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Bioorganic & Medicinal Chemistry Letters|June 22, 2010
Studies on the structure-activity relationship of 1,3,3,4-tetra-substituted pyrrolidine embodied CCR5 receptor antagonists. Part 1: Tuning the N-substituentsLi Ben, Eric Dale Jones, Enkun Zhou, et al.Proceedings of the National Academy of Sciences of the United States of America|April 25, 2002
Interactions that determine the assembly of a retinoid X receptor/corepressor complexJagadish C Ghosh, Xiaofang Yang, Aihua Zhang, et al.Acta Pharmacologica Sinica|July 18, 2017
Amyloid beta: structure, biology and structure-based therapeutic developmentGuo-Fang Chen, Ting-Hai Xu, Yan Yan, et al.Proceedings of the National Academy of Sciences of the United States of America|June 18, 2026
Structural basis for lysophosphatidic acid recognition and atypical Gα<sub>q</sub> coupling by LPAR5Xin Li, Kai Wang, Zhongliang Xing, et al.Science Advances|November 25, 2015
Structural basis for recognition of diverse transcriptional repressors by the TOPLESS family of corepressorsJiyuan Ke, Honglei Ma, Xin Gu, et al.Acta Pharmacologica Sinica|July 9, 2025
An update for AlphaFold3 versus experimental structures: assessing the precision of small molecule binding in GPCRsShi-Yi Shen, Jun-Rui Li, Yu-Song Wang, et al.Bioorganic & Medicinal Chemistry Letters|August 3, 2010
Studies on the structure-activity relationship of 1,3,3,4-tetra-substituted pyrrolidine embodied CCR5 receptor antagonists. Part 2: Discovery of highly potent anti-HIV agentsBen Li, Eric Dale Jones, Enkun Zhou, et al.Molecular and Cellular Biology|September 4, 2014
MicroRNA 34a inhibits beige and brown fat formation in obesity in part by suppressing adipocyte fibroblast growth factor 21 signaling and SIRT1 functionTing Fu, Sunmi Seok, Sunge Choi, et al.Nature Communications|April 16, 2024
Cryo-EM structures of adenosine receptor A<sub>3</sub>AR bound to selective agonistsHongmin Cai, Shimeng Guo, Youwei Xu, et al.Proceedings of the National Academy of Sciences of the United States of America|September 7, 2007
A mechanistic basis for converting a receptor tyrosine kinase agonist to an antagonistW David Tolbert, Jennifer Daugherty, ChongFeng Gao, et al.Pageof 32