Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Guangying Du"'
Autor:
Yanqun Wang, An Yan, Deyong Song, Chuangchuang Dong, Muding Rao, Yuanzhu Gao, Ruxi Qi, Xiaomin Ma, Qiaoping Wang, Hongguang Xu, Hong Liu, Jing Han, Maoqin Duan, Shuo Liu, Xiaoping Yu, Mengqi Zong, Jianxia Feng, Jie Jiao, Huimin Zhang, Min Li, Beibei Yu, Yanxia Wang, Fanhao Meng, Xiaodan Ni, Ying Li, Zhenduo Shen, Baiping Sun, Xin Shao, Haifeng Zhao, Yanyan Zhao, Rui Li, Yanan Zhang, Guangying Du, Jun Lu, Chunna You, Hua Jiang, Lu Zhang, Lan Wang, Changlin Dou, Zheng Liu, Jincun Zhao
Publikováno v:
Cell Discovery, Vol 9, Iss 1, Pp 1-16 (2023)
Abstract SARS-CoV-2 Omicron subvariants have demonstrated extensive evasion from monoclonal antibodies (mAbs) developed for clinical use, which raises an urgent need to develop new broad-spectrum mAbs. Here, we report the isolation and analysis of tw
Externí odkaz:
https://doaj.org/article/b38531d441f14db695079f6108b97685
Structure and function analysis of a potent human neutralizing antibody CA521FALA against SARS-CoV-2
Autor:
Deyong Song, Wenbo Wang, Chuangchuang Dong, Zhenfei Ning, Xiu Liu, Chuan Liu, Guangying Du, Chunjie Sha, Kailin Wang, Jun Lu, Baiping Sun, Yanyan Zhao, Qiaoping Wang, Hongguang Xu, Ying Li, Zhenduo Shen, Jie Jiao, Ruiying Wang, Jingwei Tian, Wanhui Liu, Lan Wang, Yong-Qiang Deng, Changlin Dou
Publikováno v:
Communications Biology, Vol 4, Iss 1, Pp 1-11 (2021)
Song et al describe and identify monoclonal antibodies that target the SARSCoV-2 Spike protein, including CA521FALA, which demonstrated neutralising potential in vivo and in vitro. They performed structural analysis, which revealed that CA521FALA rec
Externí odkaz:
https://doaj.org/article/abce2e8dd92d46c18256f52f67586310
Autor:
Wenyan Wang, Guangying Du, Shilan Lin, Jing Liu, Huijie Yang, Dawei Yu, Liang Ye, Fangxia Zou, Hongbo Wang, Rui Zhang, Jingwei Tian
Publikováno v:
Frontiers in Pharmacology, Vol 12 (2021)
Valbenazine and deutetrabenazine are the only two therapeutic drugs approved for tardive dyskinesia based on blocking the action of vesicular monoamine transporter 2 (VMAT2). But there exist demethylated inactive metabolism at the nine position for b
Externí odkaz:
https://doaj.org/article/515593430ba74dea8100ad61c24a8ad7
Autor:
Zhengping Hu, Pengfei Yu, Guangying Du, Wenyan Wang, Haibo Zhu, Ning Li, Huijuan Zhao, Zhaoju Dong, Liang Ye, Jingwei Tian
Publikováno v:
PLoS ONE, Vol 15, Iss 3, p e0228339 (2020)
The increased PD-L1 expression induces poorer prognosis in melanoma. The small molecule inhibitors of PD-1/PD-L1 pathways have been an encouraging drug development strategy because of good affinity and oral bioavailability without immunogenicity and
Externí odkaz:
https://doaj.org/article/f058d0fe4a77400ea8d5bb5ba1d4eb4e
Publikováno v:
Medicinal Plant; Feb2024, Vol. 15 Issue 1, p51-56, 6p
Publikováno v:
Biological Trace Element Research. 201:1006-1018
The traceability of different cultivation modes is critical for ensuring the commercial viability of high-value Dendrobium officinale. In this study, by means of polarizing microscopy, SEM-EDX, ICP-MS and ICP-AES, the possibility of combining microsc
Autor:
Jing Lu, Hui Lei, Xinfa Bai, Wenyan Wang, Chunjiao Liu, Yifei Yang, Fangxia Zou, Guangying Du, Xin Wang, Cuicui Sun, Lisha Yu, Mingxu Ma, Liang Ye, Hongbo Wang, Jingwei Tian, jianzhao zhang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0af0f7e92ffd29bde33280a56b064e1
https://doi.org/10.2139/ssrn.4329585
https://doi.org/10.2139/ssrn.4329585
Autor:
Xiaoyin Zhu, Yue Yang, Guangying Du, Bin Liu, Xin Yu, Liang Ye, Yutong Mao, Hongbo Wang, Jingwei Tian
Publikováno v:
Food and Chemical Toxicology. 176:113800
Autor:
Guangying Du, Yaqiu Zhao, Chenghong Xiao, Deqiang Ren, Yan Ding, Jiao Xu, Haijun Jin, Hongguan Jiao
Publikováno v:
Industrial Crops and Products. 195:116495
Autor:
Wenyan Wang, Shilan Lin, Guangying Du, Xinfa Bai, Jing Lu, Liang Ye, Hongbo Wang, Rui Zhang, Jingwei Tian
Publikováno v:
Future medicinal chemistry. 14(13)
Aim: To separate and evaluate 9-cyclopropylmethoxy-dihydrotetrabenazine (13a) and its stereoisomers for their high affinity for vesicular monoamine transporter-2 (VMAT2). Method: Stereoisomers of 13a were separated and configurations were ascertained