisoye, A. A., Adeva, B., Adinolfi, M., Adlarson, P., Agapopoulou, C., Aidala, C. A., Ajaltouni, Z., Akar, S., Akiba, K., Albicocco, P., Albrecht, J., Alessio, F., Alexander, M., Aliouche, Z., Cartelle, P. Alvarez, Amalric, R., Amato, S., Amey, J. L., Amhis, Y., An, L., Anderlini, L., Andersson, M., Andreianov, A., Andreola, P., Andreotti, M., Andreou, D., Anelli, A., Ao, D., Archilli, F., Argenton, M., Cuendis, S. Arguedas, Artamonov, A., Artuso, M., Aslanides, E., Da Silva, R. Ataide, Atzeni, M., Audurier, B., Bacher, D., Perea, I. Bachiller, Bachmann, S., Bachmayer, M., Back, J. J., Rodriguez, P. Baladron, Balagura, V., Baldini, W., Bao, H., Leite, J. Baptista de Souza, Barbetti, M., Barbosa, I. R., Barlow, R. J., Barnyakov, M., Barsuk, S., Barter, W., Bartolini, M., Bartz, J., Basels, J. M., Bassi, G., Batsukh, B., Bay, A., Beck, A., Becker, M., Bedeschi, F., Bediaga, I. B., Belin, S., Bellee, V., Belous, K., Belov, I., Belyaev, I., Benane, G., Bencivenni, G., Ben-Haim, E., Berezhnoy, A., Bernet, R., Andres, S. Bernet, Bertolin, A., Betancourt, C., Betti, F., Bex, J., Bezshyiko, Ia., Bhom, J., Bieker, M. S., Biesuz, N. V., Billoir, P., Biolchini, A., Birch, M., Bishop, F. C. R., Bitadze, A., Bizzeti, A., Blake, T., Blanc, F., Blank, J. E., Blusk, S., Bocharnikov, V., Boelhauve, J. A., Garcia, O. Boente, Boettcher, T., Bohare, A., Boldyrev, A., Bolognani, C. S., Bolzonella, R., Bondar, N., Borgato, F., Borghi, S., Borsato, M., Borsuk, J. T., Bouchiba, S. A., Bowcock, T. J. V., Boyer, A., Bozzi, C., Rodriguez, A. Brea, Breer, N., Brodzicka, J., Gonzalo, A. Brossa, Brown, J., Brundu, D., Buchanan, E., Buonaura, A., Buonincontri, L., Burke, A. T., Burr, C., Butkevich, A., Butter, J. S., Buytaert, J., Byczynski, W., Cadeddu, S., Cai, H., Calabrese, R., Ramirez, S. Calderon, Calefice, L., Cali, S., Calvi, M., Gomez, M. Calvo, Magalhaes, P. Camargo, Bouzas, J. I. Cambon, Campana, P., Perez, D. H. Campora, Quezada, A. F. Campoverde, Capelli, S., Capriotti, L., Caravaca-Mora, R., Carbone, A., Salgado, L. Carcedo, Cardinale, R., Cardini, A., Carniti, P., Carus, L., Vidal, A. Casais, Caspary, R., Casse, G., Godinez, J. Castro, Cattaneo, M., Cavallero, G., Cavallini, V., Celani, S., Cervenkov, D., Cesare, S., Chadwick, A. J., Chahrour, I., Charles, M., Charpentier, Ph., Chatzianagnostou, E., Barajas, C. A. Chavez, Chefdeville, M., Chen, C., Chen, S., Chen, Z., Chernov, A., Chernyshenko, S., Chobanova, V., Cholak, S., Chrzaszcz, M., Chubykin, A., Chulikov, V., Ciambrone, P., Vidal, X. Cid, Ciezarek, G., Cifra, P., Clarke, P. E. L., Clemencic, M., Cliff, H. V., Closier, J., Toapaxi, C. Cocha, Coco, V., Cogan, J., Cogneras, E., Cojocariu, L., Collins, P., Colombo, T., Comerma-Montells, A., Congedo, L., Contu, A., Cooke, N., Corredoira, I., Correia, A., Corti, G., Meldrum, J. J. Cottee, Couturier, B., Craik, D. C., Torres, M. Cruz, Rivera, E. Curras, Currie, R., Da Silva, C. L., Dadabaev, S., Dai, L., Dai, X., Dall'Occo, E., Dalseno, J., D'Ambrosio, C., Daniel, J., Danilina, A., d'Argent, P., Davidson, A., Davies, J. E., Davis, A., Francisco, O. De Aguiar, De Angelis, C., De Benedetti, F., de Boer, J., De Bruyn, K., De Capua, S., De Cian, M., Da Graca, U. De Freitas Carneiro, De Lucia, E., De Miranda, J. M., De Paula, L., De Serio, M., De Simone, P., De Vellis, F., de Vries, J. A., Debernardis, F., Decamp, D., Dedu, V., Del Buono, L., Delaney, B., Dembinski, H. -P., Deng, J., Denysenko, V., Deschamps, O., Dettori, F., Dey, B., Di Nezza, P., Diachkov, I., Didenko, S., Ding, S., Dittmann, L., Dobishuk, V., Docheva, A. D., Dong, C., Donohoe, A. M., Dordei, F., Reis, A. C. dos, Dowling, A. D., Duan, W., Duda, P., Dudek, M. W., Dufour, L., Duk, V., Durante, P., Duras, M. M., Durham, J. M., Durmus, O. D., Dziurda, A., Dzyuba, A., Easo, S., Eckstein, E., Egede, U., Egorychev, A., Egorychev, V., Eisenhardt, S., Ejopu, E., Eklund, L., Elashri, M., Ellbracht, J., Ely, S., Ene, A., Epple, E., Eschle, J., Esen, S., Evans, T., Fabiano, F., Falcao, L. N., Fan, Y., Fang, B., Fantini, L., Faria, M., Farmer, K., Fazzini, D., Felkowski, L., Feng, M., Feo, M., Gomez, M. Fernandez, Fernez, A. D., Ferrari, F., Rodrigues, F. Ferreira, Ferrillo, M., Ferro-Luzzi, M., Filippov, S., Fini, R. A., Fiorini, M., Fischer, K. M., Fitzgerald, D. S., Fitzpatrick, C., Fleuret, F., Fontana, M., Foreman, L. F., Forty, R., Foulds-Holt, D., Sevilla, M. Franco, Frank, M., Franzoso, E., Frau, G., Frei, C., Friday, D. A., Fu, J., Fuehring, Q., Fujii, Y., Fulghesu, T., Gabriel, E., Galati, G., Galati, M. D., Torreira, A. Gallas, Galli, D., Gambetta, S., Gandelman, M., Gandini, P., Ganie, B., Gao, H., Gao, R., Gao, Y., Garau, M., Martin, L. M. Garcia, Moreno, P. Garcia, Pardiñas, J. García, Garg, K. G., Garrido, L., Gaspar, C., Geertsema, R. E., Gerken, L. L., Gersabeck, E., Gersabeck, M., Gershon, T., Ghorbanimoghaddam, Z., Giambastiani, L., Giasemis, F. I., Gibson, V., Giemza, H. K., Gilman, A. L., Giovannetti, M., Gioventù, A., Gironell, P. Gironella, Giugliano, C., Giza, M. A., Gkougkousis, E. L., Glaser, F. C., Gligorov, V. V., Göbel, C., Golobardes, E., Golubkov, D., Golutvin, A., Gomes, A., Fernandez, S. Gomez, Abrantes, F. Goncalves, Goncerz, M., Gong, G., Gooding, J. A., Gorelov, I. V., Gotti, C., Grabowski, J. P., Cardoso, L. A. Granado, Graugés, E., Graverini, E., Grazette, L., Graziani, G., Grecu, A. T., Greeven, L. M., Grieser, N. A., Grillo, L., Gromov, S., Gu, C., Guarise, M., Guittiere, M., Guliaeva, V., Günther, P. A., Guseinov, A. -K., Gushchin, E., Guz, Y., Gys, T., Habermann, K., Hadavizadeh, T., Hadjivasiliou, C., Haefeli, G., Haen, C., Haimberger, J., Hajheidari, M., Halvorsen, M. M., Hamilton, P. M., Hammerich, J., Han, Q., Han, X., Hansmann-Menzemer, S., Hao, L., Harnew, N., Hartmann, M., He, J., Hemmer, F., Henderson, C., Henderson, R. D. L., Hennequin, A. M., Hennessy, K., Henry, L., Herd, J., Gascon, P. Herrero, Heuel, J., Hicheur, A., Mendizabal, G. Hijano, Hill, D., Hollitt, S. E., Horswill, J., Hou, R., Hou, Y., Howarth, N., Hu, J., Hu, W., Hu, X., Huang, W., Hulsbergen, W., Hunter, R. J., Hushchyn, M., Hutchcroft, D., Ilin, D., Ilten, P., Inglessi, A., Iniukhin, A., Ishteev, A., Ivshin, K., Jacobsson, R., Jage, H., Elles, S. J. Jaimes, Jakobsen, S., Jans, E., Jashal, B. K., Jawahery, A., Jevtic, V., Jiang, E., Jiang, X., Jiang, Y., Jiang, Y. J., John, M., Johnson, D., Jones, C. R., Jones, T. P., Joshi, S., Jost, B., Jurik, N., Juszczak, I., Kaminaris, D., Kandybei, S., Kang, Y., Kar, C., Karacson, M., Karpenkov, D., Kauniskangas, A., Kautz, J. W., Keizer, F., Kenzie, M., Ketel, T., Khanji, B., Kharisova, A., Kholodenko, S., Khreich, G., Kirn, T., Kirsebom, V. S., Kitouni, O., Klaver, S., Kleijne, N., Klimaszewski, K., Kmiec, M. R., Koliiev, S., Kolk, L., Konoplyannikov, A., Kopciewicz, P., Koppenburg, P., Korolev, M., Kostiuk, I., Kot, O., Kotriakhova, S., Kozachuk, A., Kravchenko, P., Kravchuk, L., Kreps, M., Krokovny, P., Krupa, W., Krzemien, W., Kshyvanskyi, O. K., Kubat, J., Kubis, S., Kucharczyk, M., Kudryavtsev, V., Kulikova, E., Kupsc, A., Kutsenko, B. K., Lacarrere, D., Lai, A., Lampis, A., Lancierini, D., Gomez, C. Landesa, Lane, J. J., Lane, R., Langenbruch, C., Langer, J., Lantwin, O., Latham, T., Lazzari, F., Lazzeroni, C., Gac, R. Le, Lefèvre, R., Leflat, A., Legotin, S., Lehuraux, M., Cid, E. Lemos, Leroy, O., Lesiak, T., Leverington, B., Li, A., Li, H., Li, K., Li, L., Li, P., Li, P. -R., Li, Q., Li, S., Li, T., Li, Y., Lian, Z., Liang, X., Libralon, S., Lin, C., Lin, T., Lindner, R., Lisovskyi, V., Litvinov, R., Liu, F. L., Liu, G., Liu, K., Liu, S., Liu, Y., Liu, Y. L., Salvia, A. Lobo, Loi, A., Castro, J. Lomba, Long, T., Lopes, J. H., Huertas, A. Lopez, Soliño, S. López, Lucarelli, C., Lucchesi, D., Martinez, M. Lucio, Lukashenko, V., Luo, Y., Lupato, A., Luppi, E., Lynch, K., Lyu, X. -R., Ma, G. M., Ma, R., Maccolini, S., Machefert, F., Maciuc, F., Mack, B., Mackay, I., Mackey, L. M., Mohan, L. R. Madhan, Madurai, M. M., Maevskiy, A., Magdalinski, D., Maisuzenko, D., Majewski, M. W., Malczewski, J. J., Malde, S., Malentacca, L., Malinin, A., Maltsev, T., Manca, G., Mancinelli, G., Mancuso, C., Escalero, R. Manera, Manuzzi, D., Marangotto, D., Marchand, J. F., Marchevski, R., Marconi, U., Mariani, S., Benito, C. Marin, Marks, J., Marshall, A. M., Martelli, G., Martellotti, G., Martinazzoli, L., Martinelli, M., Santos, D. Martinez, Vidal, F. Martinez, Massafferri, A., Matev, R., Mathad, A., Matiunin, V., Matteuzzi, C., Mattioli, K. R., Mauri, A., Maurice, E., Mauricio, J., Mayencourt, P., Mazurek, M., McCann, M., Mcconnell, L., McGrath, T. H., McHugh, N. T., McNab, A., McNulty, R., Meadows, B., Meier, G., Melnychuk, D., Meng, F. M., Merk, M., Merli, A., Garcia, L. Meyer, Miao, D., Miao, H., Mikhasenko, M., Milanes, D. A., Minotti, A., Minucci, E., Miralles, T., Mitreska, B., Mitzel, D. S., Modak, A., Mödden, A., Mohammed, R. A., Moise, R. D., Mokhnenko, S., Mombächer, T., Monk, M., Monteil, S., Gomez, A. Morcillo, Morello, G., Morello, M. J., Morgenthaler, M. P., Morris, A. B., Morris, A. G., Mountain, R., Mu, H., Mu, Z. M., Muhammad, E., Muheim, F., Mulder, M., Müller, K., Muñoz-Rojas, F., Murta, R., Naik, P., Nakada, T., Nandakumar, R., Nanut, T., Nasteva, I., Needham, M., Neri, N., Neubert, S., Neufeld, N., Neustroev, P., Nicolini, J., Nicotra, D., Niel, E. M., Nikitin, N., Nogarolli, P., Nogga, P., Nolte, N. S., Normand, C., Fernandez, J. Novoa, Nowak, G., Nunez, C., Nur, H. N., Oblakowska-Mucha, A., Obraztsov, V., Oeser, T., Okamura, S., Okhotnikov, A., Okhrimenko, O., Oldeman, R., Oliva, F., Olocco, M., Onderwater, C. J. G., O'Neil, R. H., Goicochea, J. M. Otalora, Owen, P., Oyanguren, A., Ozcelik, O., Padeken, K. O., Pagare, B., Pais, P. R., Pajero, T., Palano, A., Palutan, M., Panshin, G., Paolucci, L., Papanestis, A., Pappagallo, M., Pappalardo, L. L., Pappenheimer, C., Parkes, C., Passalacqua, B., Passaleva, G., Passaro, D., Pastore, A., Patel, M., Patoc, J., Patrignani, C., Paul, A., Pawley, C. J., Pellegrino, A., Peng, J., Altarelli, M. Pepe, Perazzini, S., Pereima, D., Da Costa, H. Pereira, Castro, A. Pereiro, Perret, P., Perro, A., Petridis, K., Petrolini, A., Pfaller, J. P., Pham, H., Pica, L., Piccini, M., Pietrzyk, B., Pietrzyk, G., Pinci, D., Pisani, F., Pizzichemi, M., Placinta, V., Casasus, M. Plo, Polci, F., Lener, M. Poli, Poluektov, A., Polukhina, N., Polyakov, I., Polycarpo, E., Ponce, S., Popov, D., Poslavskii, S., Prasanth, K., Prouve, C., Pugatch, V., Punzi, G., Qasim, S., Qian, Q. Q., Qian, W., Qin, N., Qu, S., Quagliani, R., Trejo, R. I. Rabadan, Rademacker, J. H., Rama, M., García, M. Ramírez, De Oliveira, V. Ramos, Pernas, M. Ramos, Rangel, M. S., Ratnikov, F., Raven, G., De Miguel, M. Rebollo, Redi, F., Reich, J., Reiss, F., Ren, Z., Resmi, P. K., Ribatti, R., Ricart, G. R., Riccardi, D., Ricciardi, S., Richardson, K., Richardson-Slipper, M., Rinnert, K., Robbe, P., Robertson, G., Rodrigues, E., Fernandez, E. Rodriguez, Lopez, J. A. Rodriguez, Rodriguez, E. Rodriguez, Rogovskiy, A., Rolf, D. L., Roloff, P., Romanovskiy, V., Lamas, M. Romero, Vidal, A. Romero, Romolini, G., Ronchetti, F., Rong, T., Rotondo, M., Roy, S. R., Rudolph, M. S., Diaz, M. Ruiz, Fernandez, R. A. Ruiz, Vidal, J. Ruiz, Ryzhikov, A., Ryzka, J., Saavedra-Arias, J. J., Silva, J. J. Saborido, Sadek, R., Sagidova, N., Sahoo, D., Sahoo, N., Saitta, B., Salomoni, M., Gras, C. Sanchez, Sanderswood, I., Santacesaria, R., Rios, C. Santamarina, Santimaria, M., Santoro, L., Santovetti, E., Saputi, A., Saranin, D., Sarnatskiy, A. S., Sarpis, G., Sarpis, M., Satriano, C., Satta, A., Saur, M., Savrina, D., Sazak, H., Smead, L. G. Scantlebury, Scarabotto, A., Schael, S., Scherl, S., Schiller, M., Schindler, H., Schmelling, M., Schmidt, B., Schmitt, S., Schmitz, H., Schneider, O., Schopper, A., Schulte, N., Schulte, S., Schune, M. H., Schwemmer, R., Schwering, G., Sciascia, B., Sciuccati, A., Sellam, S., Semennikov, A., Senger, T., Soares, M. Senghi, Sergi, A., Serra, N., Sestini, L., Seuthe, A., Shang, Y., Shangase, D. M., Shapkin, M., Sharma, R. S., Shchemerov, I., Shchutska, L., Shears, T., Shekhtman, L., Shen, Z., Sheng, S., Shevchenko, V., Shi, B., Shi, Q., Shimizu, Y., Shmanin, E., Shorkin, R., Shupperd, J. D., Coutinho, R. Silva, Simi, G., Simone, S., Skidmore, N., Skwarnicki, T., Slater, M. W., Smallwood, J. C., Smith, E., Smith, K., Smith, M., Snoch, A., Lavra, L. Soares, Sokoloff, M. D., Soler, F. J. P., Solomin, A., Solovev, A., Solovyev, I., Song, R., Song, Y., Song, Y. S., De Almeida, F. L. Souza, De Paula, B. Souza, Norella, E. Spadaro, Spedicato, E., Speer, J. G., Spiridenkov, E., Spradlin, P., Sriskaran, V., Stagni, F., Stahl, M., Stahl, S., Stanislaus, S., Stein, E. N., Steinkamp, O., Stenyakin, O., Stevens, H., Strekalina, D., Su, Y., Suljik, F., Sun, J., Sun, L., Sun, Y., Lima, D. S. Sundfeld, Sutcliffe, W., Swallow, P. N., Swystun, F., Szabelski, A., Szumlak, T., Tan, Y., Tat, M. D., Terentev, A., Terzuoli, F., Teubert, F., Thomas, E., Thompson, D. J. D., Tilquin, H., Tisserand, V., T'Jampens, S., Tobin, M., Tomassetti, L., Tonani, G., Tong, X., Machado, D. Torres, Toscano, L., Tou, D. Y., Trippl, C., Tuci, G., Tuning, N., Uecker, L. H., Ukleja, A., Unverzagt, D. J., Ursov, E., Usachov, A., Ustyuzhanin, A., Uwer, U., Vagnoni, V., Valenti, G., Canudas, N. Valls, Van Hecke, H., van Herwijnen, E., Van Hulse, C. B., Van Laak, R., van Veghel, M., Vasquez, G., Gomez, R. Vazquez, Regueiro, P. Vazquez, Sierra, C. Vázquez, Vecchi, S., Velthuis, J. J., Veltri, M., Venkateswaran, A., Vesterinen, M., Diaz, M. Vieites, Vilasis-Cardona, X., Figueras, E. Vilella, Villa, A., Vincent, P., Volle, F. C., Bruch, D. vom, Voropaev, N., Vos, K., Vouters, G., Vrahas, C., Wagner, J., Walsh, J., Walton, E. J., Wan, G., Wang, C., Wang, G., Wang, J., Wang, M., Wang, N. W., Wang, R., Wang, X., Wang, X. W., Wang, Y., Wang, Z., Ward, J. A., Waterlaat, M., Watson, N. K., Websdale, D., Wei, Y., Wendel, J., Westhenry, B. D. C., White, D. J., Whitehead, M., Wiederhold, A. R., Wiedner, D., Wilkinson, G., Wilkinson, M. K., Williams, M., Williams, M. R. J., Williams, R., Wilson, F. F., Wislicki, W., Witek, M., Witola, L., Wong, C. P., Wormser, G., Wotton, S. A., Wu, H., Wu, J., Wu, Y., Wyllie, K., Xian, S., Xiang, Z., Xie, Y., Xu, A., Xu, J., Xu, L., Xu, M., Xu, Z., Yang, D., Yang, K., Yang, S., Yang, X., Yang, Y., Yang, Z., Yeroshenko, V., Yeung, H., Yin, H., Yu, C. Y., Yu, J., Yuan, X., Zaffaroni, E., Zavertyaev, M., Zdybal, M., Zeng, C., Zeng, M., Zhang, C., Zhang, D., Zhang, J., Zhang, L., Zhang, S., Zhang, Y., Zhang, Y. Z., Zhao, Y., Zharkova, A., Zhelezov, A., Zheng, S. Z., Zheng, X. Z., Zheng, Y., Zhou, T., Zhou, X., Zhou, Y., Zhovkovska, V., Zhu, L. Z., Zhu, X., Zhukov, V., Zhuo, J., Zou, Q., Zuliani, D., and Zunica, G.
Subjects: High Energy Physics - Experiment
Abstract: A sample of $pp$ collision data, corresponding to an integrated luminosity of 5.5 fb$^{-1}$ and collected by the LHCb experiment during LHC Run 2, is used to measure the ratio of the lifetime of the $\Xi^-_b$ baryon to that of the $\Lambda^0_b$ baryon, $r_{\tau}\equiv\tau_{\Xi^-_b}/\tau_{\Lambda^0_b}$. The value ${r_{\tau}=1.076\pm0.013\pm0.006}$ is obtained, where the first uncertainty is statistical and the second systematic. This value is averaged with the corresponding value from Run 1 to obtain ${r_{\tau}^{\rm Run\,1,2} = 1.078\pm0.012\pm0.007}$. Multiplying by the world-average value of the $\Lambda^0_b$ lifetime yields $\tau_{\Xi^-_b}^{\rm Run~1,2} = 1.578\pm0.018\pm0.010\pm0.011$ ps, where the uncertainties are statistical, systematic, and due to the limited knowledge of the $\Lambda^0_b$ lifetime. This measurement improves the precision of the current world average of the $\Xi^-_b$ lifetime by about a factor of two, and is in good agreement with the most recent theoretical predictions., Comment: 12 pages, 5 figures. All figures and tables, along with any supplementary material and additional information, are available at https://cern.ch/lhcbproject/Publications/p/LHCb-PAPER-2014-010.html (LHCb public pages)
Published: 2024
Full Text: View/download PDF

225. Measurement of the branching fraction ratios $R(D^{+})$ and $R(D^{*+})$ using muonic $\tau$ decays

Author: LHCb collaboration, Aaij, R., Abdelmotteleb, A. S. W., Beteta, C. Abellan, Abudinén, F., Ackernley, T., Adefisoye, A. A., Adeva, B., Adinolfi, M., Adlarson, P., Agapopoulou, C., Aidala, C. A., Ajaltouni, Z., Akar, S., Akiba, K., Albicocco, P., Albrecht, J., Alessio, F., Alexander, M., Aliouche, Z., Cartelle, P. Alvarez, Amalric, R., Amato, S., Amey, J. L., Amhis, Y., An, L., Anderlini, L., Andersson, M., Andreianov, A., Andreola, P., Andreotti, M., Andreou, D., Anelli, A., Ao, D., Archilli, F., Argenton, M., Cuendis, S. Arguedas, Artamonov, A., Artuso, M., Aslanides, E., Atzeni, M., Audurier, B., Bacher, D., Perea, I. Bachiller, Bachmann, S., Bachmayer, M., Back, J. J., Rodriguez, P. Baladron, Balagura, V., Baldini, W., Bao, H., Leite, J. Baptista de Souza, Barbetti, M., Barbosa, I. R., Barlow, R. J., Barnyakov, M., Barsuk, S., Barter, W., Bartolini, M., Bartz, J., Baryshnikov, F., Basels, J. M., Bassi, G., Batsukh, B., Bay, A., Beck, A., Becker, M., Bedeschi, F., Bediaga, I. B., Belin, S., Bellee, V., Belous, K., Belov, I., Belyaev, I., Benane, G., Bencivenni, G., Ben-Haim, E., Berezhnoy, A., Bernet, R., Andres, S. Bernet, Bertolin, A., Betancourt, C., Betti, F., Bex, J., Bezshyiko, Ia., Bhom, J., Bieker, M. S., Biesuz, N. V., Billoir, P., Biolchini, A., Birch, M., Bishop, F. C. R., Bitadze, A., Bizzeti, A., Blake, T., Blanc, F., Blank, J. E., Blusk, S., Bocharnikov, V., Boelhauve, J. A., Garcia, O. Boente, Boettcher, T., Bohare, A., Boldyrev, A., Bolognani, C. S., Bolzonella, R., Bondar, N., Borgato, F., Borghi, S., Borsato, M., Borsuk, J. T., Bouchiba, S. A., Bowcock, T. J. V., Boyer, A., Bozzi, C., Bradley, M. J., Rodriguez, A. Brea, Breer, N., Brodzicka, J., Gonzalo, A. Brossa, Brown, J., Brundu, D., Buchanan, E., Buonaura, A., Buonincontri, L., Burke, A. T., Burr, C., Butkevich, A., Butter, J. S., Buytaert, J., Byczynski, W., Cadeddu, S., Cai, H., Calabrese, R., Ramirez, S. Calderon, Calefice, L., Cali, S., Calvi, M., Gomez, M. Calvo, Magalhaes, P. Camargo, Bouzas, J. I. Cambon, Campana, P., Perez, D. H. Campora, Quezada, A. F. Campoverde, Capelli, S., Capriotti, L., Caravaca-Mora, R., Carbone, A., Salgado, L. Carcedo, Cardinale, R., Cardini, A., Carniti, P., Carus, L., Vidal, A. Casais, Caspary, R., Casse, G., Godinez, J. Castro, Cattaneo, M., Cavallero, G., Cavallini, V., Celani, S., Cervenkov, D., Cesare, S., Chadwick, A. J., Chahrour, I., Charles, M., Charpentier, Ph., Barajas, C. A. Chavez, Chefdeville, M., Chen, C., Chen, S., Chen, Z., Chernov, A., Chernyshenko, S., Chobanova, V., Cholak, S., Chrzaszcz, M., Chubykin, A., Chulikov, V., Ciambrone, P., Vidal, X. Cid, Ciezarek, G., Cifra, P., Clarke, P. E. L., Clemencic, M., Cliff, H. V., Closier, J., Toapaxi, C. Cocha, Coco, V., Cogan, J., Cogneras, E., Cojocariu, L., Collins, P., Colombo, T., Comerma-Montells, A., Congedo, L., Contu, A., Cooke, N., Corredoira, I., Correia, A., Corti, G., Meldrum, J. J. Cottee, Couturier, B., Craik, D. C., Torres, M. Cruz, Rivera, E. Curras, Currie, R., Da Silva, C. L., Dadabaev, S., Dai, L., Dai, X., Dall'Occo, E., Dalseno, J., D'Ambrosio, C., Daniel, J., Danilina, A., d'Argent, P., Davidson, A., Davies, J. E., Davis, A., Francisco, O. De Aguiar, De Angelis, C., De Benedetti, F., de Boer, J., De Bruyn, K., De Capua, S., De Cian, M., Da Graca, U. De Freitas Carneiro, De Lucia, E., De Miranda, J. M., De Paula, L., De Serio, M., De Simone, P., De Vellis, F., de Vries, J. A., Debernardis, F., Decamp, D., Dedu, V., Del Buono, L., Delaney, B., Dembinski, H. -P., Deng, J., Denysenko, V., Deschamps, O., Dettori, F., Dey, B., Di Nezza, P., Diachkov, I., Didenko, S., Ding, S., Dittmann, L., Dobishuk, V., Docheva, A. D., Dong, C., Donohoe, A. M., Dordei, F., Reis, A. C. dos, Dowling, A. D., Duan, W., Duda, P., Dudek, M. W., Dufour, L., Duk, V., Durante, P., Duras, M. M., Durham, J. M., Durmus, O. D., Dziurda, A., Dzyuba, A., Easo, S., Eckstein, E., Egede, U., Egorychev, A., Egorychev, V., Eisenhardt, S., Ejopu, E., Eklund, L., Elashri, M., Ellbracht, J., Ely, S., Ene, A., Epple, E., Eschle, J., Esen, S., Evans, T., Fabiano, F., Falcao, L. N., Fan, Y., Fang, B., Fantini, L., Faria, M., Farmer, K., Fazzini, D., Felkowski, L., Feng, M., Feo, M., Gomez, M. Fernandez, Fernez, A. D., Ferrari, F., Rodrigues, F. Ferreira, Ferrillo, M., Ferro-Luzzi, M., Filippov, S., Fini, R. A., Fiorini, M., Fischer, K. M., Fitzgerald, D. S., Fitzpatrick, C., Fleuret, F., Fontana, M., Foreman, L. F., Forty, R., Foulds-Holt, D., Sevilla, M. Franco, Frank, M., Franzoso, E., Frau, G., Frei, C., Friday, D. A., Fu, J., Fuehring, Q., Fujii, Y., Fulghesu, T., Gabriel, E., Galati, G., Galati, M. D., Torreira, A. Gallas, Galli, D., Gambetta, S., Gandelman, M., Gandini, P., Ganie, B., Gao, H., Gao, R., Gao, Y., Garau, M., Martin, L. M. Garcia, Moreno, P. Garcia, Pardiñas, J. García, Garg, K. G., Garrido, L., Gaspar, C., Geertsema, R. E., Gerken, L. L., Gersabeck, E., Gersabeck, M., Gershon, T., Ghorbanimoghaddam, Z., Giambastiani, L., Giasemis, F. I., Gibson, V., Giemza, H. K., Gilman, A. L., Giovannetti, M., Gioventù, A., Gironell, P. Gironella, Giugliano, C., Giza, M. A., Gkougkousis, E. L., Glaser, F. C., Gligorov, V. V., Göbel, C., Golobardes, E., Golubkov, D., Golutvin, A., Gomes, A., Fernandez, S. Gomez, Abrantes, F. Goncalves, Goncerz, M., Gong, G., Gooding, J. A., Gorelov, I. V., Gotti, C., Grabowski, J. P., Cardoso, L. A. Granado, Graugés, E., Graverini, E., Grazette, L., Graziani, G., Grecu, A. T., Greeven, L. M., Grieser, N. A., Grillo, L., Gromov, S., Gu, C., Guarise, M., Guittiere, M., Guliaeva, V., Günther, P. A., Guseinov, A. -K., Gushchin, E., Guz, Y., Gys, T., Habermann, K., Hadavizadeh, T., Hadjivasiliou, C., Haefeli, G., Haen, C., Haimberger, J., Hajheidari, M., Halvorsen, M. M., Hamilton, P. M., Hammerich, J., Han, Q., Han, X., Hansmann-Menzemer, S., Hao, L., Harnew, N., Hartmann, M., He, J., Hemmer, F., Henderson, C., Henderson, R. D. L., Hennequin, A. M., Hennessy, K., Henry, L., Herd, J., Gascon, P. Herrero, Heuel, J., Hicheur, A., Mendizabal, G. Hijano, Hill, D., Hollitt, S. E., Horswill, J., Hou, R., Hou, Y., Howarth, N., Hu, J., Hu, W., Hu, X., Huang, W., Hulsbergen, W., Hunter, R. J., Hushchyn, M., Hutchcroft, D., Ilin, D., Ilten, P., Inglessi, A., Iniukhin, A., Ishteev, A., Ivshin, K., Jacobsson, R., Jage, H., Elles, S. J. Jaimes, Jakobsen, S., Jans, E., Jashal, B. K., Jawahery, A., Jevtic, V., Jiang, E., Jiang, X., Jiang, Y., Jiang, Y. J., John, M., Johnson, D., Jones, C. R., Jones, T. P., Joshi, S., Jost, B., Jurik, N., Juszczak, I., Kaminaris, D., Kandybei, S., Kang, Y., Kar, C., Karacson, M., Karpenkov, D., Kauniskangas, A., Kautz, J. W., Keizer, F., Kenzie, M., Ketel, T., Khanji, B., Kharisova, A., Kholodenko, S., Khreich, G., Kirn, T., Kirsebom, V. S., Kitouni, O., Klaver, S., Kleijne, N., Klimaszewski, K., Kmiec, M. R., Koliiev, S., Kolk, L., Konoplyannikov, A., Kopciewicz, P., Koppenburg, P., Korolev, M., Kostiuk, I., Kot, O., Kotriakhova, S., Kozachuk, A., Kravchenko, P., Kravchuk, L., Kreps, M., Krokovny, P., Krupa, W., Krzemien, W., Kshyvanskyi, O. K., Kubat, J., Kubis, S., Kucharczyk, M., Kudryavtsev, V., Kulikova, E., Kupsc, A., Kutsenko, B. K., Lacarrere, D., Lai, A., Lampis, A., Lancierini, D., Gomez, C. Landesa, Lane, J. J., Lane, R., Langenbruch, C., Langer, J., Lantwin, O., Latham, T., Lazzari, F., Lazzeroni, C., Gac, R. Le, Lefèvre, R., Leflat, A., Legotin, S., Lehuraux, M., Cid, E. Lemos, Leroy, O., Lesiak, T., Leverington, B., Li, A., Li, H., Li, K., Li, L., Li, P., Li, P. -R., Li, Q., Li, S., Li, T., Li, Y., Lian, Z., Liang, X., Libralon, S., Lin, C., Lin, T., Lindner, R., Lisovskyi, V., Litvinov, R., Liu, F. L., Liu, G., Liu, K., Liu, S., Liu, Y., Liu, Y. L., Salvia, A. Lobo, Loi, A., Castro, J. Lomba, Long, T., Lopes, J. H., Huertas, A. Lopez, Soliño, S. López, Lucarelli, C., Lucchesi, D., Martinez, M. Lucio, Lukashenko, V., Luo, Y., Lupato, A., Luppi, E., Lynch, K., Lyu, X. -R., Ma, G. M., Ma, R., Maccolini, S., Machefert, F., Maciuc, F., Mack, B., Mackay, I., Mackey, L. M., Mohan, L. R. Madhan, Madurai, M. M., Maevskiy, A., Magdalinski, D., Maisuzenko, D., Majewski, M. W., Malczewski, J. J., Malde, S., Malentacca, L., Malinin, A., Maltsev, T., Manca, G., Mancinelli, G., Mancuso, C., Escalero, R. Manera, Manuzzi, D., Marangotto, D., Marchand, J. F., Marchevski, R., Marconi, U., Mariani, S., Benito, C. Marin, Marks, J., Marshall, A. M., Martelli, G., Martellotti, G., Martinazzoli, L., Martinelli, M., Santos, D. Martinez, Vidal, F. Martinez, Massafferri, A., Matev, R., Mathad, A., Matiunin, V., Matteuzzi, C., Mattioli, K. R., Mauri, A., Maurice, E., Mauricio, J., Mayencourt, P., Mazurek, M., McCann, M., Mcconnell, L., McGrath, T. H., McHugh, N. T., McNab, A., McNulty, R., Meadows, B., Meier, G., Melnychuk, D., Meloni, S, Meng, F. M., Merk, M., Merli, A., Garcia, L. Meyer, Miao, D., Miao, H., Mikhasenko, M., Milanes, D. A., Minotti, A., Minucci, E., Miralles, T., Mitreska, B., Mitzel, D. S., Modak, A., Mödden, A., Mohammed, R. A., Moise, R. D., Mokhnenko, S., Mombächer, T., Monk, M., Monteil, S., Gomez, A. Morcillo, Morello, G., Morello, M. J., Morgenthaler, M. P., Morris, A. B., Morris, A. G., Mountain, R., Mu, H., Mu, Z. M., Muhammad, E., Muheim, F., Mulder, M., Müller, K., Muñoz-Rojas, F., Murta, R., Naik, P., Nakada, T., Nandakumar, R., Nanut, T., Nasteva, I., Needham, M., Neri, N., Neubert, S., Neufeld, N., Neustroev, P., Nicolini, J., Nicotra, D., Niel, E. M., Nikitin, N., Nogarolli, P., Nogga, P., Nolte, N. S., Normand, C., Fernandez, J. Novoa, Nowak, G., Nunez, C., Nur, H. N., Oblakowska-Mucha, A., Obraztsov, V., Oeser, T., Okamura, S., Okhotnikov, A., Okhrimenko, O., Oldeman, R., Oliva, F., Olocco, M., Onderwater, C. J. G., O'Neil, R. H., Goicochea, J. M. Otalora, Owen, P., Oyanguren, A., Ozcelik, O., Padeken, K. O., Pagare, B., Pais, P. R., Pajero, T., Palano, A., Palutan, M., Panshin, G., Paolucci, L., Papanestis, A., Pappagallo, M., Pappalardo, L. L., Pappenheimer, C., Parkes, C., Passalacqua, B., Passaleva, G., Passaro, D., Pastore, A., Patel, M., Patoc, J., Patrignani, C., Paul, A., Pawley, C. J., Pellegrino, A., Peng, J., Altarelli, M. Pepe, Perazzini, S., Pereima, D., Da Costa, H. Pereira, Castro, A. Pereiro, Perret, P., Perro, A., Petridis, K., Petrolini, A., Pfaller, J. P., Pham, H., Pica, L., Piccini, M., Pietrzyk, B., Pietrzyk, G., Pinci, D., Pisani, F., Pizzichemi, M., Placinta, V., Casasus, M. Plo, Polci, F., Lener, M. Poli, Poluektov, A., Polukhina, N., Polyakov, I., Polycarpo, E., Ponce, S., Popov, D., Poslavskii, S., Prasanth, K., Prouve, C., Pugatch, V., Punzi, G., Qasim, S., Qian, W., Qin, N., Qu, S., Quagliani, R., Trejo, R. I. Rabadan, Rademacker, J. H., Rama, M., García, M. Ramírez, De Oliveira, V. Ramos, Pernas, M. Ramos, Rangel, M. S., Ratnikov, F., Raven, G., De Miguel, M. Rebollo, Redi, F., Reich, J., Reiss, F., Ren, Z., Resmi, P. K., Ribatti, R., Ricart, G. R., Riccardi, D., Ricciardi, S., Richardson, K., Richardson-Slipper, M., Rinnert, K., Robbe, P., Robertson, G., Rodrigues, E., Fernandez, E. Rodriguez, Lopez, J. A. Rodriguez, Rodriguez, E. Rodriguez, Rogovskiy, A., Rolf, D. L., Roloff, P., Romanovskiy, V., Lamas, M. Romero, Vidal, A. Romero, Romolini, G., Ronchetti, F., Rotondo, M., Roy, S. R., Rudolph, M. S., Ruf, T., Diaz, M. Ruiz, Fernandez, R. A. Ruiz, Vidal, J. Ruiz, Ryzhikov, A., Ryzka, J., Saavedra-Arias, J. J., Silva, J. J. Saborido, Sadek, R., Sagidova, N., Sahoo, D., Sahoo, N., Saitta, B., Salomoni, M., Gras, C. Sanchez, Sanderswood, I., Santacesaria, R., Rios, C. Santamarina, Santimaria, M., Santoro, L., Santovetti, E., Saputi, A., Saranin, D., Sarpis, G., Sarpis, M., Satriano, C., Satta, A., Saur, M., Savrina, D., Sazak, H., Smead, L. G. Scantlebury, Scarabotto, A., Schael, S., Scherl, S., Schiller, M., Schindler, H., Schmelling, M., Schmidt, B., Schmitt, S., Schmitz, H., Schneider, O., Schopper, A., Schulte, N., Schulte, S., Schune, M. H., Schwemmer, R., Schwering, G., Sciascia, B., Sciuccati, A., Sellam, S., Semennikov, A., Senger, T., Soares, M. Senghi, Sergi, A., Serra, N., Sestini, L., Seuthe, A., Shang, Y., Shangase, D. M., Shapkin, M., Sharma, R. S., Shchemerov, I., Shchutska, L., Shears, T., Shekhtman, L., Shen, Z., Sheng, S., Shevchenko, V., Shi, B., Shi, Q., Shields, E. B., Shimizu, Y., Shmanin, E., Shorkin, R., Shupperd, J. D., Coutinho, R. Silva, Simi, G., Simone, S., Skidmore, N., Skwarnicki, T., Slater, M. W., Smallwood, J. C., Smith, E., Smith, K., Smith, M., Snoch, A., Lavra, L. Soares, Sokoloff, M. D., Soler, F. J. P., Solomin, A., Solovev, A., Solovyev, I., Song, R., Song, Y., Song, Y. S., De Almeida, F. L. Souza, De Paula, B. Souza, Norella, E. Spadaro, Spedicato, E., Speer, J. G., Spiridenkov, E., Spradlin, P., Sriskaran, V., Stagni, F., Stahl, M., Stahl, S., Stanislaus, S., Stein, E. N., Steinkamp, O., Stenyakin, O., Stevens, H., Strekalina, D., Su, Y., Suljik, F., Sun, J., Sun, L., Sun, Y., Lima, D. S. Sundfeld, Sutcliffe, W., Swallow, P. N., Swystun, F., Szabelski, A., Szumlak, T., Tan, Y., Tat, M. D., Terentev, A., Terzuoli, F., Teubert, F., Thomas, E., Thompson, D. J. D., Tilquin, H., Tisserand, V., T'Jampens, S., Tobin, M., Tomassetti, L., Tonani, G., Tong, X., Machado, D. Torres, Toscano, L., Tou, D. Y., Trippl, C., Tuci, G., Tuning, N., Uecker, L. H., Ukleja, A., Unverzagt, D. J., Ursov, E., Usachov, A., Ustyuzhanin, A., Uwer, U., Vagnoni, V., Valenti, G., Canudas, N. Valls, Van Hecke, H., van Herwijnen, E., Van Hulse, C. B., Van Laak, R., van Veghel, M., Vasquez, G., Gomez, R. Vazquez, Regueiro, P. Vazquez, Sierra, C. Vázquez, Vecchi, S., Velthuis, J. J., Veltri, M., Venkateswaran, A., Vesterinen, M., Diaz, M. Vieites, Vilasis-Cardona, X., Figueras, E. Vilella, Villa, A., Vincent, P., Volle, F. C., Bruch, D. vom, Voropaev, N., Vos, K., Vouters, G., Vrahas, C., Wagner, J., Walsh, J., Walton, E. J., Wan, G., Wang, C., Wang, G., Wang, J., Wang, M., Wang, N. W., Wang, R., Wang, X., Wang, X. W., Wang, Y., Wang, Z., Ward, J. A., Waterlaat, M., Watson, N. K., Websdale, D., Wei, Y., Wendel, J., Westhenry, B. D. C., White, D. J., Whitehead, M., Wiederhold, A. R., Wiedner, D., Wilkinson, G., Wilkinson, M. K., Williams, M., Williams, M. R. J., Williams, R., Wilson, F. F., Wislicki, W., Witek, M., Witola, L., Wong, C. P., Wormser, G., Wotton, S. A., Wu, H., Wu, J., Wu, Y., Wyllie, K., Xian, S., Xiang, Z., Xie, Y., Xu, A., Xu, J., Xu, L., Xu, M., Xu, Z., Yang, D., Yang, K., Yang, S., Yang, X., Yang, Y., Yang, Z., Yeroshenko, V., Yeung, H., Yin, H., Yu, C. Y., Yu, J., Yuan, X., Zaffaroni, E., Zavertyaev, M., Zdybal, M., Zeng, C., Zeng, M., Zhang, C., Zhang, D., Zhang, J., Zhang, L., Zhang, S., Zhang, Y., Zhang, Y. Z., Zhao, Y., Zharkova, A., Zhelezov, A., Zheng, X. Z., Zheng, Y., Zhou, T., Zhou, X., Zhou, Y., Zhovkovska, V., Zhu, L. Z., Zhu, X., Zhukov, V., Zhuo, J., Zou, Q., Zuliani, D., and Zunica, G.
Subjects: High Energy Physics - Experiment
Abstract: The branching fraction ratios of $\overline{B}^0\to D^+\tau^-\overline{\nu}_{\tau}$ and $\overline{B}^0\to D^{*+}\tau^-\overline{\nu}_{\tau}$ decays are measured with respect to their muonic counterparts, using a data sample corresponding to an integrated luminosity of 2.0 fb$^{-1}$ collected by the LHCb experiment in proton-proton collisions at $\sqrt{s} = 13$ TeV. The reconstructed final states are formed by combining $D^+$ mesons with $\tau^-\to\mu^-\overline{\nu}_{\mu}\nu_{\tau}$ candidates, where the $D^+$ is reconstructed via the $D^+\to K^-\pi^+\pi^+$ decay. The results are \begin{align*} R(D^{+}) &= 0.249 \pm 0.043 \pm 0.047, R(D^{*+}) &= 0.402 \pm 0.081\pm 0.085, \end{align*} where the first uncertainties are statistical and the second systematic. The two measurements have a correlation coefficient of $-0.39$ and are compatible with the Standard Model., Comment: All figures and tables, along with machine-readable versions and any supplementary material and additional information, are available at https://lhcbproject.web.cern.ch/Publications/LHCbProjectPublic/LHCb-PAPER-2024-007.html (LHCb public pages)
Published: 2024

226. Observation of new charmonium(-like) states in $B^+ \to D^{*\pm} D^{\mp} K^+$ decays

Author: LHCb collaboration, Aaij, R., Abdelmotteleb, A. S. W., Beteta, C. Abellan, Abudinén, F., Ackernley, T., Adefisoye, A. A., Adeva, B., Adinolfi, M., Adlarson, P., Agapopoulou, C., Aidala, C. A., Ajaltouni, Z., Akar, S., Akiba, K., Albicocco, P., Albrecht, J., Alessio, F., Alexander, M., Aliouche, Z., Cartelle, P. Alvarez, Amalric, R., Amato, S., Amey, J. L., Amhis, Y., An, L., Anderlini, L., Andersson, M., Andreianov, A., Andreola, P., Andreotti, M., Andreou, D., Anelli, A., Ao, D., Archilli, F., Argenton, M., Cuendis, S. Arguedas, Artamonov, A., Artuso, M., Aslanides, E., Atzeni, M., Audurier, B., Bacher, D., Perea, I. Bachiller, Bachmann, S., Bachmayer, M., Back, J. J., Rodriguez, P. Baladron, Balagura, V., Baldini, W., Leite, J. Baptista de Souza, Barbetti, M., Barbosa, I. R., Barlow, R. J., Barsuk, S., Barter, W., Bartolini, M., Bartz, J., Baryshnikov, F., Basels, J. M., Bassi, G., Batsukh, B., Battig, A., Bay, A., Beck, A., Becker, M., Bedeschi, F., Bediaga, I. B., Beiter, A., Belin, S., Bellee, V., Belous, K., Belov, I., Belyaev, I., Benane, G., Bencivenni, G., Ben-Haim, E., Berezhnoy, A., Bernet, R., Andres, S. Bernet, Bertella, C., Bertolin, A., Betancourt, C., Betti, F., Bex, J., Bezshyiko, Ia., Bhom, J., Bieker, M. S., Biesuz, N. V., Billoir, P., Biolchini, A., Birch, M., Bishop, F. C. R., Bitadze, A., Bizzeti, A., Blake, T., Blanc, F., Blank, J. E., Blusk, S., Bocharnikov, V., Boelhauve, J. A., Garcia, O. Boente, Boettcher, T., Bohare, A., Boldyrev, A., Bolognani, C. S., Bolzonella, R., Bondar, N., Borgato, F., Borghi, S., Borsato, M., Borsuk, J. T., Bouchiba, S. A., Bowcock, T. J. V., Boyer, A., Bozzi, C., Bradley, M. J., Rodriguez, A. Brea, Breer, N., Brodzicka, J., Gonzalo, A. Brossa, Brown, J., Brundu, D., Buchanan, E., Buonaura, A., Buonincontri, L., Burke, A. T., Burr, C., Bursche, A., Butkevich, A., Butter, J. S., Buytaert, J., Byczynski, W., Cadeddu, S., Cai, H., Calabrese, R., Calefice, L., Cali, S., Calvi, M., Gomez, M. Calvo, Bouzas, J. I. Cambon, Campana, P., Perez, D. H. Campora, Quezada, A. F. Campoverde, Capelli, S., Capriotti, L., Caravaca-Mora, R., Carbone, A., Salgado, L. Carcedo, Cardinale, R., Cardini, A., Carniti, P., Carus, L., Vidal, A. Casais, Caspary, R., Casse, G., Godinez, J. Castro, Cattaneo, M., Cavallero, G., Cavallini, V., Celani, S., Cerasoli, J., Cervenkov, D., Cesare, S., Chadwick, A. J., Chahrour, I., Charles, M., Charpentier, Ph., Barajas, C. A. Chavez, Chefdeville, M., Chen, C., Chen, S., Chen, Z., Chernov, A., Chernyshenko, S., Chobanova, V., Cholak, S., Chrzaszcz, M., Chubykin, A., Chulikov, V., Ciambrone, P., Vidal, X. Cid, Ciezarek, G., Cifra, P., Clarke, P. E. L., Clemencic, M., Cliff, H. V., Closier, J., Toapaxi, C. Cocha, Coco, V., Cogan, J., Cogneras, E., Cojocariu, L., Collins, P., Colombo, T., Comerma-Montells, A., Congedo, L., Contu, A., Cooke, N., Corredoira, I., Correia, A., Corti, G., Meldrum, J. J. Cottee, Couturier, B., Craik, D. C., Torres, M. Cruz, Rivera, E. Curras, Currie, R., Da Silva, C. L., Dadabaev, S., Dai, L., Dai, X., Dall'Occo, E., Dalseno, J., D'Ambrosio, C., Daniel, J., Danilina, A., d'Argent, P., Davidson, A., Davies, J. E., Davis, A., Francisco, O. De Aguiar, De Angelis, C., De Benedetti, F., de Boer, J., De Bruyn, K., De Capua, S., De Cian, M., Da Graca, U. De Freitas Carneiro, De Lucia, E., De Miranda, J. M., De Paula, L., De Serio, M., De Simone, P., De Vellis, F., de Vries, J. A., Debernardis, F., Decamp, D., Dedu, V., Del Buono, L., Delaney, B., Dembinski, H. -P., Deng, J., Denysenko, V., Deschamps, O., Dettori, F., Dey, B., Di Nezza, P., Diachkov, I., Didenko, S., Ding, S., Dittmann, L., Dobishuk, V., Docheva, A. D., Dolmatov, A., Dong, C., Donohoe, A. M., Dordei, F., Reis, A. C. dos, Dowling, A. D., Downes, A. G., Duan, W., Duda, P., Dudek, M. W., Dufour, L., Duk, V., Durante, P., Duras, M. M., Durham, J. M., Durmus, O. D., Dziurda, A., Dzyuba, A., Easo, S., Eckstein, E., Egede, U., Egorychev, A., Egorychev, V., Eisenhardt, S., Ejopu, E., Ek-In, S., Eklund, L., Elashri, M., Ellbracht, J., Ely, S., Ene, A., Epple, E., Escher, S., Eschle, J., Esen, S., Evans, T., Fabiano, F., Falcao, L. N., Fan, Y., Fang, B., Fantini, L., Faria, M., Farmer, K., Fazzini, D., Felkowski, L., Feng, M., Feo, M., Gomez, M. Fernandez, Fernez, A. D., Ferrari, F., Rodrigues, F. Ferreira, Sole, S. Ferreres, Ferrillo, M., Ferro-Luzzi, M., Filippov, S., Fini, R. A., Fiorini, M., Fischer, K. M., Fitzgerald, D. S., Fitzpatrick, C., Fleuret, F., Fontana, M., Foreman, L. F., Forty, R., Foulds-Holt, D., Sevilla, M. Franco, Frank, M., Franzoso, E., Frau, G., Frei, C., Friday, D. A., Fu, J., Fuehring, Q., Fujii, Y., Fulghesu, T., Gabriel, E., Galati, G., Galati, M. D., Torreira, A. Gallas, Galli, D., Gambetta, S., Gandelman, M., Gandini, P., Gao, H., Gao, R., Gao, Y., Garau, M., Martin, L. M. Garcia, Moreno, P. Garcia, Pardiñas, J. García, Garg, K. G., Garrido, L., Gaspar, C., Geertsema, R. E., Gerken, L. L., Gersabeck, E., Gersabeck, M., Gershon, T., Ghorbanimoghaddam, Z., Giambastiani, L., Giasemis, F. I., Gibson, V., Giemza, H. K., Gilman, A. L., Giovannetti, M., Gioventù, A., Gironell, P. Gironella, Giugliano, C., Giza, M. A., Gkougkousis, E. L., Glaser, F. C., Gligorov, V. V., Göbel, C., Golobardes, E., Golubkov, D., Golutvin, A., Gomes, A., Fernandez, S. Gomez, Abrantes, F. Goncalves, Goncerz, M., Gong, G., Gooding, J. A., Gorelov, I. V., Gotti, C., Grabowski, J. P., Cardoso, L. A. Granado, Graugés, E., Graverini, E., Grazette, L., Graziani, G., Grecu, A. T., Greeven, L. M., Grieser, N. A., Grillo, L., Gromov, S., Gu, C., Guarise, M., Guittiere, M., Guliaeva, V., Günther, P. A., Guseinov, A. -K., Gushchin, E., Guz, Y., Gys, T., Habermann, K., Hadavizadeh, T., Hadjivasiliou, C., Haefeli, G., Haen, C., Haimberger, J., Hajheidari, M., Halvorsen, M. M., Hamilton, P. M., Hammerich, J., Han, Q., Han, X., Hansmann-Menzemer, S., Hao, L., Harnew, N., Harrison, T., Hartmann, M., He, J., Hemmer, F., Henderson, C., Henderson, R. D. L., Hennequin, A. M., Hennessy, K., Henry, L., Herd, J., Gascon, P. Herrero, Heuel, J., Hicheur, A., Mendizabal, G. Hijano, Hill, D., Hollitt, S. E., Horswill, J., Hou, R., Hou, Y., Howarth, N., Hu, J., Hu, W., Hu, X., Huang, W., Hulsbergen, W., Hunter, R. J., Hushchyn, M., Hutchcroft, D., Ilin, D., Ilten, P., Inglessi, A., Iniukhin, A., Ishteev, A., Ivshin, K., Jacobsson, R., Jage, H., Elles, S. J. Jaimes, Jakobsen, S., Jans, E., Jashal, B. K., Jawahery, A., Jevtic, V., Jiang, E., Jiang, X., Jiang, Y., Jiang, Y. J., John, M., Johnson, D., Jones, C. R., Jones, T. P., Joshi, S., Jost, B., Jurik, N., Juszczak, I., Kaminaris, D., Kandybei, S., Kang, Y., Karacson, M., Karpenkov, D., Kauniskangas, A., Kautz, J. W., Keizer, F., Kenzie, M., Ketel, T., Khanji, B., Kharisova, A., Kholodenko, S., Khreich, G., Kirn, T., Kirsebom, V. S., Kitouni, O., Klaver, S., Kleijne, N., Klimaszewski, K., Kmiec, M. R., Koliiev, S., Kolk, L., Konoplyannikov, A., Kopciewicz, P., Koppenburg, P., Korolev, M., Kostiuk, I., Kot, O., Kotriakhova, S., Kozachuk, A., Kravchenko, P., Kravchuk, L., Kreps, M., Kretzschmar, S., Krokovny, P., Krupa, W., Krzemien, W., Kubat, J., Kubis, S., Kucewicz, W., Kucharczyk, M., Kudryavtsev, V., Kulikova, E., Kupsc, A., Kutsenko, B. K., Lacarrere, D., Lai, A., Lampis, A., Lancierini, D., Gomez, C. Landesa, Lane, J. J., Lane, R., Langenbruch, C., Langer, J., Lantwin, O., Latham, T., Lazzari, F., Lazzeroni, C., Gac, R. Le, Lefèvre, R., Leflat, A., Legotin, S., Lehuraux, M., Cid, E. Lemos, Leroy, O., Lesiak, T., Leverington, B., Li, A., Li, H., Li, K., Li, L., Li, P., Li, P. -R., Li, S., Li, T., Li, Y., Li, Z., Lian, Z., Liang, X., Libralon, S., Lin, C., Lin, T., Lindner, R., Lisovskyi, V., Litvinov, R., Liu, F. L., Liu, G., Liu, K., Liu, Q., Liu, S., Liu, Y., Liu, Y. L., Salvia, A. Lobo, Loi, A., Castro, J. Lomba, Long, T., Lopes, J. H., Huertas, A. Lopez, Soliño, S. López, Lucarelli, C., Lucchesi, D., Martinez, M. Lucio, Lukashenko, V., Luo, Y., Lupato, A., Luppi, E., Lynch, K., Lyu, X. -R., Ma, G. M., Ma, R., Maccolini, S., Machefert, F., Maciuc, F., Mack, B., Mackay, I., Mackey, L. M., Mohan, L. R. Madhan, Madurai, M. M., Maevskiy, A., Magdalinski, D., Maisuzenko, D., Majewski, M. W., Malczewski, J. J., Malde, S., Malecki, B., Malentacca, L., Malinin, A., Maltsev, T., Manca, G., Mancinelli, G., Mancuso, C., Escalero, R. Manera, Manuzzi, D., Marangotto, D., Marchand, J. F., Marchevski, R., Marconi, U., Mariani, S., Benito, C. Marin, Marks, J., Marshall, A. M., Marshall, P. J., Martelli, G., Martellotti, G., Martinazzoli, L., Martinelli, M., Santos, D. Martinez, Vidal, F. Martinez, Massafferri, A., Materok, M., Matev, R., Mathad, A., Matiunin, V., Matteuzzi, C., Mattioli, K. R., Mauri, A., Maurice, E., Mauricio, J., Mayencourt, P., Mazurek, M., McCann, M., Mcconnell, L., McGrath, T. H., McHugh, N. T., McNab, A., McNulty, R., Meadows, B., Meier, G., Melnychuk, D., Merk, M., Merli, A., Garcia, L. Meyer, Miao, D., Miao, H., Mikhasenko, M., Milanes, D. A., Minotti, A., Minucci, E., Miralles, T., Mitreska, B., Mitzel, D. S., Modak, A., Mödden, A., Mohammed, R. A., Moise, R. D., Mokhnenko, S., Mombächer, T., Monk, M., Monteil, S., Gomez, A. Morcillo, Morello, G., Morello, M. J., Morgenthaler, M. P., Morris, A. B., Morris, A. G., Mountain, R., Mu, H., Mu, Z. M., Muhammad, E., Muheim, F., Mulder, M., Müller, K., Muñoz-Rojas, F., Murta, R., Naik, P., Nakada, T., Nandakumar, R., Nanut, T., Nasteva, I., Needham, M., Neri, N., Neubert, S., Neufeld, N., Neustroev, P., Nicolini, J., Nicotra, D., Niel, E. M., Nikitin, N., Nogga, P., Nolte, N. S., Normand, C., Fernandez, J. Novoa, Nowak, G., Nunez, C., Nur, H. N., Oblakowska-Mucha, A., Obraztsov, V., Oeser, T., Okamura, S., Okhotnikov, A., Oldeman, R., Oliva, F., Olocco, M., Onderwater, C. J. G., O'Neil, R. H., Goicochea, J. M. Otalora, Owen, P., Oyanguren, A., Ozcelik, O., Padeken, K. O., Pagare, B., Pais, P. R., Pajero, T., Palano, A., Palutan, M., Panshin, G., Paolucci, L., Papanestis, A., Pappagallo, M., Pappalardo, L. L., Pappenheimer, C., Parkes, C., Passalacqua, B., Passaleva, G., Passaro, D., Pastore, A., Patel, M., Patoc, J., Patrignani, C., Pawley, C. J., Pellegrino, A., Altarelli, M. Pepe, Perazzini, S., Pereima, D., Castro, A. Pereiro, Perret, P., Perro, A., Petridis, K., Petrolini, A., Petrucci, S., Pfaller, J. P., Pham, H., Pica, L., Piccini, M., Pietrzyk, B., Pietrzyk, G., Pinci, D., Pisani, F., Pizzichemi, M., Placinta, V., Casasus, M. Plo, Polci, F., Lener, M. Poli, Poluektov, A., Polukhina, N., Polycarpo, E., Ponce, S., Popov, D., Poslavskii, S., Prasanth, K., Prouve, C., Pugatch, V., Punzi, G., Qian, W., Qin, N., Qu, S., Quagliani, R., Trejo, R. I. Rabadan, Rademacker, J. H., Rama, M., García, M. Ramírez, Pernas, M. Ramos, Rangel, M. S., Ratnikov, F., Raven, G., De Miguel, M. Rebollo, Redi, F., Reich, J., Reiss, F., Ren, Z., Resmi, P. K., Ribatti, R., Ricart, G. R., Riccardi, D., Ricciardi, S., Richardson, K., Richardson-Slipper, M., Rinnert, K., Robbe, P., Robertson, G., Rodrigues, E., Fernandez, E. Rodriguez, Lopez, J. A. Rodriguez, Rodriguez, E. Rodriguez, Rogovskiy, A., Rolf, D. L., Roloff, P., Romanovskiy, V., Lamas, M. Romero, Vidal, A. Romero, Romolini, G., Ronchetti, F., Rotondo, M., Roy, S. R., Rudolph, M. S., Ruf, T., Diaz, M. Ruiz, Fernandez, R. A. Ruiz, Vidal, J. Ruiz, Ryzhikov, A., Ryzka, J., Saavedra-Arias, J. J., Silva, J. J. Saborido, Sadek, R., Sagidova, N., Sahoo, D., Sahoo, N., Saitta, B., Salomoni, M., Gras, C. Sanchez, Sanderswood, I., Santacesaria, R., Rios, C. Santamarina, Santimaria, M., Santoro, L., Santovetti, E., Saputi, A., Saranin, D., Sarpis, G., Sarpis, M., Sarti, A., Satriano, C., Satta, A., Saur, M., Savrina, D., Sazak, H., Smead, L. G. Scantlebury, Scarabotto, A., Schael, S., Scherl, S., Schiller, M., Schindler, H., Schmelling, M., Schmidt, B., Schmitt, S., Schmitz, H., Schneider, O., Schopper, A., Schulte, N., Schulte, S., Schune, M. H., Schwemmer, R., Schwering, G., Sciascia, B., Sciuccati, A., Sellam, S., Semennikov, A., Senger, T., Soares, M. Senghi, Sergi, A., Serra, N., Sestini, L., Seuthe, A., Shang, Y., Shangase, D. M., Shapkin, M., Sharma, R. S., Shchemerov, I., Shchutska, L., Shears, T., Shekhtman, L., Shen, Z., Sheng, S., Shevchenko, V., Shi, B., Shi, Q., Shields, E. B., Shimizu, Y., Shmanin, E., Shorkin, R., Shupperd, J. D., Coutinho, R. Silva, Simi, G., Simone, S., Skidmore, N., Skwarnicki, T., Slater, M. W., Smallwood, J. C., Smith, E., Smith, K., Smith, M., Snoch, A., Lavra, L. Soares, Sokoloff, M. D., Soler, F. J. P., Solomin, A., Solovev, A., Solovyev, I., Song, R., Song, Y., Song, Y. S., De Almeida, F. L. Souza, De Paula, B. Souza, Norella, E. Spadaro, Spedicato, E., Speer, J. G., Spiridenkov, E., Spradlin, P., Sriskaran, V., Stagni, F., Stahl, M., Stahl, S., Stanislaus, S., Stein, E. N., Steinkamp, O., Stenyakin, O., Stevens, H., Strekalina, D., Su, Y., Suljik, F., Sun, J., Sun, L., Sun, Y., Sutcliffe, W., Swallow, P. N., Swystun, F., Szabelski, A., Szumlak, T., Tan, Y., Tat, M. D., Terentev, A., Terzuoli, F., Teubert, F., Thomas, E., Thompson, D. J. D., Tilquin, H., Tisserand, V., T'Jampens, S., Tobin, M., Tomassetti, L., Tonani, G., Tong, X., Machado, D. Torres, Toscano, L., Tou, D. Y., Trippl, C., Tuci, G., Tuning, N., Uecker, L. H., Ukleja, A., Unverzagt, D. J., Ursov, E., Usachov, A., Ustyuzhanin, A., Uwer, U., Vagnoni, V., Valassi, A., Valenti, G., Canudas, N. Valls, Van Hecke, H., van Herwijnen, E., Van Hulse, C. B., Van Laak, R., van Veghel, M., Vasquez, G., Gomez, R. Vazquez, Regueiro, P. Vazquez, Sierra, C. Vázquez, Vecchi, S., Velthuis, J. J., Veltri, M., Venkateswaran, A., Vesterinen, M., Diaz, M. Vieites, Vilasis-Cardona, X., Figueras, E. Vilella, Villa, A., Vincent, P., Volle, F. C., Bruch, D. vom, Vorobyev, V., Voropaev, N., Vos, K., Vouters, G., Vrahas, C., Wagner, J., Walsh, J., Walton, E. J., Wan, G., Wang, C., Wang, G., Wang, J., Wang, M., Wang, N. W., Wang, R., Wang, X., Wang, X. W., Wang, Y., Wang, Z., Ward, J. A., Waterlaat, M., Watson, N. K., Websdale, D., Wei, Y., Westhenry, B. D. C., White, D. J., Whitehead, M., Wiederhold, A. R., Wiedner, D., Wilkinson, G., Wilkinson, M. K., Williams, M., Williams, M. R. J., Williams, R., Wilson, F. F., Wislicki, W., Witek, M., Witola, L., Wong, C. P., Wormser, G., Wotton, S. A., Wu, H., Wu, J., Wu, Y., Wyllie, K., Xian, S., Xiang, Z., Xie, Y., Xu, A., Xu, J., Xu, L., Xu, M., Xu, Z., Yang, D., Yang, S., Yang, X., Yang, Y., Yang, Z., Yeroshenko, V., Yeung, H., Yin, H., Yu, C. Y., Yu, J., Yuan, X., Zaffaroni, E., Zavertyaev, M., Zdybal, M., Zeng, M., Zhang, C., Zhang, D., Zhang, J., Zhang, L., Zhang, S., Zhang, Y., Zhang, Y. Z., Zhao, Y., Zharkova, A., Zhelezov, A., Zheng, X. Z., Zheng, Y., Zhou, T., Zhou, X., Zhou, Y., Zhovkovska, V., Zhu, L. Z., Zhu, X., Zhukov, V., Zhuo, J., Zou, Q., Zuliani, D., and Zunica, G.
Subjects: High Energy Physics - Experiment
Abstract: A study of resonant structures in $B^{+}\rightarrow{D^{\ast+}D^{-}K^{+}}$ and $B^{+}\rightarrow{D^{\ast-}D^{+}K^{+}}$ decays is performed, using proton-proton collision data at centre-of-mass energies of $\sqrt{s}=7, 8$, and $13$ TeV recorded by the LHCb experiment, corresponding to an integrated luminosity of 9 fb$^{-1}$. A simultaneous amplitude fit is performed to the two channels with contributions from resonances decaying to $D^{\ast-}D^{+}$ and $D^{\ast+}D^{-}$ states linked by $C$ parity. This procedure allows the $C$-parities of resonances in the $D^{\ast\pm}D^{\mp}$ mass spectra to be determined. Four charmonium(-like) states are observed decaying into $D^{\ast\pm}D^{\mp}$: $\eta_c(3945)$, $h_c(4000)$, $\chi_{c1}(4010)$ and $h_c(4300)$, with quantum numbers $J^{PC}$ equal to $0^{-+}$, $1^{+-}$, $1^{++}$ and $1^{+-}$, respectively. At least three of these states have not been observed previously. In addition, the existence of the $T_{\bar{c}\bar{s}0}^{*}(2870)^{0}$ and $T_{\bar{c}\bar{s}1}^{*}(2900)^{0}$ resonances in the $D^-K^+$ mass spectrum, already observed in the $B^+ \to D^+ D^- K^+$ decay, is confirmed in a different production channel., Comment: All figures and tables, along with any supplementary material and additional information, are available at https://cern.ch/lhcbproject/Publications/p/LHCb-PAPER-2023-047.html (LHCb public pages)
Published: 2024
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227. MicroRNA-200c Nanoparticles Sensitized Gastric Cancer Cells to Radiotherapy by Regulating PD-L1 Expression and EMT

Author: Qian L, Liu F, Chu Y, Zhai Q, Wei X, Shao J, Li R, Xu Q, Yu L, Liu B, and Liu Q
Subjects: microrna-200c, gastric cancer, nanoparticle, pd-l1, radiotherapy, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
Abstract: Lingyu Qian,1,2,* Fangcen Liu,3,* Yanhong Chu,1 Qingqing Zhai,1 Xiao Wei,3 Jie Shao,1 Rutian Li,1 Qiuping Xu,1 Lixia Yu,1 Baorui Liu,1 Qin Liu1 1The Comprehensive Cancer Centre of Drum Tower Hospital, Nanjing University Medical School & Clinical Cancer Institute of Nanjing University, Nanjing, People’s Republic of China; 2Department of Oncology, Rudong Peoples’ Hospital of Jiangsu Province, Nantong, People’s Republic of China; 3Department of Pathology, Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School, Nanjing, People’s Republic of China*These authors contributed equally to this workCorrespondence: Qin LiuThe Comprehensive Cancer Centre of Drum Tower Hospital, Nanjing University Medical School & Clinical Cancer Institute of Nanjing University, Nanjing 210008, People’s Republic of ChinaEmail liuqinxh@126.comIntroduction: Immuno-checkpoint inhibitors (ICIs) in advanced gastric cancer either as monotherapy or in combining strategies are rapidly evolving but still in early phase. Various efforts have been made to provide insights into regulating immune checkpoint molecule programmed cell death ligand-1 (PD-L1) expression to improve ICIs efficacy. The aim of this study was to investigate the effect and potential mechanism of miR-200c nanoparticles combined with radiotherapy in gastric cancer cells.Methods: We prepared miR-200c-loaded nanoparticles (miR-200c NPs) to achieve targeted delivery of miR-200c to AGS cells. The roles of miR-200c NPs and radiotherapy in regulating the viability of AGS cells were assessed by CCK-8 toxicity test and Annexin V-FITC/PI apoptosis kit. Flow cytometry was used to analyze expression of PD-L1 and CD44 on the surface of AGS cells treated by miR-200c NPs and/or ionizing radiation. Enzyme-linked immunosorbent assay (ELISA) was used to test the level of transforming growth factor-beta 1 (TGF-β 1) secreted by AGS cells. The cooperation mechanism between miR-200c NPs and radiotherapy was also explored in vitro.Results: Compared with naked miR-200c mimics, miR-200c NPs significantly downregulated PD-L1 expression of gastric cancer cells. The combination of miR-200c NPs and radiotherapy showed significantly synergistic inhibitory effect on gastric cancer cells by inhibiting immune escape mediated by PD-L1, reversing EMT phenotype as well as abrogating cancer stem cells (CSCs)-associated properties of tumor cells.Conclusion: MiR-200c NPs sensitized gastric cancer cells to radiotherapy by regulating PD-L1 expression and EMT.Keywords: microRNA-200c, gastric cancer, nanoparticle, PD-L1, radiotherapy
Published: 2020

228. Prognostic Value of Gastrokine-2 (GKN2) and Its Correlation with Tumor-Infiltrating Immune Cells in Lung Cancer and Gastric Cancers

Author: Liu F and Wu H
Subjects: gkn2, lung cancer, gastric cancer, prognosis, tumor-infiltrating, biomarker, Pathology, RB1-214, Therapeutics. Pharmacology, RM1-950
Abstract: Fangteng Liu,1,2 Hengyu Wu1 1Department of Breast Surgery, The Third Hospital of Nanchang, Nanchang, Jiangxi 330009, People’s Republic of China; 2Faculty of Medicine, University of Munich, Munich 80336, GermanyCorrespondence: Hengyu Wu Tel +86-15270280590Email why_wuhengyu0590@163.comBackground: GKN2, as a secretory protein, is involved in the inflammation and immune modulation, and its aberrant expression is closely related to tumorigenesis. However, integrated studies on the value of GKN2 as a promising clinical biomarker and immunotherapy target in multiple tumors are still rare.Methodology: Multiple online databases, including ONCOMINE, SEGreg, UALCAN, GEPIA, K-M Plotter, cBioPortal, MethSurv, CellMarker, and Timer, were applied to assess the clinical significance of GKN2 and its correlation with tumor-infiltrating immune cells in differentially expressed cancers.Results: Several databases confirmed that GKN2 was significantly down-regulated in lung and gastric cancers compared that in normal samples. GKN2 was altered in 3%, 5%, and 4% of the LUAD, LUSC, and STAD samples, respectively. Hyper-methylation of GKN2 was found in LUAD and LUSC samples. For the clinical values of GKN2, we found that the low transcription level of GKN2 was associated with worse OS in lung cancer, and inferior FP and PPS in gastric cancer, and the relationships between GKN2 expression and clinical variables regarding OS/FP/PPS in lung and gastric cancers were assessed. Moreover, the prognostic value of the DNA methylation patterns of GKN2 in LUAD, LUSC, and STAD was identified. Furthermore, GKN2 expression was found to be significantly correlated with the infiltrating multiple tumor immune cells, and statistically significant differences in the correlation between GKN2 expression and multiple markers of neutrophils and macrophage polarization were observed in LUAD, LUSC, and STAD.Conclusion: The study revealed the prognosis and risk factors for deterioration in patients with low expression of GKN2. GKN2 may be used as a valuable prognostic biomarker and therapeutic target in lung and gastric cancers.Keywords: GKN2, lung cancer, gastric cancer, prognosis, tumor-infiltrating, biomarker
Published: 2020

229. Antitumor Efficacy of Oncolytic Herpes Virus Type 1 Armed with GM-CSF in Murine Uveal Melanoma Xenografts

Author: Liu S, Liu F, Zhao M, and Zhang J
Subjects: uveal melanoma, oncolytic virus, hsv-1, gm-csf, antitumor efficacy, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
Abstract: Sisi Liu,1 Fusheng Liu,2 Mingwei Zhao,1 Junwen Zhang2 1Department of Ophthalmology, Peking University People’s Hospital, Eye Diseases and Optometry Institute, Beijing Key Laboratory of Diagnosis and Therapy of Retinal and Choroid Diseases, College of Optometry, Peking University Health Science Center, Beijing, People’s Republic of China; 2Brain Tumor Research Center, Beijing Neurosurgical Institute, Beijing Laboratory of Biomedical Materials, Beijing Tiantan Hospital Affiliated to Capital Medical University, Beijing 100070, People’s Republic of ChinaCorrespondence: Junwen ZhangBrain Tumor Research Center, Beijing Neurosurgical Institute, Beijing Laboratory of Biomedical Materials, Beijing Tiantan Hospital Affiliated to Capital Medical University, No. 115 Nansihuan West Road, Fengtai District, Beijing 100070, People’s Republic of ChinaTel +86-10-59975626Email jewzhang@hotmail.comMingwei ZhaoDepartment of Ophthalmology, Peking University People’s Hospital, Eye Diseases and Optometry Institute, Beijing Key Laboratory of Diagnosis and Therapy of Retinal and Choroid Diseases, College of Optometry, Peking University Health Science Center, No. 11 Xizhimen South Street, Xi Cheng District, Beijing 100044, People’s Republic of ChinaTel +86-10-8832666Email mingwei_zhao@outlook.comBackground: Uveal melanoma (UM) is the most common primary intraocular tumor in adults with a high incidence of metastasis. Standard care therapies for UM include enucleation and radiation, which are minimally effective in prolonging patient survival. Oncolytic virus treatment has become a new trend in cancer field. Of which, oncolytic herpes simplex virus type 1 (HSV-1) therapy is one of the most effective antitumor treatments. Here, we established an oncolytic HSV-1 encoding granulocyte-macrophage colony-stimulating factor (GM-CSF), tested its efficacy in UM therapy, and investigated the innate immune response induced by this virus.Methods: Oncolytic HSV-1 expressing GM-CSF (HSV-GM-CSF) was constructed, then verified using qPCR and Western blot assays. Cell viability assays and transmission electron microscopy were conducted on three UM cell lines, MUM2B, 92.1, and MP41, to assess the cell-killing ability and virus infection of this virus. For in vivo experiments, BALB/c-nude mice in situ UM xenografts were established to testify the efficacy of the oncolytic virus, oncolytic HSV-1, and HSV-GM-CSF groups, respectively. IVIS images, ocular volumes, mice weights, and survivals were tracked to see the efficacy of the virus. Hematoxylin and eosin staining, immunohistochemistry, and flow cytometry analyses were conducted to demonstrate the immune activity after virus treatment.Results: All three tested UM cell lines were sensitive to infection by HSV-GM-CSF. In vivo xenograft experiments revealed that oncolytic virus HSV-1 reduced UM tumor volume and that oncolytic virus HSV-1 armed with GM-CSF enhanced the antitumor effect compared with unmodified HSV-1. The bodyweights of untreated control group mice were significantly lower than those of mice in either virus-treated group (HSV-1 or HSV-GM-CSF). Follow-up survivals were prolonged in the virus-treated groups compared with the control group and were prolonged to a greater extent in the HSV-GM-CSF group than in the HSV-1 group. Macrophage stimulation was observed following HSV-GM-CSF treatment.Conclusion: Our results indicate that the recombinant oncolytic virus HSV-GM-CSF is a potential therapeutic treatment for UM.Keywords: uveal melanoma, oncolytic virus, HSV-1, GM-CSF, antitumor efficacy
Published: 2020

230. Perfluorocarbons-Based 19F Magnetic Resonance Imaging in Biomedicine

Author: Wu L, Liu F, Liu S, Xu X, Liu Z, and Sun X
Subjects: fluorine-19 magnetic resonance imaging, fluorocarbons, nanoparticles, molecular imaging, neoplasms, Medicine (General), R5-920
Abstract: Lina Wu,1,2,* Fang Liu,1,3,* Shuang Liu,1,2,* Xiuan Xu,1,3 Zhaoxi Liu,1,2 Xilin Sun1,2 1NHC and CAMS Key Laboratory of Molecular Probe and Targeted Theranostics, Molecular Imaging Research Center (MIRC), Harbin Medical University, Harbin, Heilongjiang 150028, People’s Republic of China; 2TOF-PET/CT/MR Center, Harbin Medical University, Harbin, Heilongjiang 150028, People’s Republic of China; 3Department of Medical Imaging, Harbin Medical University, Harbin, Heilongjiang 150028, People’s Republic of China*These authors contributed equally to this workCorrespondence: Xilin SunMolecular Imaging Research Center of Harbin Medical University (MIRC), TOF-PET/CT/MR Center, Harbin Medical University, Harbin, Heilongjiang 150028, People’s Republic of ChinaFax +86 451-82576509Email sunxl@ems.hrbmu.edu.cnAbstract: Fluorine-19 (19F) magnetic resonance (MR) molecular imaging is a promising noninvasive and quantitative molecular imaging approach with intensive research due to the high sensitivity and low endogenous background signal of the 19F atom in vivo. Perfluorocarbons (PFCs) have been used as blood substitutes since 1970s. More recently, a variety of PFC nanoparticles have been designed for the detection and imaging of physiological and pathological changes. These molecular imaging probes have been developed to label cells, target specific epitopes in tumors, monitor the prognosis and therapy efficacy and quantitate characterization of tumors and changes in tumor microenvironment noninvasively, therefore, significantly improving the prognosis and therapy efficacy. Herein, we discuss the recent development and applications of 19F MR techniques with PFC nanoparticles in biomedicine, with particular emphasis on ligand-targeted and quantitative 19F MR imaging approaches for tumor detection, oxygenation measurement, smart stimulus response and therapy efficacy monitoring, et al.Keywords: fluorine-19 magnetic resonance imaging, fluorocarbons, nanoparticles, molecular imaging, neoplasms
Published: 2020

231. The Effects of Body Mass Index on the Use of Patient-Controlled Intravenous Analgesia After Open Gastrointestinal Tumor Surgery: A Retrospective Analysis

Author: Li TT, Xiong LL, Huang J, Wen S, Chen YJ, Wang TH, and Liu F
Subjects: postoperative nausea and vomiting (ponv), postoperative pain, sufentanil, dexmedetomidine, flurbiprofen axetil., Medicine (General), R5-920
Abstract: Ting-Ting Li,1,* Liu-Lin Xiong,2,* Jin Huang,3 Song Wen,4 Yan-Jun Chen,1 Ting-Hua Wang,1 Fei Liu1 1Department of Anesthesiology, Institute of Neurological Disease, West China Hospital, Sichuan University, Chengdu, 610044, People’s Republic of China; 2School of Pharmacy and Medical Sciences, Faculty of Health Sciences, University of South Australia, Adelaide, SA 5000, Australia; 3Laboratory Zoology Department, Institute of Neuroscience, Kunming Medical University, Kunming, People’s Republic of China; 4Department of Pain, Affiliated Hospital of Zunyi Medical University, Guizhou, People’s Republic of China*These authors contributed equally to this workCorrespondence: Ting-Hua WangInstitute of Neurological Disease, Department of Anesthesiology, Translational Neuroscience Center, West China Hospital, Sichuan University, Chengdu 610041, People’s Republic of ChinaTel +86 871-65939180Fax +86 871-65922935Email Wangth_email@163.comFei LiuDepartment of Anesthesiology, West China Hospital, Sichuan University, Chengdu 610041, People’s Republic of ChinaTel +86 18980605856Fax +86 871-85423593Email 30333870@qq.comPurpose: To investigate the impact of body mass index (BMI) on the analgesic effects and adverse reactions of patient-controlled intravenous analgesia (PCIA).Methods: From 2017 to 2018, 390 patients undergoing open gastrointestinal surgery were reviewed at West China Hospital, Sichuan University. All used PCIA of sufentanil combined with dexmedetomidine and flurbiprofen axetil. According to their BMIs, they were placed into six groups: group A (BMI < 18.5kg/m2, 29), group B (18.5kg/m2 ≤ BMI< 22kg/m2, 124), group C (22kg/m2 ≤ BMI < 24kg/m2, 99), group D (24kg/m2 ≤ BMI < 26kg/m2, 69), group E (26kg/m2 ≤ BMI < 28kg/m2, 46) and group F (BMI ≥ 28kg/m2, 23). Main data of the perioperative use of analgesics, postoperative visual analogue score (VAS), and adverse reactions were collected.Results: Twenty-four hours (h) after surgery, patients in group A had a higher resting VAS than the other groups, especially B (pA-B = 0.011). VAS of patients during activity in group B was lower than those in group C 48 h after surgery (p = 0.013). Compared with groups B to F, group A had a significantly lower incidence of hypertension (p = 0.012) and a significantly higher incidence of vomiting 24 h after surgery (p = 0.009). Binary logistic analysis found that higher age was a risk factor for vomiting 24 h after surgery (OR 1.158, p = 0.045).Conclusion: Using the same PCIA, patients with BMIs of less than 18.5 kg/m2 had worse analgesia on the first day after surgery and were more likely to vomit. Postoperative analgesia and related experiences in patients with BMIs of less than 18.5 kg/m2 need to be improved.Keywords: postoperative nausea and vomiting, PONV, postoperative pain, sufentanil, dexmedetomidine, flurbiprofen axetil
Published: 2020

232. Prognostic Nomograms for Patients with Hepatocellular Carcinoma After Curative Hepatectomy, with a Focus on Recurrence Timing and Post-Recurrence Management

Author: Xu W, Liu F, Shen X, and Li R
Subjects: hepatocellular carcinoma, hepatectomy, post-recurrence management, overall survival, nomogram, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
Abstract: Wei Xu,* Fei Liu,* Xianbo Shen,* Ruineng Li Department of Hepatobiliary Surgery, Hunan Provincial People’s Hospital, The First Hospital Affiliated with Hunan Normal University, Changsha, People’s Republic of China*These authors contributed equally to this workCorrespondence: Wei XuDepartment of Hepatobiliary Surgery, Hunan Provincial People’s Hospital, The First Hospital Affiliated with Hunan Normal University, Changsha, People’s Republic of ChinaTel +86 13873159491Fax +86 73182278012Email xuwei0209@163.comBackground: Prognoses of patients with hepatocellular carcinoma (HCC) after curative hepatectomy remain unsatisfactory because of the high incidence of postoperative recurrence. Published predictive systems focus on pre-resection oncological characteristics, ignoring post-recurrence factors.Purpose: This study aimed to develop prognostic nomograms for 3- and 5-year overall survival (OS) of patients with HCC after curative hepatectomy, focusing on potentially influential post-recurrence factors.Patients and Methods: Clinicopathological and postoperative follow-up data were extracted from 494 patients with HCC who underwent curative hepatectomy between January 2012 and June 2019. Early recurrence (ER) and late recurrence (LR) were defined as recurrence at ≤ 2 and > 2 years, respectively, after curative hepatectomy. Nomograms for the prediction of 3- and 5-year OS were established based on multivariate analysis. The areas under time-dependent receiver operating characteristic curves (AUCs) for the nomograms were calculated independently to verify predictive accuracy. The nomograms were internally validated based on 2000 bootstrap resampling of 75% of the original data.Results: In total, 494 patients with HCC who underwent curative hepatectomy met the eligibility criteria. Cox proportional hazard regression analysis identified factors potentially influencing 3- and 5-year OS. Multivariate analysis indicated that patient age, Hong Kong Liver Cancer stage, γ-glutamyl transferase (γ-GGT) level, METAVIR inflammation activity grade, ER and post-recurrence treatment modality were influencing factors for 3-year OS (AUC, 0.891; 95% CI, 0.8364– 0.9447). γ-GGT > 60 U/L, hepatectomy extent, LR and post-recurrence treatment modality were influencing factors for 5-year OS (AUC, 0.864; 95% CI, 0.8041– 0.9237). Calibration plots showed satisfactory concordance between the predicted and actual observation cohorts.Conclusion: We propose new prognostic nomograms for OS prediction with a focus on the differentiation of recurrence timing and post-recurrence management. These nomograms overcome the shortcomings of previous predictive nomograms and significantly improve predictive accuracy.Keywords: hepatocellular carcinoma, hepatectomy, post-recurrence management, overall survival, nomogram
Published: 2020

233. A Retrospective Cohort Study on Pretreated Neutrophil-to-Lymphocyte Ratio and Prognosis of Small Cell Lung Cancer: Evidence of Effect Modification by Chemotherapy Regimen

Author: Liu F, Zhou S, Tan L, Jiang H, and Huang Y
Subjects: neutrophil-to-lymphocyte ratio (nlr), overall survival, small cell lung cancer (sclc), etoposide plus carboplatin/cisplatin, mortality risk, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
Abstract: Feiwen Liu,1 Shaozhang Zhou,1,2 Liping Tan,2 Huiqin Jiang,1 Yucong Huang1 1Oncology Medical College, Guangxi Medical University, Nanning City 530021, Guangxi Zhuang Autonomous Region, People’s Republic of China; 2Department of Respiratory Oncology, Guangxi Medical University Affiliated Tumor Hospital, Nanning City 530021, Guangxi Zhuang Autonomous Region, People’s Republic of ChinaCorrespondence: Shaozhang Zhou; Liping TanDepartment of Respiratory Oncology, Guangxi Medical University Affiliated Tumor Hospital, No. 71 Heti Road, Nanning City 530021, Guangxi Zhuang Autonomous Region, People’s Republic of ChinaTel +86-13977183708; +86-18776404799Fax +86-771-5300613Email zhoushaozhang@gxmu.edu.cn; 988tan@163.comPurpose: Neutrophil-to-lymphocyte ratio (NLR) has been suggested as an independent risk factor for progression-free survival (PFS) and overall survival (OS) in small cell lung cancer (SCLC). However, it is still unknown whether there is a linear relationship between the NLR and the risk of death in SCLC. The objective of this study is to provide further results.Patients and Methods: A retrospective cohort study was performed among a total of 251 participants with SCLC. Smooth curve fitting and piecewise Cox regression model were used to determine the linear relationship between NLR and mortality risk. A multivariable Cox regression model was used to estimate the effects of NLR on OS. Interaction and stratified analyses were conducted according to covariates.Results: The analysis indicated no significant nonlinear relationship or threshold effect between NLR and hazard of death. Multivariate analysis revealed that every unit increase in NLR was associated with a 10% increase in mortality risk. High NLR (> 3.5) at baseline was associated with poor OS (hazard ratio [HR]=1.97, P=0.009). The difference in median OS duration between the high and low NLR groups was statistically significant (9.1 months vs 14.6 months, P=0.0067). Furthermore, interaction analysis identified the chemotherapy regimen to play an interactive role in the association between NLR and hazard of death.Conclusion: NLR was identified as an independent risk factor for OS in SCLC and the linear correlation was observed between them. Administration of etoposide plus cisplatin (EP) regimen in patients with low NLR resulted in better long-term outcome than that of etoposide plus carboplatin (EC) regimen, while administration of the EC regimen conferred longer OS than that of the EP regimen in patients with high NLR.Keywords: neutrophil-to-lymphocyte ratio, NLR, overall survival, small cell lung cancer, SCLC, etoposide plus carboplatin/cisplatin, mortality risk
Published: 2020

234. Pretreatment Apparent Diffusion Coefficient as a Predictor of Response to Transcatheter Arterial Chemoembolization Immediately Combined with Radiofrequency Ablation for Treatment of Solitary Large Hepatocellular Carcinoma

Author: Tang J, Liu F, Yuan H, Li X, Tian X, Ji K, and Wang W
Subjects: solitary large hepatocellular carcinoma, apparent diffusion coefficient, tace, radiofrequency ablation, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
Abstract: Jing Tang,1,2 Fengyong Liu,2 Hongjun Yuan,2 Xin Li,2 Xiaomei Tian,2 Kan Ji,2 Xueping Li,3 Wei Wang3 1Medical School of Chinese PLA, Beijing, People’s Republic of China; 2Department of Interventional Radiology, The First Medical Center, Chinese PLA General Hospital, Beijing, People’s Republic of China; 3Department of Radiology, The First Medical Center, Chinese PLA General Hospital, Beijing, People’s Republic of ChinaCorrespondence: Fengyong LiuDepartment of Interventional Radiology, The First Medical Center, Chinese PLA General Hospital, No. 28, Fuxing Road, Haidian District, Beijing 100853, People’s Republic of ChinaTel +8613371668617Fax +86-10-66939340Email liufengyong301@163.comPurpose: To evaluate whether the pretreatment apparent diffusion coefficient (ADC) measured with diffusion weighted imaging (DWI) of tumor can be used as an imaging biomarker for predicting prognosis in solitary large hepatocellular carcinomas (HCCs) treated with transcatheter arterial chemoembolization (TACE) immediately combined with radiofrequency ablation (RFA).Patients and Methods: In this single institution retrospective study, 40 solitary large HCCs that underwent treatment with TACE immediately combined with RFA were analyzed. All patients underwent abdominal dynamic contrast-enhanced magnetic resonance imaging within one month before treatment with DWI, and ADC values in the lesions were measured by two independent radiologists. Associations among patients’ preoperative ADC values and objective response (OR), progression-free survival (PFS) and overall survival (OS) were examined. Survival curves were drawn with the Kaplan–Meier method, and differences were determined with the Log rank test. The Cox proportional-hazards model was used for univariate and multivariate analyses of PFS and OS.Results: Forty solitary large HCCs (mean 9.54 cm, range 5.04– 16.06 cm) were successfully treated with TACE in immediate combination with RFA (OR 75%). The ADC values were significantly higher in the response group than the non-response group (1.51± 0.32× 10− 3 mm2/s vs 1.09± 0.17× 10− 3 mm2/s; P< 0.001). As predicted on the basis of the ADC values, the optimal cutoff value for the efficacy of TACE combined with RFA was 1.32× 10− 3 mm2/s, with a predictive sensitivity of 0.63 and a specificity of 1.00. Patients with high ADC had longer PFS than those with low ADC (14.9 months vs 5.3 months; P< 0.001) and had significantly longer survival rates (22.6 months vs 12.1 months; P=0.004).Conclusion: Preoperative ADC values < 1.32× 10− 3 mm2/s are an independent predictor of poorer prognosis in patients with solitary large HCCs who have undergone TACE immediately combined with RFA.Keywords: solitary large hepatocellular carcinoma, apparent diffusion coefficient, TACE, radiofrequency ablation
Published: 2020

235. Willingness-to-Pay and Benefit–Cost Analysis of IPL for Rosacea Treatment: A Cross-Sectional Study in China

Author: Deng Q, Zhang S, Deng YX, Liu F, Shi W, Xie H, Xiao Y, Huang YX, and Li J
Subjects: benefit-cost analysis, intense pulsed light, rosacea, willingness-to-pay, economic evaluation., Medicine (General), R5-920
Abstract: Qing Deng1,2 ,* Shu-ping Zhang1,2 ,* Yu-Xuan Deng,1,2 Fang-fen Liu,1,2 Wei Shi,1– 3 Hong-fu Xie,1– 4 Yi Xiao,1,2 Ying-Xue Huang,1,2 Ji Li1– 4 1Department of Dermatology, Xiangya Hospital, Central South University, Changsha, People’s Republic of China; 2National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan 410008, People’s Republic of China; 3Key Laboratory of Organ Injury, Aging and Regenerative Medicine of Hunan Province, Changsha, Hunan, People’s Republic of China; 4Key Laboratory of Molecular Radiation Oncology Hunan Province, Changsha, People’s Republic of China*These authors contributed equally to this workCorrespondence: Ying-Xue Huang; Ji LiDepartment of Dermatology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, Hunan 410008, People’s Republic of ChinaTel +86 186 2755 6448; +86 139 7512 3658Fax +86 0731 8432 8888Email 29103866@qq.com; liji_xy@csu.edu.cnBackground: Intense pulsed light (IPL), as a therapeutic approach for rosacea, had advantage in removing erythema and telangiectasia and was gradually accepted by rosacea patients, but there have been few studies on economic evaluation of this therapy.Purpose: This study aimed to detect willingness-to-pay (WTP) of IPL treatment for rosacea and to conduct a benefit–cost analysis (BCA) among the Chinese population, so as to provide an economic reference for doctors to make treatment decisions.Materials and Methods: An observational, cross-sectional study assessed respondent’s demographic characteristics and willingness-to-pay (WTP) of IPL and rosacea patients’ clinical data and Dermatology Life Quality Index (DLQI). WTP was obtained by contingent valuation (CV) method. In brief, contrast figures of three cases treated with IPL (Case1, Case2, and Case3 represented the increasing severity of rosacea) were showed and WTP was inquired. The costs were obtained according the market and compared with WTP (benefits) to get a benefit–cost ratio (BCR). Predictors of cost-effective WTP were identified using the multivariable logistic regression model.Results: A total of 303 rosacea patients and 202 controls were included in the study. The average cost of a single IPL treatment for rosacea was USD 208.04 in Changsha, China. The mean WTP for Case 1, Case 2, and Case 3 was USD 201.57, 214.64, and 221.74, respectively. WTP was statistically lower for Case 1 than that for Case 2 or Case 3 (P< 0.05). The BCRs were 0.85, 1.03, and 1.06 for Case 1, Case 2, and Case 3, respectively. WTP is significantly associated with household monthly income, previous treatment cost, and DLQI after adjustments for demographic characteristics (P< 0.05).Conclusion: IPL is an acceptable treatment for rosacea with moderate to severe erythema. For patients with relatively high income or severely impaired quality of life, IPL is an economically feasible therapy and deserves to be recommended.Keywords: benefit-cost analysis, intense pulsed light, rosacea, willingness-to-pay, economic evaluation
Published: 2020

236. Progress: Targeted Therapy, Immunotherapy, and New Chemotherapy Strategies in Advanced Triple-Negative Breast Cancer

Author: Shi J, Liu F, and Song Y
Subjects: advanced tnbc, targets, immune checkpoint inhibitor, refractory, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
Abstract: Jinhong Shi, Feiqi Liu, Yanqiu Song Cancer Center, The First Hospital of Jilin University, Changchun, Jilin, People’s Republic of ChinaCorrespondence: Yanqiu SongThe First Hospital of Jilin University, No. 1, Xinmin Street, Changchun, Jilin 130021, People’s Republic of ChinaTel +86 18934749569Email song_yq@jlu.edu.cnAbstract: Triple-negative breast cancer (TNBC) is one of the most aggressive subtypes of breast cancer, accounting for approximately 15% of cases, and is defined by the lack of expression of hormone receptors (estrogen and progesterone receptors) and lack of amplification or overexpression of human epidermal growth receptor 2 (HER2). Due to the lack of targets of hormone receptors and HER2, treatment of TNBC or advanced TNBC relies on conventional chemotherapeutic agents, but their efficacy and prognosis are poor. In patients with advanced TNBC, poorer outcomes are observed. Recently, with the launch of clinical trials and advancements in molecular studies, targeted therapy for signaling transduction pathways, immunotherapy for immune checkpoints, and new chemotherapy strategies have provided feasible or potential therapeutic options for advanced TNBC. This review aimed to summarize recent progress in targeted therapy, immunotherapy, and chemotherapy for advanced TNBC.Keywords: advanced TNBC, targets, immune checkpoint inhibitor, refractory
Published: 2020

237. Phoenixin 14 Inhibits High-Fat Diet-Induced Non-Alcoholic Fatty Liver Disease in Experimental Mice

Author: Yang F, Huang P, Shi L, Liu F, Tang A, and Xu S
Subjects: phoenixin 14, nonalcoholic fatty liver disease (nafld), oxidative stress, inflammation, nrf2/ho-1, sirt1/ampk, Therapeutics. Pharmacology, RM1-950
Abstract: Fan Yang,1 Ping Huang,1 Liandong Shi,2 Feng Liu,3 Aimei Tang,3 Shaohui Xu1 1Department of Endocrinology, Guilin People’s Hospital, Guilin, Guangxi 541002, People’s Republic of China; 2Department of Ultrasonography, Guilin People’s Hospital, Guilin, Guangxi 541002, People’s Republic of China; 3Department of Ministry of Health Care, Guilin People’s Hospital, Guilin, Guangxi 541002, People’s Republic of ChinaCorrespondence: Fan YangDepartment of Endocrinology, Guilin People’s Hospital, No. 12, Wenming Road, Guilin, Guangxi 541002, People’s Republic of ChinaTel/ Fax +86-773-2821218Email fanyang823@163.comIntroduction: Nonalcoholic fatty liver disease (NAFLD) is one of the most common chronic liver diseases. The development of NAFLD is closely associated with hepatic lipotoxicity, inflammation, and oxidative stress. The new concept of NAFLD treatment is to seek molecular control of lipid metabolism and hepatic redox hemostasis. Phoenixin is a newly identified neuropeptide with pleiotropic effects. This study investigated the effects of phoenixin 14 against high-fat diet (HFD)-induced NAFLD in mice.Materials and Methods: For this study, we used HFD-induced NAFLD mice models to analyze the effect of phonenixin14. The mice were fed on HFD and normal diet and also given phoenixin 14 (100 ng/g body weight) by gastrogavage for 10 weeks. The peripheral blood samples were collected for biochemical assays. The liver tissues were examined for HFD-induced tissue fibrosis, lipid deposition and oxidative activity including SOD, GSH, and MDA. The liver tissues were analyzed for the inflammatory cytokines and oxidative stress pathway genes.Results: The results indicate that phoenixin 14 significantly ameliorated HFD-induced obesity and fatty liver. The biochemical analysis of blood samples revealed that phoenixin 14 ameliorated HFD-induced elevated circulating alanine aminotransferase (ALT), aspartate aminotransferase (AST), total cholesterol, and triglyceride levels, suggesting that phoenixin 14 has a protective role in liver function and lipid metabolism. Hematoxylin-eosin (HE) and Oil Red O staining of the liver showed that phoenixin 14 alleviated HFD-induced tissue damage and lipid deposition in the liver. Furthermore, the mice administered with phoenixin 14 had increased hepatic SOD activity, increased production of GSH and reduced MDA activity, as well as reduced production of TNF-α and IL-6 suggesting that phoenixin 14 exerts beneficial effects against inflammation and ROS. The findings suggest an explanation of how mechanistically phoenixin 14 ameliorated HFD-induced reduced activation of the SIRT1/AMPK and NRF2/HO-1 pathways.Conclusion: Collectively, this study revealed that phoenixin 14 exerts a protective effect in experimental NAFLD mice. Phoenixin could be of the interest in preventive modulation of NAFLD.Keywords: phoenixin 14, nonalcoholic fatty liver disease, NAFLD, oxidative stress, inflammation, NRF2/HO-1, SIRT1/AMPK
Published: 2020

238. Knockdown of PVT1 Suppresses Colorectal Cancer Progression by Regulating MiR-106b-5p/FJX1 Axis

Author: Liu F, Wu R, Guan L, and Tang X
Subjects: colorectal cancer, pvt1, mir-106b-5p, fjx1, metastasis, apoptosis, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
Abstract: Fang Liu,1 Rong Wu,2 Lina Guan,3 Xuegui Tang1 1Anorectal Department of Integrated Traditional Chinese and Western Medicine, Affiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan, People’s Republic of China; 2Department of Clinical Medicine of Combination of Chinese and Western Medicine, North Sichuan Medical College, Nanchong, Sichuan, People’s Republic of China; 3Institute of Anorectal Diseases, North Sichuan Medical College, Nanchong, Sichuan, People’s Republic of ChinaCorrespondence: Xuegui Tang Anorectal Department of Integrated Traditional Chinese and Western MedicineAffiliated Hospital of North Sichuan Medical College, No. 1, Maoyuan South Road, Nanchong 637000, Sichuan, People’s Republic of ChinaTel +86-0817-2262120Email L29228273@163.comPurpose: Long non-coding RNA plasmacytoma variant translocation 1 (PVT1) has been revealed to involve in the progression of CRC. However, the precise mechanisms of PVT1 in action remain unclear.Methods: The expression of PVT1, microRNA-106b-5p (miR-106b-5p) and four jointed box 1 (FJX1) was measured using quantitative real-time polymerase chain reaction (qRT-PCR) or Western blot, respectively. Cell proliferation was investigated by 3-(4,5)-dimethylthiahiazo (−z-y1)-3,5-di-phenytetrazoliumromide assay. Transwell assay was used to determine cell migration and invasion. The correlation between miR-106b-5p and PVT1 or FJX1 was confirmed using luciferase reporter assay. The effects of PVT1 in vivo were assessed using mice xenograft model.Results: PVT1 was up-regulated in CRC tissues and cell lines, especially in CRC tissues with high-grade, and highly expressed PVT1 predicted worse prognosis. Functional experiments demonstrated that PVT1 deletion inhibited CRC cell proliferation, migration and invasion in vitro and suppressed tumor growth in vivo. MiR-106b-5p was confirmed to be a target of PVT1, and inhibition of miR-106b-5p reversed the inhibitory effects of PVT1 knockdown on CRC cell malignant phenotypes. In addition, we found miR-106b-5p directly targeted FJX1, and miR-106b-5p-mediated inhibition on CRC cell proliferation, migration and invasion was attenuated by FJX1 up-regulation. Importantly, it was also proved that PVT1 could indirectly regulate FJX1 expression via targeting miR-106b-5p.Conclusion: Knockdown of PVT1 impaired cell proliferation, migration and invasion in CRCs via regulating miR-106b-5p/FJX1 axis, which provided a novel insight into the development of therapeutic strategies for CRC patients.Keywords: colorectal cancer, PVT1, miR-106b-5p, FJX1, metastasis, apoptosis
Published: 2020

239. CREB1 Suppresses Transcription of microRNA-186 to Promote Growth, Invasion and Epithelial–Mesenchymal Transition of Gastric Cancer Cells Through the KRT8/HIF-1α Axis

Author: Huang X, Liu F, Jiang Z, Guan H, and Jia Q
Subjects: creb1, transcription suppression, microrna-186, krt-8, hif-1α, gastric cancer, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
Abstract: Xue Huang, Fujian Liu, Zhiyong Jiang, Hang Guan, Qiuhong Jia Department of Gastroenterology, The Eighth Affiliated Hospital of Guangxi Medical University, Guigang 537100, Guangxi, People’s Republic of ChinaCorrespondence: Qiuhong JiaDepartment of Gastroenterology, The Eighth Affiliated Hospital of Guangxi Medical University, No. 1, Zhongshan Middle Road, Gangbei District, Guigang 537100, Guangxi, People’s Republic of ChinaTel/Fax +86-775-4200168Email qiuhongjia211@163.comBackground: The cAMP response element-binding protein 1 (CREB1) was initiated as a potential target for cancer treatment. This research was conducted to probe the effect of CREB1 in the progression of gastric cancer (GC) and the molecules involved.Materials and Methods: CREB1 expression in GC tissues and cell lines (AGS and MKN-45) as well as that in normal tissues and in gastric mucosa cell line (GES-1) was detected. The correlation between CREB1 expression and prognosis of GC patients was determined. Artificial silencing of CREB1 was introduced to evaluate its effect on biological behaviors of GC cells. The target microRNA (miRNA) of CREB1 and the target mRNA of miR-186 were predicted and validated. Altered expression of miR-186, KRT8 and HIF-1α was introduced to confirm their functions in GC progression.Results: CREB1 was abundantly expressed in GC tissues and cells and linked to dismal prognosis in patients. Silencing of CREB1 or upregulation of miR-186 suppressed the malignant behaviors such as growth, epithelial–mesenchymal transition (EMT) and invasion of GC cells, while artificial overexpression of KRT8 led to reversed trends. KRT8 was a target mRNA of miR-186, and CREB1 transcriptionally suppressed miR-186 expression to further up-regulate KRT8. KRT8 was also found to increase HIF-1α expression. Upregulation of HIF-1α was found to block the suppressing role of CREB1 silencing in GC cell malignancy.Conclusion: This study evidenced that silencing of CREB1 inhibits growth, invasion, EMT and resistance to apoptosis of GC cells involving the upregulation of miR-186 and the following downregulation of KRT8 and HIF-1α.Keywords: CREB1, transcription suppression, microRNA-186, KRT-8, HIF-1α, gastric cancer
Published: 2020

240. Clinico-Radiological Features and Outcomes in Pregnant Women with COVID-19 Pneumonia Compared with Age-Matched Non-Pregnant Women

Author: Liu F, Liu H, Hou L, Li J, Zheng H, Chi R, Lan W, and Wang D
Subjects: covid-19, pregnancy, computed tomography, outcome, Infectious and parasitic diseases, RC109-216
Abstract: Fang Liu, 1,* Huanhuan Liu, 2,* Liang Hou, 2,* Jinning Li, 2 Hui Zheng, 2 Runmin Chi, 2 Weishun Lan, 1 Dengbin Wang 2 1Department of Radiology, Maternal and Child Health Hospital of Hubei Province, Wuhan 430070, People’s Republic of China; 2Department of Radiology, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200092, People’s Republic of China*These authors contributed equally to this workCorrespondence: Dengbin WangDepartment of Radiology, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, No. 1665 Kongjiang Road, Shanghai 200092, People’s Republic of ChinaTel +86-21-25077030Fax +86-21-65795173Email wangdengbin@xinhuamed.com.cnWeishun LanDepartment of Radiology, Maternal and Child Health Hospital of Hubei Province, No. 745 Wuluo Road, Wuhan 430070, People’s Republic of ChinaTel +86-21-13349995888Fax +86-27-87882324Email lws7375@126.comPurpose: To investigate the clinico-radiological findings and outcomes in pregnant women with COVID-19 pneumonia compared to age-matched non-pregnant women.Methods: A retrospective case-controlled study was conducted to review clinical and CT data of 21 pregnant and 19 age-matched non-pregnant women with COVID-19 pneumonia. Four stages of CT images were analyzed and compared based on the time interval from symptom onset: stage 1 (0– 6 days), stage 2 (7– 9 days), stage 3 (10– 16 days), and stage 4 (> 16 days). The initial and follow-up data were analyzed and compared.Results: Compared with age-matched non-pregnant women, initial absence of fever (13/21, 62%) and normal lymphocyte count (11/21, 52%) were more frequent in pregnant group. The predominant patterns of lung lesions were pure ground-glass opacity (GGO), GGO with consolidation or reticulation, and pure consolidation in both groups. Pure consolidation on chest CT was more common at presentation in pregnant cases. Pregnant women progressed with a higher consolidation frequency compared with non-pregnant group in stage 2 (95% vs 82%). Improvement was identified in stages 3 and 4 for both groups, but consolidation was still more frequent for pregnant women in stage 4. Most patients (38/40, 95%) were grouped as mild or common type. The length of hospitalization between the two groups was similar.Conclusion: Pregnant women with COVID-19 pneumonia did not present typical clinical features, while developing a relatively more severe disease at imaging with a slower recovery course and experiencing similar outcomes compared with the non-pregnant women.Keywords: COVID-19, pregnancy, computed tomography, outcome
Published: 2020

241. Glucagon-Like Peptide 1 Attenuates Lipotoxicity-Induced Islet Dysfunction in ApoE–/– Mice

Author: Liu F, Gong L, Qin W, Cui C, Chen L, and Zhang M
Subjects: glp-1, islet function, parp-1, Specialties of internal medicine, RC581-951
Abstract: Fuqiang Liu,1– 4 Lei Gong,1– 4 Weidong Qin,5 Chen Cui,1– 4 Li Chen,1– 4 Mingxiang Zhang5 1Department of Endocrinology, Qilu Hospital, Shandong University, Jinan 250012, People’s Republic of China; 2Institute of Endocrine and Metabolic Diseases, Shandong University, Jinan 250012, People’s Republic of China; 3Key Laboratory of Endocrine and Metabolic Diseases, Shandong Province Medicine and Health, Jinan, People’s Republic of China; 4Jinan Clinical Research Center for Endocrine and Metabolic Diseases, Jinan, People’s Republic of China; 5Key Laboratory of Cardiovascular Remodeling and Function Research, Chinese Ministry of Education and Chinese Ministry of Public Health, Qilu Hospital, Shandong University, Jinan Shandong 250012, People’s Republic of ChinaCorrespondence: Li ChenDepartment of Endocrinology, Qilu Hospital of Shandong University, 107 Wen Hua Xi Road, Jinan, Shandong 250012, People’s Republic of China, Tel +86-531-8216-9255Fax +86-531-86169356Email chenli191125@126.comMingxiang ZhangKey Laboratory of Cardiovascular Remodeling and Function Research, Chinese Ministry of Education and Chinese Ministry of Public Health, Qilu Hospital, Shandong University, 107 Wen Hua Xi Road, Jinan, Shandong 250012, People’s Republic of China, Tel +86-531-8216-9255Fax +86-531-86169356Email zhangmingxiang2019@126.comAim: Glucagon-like peptide-1 (GLP1) is known to decrease glucagon release and may be beneficial for the reduction of elevated blood glucose. However, its role and mechanism of action in diabetes remain elusive. This study aimed to examine the function of GLP1 and analyze the mechanism of effect that GLP1exerts on inducible nitric oxide synthase (iNOS) in diabetic mice.Methods: A diabetes model was established in ApoE–/– mice fed a high-fat diet and treated with GLP1 and/or lentivirus-expressing PARP1. PARP1, iNOS, and inflammatory factors in islets were detected by Western blot and ELISA. Islet α cells and β cells and CD8+ T lymphocytes were detected by immunostaining. Islet-cell apoptosis was detected by TUNEL.Results: GLP1 inhibited the expression of PARP1 and iNOS in islets, alleviated decrease in β cells, and suppressed cell apoptosis induced by the high-fat diet. Moreover, GLP1 recovered the decline in insulin sensitivity and glucose tolerance in ApoE–/– mice fed the high-fat diet, and the effects of GLP1 were related to the inhibition of COX2 and NFκB expression.Conclusion: GLP1 significantly alleviated the decrease in β-cell numbers, suppressed β-cell apoptosis induced by the high-fat diet, inhibited the expression of iNOS, and alleviated inflammatory islet injury via inhibiting the COX2–NFκB pathway.Keywords: GLP1, islet function, PARP1
Published: 2020

242. Longitudinal Progression of Estimated GFR in HIV-1-Infected Patients with Normal Renal Function on Tenofovir-Based Therapy in China

Author: Liu F, Xu A, Zhao H, Yang Z, Chen C, Ranieri B, Bao J, Zheng G, Wang M, Wang Y, and Xun Y
Subjects: nonlinear trajectory, renal function, human immunodeficiency virus-1, Therapeutics. Pharmacology, RM1-950
Abstract: Fang Liu,1 Aifang Xu,1 Huaqing Zhao,2 Zongxing Yang,3 Chen Chen,4 Brona Ranieri,4 Jianfeng Bao,5 Guoxiang Zheng,3 Miaochan Wang,1 Ying Wang,1 Yunhao Xun5 1Medical Laboratory, Xixi Hospital of Hangzhou, Hangzhou, People’s Republic of China; 2Temple University School of Medicine, Department of Clinical Sciences, Philadelphia, PA, USA; 3Department of Infectious Diseases, Xixi Hospital of Hangzhou, Hangzhou, People’s Republic of China; 4Department of Neuroscience, Temple University, Philadelphia, PA, USA; 5Department of Integrated Chinese and Western Medicine, Xixi Hospital of Hangzhou, Hangzhou, People’s Republic of ChinaCorrespondence: Yunhao XunDepartment of Integrated Chinese and Western Medicine, Xixi Hospital of Hangzhou, Zhejiang Chinese Medical University Affiliated Sixth Hospital, 2 Hengbu Road, Hangzhou 310023, People’s Republic of ChinaTel +86-571-86481581Fax +86-571-86481822Email hzxxgb@outlook.comPurpose: Estimated glomerular filtration rate (eGFR) decline in HIV-1-infected patients exposure to tenofovir disoproxil fumarate (TDF) has been widely assessed using linear models, but nonlinear assumption is not well validated. We constructed a retrospective cohort study to assess whether eGFR decline follows nonlinearity during antiviral therapy.Patients and Methods: We examined 823 (299 of TDF users and 524 of non-TDF users) treatment-naïve HIV-1-infected participants (age ≥ 17 years, initial eGFR ≥ 90 mL/min/1.73m2). Estimated GFR trajectories were compared by one-linear and piecewise-linear mixed effects models, before and after propensity score matching, respectively. Whether the incidence of renal dysfunction (reduced renal function [RRF], eGFR < 90 mL/min/1.73 m2 and rapid kidney function decline [RKFD], eGFR > − 3 mL/min/1.73 m2/year) follows nonlinearity was assessed by logistic regression.Results: The median follow-up time of this study was 10 (interquartile range, 2– 20) months, during which 178 (21.6%) experienced RRF, and 451 (54.8%) experienced RKFD. The slopes (mL/min/1.73 m2/year) of eGFR were − 5.31 (95% CI: − 6.57, − 4.06) before 1.40 years, 4.83 (95% CI: 1.38, 8.28) from years 1.40 to 2.30 and − 3.71 (95% CI: − 5.97, − 1.45) after 2.30 years among TDF users. Within years 1.40– 2.30, each year of TDF exposure was associated with a 78% decreased risk of RKFD (95% CI: − 91%, − 49%). In comparison, eGFR increased slightly at the initiation of antiviral therapy, declined after 2.15 years (− 4.96; 95% CI: − 5.76, − 4.17) among non-TDF users. Such a progression nonlinear trajectory was missed on the assumption of one-linearity, whether in TDF or non-TDF users.Conclusion: Over the piecewise mixed-effects analyses with the advantage of revealing the true nature of the exposure outcome relationships, an interesting reverse S-shaped relationship was observed. A routine screen based on nonlinearity could be more helpful for patient management.Keywords: nonlinear trajectory, renal function, human immunodeficiency virus-1
Published: 2020

243. Comparative Diagnostic Evaluation with Contrast-Enhanced Ultrasound, Computed Tomography and Magnetic Resonance Imaging in Patients with Pancreatic Cystic Neoplasms

Author: Sun Y, Yang S, Qi E, Liu F, Zhou F, Lu Y, Liang P, Ye H, and Yu X
Subjects: contrast-enhanced ultrasound, computed tomography, magnetic resonance imaging, pancreatic cystic neoplasms, diagnostic evaluation, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
Abstract: Ya Sun,1,2,* Shuo Yang,3,* Erpeng Qi,1 Fangyi Liu,1 Fubo Zhou,1 Yuhan Lu,1 Ping Liang,1 Huiyi Ye,4 Xiaoling Yu1 1Department of Interventional Ultrasound, Chinese PLA General Hospital, Beijing 100853, People’s Republic of China; 2Department of Ultrasound, Aerospace Central Hospital, Beijing 100049, People’s Republic of China; 3Chinese PLA Medical School, Beijing, 100853, People’s Republic of China; 4Radiology Department, Chinese PLA General Hospital, Beijing 100853, People’s Republic of China*These authors contributed equally to this workCorrespondence: Xiaoling YuDepartment of Interventional Ultrasound, Chinese PLA General Hospital, 28 Fuxing Road, Beijing 100853, People’s Republic of ChinaEmail dyuxl301@aliyun.comPurpose: The purpose of our study was to evaluate the role of contrast-enhanced ultrasound (CEUS) with magnetic resonance imaging (MRI) and computed tomography (CT) in the pathological diagnosis of pancreatic cystic neoplasms (PCNs).Methods: A total of 90 patients (66 women, 24 men) aged 18– 71 years were studied prospectively. CEUS was performed in all patients, whereas MRI was performed in 85 patients and CT in 69 patients. We analyzed the sensitivity and accuracy of these three imaging modalities to diagnose the PCNs. Neoplasm size, location, shape, intralesional mural nodules, septa and duct dilatation were also assessed by different radiologists.Results: There were no significant differences in sensitivity for discriminating PCNs from pancreatic cystic lesions between CEUS and MRI (p=0.614) or between CEUS and CT (p=0.479). The diagnostic accuracy of CEUS for classifying PCNs was 64.4% (58/90), which was higher than that of CT (53.6%, 37/69, P=0.017), and lower than that of MRI (70.6%, 60/85, p=0.791). Regarding tumor size for lesions larger than 3 cm, CEUS was superior to CT in differentiating the specific type of PCN (p=0.041), and CEUS had the same value as MRI (p=0.774). Furthermore, CEUS is valuable for precisely characterizing internal structures, for instance, septa (p=0.003, compared with CT; p=0.443, compared with MRI) and nodules (p= 0.018, compared with CT; p=0.033, compared with MRI). The number of septa (p=0.033) and cyst morphology (p=0.016) were meaningful indicators in differentiating serous and mucinous adenoma. There was no significant difference in evaluating size and detecting duct dilatation among the three imaging methods.Conclusion: CEUS compares favorably with MRI in displaying the inner structure of PCNs and offers advantages over CT. CEUS can contribute in an important way to the diagnosis of pancreatic cystic neoplasms.Keywords: contrast-enhanced ultrasound, computed tomography, magnetic resonance imaging, pancreatic cystic neoplasms, diagnostic evaluation
Published: 2020

244. Gut Microbiota Regulates Depression-Like Behavior in Rats Through the Neuroendocrine-Immune-Mitochondrial Pathway

Author: Liu S, Guo R, Liu F, Yuan Q, Yu Y, and Ren F
Subjects: gut microbiota, depression, neurotransmitter, hpa axis, immune, mitochondrial, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571, Neurology. Diseases of the nervous system, RC346-429
Abstract: Shuhan Liu,1 Rongjuan Guo,2 Fei Liu,3 Qingjie Yuan,4 Yao Yu,1 Feifei Ren1 1Second Clinical Medical College, Beijing University of Chinese Medicine, Beijing 100029, People’s Republic of China; 2Department of Neurology, Dongfang Hospital Beijing University of Chinese Medicine, Beijing 100078, People’s Republic of China; 3College of Acupuncture and Massage, Changchun University of Chinese Medicine, Changchun 130117, People’s Republic of China; 4Department of Traditional Chinese Medicine, Tsinghua University Yuquan Hospital, Beijing 100040, People’s Republic of ChinaCorrespondence: Rongjuan GuoDepartment of Neurology, Dongfang Hospital Beijing University of Chinese Medicine, No. 6 Fangxingyuan 1st Block, Fengtai District, Beijing City, People’s Republic of ChinaTel +86 1 861 137 7633Fax +86 1064286498Email dfguorongjuan@163.comPurpose: Gut microbiota affects various physiological functions in the host and has crucial effects on the nervous system. There is increasing evidence of a correlation between gut microbiota and depression; however, the mechanisms underlying the regulation of depression-like behavior by gut microbiota remain unclear. In this study, we assessed the regulatory mechanism of gut microbiota on depression-like behavior in rats.Methods: We transplanted fecal microbiota obtained from patients with depression and healthy individuals into germ-free (GF) rats (n=18) through fecal microbiota transplantation technology. Next, we assessed the affective behavior in the rats using the forced swimming test and a sucrose preference test. We used enzyme-linked immunosorbent assay (ELISA) to determine the hippocampal levels of 5-hydroxytryptamine (5-HT), dopamine (DA), and noradrenaline (NE) and the serum levels of corticosterone (CORT), adrenocorticotropic hormone (ACTH), corticotropin-releasing hormone (CRH), tumor necrosis factor-α (TNF-α), interferon-γ (IFN-γ), interleukin-6 (IL-6), interleukin-1 (IL-1), interleukin-1 (IL-4), and interleukin-1 (IL-10). The mitochondrial morphology of small intestinal epithelial cells was observed through transmission electron microscopy.Results: Rats that received fecal microbiota from patients with depression (depression microbiota) exhibited depression-like behavior. They presented decreased levels of hippocampal neurotransmitters, serum CORT levels, and anti-inflammatory cytokine levels, as well as increased ACTH, CRH, and serum levels of multiple pro-inflammatory cytokines. Observation of the mitochondria ultrastructure showed damaged mitochondria in the intestinal epithelial cells, significant endoplasmic reticulum expansion, and border aggregation of nuclear chromatin.Conclusion: Our findings suggested that the depression-like behaviors induced by the depression microbiota through the neuroendocrine-immune-mitochondrial pathway, which were associated with neuroendocrine disorders, inflammatory responses, and mitochondrial damage.Keywords: gut microbiota, depression, neurotransmitter, HPA axis, immune, mitochondrial
Published: 2020

245. A Study of Antidepressant Effect and Mechanism on Intranasal Delivery of BDNF-HA2TAT/AAV to Rats with Post-Stroke Depression

Author: Chen C, Dong Y, Liu F, Gao C, Ji C, Dang Y, Ma X, and Liu Y
Subjects: post stroke depression (psd), bdnf-ha2tat/aav, nasal-brain pathway, hippocampus, prefrontal cortex, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571, Neurology. Diseases of the nervous system, RC346-429
Abstract: Ce Chen,1,* Yingying Dong,1,* Fei Liu,2 Chengge Gao,1 Cui Ji,3 Yonghui Dang,4 Xiancang Ma,1 Yong Liu5 1Department of Psychiatry, First Affiliated Hospital of Medical College Xi’an Jiaotong University, Xi’an 710061, Shaanxi, People’s Republic of China; 2Clinical Research Center of Shaanxi Province for Dental and Maxillofacial Diseases, College of Stomatology, Xi’an Jiaotong University, Xi’an 710004, Shaanxi, People’s Republic of China; 3The Hospital of Xidian University, Xi’an 710071, Shaanxi, People’s Republic of China; 4College of Medicine & Forensics, Xi’an Jiaotong University Health Science Center, Xi’an 710061, Shaanxi, People’s Republic of China; 5The Institute of Neurobiology, Xi’an Jiaotong University, Xi’an 710061, Shaanxi, People’s Republic of China*These authors contributed equally to this workCorrespondence: Yong LiuThe Institute of Neurobiology, Xi’an Jiaotong University, Yanta Road W. 76#, Xi’an, Shaanxi 710061, People’s Republic of ChinaTel +8618189236156Email liuy5599@mail.xjtu.edu.cnAim: Post-stroke depression (PSD) is one of the most frequent neuropsychiatric disorders associated with stroke characterized by depression. The neuroplasticity hypothesis postulates that loss of brain-derived neurotrophic factor (BDNF) plays a major role in pathophysiology of PSD, and restoration of it may represent a critical mechanism underlying antidepressant efficacy.Methods: In previous studies, we designed a new fusion gene, HA2TAT-BDNF, and cloned it into adenovirus associated virus (AAV) to construct the BDNF-HA2TAT/AAV for the delivery of BDNF to central nervous system (CNS) via nose-brain pathway. In this study, we used it to explore the antidepressant effects on PSD rats through behavioral and various histological methods, and try to find out its specific mechanism.Results: Compared with the control group, the PSD+AAV group showed decreased sucrose consumption percentage in the sucrose preference test (SPT) (P < 0.001) and prolonged immobility in the forced swimming test (FST) (P=0.000). However, the nasal administration of BDNF-HA2TAT/AAV reversed results of these two behavioral tests (P> 0.05, P > 0.05), showing an adequate antidepressant effect. Compared with the control group, the concentrations of BDNF mRNA and protein in the hippocampus (P< 0.05, P < 0.01) and prefrontal cortex (P < 0.01, P < 0.01) of PSD rats both decreased. Increased BDNF mRNA and protein expression was observed in the prefrontal cortex (P > 0.05, P < 0.05), without notable change in the hippocampus (P < 0.05, P < 0.001) of PSD+BDNF rats.Conclusion: These results suggest that BDNF reductions in the prefrontal cortex and hippocampus are associated with the development of post-stroke depression, and that increased levels of BDNF in the prefrontal cortex could be used as a therapeutic target to treat PSD. However, the exact mechanism of BDNF action remains unclear in this regard, hindering the wider application of our method. We expect that our research could facilitate the exploration of pathogenesis and the new treatment method of PSD.Keywords: post-stroke depression, PSD, BDNF-HA2TAT/AAV, nasal-brain pathway, hippocampus, prefrontal cortex
Published: 2020

246. Novel Prognostic Nomograms for Predicting Early and Late Recurrence of Hepatocellular Carcinoma After Curative Hepatectomy

Author: Xu W, Li R, and Liu F
Subjects: hepatocellular carcinoma, hepatectomy, risk factor, prognosis, pomogram, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
Abstract: Wei Xu, Ruineng Li, Fei Liu Department of Hepatobiliary Surgery, Hunan Provincial People’s Hospital, The First Hospital Affiliated with Hunan Normal University, Changsha 410005, People’s Republic of ChinaCorrespondence: Wei XuDepartment of Hepatobiliary Surgery, Hunan Provincial People’s Hospital, The First Hospital Affiliated with Hunan Normal University, No. 61 West Jiefang Road, Changsha 410005, People’s Republic of ChinaTel +8613873159491Fax +8673182278012Email xuwei0209@163.comAim: Hepatectomy is the main curative method for patients with hepatocellular carcinoma (HCC) in China. Unfortunately, high recurrence rate after hepatectomy poses negative impact on the prognosis of patients. This study aimed to develop prognostic nomograms to predict early recurrence (ER) and late recurrence (LR) of HCC after curative hepatectomy.Patients and Methods: Total of 318 HCC patients undergoing curative hepatectomy from January 2012 to January 2018 were retrospectively recruited. Potential risk factors that were significant for predicting ER and LR in univariate analysis were selected for multivariate survival model analysis using the backward stepwise method. Risk factors identified in multivariate analysis were used to develop nomograms to predict ER and LR. The nomogram was internally validated using 2,000 bootstrap samples from 75% of the original data.Results: Among 318 patients, 164 showed postoperative recurrence, of which 140 and 24 had ER (≤ 2 years) and LR (> 2 years), respectively. Multivariate analysis showed that age, Hong Kong Liver Cancer Stage, albumin-bilirubin, METAVIR fibrosis grade, and microvascular invasion were risk factors of ER for HCC after curative hepatectomy. The AUC of the ROC curve for ER in the development set (D-set) was 0.888 while that in the validation set (V-set) was 0.812. Neutrophil/lymphocyte ratio and glypican-3 (+) were risk factors for LR in HCC patients after curative hepatectomy. The AUC of the ROC curve for LR predictive nomogram that integrated all independent predictors was 0.831. The AUC of the ROC curve for LR in the D-set was 0.833, while that for LR in the V-set was 0.733. The C-index and AUC of ROC for the proposed nomograms were more satisfactory than three conventional HCC staging systems used in this study.Conclusion: We developed novel nomograms to predict ER and LR of HCC patients after curative hepatectomy for clinical use to individualize follow-up and therapeutic strategies.Keywords: hepatocellular carcinoma, hepatectomy, risk factor, prognosis, nomogram
Published: 2020

247. Long Non-Coding RNA CASC19 Sponges microRNA-532 and Promotes Oncogenicity of Clear Cell Renal Cell Carcinoma by Increasing ETS1 Expression

Author: Luo Y, Liu F, Yan C, Qu W, Zhu L, Guo Z, Zhou F, and Zhang W
Subjects: cancer, mtt assay, cell migration, invasiveness, xenograft, knockdown, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
Abstract: Yu Luo, Feng Liu, Chunhui Yan, Wei Qu, Liang Zhu, Zheng Guo, Fan Zhou, Wei Zhang Department of Urology, The 161st Hospital of the People’s Liberation Army, Wuhan, Hubei 430010, People’s Republic of ChinaCorrespondence: Feng LiuDepartment of Urology, The 161st Hospital of the People’s Liberation Army, No. 68, Huangpu Road, Wuhan, Hubei 430010, People’s Republic of ChinaEmail liufwh@163.comPurpose: The long non-coding RNA cancer susceptibility 19 (CASC19) is recognized as an important regulator in gastric cancer, colorectal cancer, and non-small cell lung cancer. Nevertheless, to the best of our knowledge, the expression status and detailed roles of CASC19 in clear cell renal cell carcinoma (ccRCC) have not been elucidated. Hence, we aimed to determine CASC19 expression in ccRCC and investigate its roles in ccRCC oncogenicity. The molecular mechanisms underlying CASC19 functions in ccRCC were also determined.Methods: CASC19 expression was measured by using reverse transcription-quantitative polymerase chain reaction. The effects of CASC19 on ccRCC cell proliferation, colony formation, migration, and invasiveness in vitro, as well as on tumor growth in vivo, were examined by the MTT assay, colony formation assay, cell migration and invasiveness assays, and tumor xenograft in nude nice, respectively.Results: CASC19 was overexpressed in ccRCC tissues and cell lines. High expression of CASC19 was closely associated with unfavorable clinicopathological parameters and predicted negative clinical outcomes in patients with ccRCC. Knockdown of CASC19 decreased ccRCC cell proliferation, colony formation, migration, and invasiveness, as well as attenuated tumor growth in vivo. Mechanistically, CASC19 functioned as a competing endogenous RNA and upregulated the expression of ETS proto-oncogene 1 (ETS1) through sponging microRNA-532 (miR-532). Furthermore, rescue assays revealed that inhibiting miR-532 or restoring ETS1 expression partially abolished the impacts of CASC19 knockdown on ccRCC cells.Conclusion: The CASC19/miR-532/ETS1 regulatory pathway is crucial for the malignant manifestations of ccRCC, which makes it an attractive target for potential treatments of ccRCC.Keywords: cancer, MTT assay, cell migration, invasiveness, xenograft, knockdown
Published: 2020

248. Perioperative Circulating Tumor DNA in Colorectal Liver Metastases: Concordance with Metastatic Tissue and Predictive Value for Tumor Burden and Prognosis

Author: He Y, Ma X, Chen K, Liu F, Cai S, Han-Zhang H, Hou T, Xiang J, and Peng J
Subjects: colorectal liver metastases (clm), circulating tumor dna (ctdna), tumor burden, prognosis., Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
Abstract: Yiping He,1,2,* Xiaoji Ma,1,2,* Ke Chen,2,3,* Fangqi Liu,1,2 Sanjun Cai,1,2 Han Han-Zhang,4 Ting Hou,4 Jianxing Xiang,4 Junjie Peng1,2 1Department of Colorectal Surgery, Fudan University Shanghai Cancer Center, Shanghai 200032, People’s Republic of China; 2Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, People’s Republic of China; 3Department of Endoscopy, Fudan University Shanghai Cancer Center, Shanghai 200032, People’s Republic of China; 4Burning Rock Biotech, Guangzhou, Guangdong, People’s Republic of China*These authors contributed equally to this workCorrespondence: Junjie PengDepartment of Colorectal Surgery, Fudan University Shanghai Cancer Center, 270 Dong’An Road, Shanghai 200032, People’s Republic of ChinaTel +86 21 64175590Email pengjj67@hotmail.comBackground: The surgical resection of colorectal cancer with liver metastases (CLM) has proven to be the most important modality for long-term survival, while effective biomarkers for outcome prediction or postoperative surveillance are still lacking. Currently, circulating biomarkers obtained from a liquid biopsy are widely used to assess the treatment response, disease recurrence and progression. In this study, we analyzed the value of the liquid biopsy, which includes circulating tumor DNA (ctDNA) and cell-free DNA (cfDNA), in patients with CLM.Methods: Capture-based targeted deep sequencing was performed on matched pre-surgery, post-surgery and liver metastatic tissues of 20 CRC patients who underwent the resection of liver metastases between May and September 2017 using a panel consisting of 41 genes. Mutation landscapes obtained from pre-surgery plasma samples and metastatic tissue samples were compared.Results: Collectively, we identified 47 mutations from 17 pre-surgery plasma samples (85%), and the remaining 3 patients had no mutation detected from the panel. We revealed a high by-variant concordance rate of 82.14% between pre-surgery plasma samples and liver metastatic tissue samples. We further analyzed the correlation between ctDNA, cfDNA, CEA and tumor burden and revealed a positive correlation between ctDNA and tumor burden (R=0.69, p=0.002). As of the date for data cutoff, 8/20 patients experienced relapse. Our study also demonstrated that pre-surgery ctDNA (p< 0.001), cfDNA (p=0.001) and CEA (p=0.012) levels had predictive value for relapse. Patients with low pre-surgery ctDNA (p< 0.001), cfDNA (p=0.001) or CEA (p=0.012) levels were more likely to experience prolonged progression-free survival.Conclusion: Our data demonstrate that the genomic profile obtained from ctDNA is comparable with the genomic profile obtained from metastatic liver tumors. Furthermore, our study also show that pre-surgery ctDNA levels are positively correlated with tumor burden. In addition, pre-surgery ctDNA, cfDNA and CEA levels have predictive value for relapse.Keywords: colorectal liver metastases, CLM, circulating tumor DNA, ctDNA, tumor burden, prognosis
Published: 2020

249. Enhanced and Prolonged Antitumor Effect of Salinomycin-Loaded Gelatinase-Responsive Nanoparticles via Targeted Drug Delivery and Inhibition of Cervical Cancer Stem Cells

Author: Wang Q, Liu F, Wang L, Xie C, Wu P, Du S, Zhou S, Sun Z, Liu Q, Yu L, Liu B, and Li R
Subjects: nanoparticles, salinomycin, tumor targeted delivery, cancer stem cells, epithelial interstitial transformation, Medicine (General), R5-920
Abstract: Qin Wang,1,* Fangcen Liu,2,* Lifeng Wang,1 Chen Xie,3 Puyuan Wu,1 Shiyao Du,1 Shujuan Zhou,1 Zhichen Sun,1 Qin Liu,1 Lixia Yu,1 Baorui Liu,1 Rutian Li1 1The Comprehensive Cancer Centre of Drum Tower Hospital, Medical School of Nanjing University, Clinical Cancer Institute of Nanjing University, Nanjing 210008, People’s Republic of China; 2The Comprehensive Cancer Centre, Nanjing Drum Tower Hospital, Clinical College of Nanjing Medical University, Nanjing, People’s Republic of China; 3Key Laboratory for Organic Electronics and Information Displays, Institute of Advanced Materials (IAM), Jiangsu National Synergetic Innovation Center for Advanced Materials (SICAM), Nanjing University of Posts & Telecommunications, Nanjing 210023, People’s Republic of China*These authors contributed equally to this workCorrespondence: Rutian Li; Baorui LiuThe Comprehensive Cancer Centre of Drum Tower Hospital, Medical School of Nanjing University, Clinical Cancer Institute of Nanjing University, 321 Zhongshan Road, Nanjing 210008, People’s Republic of ChinaTel +86-25-83107081Fax +86-25-83317016Email rutianli@nju.edu.cn; baoruiliu@nju.edu.cnBackground: Cervical cancer stem cells (CCSCs) represent a subpopulation of tumor cells that possess self-renewal capacity and numerous intrinsic mechanisms of resistance to conventional chemotherapy and radiotherapy. These cells play a crucial role in relapse and metastasis of cervical cancer. Therefore, eradication of CCSCs is the primary objective in cervical cancer therapy. Salinomycin (Sal) is an agent used for the elimination of cancer stem cells (CSCs); however, the occurrence of several side effects hinders its application. Nanoscale drug-delivery systems offer great promise for the diagnosis and treatment of tumors. These systems can be used to reduce the side effects of Sal and improve clinical benefit.Methods: Sal-loaded polyethylene glycol-peptide-polycaprolactone nanoparticles (Sal NPs) were fabricated under mild and non-toxic conditions. The real-time biodistribution of Sal NPs was investigated through non-invasive near-infrared fluorescent imaging. The efficacy of tumor growth inhibition by Sal NPs was evaluated using tumor xenografts in nude mice. Flow cytometry, immunohistochemistry, and Western blotting were used to detect the apoptosis of CSCs after treatment with Sal NPs. Immunohistochemistry and Western blotting were used to examine epithelial–mesenchymal transition (epithelial interstitial transformation) signal-related molecules.Results: Sal NPs exhibited antitumor efficacy against cervical cancers by inducing apoptosis of CCSCs and inhibiting the epithelial–mesenchymal transition pathway. Besides, tumor pieces resected from Sal NP-treated mice showed decreased reseeding ability and growth speed, further demonstrating the significant inhibitory ability of Sal NPs against CSCs. Moreover, owing to targeted delivery based on the gelatinase-responsive strategy, Sal NPs was more effective and tolerable than free Sal.Conclusion: To the best of our knowledge, this is the first study to show that CCSC-targeted Sal NPs provide a potential approach to selectively target and efficiently eradicate CCSCs. This renders them a promising strategy to improve the therapeutic effect against cervical cancer.Keywords: nanoparticles, salinomycin, tumor-targeted delivery, cancer stem cells, epithelial interstitial transformation
Published: 2020

250. LINC01410 Knockdown Suppresses Cervical Cancer Growth and Invasion via Targeting miR-2467-3p/VOPP1 Axis

Author: Liu F and Wen C
Subjects: linc01410, mir-2467-3p, vopp1, cervical cancer, progression, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
Abstract: Fengjuan Liu, Chuansong Wen Department of Gynecology, Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine, Hangzhou 310006, People’s Republic of ChinaCorrespondence: Chuansong WenDepartment of Gynecology, Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine, No. 4 Xueshi Road, Shangcheng District, Hangzhou, Zhejiang 310006, People’s Republic of ChinaTel +86-15867187766Email chuansong_wen@163.comBackground: Long noncoding RNAs have essential roles in human diseases, including cancer. Our work aims to assess the function and mechanisms of LINC01410 in cervical cancer (CC) development.Methods: Expression analyses were performed using qRT-PCR. Proliferation was determined through CCK8 and colony formation assays. Cell migration and invasion were determined by Transwell assay. The interactions among LINC01410, miR-2467-3p and VOPP1 were analyzed via luciferase reporter assay.Results: LINC01410 was upregulated in CC tissues and cell lines. LINC01410 upregulation correlated with poor prognosis. LINC01410 silencing suppressed proliferation, migration and invasion of CC cells. LINC01410 was the sponge for miR-2467. And LINC01410 promoted VOPP1 expression through inhibiting miR-2467.Conclusion: Our findings demonstrated that LINC01410 contributed to CC progression through regulating miR-2467/VOPP1 axis and suggested that LINC01410/miR-2467/VOPP1 cascade may be a potential therapeutic target.Keywords: LINC01410, miR-2467-3p, VOPP1, cervical cancer, progression
Published: 2020

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