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Nature Structural Biology|December 14, 2001
Crystal structure of a bacterial cocaine esteraseNicholas A Larsen, James M Turner, James Stevens, et al.Nature Communications|July 24, 2021
Structural basis of intron selection by U2 snRNP in the presence of covalent inhibitorsConstantin Cretu, Patricia Gee, Xiang Liu, et al.Molecular Pharmacology|September 14, 2006
Rapid and robust protection against cocaine-induced lethality in rats by the bacterial cocaine esteraseZiva D Cooper, Diwahar Narasimhan, Roger K Sunahara, et al.The Biochemical Journal|June 23, 2012
An aminoquinazoline inhibitor of the essential bacterial cell wall synthetic enzyme GlmU has a unique non-protein-kinase-like binding modeNicholas A Larsen, Tory J Nash, Marshall Morningstar, et al.ACS Chemical Biology|January 1, 2013
Mechanism and in vitro pharmacology of TAK1 inhibition by (5Z)-7-OxozeaenolJiaquan Wu, Francoise Powell, Nicholas A Larsen, et al.Bioorganic & Medicinal Chemistry Letters|January 24, 2012
Discovery of aminopiperidine-based Smac mimetics as IAP antagonistsEdward J Hennessy, Jamal C Saeh, Li Sha, et al.Structure (London, England : 1993)|July 26, 2011
Structural basis of substrate methylation and inhibition of SMYD2Andrew D Ferguson, Nicholas A Larsen, Tina Howard, et al.ACS Medicinal Chemistry Letters|June 20, 2020
Discovery of 2,6-Dimethylpiperazines as Allosteric Inhibitors of CPS1Alan Rolfe, Shihua Yao, Toung-Vi Nguyen, et al.ACS Medicinal Chemistry Letters|March 18, 2016
Potent and Selective CK2 Kinase Inhibitors with Effects on Wnt Pathway Signaling in VivoJames E Dowling, Marat Alimzhanov, Larry Bao, et al.The Journal of Biological Chemistry|October 5, 2019
The R882H DNMT3A hot spot mutation stabilizes the formation of large DNMT3A oligomers with low DNA methyltransferase activityTuong-Vi Nguyen, Shihua Yao, Yahong Wang, et al.Pageof 4