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Proceedings of the National Academy of Sciences of the United States of America|March 15, 2020
Inhibition mechanisms of AcrF9, AcrF8, and AcrF6 against type I-F CRISPR-Cas complex revealed by cryo-EMKaiming Zhang, Shuo Wang, Shanshan Li, et al.Proceedings of the National Academy of Sciences of the United States of America|August 2, 2017
Structural basis of subunit selectivity for competitive NMDA receptor antagonists with preference for GluN2A over GluN2B subunitsGenevieve E Lind, Tung-Chung Mou, Lucia Tamborini, et al.Molecular Pharmacology|April 19, 2011
Structural basis for the high-affinity inhibition of mammalian membranous adenylyl cyclase by 2',3'-o-(N-methylanthraniloyl)-inosine 5'-triphosphateMelanie Hübner, Anshuman Dixit, Tung-Chung Mou, et al.Structure (London, England : 1993)|June 4, 2019
Structure, Function, and Dynamics of the Gα Binding Domain of Ric-8ABaisen Zeng, Tung-Chung Mou, Tzanko I Doukov, et al.Journal of the American Chemical Society|December 20, 2016
Cytochrome c Can Form a Well-Defined Binding Pocket for HydrocarbonsLevi J McClelland, Harmen B B Steele, Frank G Whitby, et al.Proceedings of the National Academy of Sciences of the United States of America|March 22, 2019
Cryo-EM structures of <i>Helicobacter pylori</i> vacuolating cytotoxin A oligomeric assemblies at near-atomic resolutionKaiming Zhang, Huawei Zhang, Shanshan Li, et al.Nature Communications|February 28, 2020
Structure of the G protein chaperone and guanine nucleotide exchange factor Ric-8A bound to Gαi1Levi J McClelland, Kaiming Zhang, Tung-Chung Mou, et al.Journal of Medicinal Chemistry|May 31, 2024
Discovery of Potent and Selective Covalent Inhibitors of HER2<sup>WT</sup> and HER2<sup>YVMA</sup>Erik J Hicken, Karin Brown, Natalie C Dwulet, et al.Cancer Discovery|May 1, 2024
A Next-Generation BRAF Inhibitor Overcomes Resistance to BRAF Inhibition in Patients with BRAF-Mutant Cancers Using Pharmacokinetics-Informed Dose EscalationRona Yaeger, Meredith A McKean, Rizwan Haq, et al.Journal of Medicinal Chemistry|August 1, 2024
Discovery of Pyrazolopyrazines as Selective, Potent, and Mutant-Active MET Inhibitors with Intracranial EfficacyQuinn A Bumpers, Robert W Pipal, Anna M Benz-Weeden, et al.Pageof 5