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51. Supplementary Figure Legend from DNA Methylation-Mediated Repression of miR-886-3p Predicts Poor Outcome of Human Small Cell Lung Cancer

Author

Cao, Jianzhong, primary, Song, Yongmei, primary, Bi, Nan, primary, Shen, Jie, primary, Liu, Wenyang, primary, Fan, Jing, primary, Sun, Guogui, primary, Tong, Tong, primary, He, Jie, primary, Shi, Yuankai, primary, Zhang, Xun, primary, Lu, Ning, primary, He, Yinghua, primary, Zhang, Hongyu, primary, Ma, Kelong, primary, Luo, Xiaoying, primary, Lv, Lei, primary, Deng, Hui, primary, Cheng, Jing, primary, Zhu, Jingde, primary, Wang, Luhua, primary, and Zhan, Qimin, primary

Published
2023
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52. Supplementary Table 2 from DNA Methylation-Mediated Repression of miR-886-3p Predicts Poor Outcome of Human Small Cell Lung Cancer

Author

Cao, Jianzhong, primary, Song, Yongmei, primary, Bi, Nan, primary, Shen, Jie, primary, Liu, Wenyang, primary, Fan, Jing, primary, Sun, Guogui, primary, Tong, Tong, primary, He, Jie, primary, Shi, Yuankai, primary, Zhang, Xun, primary, Lu, Ning, primary, He, Yinghua, primary, Zhang, Hongyu, primary, Ma, Kelong, primary, Luo, Xiaoying, primary, Lv, Lei, primary, Deng, Hui, primary, Cheng, Jing, primary, Zhu, Jingde, primary, Wang, Luhua, primary, and Zhan, Qimin, primary

Published
2023
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53. Supplementary Table 3 from DNA Methylation-Mediated Repression of miR-886-3p Predicts Poor Outcome of Human Small Cell Lung Cancer

Author

Cao, Jianzhong, primary, Song, Yongmei, primary, Bi, Nan, primary, Shen, Jie, primary, Liu, Wenyang, primary, Fan, Jing, primary, Sun, Guogui, primary, Tong, Tong, primary, He, Jie, primary, Shi, Yuankai, primary, Zhang, Xun, primary, Lu, Ning, primary, He, Yinghua, primary, Zhang, Hongyu, primary, Ma, Kelong, primary, Luo, Xiaoying, primary, Lv, Lei, primary, Deng, Hui, primary, Cheng, Jing, primary, Zhu, Jingde, primary, Wang, Luhua, primary, and Zhan, Qimin, primary

Published
2023
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54. Supplementary Figure 5 from DNA Methylation-Mediated Repression of miR-886-3p Predicts Poor Outcome of Human Small Cell Lung Cancer

Author

Cao, Jianzhong, primary, Song, Yongmei, primary, Bi, Nan, primary, Shen, Jie, primary, Liu, Wenyang, primary, Fan, Jing, primary, Sun, Guogui, primary, Tong, Tong, primary, He, Jie, primary, Shi, Yuankai, primary, Zhang, Xun, primary, Lu, Ning, primary, He, Yinghua, primary, Zhang, Hongyu, primary, Ma, Kelong, primary, Luo, Xiaoying, primary, Lv, Lei, primary, Deng, Hui, primary, Cheng, Jing, primary, Zhu, Jingde, primary, Wang, Luhua, primary, and Zhan, Qimin, primary

Published
2023
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55. Supplementary Figure 2 from DNA Methylation-Mediated Repression of miR-886-3p Predicts Poor Outcome of Human Small Cell Lung Cancer

Author

Cao, Jianzhong, primary, Song, Yongmei, primary, Bi, Nan, primary, Shen, Jie, primary, Liu, Wenyang, primary, Fan, Jing, primary, Sun, Guogui, primary, Tong, Tong, primary, He, Jie, primary, Shi, Yuankai, primary, Zhang, Xun, primary, Lu, Ning, primary, He, Yinghua, primary, Zhang, Hongyu, primary, Ma, Kelong, primary, Luo, Xiaoying, primary, Lv, Lei, primary, Deng, Hui, primary, Cheng, Jing, primary, Zhu, Jingde, primary, Wang, Luhua, primary, and Zhan, Qimin, primary

Published
2023
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56. Effects of sodium tanshinone IIA sulfonate injection on inflammatory factors and vascular endothelial function in patients with acute coronary syndrome undergoing percutaneous coronary intervention: A systematic review and meta-analysis of randomized clinical trials

Author

Kan, Zunqi, primary, Yan, Wenli, additional, Yang, Mengqi, additional, Gao, Huanyu, additional, Meng, Dan, additional, Wang, Ning, additional, Fang, Yuqing, additional, Wu, Lingyu, additional, and Song, Yongmei, additional

Published
2023
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60. Genomic Analyses Reveal Mutational Signatures and Frequently Altered Genes in Esophageal Squamous Cell Carcinoma

Author

Zhang, Ling, Zhou, Yong, Cheng, Caixia, Cui, Heyang, Cheng, Le, Kong, Pengzhou, Wang, Jiaqian, Li, Yin, Chen, Wenliang, Song, Bin, Wang, Fang, Jia, Zhiwu, Li, Lin, Li, Yaoping, Yang, Bin, Liu, Jing, Shi, Ruyi, Bi, Yanghui, Zhang, Yanyan, Wang, Juan, Zhao, Zhenxiang, Hu, Xiaoling, Yang, Jie, Li, Hongyi, Gao, Zhibo, Chen, Gang, Huang, Xuanlin, Yang, Xukui, Wan, Shengqing, Chen, Chao, Li, Bin, Tan, Yongkai, Chen, Longyun, He, Minghui, Xie, Sha, Li, Xiangchun, Zhuang, Xuehan, Wang, Mengyao, Xia, Zhi, Luo, Longhai, Ma, Jie, Dong, Bing, Zhao, Jiuzhou, Song, Yongmei, Ou, Yunwei, Li, Enming, Xu, Liyan, Wang, Jinfen, Xi, Yanfeng, Li, Guodong, Xu, Enwei, Liang, Jianfang, Yang, Xiaofeng, Guo, Jiansheng, Chen, Xing, Zhang, Yanbo, Li, Qingshan, Liu, Lixin, Li, Yingrui, Zhang, Xiuqing, Yang, Huanming, Lin, Dongxin, Cheng, Xiaolong, Guo, Yongjun, Wang, Jun, Zhan, Qimin, and Cui, Yongping

Published
2015
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67. A widespread length-dependent splicing dysregulation in cancer

Author

Zhang, Sirui, primary, Mao, Miaowei, additional, Lv, Yuesheng, additional, Yang, Yingqun, additional, He, Weijing, additional, Song, Yongmei, additional, Wang, Yongbo, additional, Yang, Yun, additional, Al Abo, Muthana, additional, Freedman, Jennifer A., additional, Patierno, Steven R., additional, Wang, Yang, additional, and Wang, Zefeng, additional

Published
2022
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74. Additional file 1 of S6K1 amplification confers innate resistance to CDK4/6 inhibitors through activating c-Myc pathway in patients with estrogen receptor-positive breast cancer

Author

Mo, Hongnan, Liu, Xuefeng, Xue, Yu, Chen, Hongyan, Guo, Shichao, Li, Zhangfu, Wang, Shuang, Li, Caiming, Han, Jiashu, Fu, Ming, Song, Yongmei, Li, Dan, and Ma, Fei

Abstract

Additional file 1: Supplementary Table S1. List of target region genes in the 1021-gene panel.

Published
2022
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75. Efficacy and Safety of Transcutaneous Electrical Acupoint Stimulation (TEAS) for Postoperative Pain in Laparoscopy: A Systematic Review and Meta-Analysis of Randomized Controlled Trials

Author

Meng, Dan, Mao, Yifei, Song, Quan-mei, Yan, Chun-chun, Zhao, Qin-yu, Yang, Mengqi, Xiang, Guangxin, and Song, Yongmei

Subjects
Article Subject
Abstract

Objectives. This meta-analysis aimed to assess the efficacy and safety of transcutaneous acupoint electrical stimulation (TEAS) for postoperative pain in laparoscopy. The review has been registered on the “INPLASY” website and the registration number is INPLASY202150101. Methods. Relevant randomized controlled trials are selected from seven electronic databases (PubMed, the Cochrane Library, Embase, China National Knowledge Infrastructure, Chongqing VIP Information, WanFang Data, and Chinese Biomedical Database) from their inception up to November 30, 2020. Twenty-eight studies were included in this meta-analysis, and the statistical analyses and the exploration of heterogeneity sources were conducted by Stata 15.0 software. Besides, the bias assessment of the included studies was evaluated using the Cochrane risk of bias tool. Results. In total, 28 RCTs covering 2787 participants were included. The meta-analysis suggested that TEAS can effectively relieve pain in the short term after laparoscopy, reduce the postoperative consumption of rescue analgesics, improve the quality of life of patients, and shorten the length of hospitalization. And no serious adverse events are related to TEAS. Therefore, TEAS is relatively safe and efficacy for clinical application. The most used acupoints were Hegu (LI14), Neiguan (PC6), and Zusanli (ST36). Conclusions. TEAS can be recommended as a complementary and alternative therapy for the treatment of postoperative pain after laparoscopy. However, the included RCTs had some methodological limitations. Therefore, larger-size, more rigorous, and higher-quality RCTs are needed in the future to further explore the efficacy and safety of TEAS for postoperative pain after laparoscopy.

Published
2022
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76. Additional file 3 of S6K1 amplification confers innate resistance to CDK4/6 inhibitors through activating c-Myc pathway in patients with estrogen receptor-positive breast cancer

Author

Mo, Hongnan, Liu, Xuefeng, Xue, Yu, Chen, Hongyan, Guo, Shichao, Li, Zhangfu, Wang, Shuang, Li, Caiming, Han, Jiashu, Fu, Ming, Song, Yongmei, Li, Dan, and Ma, Fei

Abstract

Additional file 3: Supplementary Table S3. Baseline clinical and pathological characteristics of patients in the discovery cohort.

Published
2022
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81. The efficacy and safety of transcutaneous electrical acupoint stimulation (TEAS) for postoperative pain in laparoscopy

Author

Meng, Dan, Mao, Yifei, Song, Quanmei, Yan, Chunchun, Zhao, Qinyu, Yang, Mengqi, and Song, Yongmei

Subjects
Pain, Postoperative, transcutaneous electrical acupoint Stimulation, Length of Stay, systematic review and meta-analysis, Electroacupuncture, Treatment Outcome, Meta-Analysis as Topic, Study Protocol Systematic Review, Quality of Life, Humans, Pain Management, Laparoscopy, protocol, postoperative pain, Acupuncture Points, Research Article, Pain Measurement, Randomized Controlled Trials as Topic, Systematic Reviews as Topic
Abstract

Background: With the promotion of the concept of “minimally invasive” surgery, the advantages of laparoscopic surgery are increasingly manifested. However, the postoperative pain of laparoscopic surgery brings difficulties and challenges to patients’ rehabilitation. Transcutaneous electrical acupoint stimulation (TEAS) is a non-invasive treatment, which can exert the dual efficacy of acupuncture and electrical stimulation. The efficacy and safety of TEAS for postoperative pain after laparoscopy based on randomized controlled trials (RCTs) need to further evaluate. Methods: A comprehensive and systematic literature searching will mainly perform on 7 electronic databases (PubMed, the Cochrane Library, Embase, China National Knowledge Infrastructure, Chongqing VIP Information, WanFang Data, and Chinese Biomedical Database) from their inception up to November 30, 2020. We will also search for ongoing or unpublished studies from other websites (eg, PROSPERO, ClinicalTrials.gov, and Chinese Clinical Trial Registry) and do manual retrieval for potential gray literature. Only the relevant RCTs published in English or Chinese were included. Two independent investigators will independently complete literature selection, assessment of risk bias, and data extraction, the disagreements will be discussed with the third party for final decisions. The primary outcome measures: the pain intensity (eg, VAS) and the consumption of postoperative analgesics. The secondary outcome measures: the postoperative quality of life, the duration of hospitalization, and the incidence of adverse reactions and serious events. Assessment of bias risk will follow the Cochrane risk of bias tool. Data processing will be conducted by Stata 15.0 software. Results: We will evaluate the efficacy and safety of TEAS for postoperative pain after laparoscopy based on RCTs. Conclusion: This study can provide more comprehensive and strong evidence of whether TEAS is efficacy and safe for postoperative pain in laparoscopic surgery.

Published
2021

85. Centrosomal Nlp is an oncogenic protein that is gene-amplified in human tumors and causes spontaneous tumorigenesis in transgenic mice

Author

Shao, Shujuan, Liu, Rong, Wang, Yang, Song, Yongmei, Zuo, Lihui, Xue, Liyan, Lu, Ning, Hou, Ning, Wang, Mingrong, Yang, Xiao, and Zhan, Qimin

Subjects
Genetically modified mice -- Research -- Physiological aspects, Carcinogenesis -- Physiological aspects -- Research, Cancer -- Genetic aspects, Health care industry
Abstract

Disruption of mitotic events contributes greatly to genomic instability and results in mutator phenotypes. Indeed, abnormalities of mitotic components are closely associated with malignant transformation and tumorigenesis. Here we show that ninein-like protein (Nlp), a recently identified BRCA1-associated centrosomal protein involved in microtubule nucleation and spindle formation, is an oncogenic protein. Nlp was found to be overexpressed in approximately 80% of human breast and lung carcinomas analyzed. In human lung cancers, this deregulated expression was associated with NLP gene amplification. Further analysis revealed that Nlp exhibited strong oncogenic properties; for example, it conferred to NIH3T3 rodent fibroblasts the capacity for anchorage-independent growth in vitro and tumor formation in nude mice. Consistent with these data, transgenic mice overexpressing Nlp displayed spontaneous tumorigenesis in the breast, ovary, and testicle within 60 weeks. In addition, Nlp overexpression induced more rapid onset of radiation-induced lymphoma. Furthermore, mouse embryonic fibroblasts (MEFs) derived from Nlp transgenic mice showed centrosome amplification, suggesting that Nlp overexpression mimics BRCA1 loss. These findings demonstrate that Nlp abnormalities may contribute to genomic instability and tumorigenesis and suggest that Nlp might serve as a potential biomarker for clinical diagnosis and therapeutic target., Introduction The centrosome is a small cytoplasmic nonmembranous organelle involved in the nucleation and organization of microtubules and critical for proper cell cycle progression. It establishes polarity and orientation of [...]

Published
2010
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87. Identification of genomic alterations in oesophageal squamous cell cancer

Author

Song, Yongmei, Li, Lin, Ou, Yunwei, Gao, Zhibo, Li, Enmin, Li, Xiangchun, Zhang, Weimin, Wang, Jiaqian, Xu, Liyan, Zhou, Yong, Ma, Xiaojuan, Liu, Lingyan, Zhao, Zitong, Huang, Xuanlin, Fan, Jing, Dong, Lijia, Chen, Gang, Ma, Liying, Yang, Jie, Chen, Longyun, He, Minghui, Li, Miao, Zhuang, Xuehan, Huang, Kai, Qiu, Kunlong, Yin, Guangliang, Guo, Guangwu, Feng, Qiang, Chen, Peishan, Wu, Zhiyong, Wu, Jianyi, Ma, Ling, Zhao, Jinyang, Luo, Longhai, Fu, Ming, Xu, Bainan, Chen, Bo, Li, Yingrui, Tong, Tong, Wang, Mingrong, Liu, Zhihua, Lin, Dongxin, Zhang, Xiuqing, Yang, Huanming, Wang, Jun, and Zhan, Qimin

Published
2014
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89. Polyphyllin VI Induces Apoptosis and Autophagy via Reactive Oxygen Species Mediated JNK and P38 Activation in Glioma

Author

Liu, Wei, Chai, Yi, Hu, Libo, Wang, Junhua, Pan, Xin, Yuan, Hongyu, Zhao, Zitong, Song, Yongmei, and Zhang, Yuqi

Subjects
reactive oxygen species, autophagy, polyphyllin VI, glioma, apoptosis, OncoTargets and Therapy, Original Research
Abstract

Wei Liu,1 Yi Chai,1 Libo Hu,1 Junhua Wang,2 Xin Pan,2 Hongyu Yuan,3 Zitong Zhao,3 Yongmei Song,3 Yuqi Zhang1 1School of Clinical Medicine, Tsinghua University, Beijing 10084, People’s Republic of China; 2Department of Neurosurgery, Yuquan Hospital, School of Clinical Medicine, Tsinghua University, Beijing 100040, People’s Republic of China; 3State Key Laboratory of Molecular Oncology, National Cancer Center, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, People’s Republic of ChinaCorrespondence: Yuqi ZhangSchool of Clinical Medicine, Tsinghua University, No. 1, Tsinghua Yuan, Haidian District, Beijing 10084, People’s Republic of ChinaEmail doctorzyq@126.comYongmei SongState Key Laboratory of Molecular Oncology,National Cancer Center, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, 17 Panjiayuannanli, Chaoyang, Beijing 100021, People’s Republic of ChinaEmail symlh2006@163.comBackground: Polyphyllin VI (PPVI), a bioactive component derived from a traditional Chinese herb Paris polyphylla, exhibits potential antitumor activity against hepatocellular carcinoma, as well as breast and lung cancers. However, its effect on glioma remains unknown.Methods: Five glioma cell lines (U251, U343, LN229, U87 and HEB) and an animal model were employed in the study. Anti-proliferation effects of PPVI were first determined using CCK-8 cell proliferation and clone formation assays, then reactive oxygen species (ROS), cell cycle progression and apoptosis effects measured by flow cytometry. The effect of PPVI on protein expression was quantified by Western blot analysis.Results: Data showed that PPVI inhibited the proliferation of glioma cell lines by modulating the G2/M phase. Additionally, incubation of cells with PPVI promoted apoptosis, autophagy, increased accumulation of ROS and activated ROS-modulated JNK and p38 pathways. On the other hand, N-acetyl cysteine, a ROS inhibitor, attenuated PPVI-triggered effects. Furthermore, JNK and p38 inhibitors ameliorated PPVI-triggered autophagy and apoptosis in glioma cells. In vivo assays showed that PPVI inhibited tumor growth of U87 cell line in nude mice.Conclusion: Overall, these data suggested that PPVI might be an effective therapeutic agent for glioma.Keywords: polyphyllin VI, glioma, autophagy, apoptosis, reactive oxygen species

Published
2020

90. Polyphyllin VI Induces Apoptosis and Autophagy via Reactive Oxygen Species Mediated JNK and P38 Activation in Glioma

Author

Liu,Wei, Chai,Yi, Hu,Libo, Wang,Junhua, Pan,Xin, Yuan,Hongyu, Zhao,Zitong, Song,Yongmei, Zhang,Yuqi, Liu,Wei, Chai,Yi, Hu,Libo, Wang,Junhua, Pan,Xin, Yuan,Hongyu, Zhao,Zitong, Song,Yongmei, and Zhang,Yuqi

Abstract

Wei Liu,1 Yi Chai,1 Libo Hu,1 Junhua Wang,2 Xin Pan,2 Hongyu Yuan,3 Zitong Zhao,3 Yongmei Song,3 Yuqi Zhang1 1School of Clinical Medicine, Tsinghua University, Beijing 10084, People’s Republic of China; 2Department of Neurosurgery, Yuquan Hospital, School of Clinical Medicine, Tsinghua University, Beijing 100040, People’s Republic of China; 3State Key Laboratory of Molecular Oncology, National Cancer Center, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, People’s Republic of ChinaCorrespondence: Yuqi ZhangSchool of Clinical Medicine, Tsinghua University, No. 1, Tsinghua Yuan, Haidian District, Beijing 10084, People’s Republic of ChinaEmail doctorzyq@126.comYongmei SongState Key Laboratory of Molecular Oncology,National Cancer Center, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, 17 Panjiayuannanli, Chaoyang, Beijing 100021, People’s Republic of ChinaEmail symlh2006@163.comBackground: Polyphyllin VI (PPVI), a bioactive component derived from a traditional Chinese herb Paris polyphylla, exhibits potential antitumor activity against hepatocellular carcinoma, as well as breast and lung cancers. However, its effect on glioma remains unknown.Methods: Five glioma cell lines (U251, U343, LN229, U87 and HEB) and an animal model were employed in the study. Anti-proliferation effects of PPVI were first determined using CCK-8 cell proliferation and clone formation assays, then reactive oxygen species (ROS), cell cycle progression and apoptosis effects measured by flow cytometry. The effect of PPVI on protein expression was quantified by Western blot analysis.Results: Data showed that PPVI inhibited the proliferation of glioma cell lines by modulating the G2/M phase. Additionally, incubation of cells with PPVI promoted apoptosis, autophagy, increased accumulation of ROS and activated ROS-modulated JNK and p38 pathways. On the other ha

Published
2020

91. Long Noncoding RNA VESTAR Regulates Lymphangiogenesis and Lymph Node Metastasis of Esophageal Squamous Cell Carcinoma by Enhancing VEGFC mRNA Stability

Author

Wang, Yali, primary, Zhang, Weimin, additional, Liu, Wenzhong, additional, Huang, Lijie, additional, Wang, Yan, additional, Li, Dan, additional, Wang, Guangchao, additional, Zhao, Zitong, additional, Chi, Xinming, additional, Xue, Yu, additional, Song, Yongmei, additional, Liu, Xuefeng, additional, and Zhan, Qimin, additional

Published
2021
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92. Extracellular vesicles derived from oesophageal cancer containing P4HB promote muscle wasting via regulating PHGDH/Bcl‐2/caspase‐3 pathway

Author

Gao, Xiaohan, primary, Wang, Yan, additional, Lu, Fang, additional, Chen, Xu, additional, Yang, Di, additional, Cao, Yiren, additional, Zhang, Weimin, additional, Chen, Jie, additional, Zheng, Leilei, additional, Wang, Guangchao, additional, Fu, Ming, additional, Ma, Liying, additional, Song, Yongmei, additional, and Zhan, Qimin, additional

Published
2021
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98. Correction: Molecular predictors of brain metastasis-related microRNAs in lung adenocarcinoma

Author

Sun, Guogui, primary, Ding, Xiao, additional, Bi, Nan, additional, Wang, Zhiwu, additional, Wu, Lihong, additional, Zhou, Wei, additional, Zhao, Zitong, additional, Wang, Jingbo, additional, Zhang, Weimin, additional, Fan, Jing, additional, Zhang, WenJue, additional, Dong, Xin, additional, Lv, Ning, additional, Song, Yongmei, additional, Zhan, Qimin, additional, and Wang, LuHua, additional

Published
2020
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99. Genomic Analyses Reveal Mutational Signatures and Frequently Altered Genes in Esophageal Squamous Cell Carcinoma

Author

Zhang, Ling, primary, Zhou, Yong, additional, Cheng, Caixia, additional, Cui, Heyang, additional, Cheng, Le, additional, Kong, Pengzhou, additional, Wang, Jiaqian, additional, Li, Yin, additional, Chen, Wenliang, additional, Song, Bin, additional, Wang, Fang, additional, Jia, Zhiwu, additional, Li, Lin, additional, Li, Yaoping, additional, Yang, Bin, additional, Liu, Jing, additional, Shi, Ruyi, additional, Bi, Yanghui, additional, Zhang, Yanyan, additional, Wang, Juan, additional, Zhao, Zhenxiang, additional, Hu, Xiaoling, additional, Yang, Jie, additional, Li, Hongyi, additional, Gao, Zhibo, additional, Chen, Gang, additional, Huang, Xuanlin, additional, Yang, Xukui, additional, Wan, Shengqing, additional, Chen, Chao, additional, Li, Bin, additional, Tan, Yongkai, additional, Chen, Longyun, additional, He, Minghui, additional, Xie, Sha, additional, Li, Xiangchun, additional, Zhuang, Xuehan, additional, Wang, Mengyao, additional, Xia, Zhi, additional, Luo, Longhai, additional, Ma, Jie, additional, Dong, Bing, additional, Zhao, Jiuzhou, additional, Song, Yongmei, additional, Ou, Yunwei, additional, Li, Enming, additional, Xu, Liyan, additional, Wang, Jinfen, additional, Xi, Yanfeng, additional, Li, Guodong, additional, Xu, Enwei, additional, Liang, Jianfang, additional, Yang, Xiaofeng, additional, Guo, Jiansheng, additional, Chen, Xing, additional, Zhang, Yanbo, additional, Li, Qingshan, additional, Liu, Lixin, additional, Li, Yingrui, additional, Zhang, Xiuqing, additional, Yang, Huanming, additional, Lin, Dongxin, additional, Cheng, Xiaolong, additional, Guo, Yongjun, additional, Wang, Jun, additional, Zhan, Qimin, additional, and Cui, Yongping, additional

Published
2020
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