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ACS Chemical Biology|March 22, 2014
Identification and characterization of an allosteric inhibitory site on dihydropteroate synthaseDalia I Hammoudeh, Mihir Daté, Mi-Kyung Yun, et al.ACS Pharmacology & Translational Science|April 21, 2023
Design, Synthesis, and Biological Evaluation of Pyrimidine Dihydroquinoxalinone Derivatives as Tubulin Colchicine Site-Binding Agents That Displayed Potent Anticancer Activity Both In Vitro and In VivoSatyanarayana Pochampally, Kelli L Hartman, Rui Wang, et al.Structure (London, England : 1993)|June 5, 2012
The T4 phage SF1B helicase Dda is structurally optimized to perform DNA strand separationXiaoping He, Alicia K Byrd, Mi-Kyung Yun, et al.Chemistry & Biology|August 28, 2010
Modulation of pantothenate kinase 3 activity by small molecules that interact with the substrate/allosteric regulatory domainRoberta Leonardi, Yong-Mei Zhang, Mi-Kyung Yun, et al.Journal of Medicinal Chemistry|March 2, 2026
Discovery of Sulfonamide Pantothenate Kinase Activators and Elucidation of the Role of Isoform Selectivity in Cellular Pantothenate Kinase ActivationAshton L Coker, Rajendra Tangallapally, Mi-Kyung Yun, et al.Journal of Medicinal Chemistry|August 13, 2024
Development of Brain Penetrant Pyridazine Pantothenate Kinase ActivatorsRajendra Tangallapally, Chitra Subramanian, Mi-Kyung Yun, et al.Cancer Letters|January 3, 2023
SB226, an inhibitor of tubulin polymerization, inhibits paclitaxel-resistant melanoma growth and spontaneous metastasisShanshan Deng, Souvik Banerjee, Hao Chen, et al.Proceedings of the National Academy of Sciences of the United States of America|March 12, 2014
Structural polymorphism in the N-terminal oligomerization domain of NPM1Diana M Mitrea, Christy R Grace, Marija Buljan, et al.Journal of Medicinal Chemistry|August 11, 2021
Design, Synthesis, and Biological Evaluation of Stable Colchicine-Binding Site Tubulin Inhibitors 6-Aryl-2-benzoyl-pyridines as Potential Anticancer AgentsHao Chen, Shanshan Deng, Najah Albadari, et al.Nature Chemical Biology|January 24, 2013
PUMA binding induces partial unfolding within BCL-xL to disrupt p53 binding and promote apoptosisAriele Viacava Follis, Jerry E Chipuk, John C Fisher, et al.Pageof 4