Showing results (41-50 of 54) with videos related to
Sort By:
Pageof 6
Journal of Environmental Management|June 25, 2022
A Global review of cumulative effects assessments of disturbances on forest ecosystemsEffah Kwabena Antwi, John Boakye-Danquah, Wiafe Owusu-Banahene, et al.Human Mutation|July 4, 2012
Functional characterization of MLH1 missense variants identified in Lynch syndrome patientsSofie Dabros Andersen, Sascha Emilie Liberti, Anne Lützen, et al.Journal of Medicinal Chemistry|November 15, 2019
Biphenyl Acid Derivatives as APJ Receptor AgonistsShun Su, Adam Clarke, Ying Han, et al.Chimia|August 12, 2020
Analytical Platforms at Swiss Universities of Applied SciencesChristian Berchtold, Jean-Pascal Bourgeois, Verena Christen, et al.Nature|December 8, 2016
Structure of CC chemokine receptor 2 with orthosteric and allosteric antagonistsYi Zheng, Ling Qin, Natalia V Ortiz Zacarías, et al.Bioorganic & Medicinal Chemistry Letters|February 10, 2020
Discovery and SAR of aryl hydroxy pyrimidinones as potent small molecule agonists of the GPCR APJMichael C Myers, Donna M Bilder, Cullen L Cavallaro, et al.ACS Medicinal Chemistry Letters|March 21, 2019
Use of a Conformational-Switching Mechanism to Modulate Exposed Polarity: Discovery of CCR2 Antagonist BMS-741672Michael G Yang, Zili Xiao, Robert J Cherney, et al.ACS Medicinal Chemistry Letters|March 18, 2016
Identification and Preclinical Pharmacology of BMS-986104: A Differentiated S1P1 Receptor Modulator in Clinical TrialsT G Murali Dhar, Hai-Yun Xiao, Jenny Xie, et al.Journal of Medicinal Chemistry|September 19, 2023
Discovery of <b>12</b> (BMS-986172) as a Highly Potent MGAT2 Inhibitor that Achieved Targeted Efficacious Exposures at a Low Human Dose for the Treatment of Metabolic DisordersWei Meng, Robert Brigance, James Mignone, et al.Bioorganic & Medicinal Chemistry Letters|December 14, 2017
Identification of bicyclic hexafluoroisopropyl alcohol sulfonamides as retinoic acid receptor-related orphan receptor gamma (RORγ/RORc) inverse agonists. Employing structure-based drug design to improve pregnane X receptor (PXR) selectivityHua Gong, David S Weinstein, Zhonghui Lu, et al.Pageof 6