180 results on '"Shu,Guan"'
Search Results
152. Intestinal microecology in rats with ulcerative colitis
- Author
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Han, Xiao-Xia, primary, Hou, Tian-Shu, additional, Yang, Yang, additional, Zhao, Ji-Lan, additional, Wu, Qiao-Feng, additional, and Yu, Shu-Guan, additional
- Published
- 2012
- Full Text
- View/download PDF
153. Multi-landscape
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Chen, Shaoxiong, Vitamin Creative Space, Guangdong mei shu guan, Guangzhou Photo Biennial (1st : 2005), Chen, Shaoxiong, Vitamin Creative Space, Guangdong mei shu guan, and Guangzhou Photo Biennial (1st : 2005)
- Abstract
Joan Flasch Artists' Book Collection
- Published
- 2004
154. Intestinal microecology in rats with ulcerative colitis
- Author
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Tian-Shu Hou, Ji-Lan Zhao, Shu-Guan Yu, Yang Yang, Qiaofeng Wu, and Xiao-Xia Han
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medicine.medical_specialty ,business.industry ,Internal medicine ,Medicine ,business ,medicine.disease ,Microecology ,Ulcerative colitis ,Gastroenterology - Published
- 2012
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- View/download PDF
155. Combined expression of aldehyde dehydrogenase 1A1 and β-catenin is associated with lymph node metastasis and poor survival in breast cancer patients following cyclophosphamide treatment.
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MINGLI SUN, HAISHAN ZHAO, QINGHUAN XIAO, ZHAOJIN YU, ZHIGUO SONG, WEIFAN YAO, HONGTAO TANG, SHU GUAN, FENG JIN, and MINJIE WEI
- Published
- 2015
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156. Epidemiological survey of low pathogenic avian influenza viruses in poultry in Eastern China.
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Zhao Kun-Kun, Zhong Shu-Guan, Zhao Guo, Ruan Li-Sha, Zhu Yan-Mei, Zhang Yan, Duan Zhi-Qiang, Liu Xiao-Wen, Liu Wen-Bo, Peng Da-Xin, and Liu Xiu-Fan
- Published
- 2012
157. Expression of tissue inhibitor of metalloproteinases-3 messenger RNA and protein in porcine endometrium during implantation.
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Qian Ren, Shu Guan, Jinluan Fu, and Aiguo Wang
- Abstract
Recent evidence points to a stromal decidualization-like response in the pregnant porcine uterus. The objective of this study was to evaluate expression of tissue inhibitors of metalloproteinase-3 (TIMP-3), a sensitive indicator of endometrial stromal decidualization, in endometrium of pregnant sows and to further investigate this phenomenon. Real-time PCR, Western blot and immunostaining analysis were used to study TIMP-3 expression between/at attachment sites of endometrium of Days 13, 18 and 24 pregnant sows. The results indicate that TIMP-3 protein expression was lowest by Day 13 compared with Day 18 ( P < 0.01) and 24 ( P < 0.01), and the expression was higher at attachment sites than between attachment sites on Day 13 ( P < 0.01) and 18 ( P < 0.01). TIMP-3 intensive immunostaining was observed in stroma of endometrium on Days 13, 18 and 24, and the staining at attachment sites was stronger than between attachment sites. Collectively, these results suggest the crucial role of TIMP-3 in successful implantation and embryo survival and indicate the endometrial stromal decidualization-like in pigs. [ABSTRACT FROM AUTHOR]
- Published
- 2011
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158. In Vitro Efficacy of Myxococcus fulvus ANSM068 to Biotransform Aflatoxin B1.
- Author
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Shu Guan, Lihong Zhao, Qiugang Ma, Ting Zhou, Ning Wang, Xinxu Hu, and Cheng Ji
- Subjects
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MYXOCOCCUS , *BIOTRANSFORMATION (Metabolism) , *AFLATOXINS , *LIQUID chromatography , *MASS spectrometry - Abstract
Aflatoxin B1 (AFB1) is commonly found in cereals and animal feeds and causes a significant threat to the food industry and animal production. Several microbial isolates with high AFB1 transformation ability have been identified in our previous studies. The aim of this research was to characterize one of those isolates, Myxococcus fulvus ANSM068, and to explore its biotransformation mechanism. The bacterial isolate of M. fulvus ANSM068, isolated from deer feces, was able to transform AFB1 by 80.7% in liquid VY/2 medium after incubation at 30 °C for 72 h. The supernatant of the bacterial culture was more effective in transforming AFB1 as compared to the cells alone and the cell extract. The transformation activity was significantly reduced and eradicated after the culture supernatant was treated with proteinase K, proteinase K plus SDS and heating. Culture conditions, including nitrogen source, initial pH and incubation temperature were evaluated for an optimal AFB1 transformation. Liquid chromatography mass spectrometry (LCMS) analyses showed that AFB1 was transformed to a structurally different compound. Infrared analysis (IR) indicated that the lactone ring on the AFB1 molecule was modified by the culture supernatant. Chromatographies on DEAE-Ion exchange and Sephadex-Molecular sieve and SDS-PAGE electrophoresis were used to determine active components from the culture supernatant, indicating that enzyme(s) were responsible for the AFB1 biotransformation. This is the first report on AFB1 transformation by a strain of myxobacteria through enzymatic reaction(s). [ABSTRACT FROM AUTHOR]
- Published
- 2010
- Full Text
- View/download PDF
159. In Vitro Efficacy of Myxococcus fulvus ANSM068 to Biotransform Aflatoxin B1.
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Shu Guan, Lihong Zhao, Qiugang Ma, Ting Zhou, Ning Wang, Xinxu Hu, and Cheng Ji
- Subjects
MYXOCOCCUS ,BIOTRANSFORMATION (Metabolism) ,AFLATOXINS ,LIQUID chromatography ,MASS spectrometry - Abstract
Aflatoxin B
1 (AFB1 ) is commonly found in cereals and animal feeds and causes a significant threat to the food industry and animal production. Several microbial isolates with high AFB1 transformation ability have been identified in our previous studies. The aim of this research was to characterize one of those isolates, Myxococcus fulvus ANSM068, and to explore its biotransformation mechanism. The bacterial isolate of M. fulvus ANSM068, isolated from deer feces, was able to transform AFB1 by 80.7% in liquid VY/2 medium after incubation at 30 °C for 72 h. The supernatant of the bacterial culture was more effective in transforming AFB1 as compared to the cells alone and the cell extract. The transformation activity was significantly reduced and eradicated after the culture supernatant was treated with proteinase K, proteinase K plus SDS and heating. Culture conditions, including nitrogen source, initial pH and incubation temperature were evaluated for an optimal AFB1 transformation. Liquid chromatography mass spectrometry (LCMS) analyses showed that AFB1 was transformed to a structurally different compound. Infrared analysis (IR) indicated that the lactone ring on the AFB1 molecule was modified by the culture supernatant. Chromatographies on DEAE-Ion exchange and Sephadex-Molecular sieve and SDS-PAGE electrophoresis were used to determine active components from the culture supernatant, indicating that enzyme(s) were responsible for the AFB1 biotransformation. This is the first report on AFB1 transformation by a strain of myxobacteria through enzymatic reaction(s). [ABSTRACT FROM AUTHOR]- Published
- 2010
- Full Text
- View/download PDF
160. Preparation of a composite film electrochemically deposited with chitosan and gold nanoparticles for the determination of α-1-fetoprotein.
- Author
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Yaxi Liu, Ruo Yuan, Yaqin Chai, Chenglin Hong, and Shu Guan
- Abstract
A novel amperometric immunosensor based on chitosan–gold nanoparticles (Chit–GNPs) composite film and thionine (Thi) was prepared for the determination of α-1-fetoprotein (AFP). The immunosensor was prepared by electro-depositing a Chit–GNPs composite matrix on the surface of the glass carbon electrode, then Thi was immobilized onto the Chit–GNPs film using glutaraldehyde as a cross-linker. Furthermore, the GNPs were chemisorbed onto Thi film for immobilization of α-1-fetoprotein antibody. The procedure of the immunosensor was characterized by means of cyclic voltammograms. The performance and influencing factors of the resulting immunosensor were studied in details. Under optimal conditions, the immunosensor was highly sensitive to AFP and the linear range covered from 0.40 to 200.0 ng mL
−1 with a detection limit of 0.24 ng mL−1 at three times background noise. Moreover, the simple and controllable electro-deposition method overcame the irreproducibility for preparing Chit-based immunosensor systems and the proposed immunosensor displayed a satisfactory reproducibility and stability. [ABSTRACT FROM AUTHOR]- Published
- 2010
- Full Text
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161. Ultrasensitive amperometric immunosensor for the determination of carcinoembryonic antigen based on a porous chitosan and gold nanoparticles functionalized interface.
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Yaxi Liu, Ruo Yuan, Yaqin Chai, Chenglin Hong, Kaige Liu, and Shu Guan
- Subjects
CARCINOEMBRYONIC antigen ,NANOPARTICLES ,ELECTROCHEMICAL analysis ,SPECTRUM analysis ,CARBON electrodes - Abstract
An immunosensor has been fabricated for direct amperometric determination of carcinoembryonic antigen. It is based on a biocompatible composite film composed of porous chitosan (pChit) and gold nanoparticles (GNPs). Firstly, a pChit film was formed on a glassy carbon electrode by means of electrodeposition. Then, thionine as a redox probe was immobilized on the pChit film modified electrode using glutaraldehyde as a cross-linker. Finally, GNPs were adsorbed on the electrode surface to assemble carcinoembryonic antibody (anti-CEA). The surface morphology of the pChit films was studied by means of a scanning electron microscope. The immunosensor was further characterized by cyclic voltammetry and electrochemical impedance spectroscopy. The electrochemical behaviors and factors influencing the performance of the resulting immunosensors were studied in detail. Results showed that the pChit films can enhance the surface coverage of antibodies and improve the sensitivity of the immunosensor. Under optimal conditions, the immunosensor was highly sensitive to CEA with a detection limit of 0.08 ng·mL
−1 at three times the background noise and linear ranges of 0.2∼10.0 ng·mL−1 and 10.0∼160 ng·mL−1 . Moreover, the immunosensor exhibited high selectivity, good reproducibility and stability. [ABSTRACT FROM AUTHOR]- Published
- 2009
- Full Text
- View/download PDF
162. CXCL12-CXCR4 axis promotes the natural selection of breast cancer cell metastasis
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Feng Jin, Fan Yao, Yanan Sun, Ayao Guo, Chong Liu, Quanxiu Jin, Chuifeng Fan, Xiaoyun Mao, Bo Li, and Shu Guan
- Subjects
Adult ,Receptors, CXCR4 ,Cancer Research ,Cell ,Apoptosis ,Breast Neoplasms ,Biology ,Transfection ,CXCR4 ,Metastasis ,Chemokine receptor ,Breast cancer ,Cell Line, Tumor ,medicine ,Humans ,Neoplasm Invasiveness ,Neoplasm Metastasis ,Aged ,Cell growth ,General Medicine ,Middle Aged ,CXCL12 ,medicine.disease ,Immunohistochemistry ,Chemokine CXCL12 ,biological factors ,medicine.anatomical_structure ,Cancer cell ,embryonic structures ,Cancer research ,Female ,biological phenomena, cell phenomena, and immunity ,Research Article - Abstract
CXCR4 and its ligand CXCL12 can promote the proliferation, survival, and invasion of cancer cells. They have been shown to play an important role in regulating metastasis of breast cancer to specific organs. High CXCR4 expression was also correlated to poor clinical outcome. Previous study also showed that tumor cells express a high level of CXCR4 and that tumor metastasis target tissues (lung, liver, and bone) express high levels of the ligand CXCL12, allowing tumor cells to directionally migrate to target organs via a CXCL12-CXCR4 chemotactic gradient. However, the exact mechanisms of how CXCR4 and CXCL12 enhance metastasis and/or tumor growth and their full implications on breast cancer progression are unknown. Yet it is likely that chemokine receptor signaling may provide more than just a migrational advantage by also helping the metastasized cells establish and survive in secondary environments. In this study, we investigated CXCR4 and CXCL12 expression in breast cancer and analyzed its association with clinicopathological factors by immunohistochemistry first. Then, we detected the mRNA and protein expression of CXCR4 and CXCL12 in breast cancer cell lines by Western blot and RT-PCR. The MDA-MB-231 has CXCR4 expression and very weak CXCL12 expression. So, we constructed the functional CXCL12 expression in MDA-MB-231 using a gene transfection technique. Further experiments were conducted to evaluate the effect of CXCL12 transfection on the biological behaviors of MDA-MB-231. The cell proliferation of MDA-MB-231–CXCL12 was accessed by MTT assay; the apoptosis was analyzed by an AnnexinV-FITC/propidium iodide double staining of flow cytometry method; and the cell invasive ability was examined by Matrigel invasion assay. Immunohistochemical analysis showed the co-expression of CXCR4 and CXCL12 correlated with lymph node metastasis and TNM stage (p
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163. z . Pratical map of Kwangtung province
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Shang wu yin shu guan. Auteur du texte and Shang wu yin shu guan. Auteur du texte
- Abstract
Échelle(s) : 1:1 450 000
- Published
- 1915
164. Slit-Based Slice Emittance Measurements Optimization at PITZ
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Niemczyk, Raffael, Boonpornprasert, Prach, Chen, Ye, Good, James, Groß, Matthias, Hillert, Wolfgang, Huck, Holger, Isaev, Igor, Koschitzki, Christian, Krasilnikov, Mikhail, Lal, Shankar, Li, Xiangkun, Lishilin, Osip, Loisch, Gregor, Melkumyan, David, Oppelt, Anne, Qian, Houjun, Shaker, Seyd Hamed, Shu, Guan, Stephan, Frank, and Vashchenko, Grygorii
- Subjects
Transverse profile and emittance monitors ,Physics::Accelerator Physics ,Accelerator Physics - Abstract
At the Photo Injector Test Facility at DESY in Zeuthen (PITZ) high-brightness electron sources are optimized for use at the X-ray free-electron lasers FLASH and European XFEL. Transverse projected emittance measurements are carried out by a single-slit scan technique in order to suppress space charge effects at an energy of ~20 MeV. Previous slice emittance measurements, which employed the emittance measurement in conjunction with a transverse deflecting structure, suffer from limited time resolution and low signal-to-noise ratio (SNR) due to a long drift space from the mask to the observation screen. Recent experimental studies at PITZ show improvement of the temporal resolution and SNR by utilizing quadrupole magnets between the mask and the screen. The measurement setup is described and first results are shown., Proceedings of the 8th International Beam Instrumentation Conference, IBIC2019, Malmö, Sweden
165. 日文補充讀本 / 北京近代科學圖書館編纂部編
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bei jing jin dai ke xue du shu guan
166. CEPC Conceptual Design Report: Volume 2 - Physics & Detector
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Guimarães Da Costa, João Barreiro, Gao, Yuanning, Jin, Shan, Qian, Jianming, Tully, Christopher G., Young, Charles, Wang, Lian-Tao, Ruan, Manqi, Zhu, Hongbo, Dong, Mingyi, Ouyang, Qun, Wu, Zhigang, Deng, Zhi, Li, Yulan, Qi, Huirong, Wang, Meng, Fu, Chengdong, Yao, Wei-Ming, Grancagnolo, Franco, Liu, Jianbei, Hu, Tao, Yang, Haijun, Bedeschi, Franco, Ferrari, Roberto, Zhao, Wei, Zhu, Zian, Giacomelli, Paolo, Li, Liang, Li, Fei, Liu, Zhenan, Zhu, Kejun, Hou, Suen, Bozovic Jelisavcic, Ivanka, Li, Gang, Fang, Yaquan, Li, Qiang, Boonekamp, Maarten, Liang, Zhijun, Piccinini, Fulvio, Shi, Xin, Abbrescia, Marcello, Ahmad, Muhammad, Ai, Xiaocong, Albergo, Sebastiano, Aleem, Muhammad Abid, Alexeev, Maxim, Aliev, Malik, Altmannshofer, Wolfgang, Alves, Fábio, An, Fenfen, An, Guangpeng, An, Haipeng, An, Qi, An, Rui, Andreazza, Attilio, Anduze, Marc, Antonello, Massimiliano, Garcia Pascual, Juan Antonio, Antusch, Stefan, Arhrib, Abdesslam, Arkani-Hamed, Nima, Arndt, Kirk, Azzi, Patrizia, Azzurri, Paolo, Palmer, Robert B., Bai, Bowen, Bai, Sha, Bai, Yang, Bai, Yu, Balagura, Vladislav, Balossino, Ilaria, Ban, Yong, Barger, Vernon, Barklow, Timothy, Bartalini, Paolo, Becattini, Francesco, Bellagamba, Lorenzo, Belloni, Alberto, Bencivenni, Giovanni, Berg, J. Scott, Bernius, Catrin, Bertani, Monica, Bertella, Claudia, Bertucci, Michele, Bi, Xiaojun, Bi, Yuanjie, Bian, Ligong, Bian, Tianjian, Bianchi, Fabrizio, Bigi, Ikaros I., Biglietti, Michela, Bignami, Andrea, Bilei, Gianmario, Borgonovi, Lisa, Bortoletto, Daniela, Bortone, Alberto, Boscherini, Davide, Bosotti, Angelo, Boudry, Vincent, Braibant, Sylvie, Bramante, Joseph, Branchini, Paolo, Brient, Jean-Claude, Caccia, Massimo, Cai, Chengfeng, Cai, Hao, Cai, Wenyong, Cai, Xiao, Cai, Yiming, Cai, Yuchen, Cai, Yunhai, Cai, Zhiqiang, Cano Bret, Marc, Cao, Bo, Cao, Dewen, Cao, Jianshe, Cao, Junjie, Cao, Qing-Hong, Carloni Calame, Carlo Michel, Casanova, Raimon, Cavasinni, Vincenzo, Chai, Junying, Chai, Weiping, Chang, Ningbo, Chang, Qin, Chang, Spencer, Chang, We-Fu, Chang, Xuejun, Chang, Yuan-Hann, Chekanov, Sergei, Chen, Bin, Chen, Chunhui, Chen, Fusan, Chen, Gang, Chen, Guoming, Chen, Huan, Chen, Huirun, Chen, Lei, Chen, Liejian, Chen, Mingjun, Chen, Mingshui, Chen, Nian, Chen, Ning, Chen, Shanhong, Chen, Shanzhen, Chen, Shao-Long, Chen, Shaomin, Chen, Shenjian, Chen, Shi, Chen, Wei, Chen, Wen, Chen, Xin, Chen, Xun, Chen, Xurong, Chen, Ye, Chen, Yu, Chen, Yuan, Chen, Yuanbai, Chen, Yukai, Chen, Zhenxing, Cheng, Hao, Cheng, Hsin-Chia, Cheng, Huajie, Cheng, Jian, Cheng, Shan, Cheng, Tongguang, Cheng, Weishuai, Cheong, Sanha, Chi, Yunlong, Chiarello, Gianluigi, Chiesa, Mauro, Chiu, Wen Han, Chou, Weiren, Chu, Chungming Paul, Chu, Ming-Chung, Chu, Xiaotong, Chu, Zhaolin, Chua, Chun-Khiang, Cibinetto, Gianluigi, Ciuchini, Marco, Cobal, Marina, Cochran, James, Coelho Lopes Sa, Rafael, Cossio, Fabio, Craig, Nathaniel, Cui, Han, Cui, Hanhua, Cui, Xiaohao, Cui, Zhaoyuan, Curtin, David, D Agnolo, Raffaele Tito, Dai, Jian-Ping, Dai, Jianping, Dai, Jin, Dai, Lei, Dai, Wei, Dai, Xuwen, Curtis, Stefania, Filippis, Nicola, Lucia, Erika, Mori, Francesca, Delgado, Antonio, Demarteau, Marcel, Deng, Changdong, Deng, Wei-Tian, Destefanis, Marco, Dev, P. S. Bhupal, Di Micco, Biagio, Ding, Ran, Ding, Xuefeng, Ding, Yadong, Da Rocha Rolo, Manuel Dionisio, Domenici, Danilo, Dong, Bingbing, Dong, Chongmin, Dong, Dong, Dong, Haiyi, Dong, Jianing, Dong, Jing, Dong, Lan, Dopke, Jens, Dordevic, Milos, Dos Santos Ramos, Tiago, Draper, Patrick, Drewes, Marco, Du, Mingxuan, Duan, Guang Hua, Eklund, Lars, Eno, Sarah, Erler, Jens, Essig, Rouven, Fan, Jiji, Fan, Shenghong, Fan, Wenjie, Fan, Xiangning, Fang, Shuangshi, Fano, Livio, Farilla, Addolarata, Farinelli, Riccardo, Faus-Golfe, Angeles, Fedderke, Michael A., Felici, Giulietto, Feng, Changqing, Feng, Cunfeng, Feng, Feng, Feng, Jianxin, Feng, Jun, Feng, Tai-Fu, Fischer, Oliver, Flores Castillo, Luis Roberto, Fontanesi, Elisa, Freitas, Ayres, Frotin, M., Frugiuele, Claudia, Fu, Jinyu, Fu, Qibin, Fu, Shinian, Fuchs, Elina, Fukuda, Shigeki, Gabrielli, Emidio, Gaido, Luciano, Gan, Pingping, Gao, Jie, Gao, Jun, Gao, Wu, Gao, Yanyan, Gao, Yu, Garzia, Isabella, Gaudio, Gabriella, Ge, Shao-Feng, Geng, Chao-Qiang, Geng, Huiping, Li-Sheng Geng, Gentile, Simonetta, Giraud, J., Giudice, Gian, Godbole, Rohini M., Gong, Dianjun, Gong, Guanghua, Gong, Hui, Gong, Li, Gong, Lingling, Gori, Stefania, Gou, Quanbu, Greco, Mario, Greco, Michela, Gribanov, Sergei S., Grinstein, Sebastian, Grondin, D., Gu, Jiayin, Gu, Limin, Gu, Pei-Hong, Guidi, Vincenzo, Guo, Fangyi, Guo, Jingyuan, Guo, Jun, Guo, Lei, Guo, Xin, Guo, Yuanyuan, Guo, Zhigang, Gupta, Ramesh, Han, Chengcheng, Han, Dejun, Han, Jinzhong, Han, Liangliang, Han, Ran, Han, Ruixiong, Han, Shuang, Han, Yanliang, Han, Yubo, Hang, Yanfeng, Hao, Jiankui, Hao, Xiqing, He, Dayong, He, Hong-Jian, He, Jibo, He, Jun, He, Min, He, Xiang, He, Xianke, He, Xiaogang, He, Yangle, He, Zhenqiang, Heinemeyer, Sven, Heng, Yuekun, Hong, Daojin, Hong, Jiangliu, Hong, Yang, Hor, Yuenkeung, Hostachy, J. -Y, Hou, Qingbo, Hou, Zhilong, Hsu, Shih-Chieh, Hu, Bitao, Hu, Jifeng, Hu, Jun, Hu, Shouyang, Hu, Shuyang, Hu, Yongcai, Hu, Yu, Hu, Zhen, Hu, Zhongjun, Huang, Chao-Shang, Huang, Fapeng, Huang, Guangshun, Huang, Guo-Yuan, Huang, Jinghui, Huang, Jinshu, Huang, Junjie, Huang, Liangsheng, Huang, Rijun, Huang, Shuhui, Huang, Tongming, Huang, Tuchen, Huang, Xiaozhong, Huang, Xingtao, Huang, Xuguang, Huang, Yanping, Huang, Yongsheng, Huang, Yuyan, Huo, Ran, Ignatov, Fedor V., Iqbal, Munawar, Jackson, Paul, Javaid, Tahir, Ji, Daheng, Ji, Qingping, Ji, Xiaoli, Jia Jia, Jia, Junji, Jia, Yu, Jia, Zihang, Jiang, Jiechen, Jiang, Yun, Jiao, Jianbin, Jin, Dapeng, Jin, Mingjie, Jin, Song, Jin, Yanli, Jin, Yi, Jing, Maoqiang, John, Jaya, Jones, Tim, Ju, Xudong, Jueid, Adil, Jung, Sunghoon, Jyotishmati, Susmita, Kacarevic, Goran, Kane, Gordon, Kang, Wen, Karagoz, Muge, Kato, Chikuma, Ke, Zhiyong, Kharzeev, Dmitri, Khoze, Valentin, Kilic, Can, Kiuchi, Ryuta, Ko, Pyungwon, Kobayashi, Tetsuya, Kong, Panyu, Kong, Shibei, Kopp, Joachim, Kotwal, Ashutosh, Kozaczuk, Jonathan, Kozyrev, Evgeny A., Krasnov, Alexander, Kuflik, Eric, Kuo, Chia-Ming, Kwok, King Wai, Lagarde, Francois, Lai, Pei-Zhu, Laktineh, Imad, Lan, Boyang, Lan, Xiaofei, Lavezzi, Lia, Lee, Seung J., Lei, Ge, Leng, Yongbin, Leung, Sze Ching, Li, Bingzhi, Li, Bo, Li, Boyang, Li, Changhong, Li, Cheng, Li, Congqiao, Li, Dazhang, Li, Dikai, Li, Fengyun, Li, Gexing, Li, Guangrui, Li, Hai-Bo, Li, Haifeng, Li, Haoqing, Li, Hengne, Li, Honglei, Li, Huijing, Li, Jin, Li, Jing, Li, Jinmian, Li, Jinyan, Li, Jungang, Li, Kang, Li, Ke, Li, Li, Li, Lianming, Li, Long, Li, Mengran, Li, Minxian, Li, Peirong, Li, Peiyu, Li, Peng, Li, Qiaodan, Li, Quansheng, Li, Rui, Li, Shaopeng, Li, Shiyuan, Li, Shu, Li, Tianjun, Li, Tong, Li, Weiguo, Li, Wenjun, Li, Xiaoling, Li, Xiaomei, Li, Xiaoping, Li, Xin, Li, Xingguo, Li, Xin-Qiang, Li, Yanwei, Li, Yiming, Ying Li, Li, Ying-Ying, Li, Yufeng, Li, Zhao, Li, Zhenghua, Li, Zhihui, Li, Zhongquan, Li, Ziyuan, Liang, Chaohui, Liang, Hao, Liang, Jing, Liang, Jinhan, Liang, Zuotang, Liao, Hean, Liao, Hongbo, Liao, Jinfeng, Liao, Libo, Liao, Wei, Liao, Yi, Liao, Yunfeng, Lin, Chuangxin, Lin, Hai, Lin, Haiying, Ling, Jiajie, Ling, Pan, Lisanti, Mariangela, Liu, Ao, Liu, Baiqi, Liu, Beijiang, Liu, Bing, Liu, Bo, Liu, Dianyu, Liu, Dong, Liu, Fu-Hu, Liu, Hongbang, Liu, Hu, Liu, Jia, Liu, Jiaming, Liu, Jian, Liu, Jianfei, Liu, Jiangtao, Liu, Jie, Liu, Jindong, Liu, Kexin, Liu, Ling, Liu, Liqiang, Liu, Ming, Liu, Ning, Liu, Peilian, Liu, Qian, Liu, Qingyuan, Liu, Shubin, Liu, Shulin, Liu, Tao, Liu, Weitao, Liu, Wendi, Liu, Xiang, Liu, Xiaohui, Liu, Xin, Liu, Xuesong, Liu, Xuewen, Liu, Xuyang, Liu, Yandong, Liu, Yang, Liu, Yanlin, Liu, Yi, Liu, Yong, Liu, Yudong, Liu, Zengqiang, Liu, Zeyuan, Liu, Zhanfeng, Liu, Zhaofeng, Liu, Zhen, Liu, Zhenchao, Liu, Zhongxiu, Liu, Zuowei, Llorente Merino, Javier, Lo, Cheuk Yee, Logashenko, Ivan B., Long, Andrew, Lou, Xinchou, Low, Ian, Low, Matthew, Lu, Cai-Dian, Lu, Wei, Lu, Weiguo, Lu, Yuanrong, Lu, Yunpeng, Lu, Zhijun, Lukic, Strahinja, Luo, Mingcheng, Luo, Pengwei, Luo, Qing, Luo, Tao, Luo, Xiaofeng, Luo, Yanting, Luo, Zhenhuan, Lyu, Kunfeng, Lyu, Xiaorui, Ma, Huizhou, Ma, Kai, Ma, Lianliang, Ma, Na, Ma, Qiang, Ma, Rui, Ma, Wen-Gan, Ma, Xiao, Ma, Xiaotian, Ma, Xinpeng, Ma, Yanling, Ma, Yanqing, Ma, Yongsheng, Ma, Yue, Ma, Zhongjian, Maggiora, Marco, Magniette, Frédéric, Malamud, Ernie, Mangano, Michelangelo, Mao, Lijun, Mao, Mingling, Mao, Yajun, Mao, Yanmin, Mao, Yanyan, Martin, Adam, Martinez Outschoorn, Verena Ingrid, Matsumoto, Shigeki, Mccullough, Matthew, Mcmahon, Steve, Meade, Patrick, Mele, Barbara, Mellado, Bruce, Men, Lingling, Meng, Cai, Meng, Fanbo, Mezzadri, Giulio, Mi, Zhenghui, Michelato, Paolo, Min, Tianjue, Ming, Lei, Mittal, Monika, Molson, James, Monaco, Laura, Montagna, Guido, Morello, Gianfranco, Moretti, Mauro, Mu, Zhihui, Nanni, Jérome, Neubert, Matthias, Nicrosini, Oreste, Nie, Changshan, Nikitin, Sergei, Ning, Feipeng, Ning, Guo-Zhu, Nishu, Nishu, Niu, Yazhou, Ojalvo, Isobel, Okunev, Ivan, Ospanov, Rustem, Pagani, Carlo, Paganis, Stathes, Panareo, Marco, Pandurovic, Mila, Pang, Tong, Panizzo, Giancarlo, Paparella, Rocco, Parida, Bibhuti, Passemar, Emilie, Pei, Guoxi, Pei, Shilun, Peng, Quanling, Peng, Xiaohua, Peng, Yuemei, Petrov, Alexey, Pezzotti, Lorenzo, Pierre-Émile, Thomas, Ping, Rong-Gang, Plackett, Richard, Polesello, Giacomo, Poli Lener, Marco, Polini, Alessandro, Popov, Alexandr S., Prell, Soeren, Qi, Ming, Qian, Sen, Qian, Zhuoni, Qiao, Cong-Feng, Qiao, Yusi, Qin, Guang-You, Qin, Qin, Qin, Qing, Qin, Zhonghua, Qu, Huamin, Ramani, Harikrishnan, Ramsey-Musolf, Michael, Redaelli, Stefano, Reece, Matthew, Ren, Jing, Rischke, Dirk, Rivetti, Angelo, Roda, Chiara, Rolandi, Luigi, Rompotis, Nikolaos, Ruan, Xifeng, Ruiz, Richard, Sabbi, Gianluca, Sang, Wen-Long, Santoro, Romualdo, Sanz-Cillero, Juan J., Schlaffer, Matthias, Schmid, Frank, Schuster, Philip, Schuy, Alex, Schwaller, Pedro, Sciuto, Antonella, Sen, Tanaji, Sertore, Daniele, Sha, Peng, Shan, Lianyou, Shang, Feng, Shao, Dingyu, Shao, Jianxiong, Shashkov, Yaroslav, Shelton, Jessie, Shen, Cheng-Ping, Shen, Peixun, Shen, Qiuping, Shen, Yang, Shen, Yuqiao, Shen, Zhongtao, Shi, Can, Shi, Haoyu, Shi, Jingyuan, Shi, Liaoshan, Shi, Renjie, Shi, Yu-Ji, Shi, Yukun, Shi, Yulong, Shin, Seodong, Shipsey, Ian, Shiu, Gary, Shu, Guan, Shu, Jing, Si, Zonguo, Silvestrini, Luca, Sinyatkin, Sergey, Song, Hong, Song, Mao, Song, Weimin, Stamou, Emannuel, Stratakis, Diktys, Su, Dong, Su, Feng, Su, Shufang, Su, Wanyun, Su, Wei, Su, Yangjie, Sui, Yanfeng, Sullivan, Michael, Sun, Baogeng, Sun, Daming, Sun, Guoqiang, Sun, Hao, Sun, Junfeng, Sun, Liang, Sun, Peng, Sun, Qingfeng, Sun, Shengsen, Sun, Sichun, Sun, Tingting, Sun, Xiangming, Sun, Xianjing, Sun, Xilei, Sun, Yanjun, Sun, Yongzhao, Sundrum, Raman, Tang, Chuanxiang, Tang, Guangyi, Tang, Jian, Tang, Jiannan, Tang, Jingyu, Tang, Songzhi, Tang, Yi-Lei, Tao, Jia, Tao, Junquan, Tassielli, Giovanni, Tenchini, Roberto, Teytelman, Dmitry, Thaler, Jesse, Tian, Saike, Tian, Xingcheng, Tonelli, Guido, Tong, Xinyu, Trentadue, Luca, Tsai, Yuhsin, Tsybychev, Dmitri, Tu, Yanjun, Tweedie, Brock, Unwin, James, Verducci, Monica, Vicini, Alessandro, Videau, Henri, Viehhauser, Georg, Vivarelli, Iacopo, Vossebeld, Joost, Vukasinovic, Natasa, Wan, Xia, Wang, Biao, Wang, Bin, Wang, Binlong, Wang, Bo, Wang, Chengtao, Wang, Chengwei, Wang, Chenliang, Wang, Dayong, Wang, Dou, Wang, Fei, Wang, Feng, Wang, Gang, Wang, Haijing, Wang, Haiyun, Wang, Hui, Wang, Jian, Wang, Jianchun, Wang, Jianli, Wang, Jianxiong, Wang, Jiawei, Wang, Jie, Wang, Jin, Wang, Jing, Wang, Jinwei, Wang, Ke, Wang, Kechen, Wang, Kunfu, Wang, Liangliang, Wang, Lijiao, Wang, Linlin, Wang, Longge, Wang, Lu, Wang, Meifen, Wang, Na, Wang, Pengcheng, Wang, Qun, Wang, Qunyao, Wang, Ran, Wang, Ren-Jie, Wang, Rongkun, Wang, Shaobo, Wang, Shaozhe, Wang, Shengchang, Wang, Shuzheng, Wang, Siguang, Wang, Tianhong, Wang, Tong, Wang, Wei, Wang, Weiping, Wang, Wenyu, Wang, Xi, Wang, Xiangjian, Wang, Xiangqi, Wang, Xiaolong, Wang, Xiaoning, Wang, Xiaoping, Wang, Xin, Wang, Xingze, Wang, Xiongfei, Wang, Yan, Wang, Yaqian, Wang, Yi, Wang, Yifang, Wang, Ying, Wang, Yiwei, Wang, Yong, Wang, Youkai, Wang, Yu, Wang, Yufeng, Wang, Yuhao, Wang, Zhaofeng, Wang, Zhigang, Wang, Zhipeng, Wang, Zhiyong, Wang, Zirui, Wang, Zixun, Wang, Zongyuan, Wei, Runing, Wei, Shujun, Wei, Wei, Wei, Xiaomin, Wei, Yuanyuan, Wei, Yuqian, Wen, Shuopin, Wen, Zhiwen, Willocq, Stephane, Witte, Holger, Wu, Jinfei, Wu, Juan, Wu, Kewei, Wu, Lei, Wu, Linghui, Wu, Mengqing, Wu, Peiwen, Wu, Tianya, Wu, Wenhuan, Wu, Xi, Wu, Xiao-Hong, Wu, Xing-Gang, Wu, Xu, Wu, Xueting, Wu, Ye, Wu, Yuwen, Wu, Zhi, Xia, Wenhao, Xiang, Dao, Xiang, Qian-Fei, Xianyu, Zhong-Zhi, Xiao, Bo-Wen, Xiao, Dengjie, Xiao, Ning, Xiao, Ouzheng, Xiao, Rui-Qing, Xiao, Yu, Xiao, Zhen-Jun, Xie, Ke-Pan, Xie, Xinhai, Xie, Yuehong, Xie, Yuguang, Xie, Zongtai, Xing, Qingzhi, Xing, Zhizhong, Xiu, Qinglei, Xu, Chang, Xu, Da, Xu, Fanrong, Xu, Guanglei, Xu, Guangzhi, Xu, Haocheng, Xu, Hongge, Xu, Hongliang, Xu, Hui, Xu, Ji, Xu, Nu, Xu, Qing, Xu, Qingjin, Xu, Qingjun, Xu, Wei, Xu, Yin, Xu, Yongheng, Xu, Zijun, Xue, Wei, Yan, Bin, Yan, Jun, Yan, Liang, Yan, Mingyang, Yan, Qi-Shu, Yan, Tian, Yan, Wenbiao, Yan, Yingbing, Yang, Bingfang, Yang, Huan, Yang, Jiancheng, Yang, Jianquan, Yang, Jin Min, Yang, Jing, Yang, Junfeng, Yang, Li, Yang, Liu, Yang, Mei, Yang, Ping, Yang, Qianwen, Yang, Xingwang, Yang, Xuan, Yang, Ye, Yang, Ying, Yang, Yong, Yang, Yongliang, Yang, Yueling, Yang, Zhenwei, Yao, Weichao, Yatsenko, Elena, Ye, Hanfei, Ye, Jingbo, Ye, Mei, Ye, Qiang, Ye, Ziping, Yi, Fang, Yi, Kai, Yilun, Xue, Yin, Hang, Yin, Pengfei, Yin, Xiangwei, Yin, Ze, Yin, Zhongbao, You, Zhengyun, Yu, Boxiang, Yu, Chenghui, Yu, Chunxu, Yu, Dan, Yu, Felix, Yu, Fusheng, Yu, Lingda, Yu, Lu, Yu, Yue, Yu, Zhao-Huan, Yuan, Li, Yuan, Siyu, Yuan, Ye, Yuan, Youjin, Yuan, Zhiyang, Yue, Chongxing, Yue, Junhui, Yue, Qian, Zaib, Un-Nisa, Zhai, Jian, Zhai, Jiyuan, Zhang, Baotang, Zhang, Ben-Wei, Zhang, Bo, Zhang, Bowen, Zhang, Cen, Zhang, Chad, Zhang, Chunlei, Zhang, Di, Zhang, Gang, Zhang, Guangyi, Zhang, Guoqing, Zhang, Hai-Bin, Zhang, Hao, Zhang, Honghao, Zhang, Hongyu, Zhang, Huaqiao, Zhang, Hui, Zhang, Jian, Zhang, Jianhui, Zhang, Jianqin, Zhang, Jielei, Zhang, Jingru, Zhang, Jinlong, Zhang, Junrui, Zhang, Kaili, Zhang, Lei, Zhang, Liang, Zhang, Liming, Zhang, Linhao, Zhang, Ren-You, Zhang, Rui, Zhang, Sifan, Zhang, Tianjiao, Zhang, Wenchao, Zhang, Xiangke, Zhang, Xiaohui, Zhang, Xinmin, Zhang, Xinying, Zhang, Xueyao, Zhang, Yang, Zhang, Yao, Zhang, Yi, Zhang, Ying, Zhang, Yongchao, Zhang, Yu, Zhang, Yuan, Zhang, Yuhong, Zhang, Yu-Jie, Zhang, Yulei, Zhang, Yulian, Zhang, Yumei, Zhang, Yunlong, Zhang, Yuxuan, Zhang, Zhaoru, Zhang, Zhen, Zhang, Zhenyu, Zhang, Zhiqing, Zhang, Zhiyong, Zhao, Chen, Zhao, Hang, Zhao, Jingxia, Zhao, Jingyi, Zhao, Ling, Zhao, Mei, Zhao, Minggang, Zhao, Mingrui, Zhao, Peng, Zhao, Qiang, Zhao, Shensen, Zhao, Shuai, Zhao, Shu-Min, Zhao, Tongxian, Zhao, Xianghu, Zhao, Xiaoran, Zhao, Xiaoyan, Zhao, Ying, Zhao, Yu, Zhao, Yue, Zhao, Zhengguo, Zhao, Zhen-Xing, Zhao, Zhuo, Zheng, Bo, Zheng, Hongjuan, Zheng, Liang, Zheng, Ran, Zheng, Shuxin, Zheng, Taifan, Zheng, Xuxing, Zheng, Ya-Juan, Zheng, Yangheng, Zhi, Yu, Zhong, Bin, Zhong, Yiming, Zhou, Bing, Zhou, Hai-Qing, Zhou, Hang, Zhou, Jia, Zhou, Jianxin, Zhou, Jing, Zhou, Maosen, Zhou, Nan, Zhou, Ning, Zhou, Ningchuang, Zhou, Shiyu, Zhou, Shun, Zhou, Sihong, Zhou, Siyi, Zhou, Xiang, Zhou, Yang, Zhou, Yi, Zhou, Yu-Feng, Zhou, Zusheng, Zhu, Changhe, Zhu, Chengguang, Zhu, Chenzheng, Zhu, Dechong, Zhu, Hongyan, Zhu, Hua-Xing, Zhu, Jiamin, Zhu, Jiang, Zhu, Jingya, Zhu, Jingyu, Zhu, Junjie, Zhu, Kai, Zhu, Kun, Zhu, Li, Zhu, Ruilin, Zhu, Xianglei, Zhu, Xuezheng, Zhu, Yifan, Zhu, Yingshun, Zhu, Yongfeng, Zhuang, Xuai, Zong, Hongshi, Zou, Cong, Zou, Jiaheng, Zou, Ye, Zupan, Jure, Institut de Recherches sur les lois Fondamentales de l'Univers (IRFU), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université Paris-Saclay, Laboratoire Leprince-Ringuet (LLR), Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-École polytechnique (X)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de l'Accélérateur Linéaire (LAL), Université Paris-Sud - Paris 11 (UP11)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS), Galaxies, Etoiles, Physique, Instrumentation (GEPI), Institut national des sciences de l'Univers (INSU - CNRS)-Observatoire de Paris, Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Université Paris Diderot - Paris 7 (UPD7)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Physique Subatomique et de Cosmologie (LPSC), Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP )-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes [2016-2019] (UGA [2016-2019]), Institut de Physique Nucléaire de Lyon (IPNL), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de Physique Nucléaire et de Hautes Énergies (LPNHE (UMR_7585)), Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), CEPC Study Group, Centre National de la Recherche Scientifique (CNRS)-École polytechnique (X)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3), Centre National de la Recherche Scientifique (CNRS)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Université Paris-Sud - Paris 11 (UP11), Centre National de la Recherche Scientifique (CNRS)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Paris Diderot - Paris 7 (UPD7)-Observatoire de Paris, Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL), Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes (UGA)-Institut polytechnique de Grenoble - Grenoble Institute of Technology (Grenoble INP ), Université Grenoble Alpes (UGA), Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3), Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Université de Paris (UP), and HEP, INSPIRE
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detector: technology ,Higgs particle: particle source ,electron positron: storage ring ,[PHYS.HEXP] Physics [physics]/High Energy Physics - Experiment [hep-ex] ,engineering ,FOS: Physical sciences ,threshold: production ,electron positron: annihilation ,B-factory ,High Energy Physics - Experiment ,High Energy Physics - Experiment (hep-ex) ,High Energy Physics - Phenomenology (hep-ph) ,[PHYS.HEXP]Physics [physics]/High Energy Physics - Experiment [hep-ex] ,accelerator: technology ,detector: design ,Particle Physics - Phenomenology ,new physics ,hep-ex ,Z0: decay ,Higgs-factory ,High Energy Physics::Phenomenology ,Z0: particle source ,hep-ph ,electron positron: colliding beams ,sensitivity ,CEPC ,High Energy Physics - Phenomenology ,tau: particle source ,240 GeV-cms ,vertex: primary ,Higgs particle: electroproduction ,charm: particle source ,High Energy Physics::Experiment ,proposed experiment ,numerical calculations: Monte Carlo ,Z0-factory ,performance ,Particle Physics - Experiment - Abstract
The Circular Electron Positron Collider (CEPC) is a large international scientific facility proposed by the Chinese particle physics community to explore the Higgs boson and provide critical tests of the underlying fundamental physics principles of the Standard Model that might reveal new physics. The CEPC, to be hosted in China in a circular underground tunnel of approximately 100 km in circumference, is designed to operate as a Higgs factory producing electron-positron collisions with a center-of-mass energy of 240 GeV. The collider will also operate at around 91.2 GeV, as a Z factory, and at the WW production threshold (around 160 GeV). The CEPC will produce close to one trillion Z bosons, 100 million W bosons and over one million Higgs bosons. The vast amount of bottom quarks, charm quarks and tau-leptons produced in the decays of the Z bosons also makes the CEPC an effective B-factory and tau-charm factory. The CEPC will have two interaction points where two large detectors will be located. This document is the second volume of the CEPC Conceptual Design Report (CDR). It presents the physics case for the CEPC, describes conceptual designs of possible detectors and their technological options, highlights the expected detector and physics performance, and discusses future plans for detector R&D and physics investigations. The final CEPC detectors will be proposed and built by international collaborations but they are likely to be composed of the detector technologies included in the conceptual designs described in this document. A separate volume, Volume I, recently released, describes the design of the CEPC accelerator complex, its associated civil engineering, and strategic alternative scenarios., 424 pages
167. NA China
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Shi dai mei shu guan (Guangzhou Shi, China), production company., Films du Bilboquet, production company., Grasshopper Film (Firm), publisher, film distributor., Voignier, Marie, 1974- director., and Michel-Villette, Eugénie, producer.
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- 2020
168. Organic pollutant degradation for micro-molecule product emission over SiO 2 layers-coated g-C 3 N 4 photocatalysts.
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Ma Y, Wu P, Ku M, Guo M, Yang Y, Li X, and Chen H
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In this study, a SiO
2 layer-coated g-C3 N4 catalyst was prepared by a sol-gel method to overcome the poor adsorption ability and high recombination rate of charge carriers of pristine g-C3 N4 . SEM and TEM images indicated that SiO2 nanoparticles were coated on the surface of g-C3 N4 nanoparticles with a layered structure and the layers were tightly contacted with g-C3 N4 . XRD patterns, FTIR spectra, UV-vis spectra and XPS spectra revealed that the structure of g-C3 N4 was not destroyed and its photoelectric catalytic properties were not suppressed by the coating of SiO2 layers. Adsorption experiments revealed that the SiO2 layers improved the adsorption performance of g-C3 N4 and their ratios were adjusted. The molecular weights of the final products of the degradation of RhB and antibiotics were at the micro-molecule level while the amount of g-C3 N4 reached 1.2% of the mass fraction, which were more suitable for pollutant degradation compared with those of g-C3 N4 due to its poor adsorption ability. The reason for this was likely that the SiO2 layers were not only beneficial for the adsorption of pollutants and intermediate products but also for prolonging the life time of the separated electrons and holes. Finally, active trapping experiments confirmed that both the holes and superoxide radicals were the main factors in the degradation of RhB and antibiotics, with the superoxides being the most active species., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)- Published
- 2024
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169. Development and validation of a risk nomogram model for predicting pulmonary hypertension in patients with stage 3-5 chronic kidney disease.
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Hu Y, Wang X, Xiao S, Wu H, Huan C, Xu T, Guo M, Liu A, Jiang X, Wang J, Zhu H, and Pan D
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- Humans, Nomograms, Stroke Volume, Ventricular Function, Left, Retrospective Studies, Hypertension, Pulmonary complications, Hypertension, Pulmonary diagnosis, Kidney Failure, Chronic, Renal Insufficiency, Chronic complications
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Objectives: The occurrence of pulmonary arterial hypertension (PAH) can greatly affect the prognosis of patients with chronic kidney disease (CKD). We aimed to construct a nomogram to predict the probability of PAH development in patients with stage 3-5 CKD to guide early intervention and to improve prognosis., Methods: From August 2018 to December 2021, we collected the data of 1258 patients with stage 3-5 CKD hospitalized at the Affiliated Hospital of Xuzhou Medical University as a training set and 389 patients hospitalized at Zhongda Hospital as a validation set. These patients were divided into PAH and N-PAH groups with pulmonary arterial systolic pressure ≥ 35 mmHg as the cutoff. The results of univariate and multivariate logistic regression analyses were used to establish the nomogram. Then, areas under the receiver operating characteristic curve (AUC-ROCs), a calibration plot, and decision curve analysis (DCA) were used to validate the nomogram., Results: The nomogram included nine variables: age, diabetes mellitus, hemoglobin, platelet count, serum creatinine, left ventricular end-diastolic diameter, left atrial diameter, main pulmonary artery diameter and left ventricular ejection fraction. The AUC-ROCs of the training set and validation set were 0.801 (95% confidence interval (CI) 0.771-0.830) and 0.760 (95% CI 0.699-0.818), respectively, which showed good discriminative ability of the nomogram. The calibration diagram showed good agreement between the predicted and observed results. DCA also demonstrated that the nomogram could be clinically useful., Conclusion: The evaluation of the nomogram model for predicting PAH in patients with CKD based on risk factors showed its ideal efficacy. Thus, the nomogram can be used to screen for patients at high risk for PAH and has guiding value for the subsequent formulation of prevention strategies and clinical treatment., (© 2022. The Author(s).)
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- 2023
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170. Effect of finerenone on cardiovascular events in kidney disease and/or diabetes: a meta analysis of randomized control trials.
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Zhu Y, Song M, Chen T, Yang Z, and Liu Y
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- Humans, Randomized Controlled Trials as Topic, Cardiovascular Diseases epidemiology, Cardiovascular Diseases etiology, Cardiovascular Diseases prevention & control, Diabetes Mellitus, Type 2, Diabetic Nephropathies drug therapy, Heart Failure, Myocardial Infarction epidemiology, Myocardial Infarction etiology, Myocardial Infarction prevention & control
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Objective: To evaluate the effect of finerenone on cardiovascular events in Kidney Disease and/or Diabetes., Methods: The ClinicalTrials.gov, Medline, EMBASE, Web of Science, Cochrane Library databases were systematically searched from the inception dates to December 20, 2021 in order to identify randomized controlled trials that evaluated the effect of finerenone on cardiovascular events in Kidney Disease and/or Diabetes, without language restriction. This meta-analysis collected data from 7 randomized clinical trials that evaluated the effect of finrrenone in 15,618 patients with kidney disease and/or diabetes. Risk of bias was assessed by Cochrane Risk of Bias Assessment Tool. Inconsistency among trial results was assessed by I
2 statistic. The main endpoints included death from cardiovascular causes, death from any cause, incidence of myocardial infarction, rate of heart failure, hospitalization for any cause, rate of total advent events and study-drug-related adverse events., Results: A total of 7 randomized controlled trials involving 15,618 fulfilled the inclusion criteria. The outcomes of this meta-analysis presented that finerenone significantly reduced the death from any cause (95% CI 0.82-0.99; P = 0.031), risk of heart failure (95% CI 0.67-0.92; P = 0.002) among patients with kidney disease and/or diabetes when compared to control group. Besides, finerenone could not reduce the incidence of death from cardiovascular, myocardial infarction and hospitalization for any cause among patients with kidney disease and/or diabetes (p > 0.05). In terms of safety, finerenone shared the same risk of total advent events with placebo among patients with kidney disease and/or diabetes (p > 0.05). However, finerenone had higher risk of study-drug-related advent events than placebo among patients with kidney disease and/or diabetes (95% CI 1.27-1.48; P < 0.001)., Conclusions: In patients with kidney disease and/or diabetes, treatment with finerenone resulted in lower risk of death from any cause and heart failure than placebo. However, the study-drug-related advent events also increased significantly at the same time., (© 2022. The Author(s), under exclusive licence to Springer Nature B.V.)- Published
- 2023
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171. Comparing outcomes of single-port insufflation endoscopic breast-conserving surgery and conventional open approach for breast cancer.
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Xie F, Wang ZH, Wu SS, Gang TR, Gao GX, Qu X, and Zhang ZT
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- Endoscopy, Female, Humans, Mastectomy, Segmental adverse effects, Mastectomy, Segmental methods, Quality of Life, Breast Neoplasms pathology, Insufflation
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Background: In the surgical treatment of breast cancer, the goal of surgeons is to continually create and improve minimally invasive surgical techniques to increase patients' quality of life. Currently, routine breast-conserving surgery is often performed using two obvious incisions. Here, we compare the clinical efficacy and aesthetic outcomes of a novel technique using one incision, called 'single-port insufflation endoscopic breast-conserving surgery' (SIE-BCS), vs. conventional breast-conserving surgery (C-BCS) in patients with early-stage breast cancer., Methods: A total of 180 patients with stage I or stage II breast cancer participated in this study, of whom 63 underwent SIE-BCS and 117 underwent C-BCS. Logistic regression analysis was conducted to assess the risk of local recurrence and metastasis. Aesthetic outcomes were evaluated using the BREAST-Q scale., Results: The mean operation time was significantly longer for SIE-BCS (194.9 ± 71.5 min) than for C-BCS (140.3 ± 56.9 min), but the mean incision length was significantly shorter for SIE-BCS than for C-BCS (3.4 ± 1.2 cm vs. 8.6 ± 2.3 cm). While both surgeries yielded similar BREAST-Q ratings for satisfaction with breasts and sexual well-being, SIE-BCS was associated with significantly better ratings for physical well-being (chest area) and psychological well-being. Additionally, SIE-BCS was associated with decreased rates of adverse effects of radiation. The preliminary analysis showed that SIE-BCS did not increase the risk of local recurrence or metastasis., Conclusion: The novel single-port insufflation endoscopic assisted BCS technique is feasible, safe, and improves patients' postoperative comfort and psychological well-being, as compared to the conventional technique., (© 2022. The Author(s).)
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- 2022
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172. Anterior chest wall in SAPHO syndrome: magnetic resonance imaging findings.
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Yu M, Cao Y, Li J, Zhang Y, Ye Y, Wang L, Huang Z, Lu X, Li C, and Huo J
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- Cross-Sectional Studies, Humans, Magnetic Resonance Imaging, Acquired Hyperostosis Syndrome diagnostic imaging, Osteitis, Thoracic Wall diagnostic imaging
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Background: The anterior chest wall (ACW) involvement is characteristic of synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome, yet little research has focused on its magnetic resonance imaging (MRI) findings., Purpose: To characterize the MRI features of the ACW in patients with SAPHO syndrome., Methods: Seventy-one patients with SAPHO syndrome and ACW involvement evidenced by bone scintigraphy were recruited in this cross-sectional study. The ACW region was scanned using sagittal, axial, and oblique coronal Dixon T2-weighted sequences and axial Dixon T1-weighted sequences. The characteristics of both active inflammatory and chronic structural lesions were evaluated., Results: The ACW lesions exhibited an asymmetrical distribution and a predilection for the sternocostoclavicular region (93.0%). Notably, 91.5% of the patients had lesions in the area of the anterior first ribs. Bone marrow edema (BME) was observed in 63 (88.7%) patients, which mainly affected the sternocostal joints (87.3%) and the manubrium sterni (84.5%). All of the BMEs were distributed under the articular surface or the bone cortex, consistent with the distribution of the ligaments and joint capsules. Synovitis was detected in 64 (90.1%) patients, with a predilection for the sternoclavicular joints (76.1%). A soft tissue mass or infiltration was found in all the patients who had bone marrow edema. Thirteen (18.3%) patients showed venous stenosis. Structural changes included bone bridge formation (80.3%), hyperostosis (43.7%), and fat infiltration (39.4%). Four common patterns of involvement were observed: the first rib area, the sternoclavicular area, the sternal angle area, and the areas of the second to sixth sternocostal joints., Conclusion: The ACW lesions of SAPHO syndrome demonstrated a triad of enthesitis, synovitis, and osteitis, suggesting complex interactions among the ligaments, synovium, and bones in the region. The inflammatory changes in the first rib area were highlighted in SAPHO syndrome.
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- 2020
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173. Indirubin ameliorates imiquimod-induced psoriasis-like skin lesions in mice by inhibiting inflammatory responses mediated by IL-17A-producing γδ T cells.
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Xie XJ, Di TT, Wang Y, Wang MX, Meng YJ, Lin Y, Xu XL, Li P, and Zhao JX
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- Animals, Cell Proliferation drug effects, Cytokines genetics, Cytokines metabolism, Disease Models, Animal, Indoles chemistry, Indoles pharmacology, Indoles therapeutic use, Inflammation Mediators metabolism, Interleukin-17 biosynthesis, Janus Kinase 3 metabolism, Keratinocytes drug effects, Keratinocytes pathology, Lymph Nodes drug effects, Lymph Nodes metabolism, Male, Mice, Inbred BALB C, Phosphorylation drug effects, Psoriasis chemically induced, Psoriasis genetics, RNA, Messenger genetics, RNA, Messenger metabolism, STAT3 Transcription Factor metabolism, Signal Transduction drug effects, Imiquimod adverse effects, Inflammation pathology, Psoriasis drug therapy, Psoriasis immunology, Receptors, Antigen, T-Cell, gamma-delta metabolism, Skin pathology, Th17 Cells immunology
- Abstract
Objectives: Indirubin (IR) is a bisindole compound extracted from the leaves of Chinese herb Indigo Naturalis. Indigo Naturalis has been widely used in traditional Chinese medicine to treat inflammatory and autoimmune diseases. Psoriasis is a chronic immune-mediated inflammatory skin disease in which γδ T cells play an important role. This study aims to determine the immunoregulatory effects and the underlying mechanisms of Indirubin in psoriasis-related inflammatory responses., Methods: BALB/c mice with imiquimod (IMQ)-induced psoriasis-like dermatitis were treated with saline (Model), 1 mg/kg methotrexate (MTX) that serves as a positive control, or 12.5, 25 and 50 mg/kg Indirubin(IR) intragastrically. Keratinocytes proliferation, inflammatory cells infiltration, the expression of inflammatory cytokines and Jak/Stat pathway-related proteins in the skin lesion were examined. The abundance of γδ T cells in lymph nodes and spleen was determined by flow cytometry. The IL-17 expression and secretion, and the activation of Jak3/Stat3 pathways in in vitro cultured γδ T cell were tested., Results: Indirubin ameliorated keratinocyte proliferation, reduced the infiltration of CD3
+ T cells, IL-17 A-producing γδ T cells, and CD11b+ neutrophils, inhibited the mRNA expression of Il1, Il6, Il23, Il17a and Il22, and the protein expression of Jak/Stat pathway-related molecules in the skin lesion. Indirubin also reduced the abundance of γδ T cell and CCR6+ γδ T cells (the major IL-17 A producer) in spleen and lymph nodes. In cultured γδ T cells, Indirubin inhibited the mRNA expression of Il17a and Ifng, and the secretion of IL-17 A, while suppressed the activation of Jak3/Stat3 pathways., Conclusion: Indirubin alleviates IMQ-induced psoriasis-like dermatitis mainly through reducing the inflammatory responses mediated by IL-17 A-producing γδ T cells involving Jak3/Stat3 activation. Our results highlighted the novel mechanisms by which Indirubin ameliorates psoriasis-related inflammatory responses, supporting its therapeutic potential., (Copyright © 2018 Elsevier Ltd. All rights reserved.)- Published
- 2018
- Full Text
- View/download PDF
174. Acupuncture as an early treatment for idiopathic sudden sensorineural hearing loss (ISSNHL) patients with flat or high-frequency drop audiograms: study protocol for a randomized controlled trial.
- Author
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Shang K, Ma X, Liu HL, Jing YY, Zeng L, Li N, Zhou DA, Wei J, and Zhang C
- Subjects
- Adult, Aged, Audiometry, Humans, Middle Aged, Outcome Assessment, Health Care, Quality Control, Research Design, Acupuncture Therapy methods, Hearing Loss, Sensorineural therapy, Randomized Controlled Trials as Topic
- Abstract
Background: Idiopathic sudden sensorineural hearing loss (ISSNHL) is a common form of deafness. Acupuncture has been used as a salvage therapy for ISSNHL in China since 200 BCE. However, the efficacy of acupuncture has not been confirmed in strictly controlled trials. We designed a randomized controlled clinical trial to evaluate the efficacy and long-term effects of acupuncture in patients with early ISSNHL., Methods/design: In this randomized controlled clinical trial, we will enroll 124 participants with ISSNHL diagnosed 2 to 4 weeks prior to enrollment, who have shown little hearing improvement after routine Western medical treatment (i.e., corticosteroids). 62 of these participants will have flat audiogram and the other 62 will have a high-frequency drop audiogram; they will all take Methycobal while half of the flat type and half of the high-frequency drop type will also receive acupuncture treatments for 4 weeks in a four-group design. The primary outcome measure will be the effective rate of hearing improvement (defined as the proportion of patients with at least 15-dB improvement in the hearing loss frequency band). The secondary outcome will measure the improvements in Pure Tone Average, Word Recognition Score, and Tinnitus Handicap Inventory. The assessments of the participants will be made at baseline, after treatment (week 4), and at follow-up (week 28)., Discussion: This study aims to explore the efficacy and long-term effects of acupuncture in patients with ISSNHL. This study will be a randomized controlled trial with strict methodology and few design deficits. If our study yields positive results, acupuncture could be recommended as a salvage therapy for patients with ISSNHL., Trial Registration: Chinese Clinical Trial Registry, ChiCTR-ICR-15006787 . Registered on 12 July 2015.
- Published
- 2018
- Full Text
- View/download PDF
175. Cardioprotective Effects of Serca2a Overexpression Against Ischemiareperfusion- induced Injuries in Rats.
- Author
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Jiang Y, Tian LL, Wang LH, Zhao XD, Chen JW, Murao K, Zhu W, Dong L, Wang GQ, Sun WP, and Zhang GX
- Subjects
- Animals, Apoptosis, Myocardial Infarction genetics, Myocardial Infarction pathology, Rats, Rats, Transgenic, Rats, Wistar, Reperfusion Injury genetics, Reperfusion Injury pathology, Signal Transduction, Cardiotonic Agents administration & dosage, Gene Expression Regulation, Genetic Vectors administration & dosage, Myocardial Infarction prevention & control, Reperfusion Injury prevention & control, Sarcoplasmic Reticulum Calcium-Transporting ATPases genetics
- Abstract
Aims: The aim of the present study was to assess how genetically increased Sarcoplasmic reticulum Ca2+-ATPase (Serca2a) expression affects cardiac injury after Ischemia/Reperfusion (I/R) exposure and the related mechanisms involved., Methods and Results: Rats were subjected to Left Anterior Descending coronary artery (LAD) occlusion for 30 min followed by a 24-hour reperfusion. Cardiac function analysis revealed that cardiac function dramatically improved in Serca2a transgenic rats, (Serca2aTG) rats, compared to Wild Type (WT) rats. Serca2aTG rats developed a significantly smaller myocardial infarction size compared to those in WT group. The expression of the Bcl-2 was lower in Serca2aTG rats compared with WT rats; but, Bcl-2 expression was markedly increased in Serca2aTG rats compared with WT after I/R. In addition, Bax was markedly downregulated in Serca2aTG rats compared to WT group after I/R. Meanwhile, autophagy marker LC-3B was increased in Serca2aTG group, and p62 was only increased in WT group but not in Serca2aTG group in response to I/R. Electron microscope observation confirmed that there were more autophagosomes in Serca2aTG group than in WT rats after I/R., Conclusion: our findings demonstrated that the overexpression of Serca2a plays an important role in myocardial protection from I/R injury and postischemic functional recovery, which may be via antinecrotic, anti-apoptotic and pro-autophagy signal pathways. Our research provides solid basic data and new perspective on clinical treatment in heart failure patients with long-term over-expression of Serca2a., (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.)
- Published
- 2017
- Full Text
- View/download PDF
176. Contribution of the renin-angiotensin system in chronic foot-shock induced hypertension in rats.
- Author
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Wang LH, Dong T, Liu BB, Zhao XD, Chen JW, Murao K, Zhu W, and Zhang GX
- Subjects
- Animals, Cerebral Cortex metabolism, Chronic Disease, Drinking, Eating, Electrolytes blood, Hormones blood, Hypertension psychology, Hypothalamus metabolism, Male, Oxidative Stress, Rats, Rats, Sprague-Dawley, Weight Gain, Electroshock, Hypertension physiopathology, Renin-Angiotensin System
- Abstract
Aims: Chronic foot shock has been demonstrated to induce hypertension. The present study was designed to explore whether the renin-angiotensin system (RAS) plays a role in this process and the possible mechanisms involved in chronic-foot-shock-induced hypertension., Main Methods: Male Sprague-Dawley rats were subjected to a two-week foot shock with or without an angiotensin II (Ang II) type 1 receptor blocker (ARB, candesartan) or an angiotensin I converting enzyme inhibitor (ACEI, captopril). The expression of RAS components in the central nervous and circulatory systems was examined. Antioxidant levels in the plasma were monitored., Key Findings: Two-week foot shock significantly increased systolic blood pressure (SBP). Angiotensinogen, angiotensin I converting enzyme (ACE)-1, ACE-2, angiotensin type 1a and type 1b receptors, and vasopressin (VAP) mRNA expression in the cerebral cortex and hypothalamus were increased along with the concentration of renin and Ang II in the plasma; these changes were accompanied by decreased glutathione peroxidase activity and increased lipid peroxidation levels and plasma corticosterone concentrations. Both candesartan and captopril suppressed not only the increases in SBP but also the increases in VAP expression in the hypothalamus and RAS components in the central nervous system and the circulatory system. The decreases in antioxidant levels and the increases in lipid peroxidation and corticosterone levels were also partially reversed by candesartan or captopril treatment., Significance: Chronic foot shock increases expression of the main RAS components, which play an important role in the development of high blood pressure through increased VAP levels, oxidative stress levels and stress hormone levels., (Copyright © 2014 Elsevier Inc. All rights reserved.)
- Published
- 2015
- Full Text
- View/download PDF
177. [Genome sequencing and phylogenetic analysis of avian influenza viruses subtype H9N2].
- Author
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Li SC, Li XH, Zhong SG, Sun HL, Pan JJ, Chen SJ, Peng DX, and Liu XF
- Subjects
- Hemagglutinin Glycoproteins, Influenza Virus genetics, Influenza A Virus, H9N2 Subtype classification, Neuraminidase genetics, Sequence Analysis, DNA, Genome, Viral, Influenza A Virus, H9N2 Subtype genetics, Phylogeny
- Abstract
Samples of chicken, duck, quail, and pigeon were collected from Jiangsu, Anhui, and Hebei in 2009-2011, and sixteen H9N2 subtype isolates of avian influenza virus (AIV) were identified. The eight full-length genes of 16 AIV isolates were amplified by RT-PCR and sequenced. Genome sequence analysis showed that the amino acid motif of cleavage sites in the HA gene was P-S-R/K-S-S-R, which was consistent with the characterization of the LPAIV, and the Leucine (L) at the amino acid position 226 in the HA genes of all isolates indicated the potential of binding with SAalpha, 2-6 receptor. All isolates had a S to N substitution at residue 31 in the M2 gene, which is related to the resistance phenotype of adamantanes. The key molecular features of 16 AIV isolates from different hosts were same. Genome phylogenetic analysis revealed that all 16 H9N2 subtype AIVs originated from F98-like virus as backbone and formed two new genotypes through reassortment with HA gene of Y280-like virus and PB2 and M genes of G1-like virus. Our findings suggest that more attention should be paid to the surveillance of H9N2 influenza virus and its direction of reassortment.
- Published
- 2012
178. [The production of gastrodin through biotransformation of p-hydroxybenzaldehyde by cell suspension culture of Datura stramonium].
- Author
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Gong JS, Ma WP, Pu JX, Xu SG, Zheng SQ, and Xiao CJ
- Subjects
- Benzyl Alcohols isolation & purification, Benzyl Alcohols metabolism, Biotransformation, Cell Culture Techniques methods, Cells, Cultured, Datura stramonium cytology, Glucosides isolation & purification, Plant Stems cytology, Plants, Medicinal cytology, Plants, Medicinal metabolism, Benzaldehydes metabolism, Datura stramonium metabolism, Glucosides biosynthesis
- Abstract
Aim: To investigate the production of p-hydroxymethylphenol-beta-D-glucoside (gastrodin) through biotransformation by plant cell suspension cultures., Methods: Using cell suspension cultures of Datura stramonium to convert the exogenous p-hydroxybenzaldehyde into gastrodin was conducted and the converted compounds were separated with a combination of multi-chromatography. Their chemical structures were determined on the basis of spectral analysis and chemical evidence., Results: The conversion procedure of p-hydroxybenzaldehyde into gastrodin by Datura stramonium cell suspension cultures was established. The synthesized gastrodin (II) was isolated from the fermental liquor and identified by spectral analysis. At the same time, the p-hydroxybenzyl alcohol (I) converted through biotransformation of p-hydroxybenzaldehyde by cell suspension cultures of Datura stramonium was also isolated and identified. Two compounds were also isolated from the cell cultures and they were identified as beta-D-furanoallulose (III) and n-butyloxystyryl-beta-D-pyranoallulose (IV)., Conclusion: Datura stramonium grown in suspension cultures can convert exogenous p-hydroxybenzaldehyde into the corresponding gastrodin.
- Published
- 2006
179. [Childhood and adolescent thyroid carcinoma: a clinical analysis of 86 cases].
- Author
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Jin GP, Meng ZZ, Luo RH, Yang H, and Yu SG
- Subjects
- Adolescent, Adult, Cell Differentiation, Child, Child, Preschool, Female, Humans, Male, Prognosis, Thyroid Neoplasms mortality, Thyroid Neoplasms surgery, Thyroid Neoplasms pathology
- Abstract
Objective: To investigate the clinico-pathologic characteristics, treatment and prognosis of thyroid carcinoma in childhood and adolescents., Methods: From 1984 to 1997, 86 cases with thyroid carcinoma in childhood and adolescent treated were summarized., Results: All cases underwent operation with adjuvant therapy. Pathologically, papillary carcinoma was diagnosed in 73 (84.9%), follicular carcinoma in 6 (7%), papillary-follicular carcinoma in 4 (4.7%) and medullary carcinoma in 3 (3.5%). Cervical lymph node metastasis was found in 59 cases (68.6%), 16 of which with both thyroid carcinoma and bilateral cervical lymph node metastasis (27.1%). Lung metastasis was found in 11 cases. Recurrence occurred in 6 cases after operation. Compared with the thyroid carcinoma in adult patients, cervical lymph node metastasis, bilateral involvement of the thyroid gland with bilateral cervical nodes and lung metastasis rate were more commonly seen in childhood and adolescence. All but 2 patients had been followed up for more than 5 years, 41 patients for more than 10 years. The 5-year and 10-year survival rate was 95.3% (82/86) and 87.8% (36/41), respectively., Conclusion: The clinical manifestations of childhood and adolescent thyroid cancer are generally not pathognostic which may lead to misdiagnosis. Surgery is the main method in the comprehensive treatment with a good prognosis. The therapy with (131)I after operation was beneficial for some patients accompanied with lung metastasis.
- Published
- 2004
180. [Malignant fibrous histiocytoma of head and neck: clinical analysis of 21 cases].
- Author
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Jin GP, Zhao M, Qi JX, Jiang HG, and Yu SG
- Subjects
- Adolescent, Adult, Aged, Female, Follow-Up Studies, Head and Neck Neoplasms pathology, Histiocytoma, Benign Fibrous pathology, Histiocytoma, Benign Fibrous secondary, Humans, Lymphatic Metastasis, Male, Middle Aged, Neoplasm Staging, Treatment Outcome, Head and Neck Neoplasms surgery, Histiocytoma, Benign Fibrous surgery, Neoplasm Recurrence, Local
- Abstract
Background & Objective: Malignant fibrous histiocytoma (MFH) is a type of pleomorphic neoplastic diseases with complex pathological structure. Its histological origin is uncertain. It was often classified as other carcinoma. This study was designed to investigate the clinical and pathological features and improve the diagnosis and treatment., Methods: To summarize and analyze the clinical experiences of 21 cases of MFH at head and neck proved histologically from June 1984 to June 1999 treated in Department of Head and Neck Surgery, Henan Tumor Hospital., Results: Twenty cases were followed up more than 3 years; one case was lost. The 3-year survival rate was 42.9%(9/21). Nineteen cases were treated with surgery. Two cases in advanced stage were treated by non-surgery who died in 2 and 5 months. Among the patients treated with surgery, 6 cases survived without evidence of recurrence more than 3 years, 13 cases recurred within 2 years and 9 cases with metastasis. Seven cases received second surgery after recurrence. Among them,3 cases survived more than 3 years after second surgery. Of all 21 patients, 12 were proved with cervical lymph node metastasis., Conclusion: MFH at head and neck region is a kind of malignant disease with high recurrent rate and the cervical lymph node metastasis rate was 57.1%. Amplified radical surgery is the first choice of treatment. The second surgery has special value to the recurrent patients. Radiotherapy alone or chemotherapy alone is not effective to MFH of head and neck region.
- Published
- 2003
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