Showing results (61-70 of 304) with videos related to
Sort By:
Pageof 31
International Journal of Biological Macromolecules|March 5, 2026
Molecular and functional characterization of a SUR1 mutation underlying dual glucose dysregulationDavoud Amirkashani, P V Migisha Ntwali, Behnoosh Tasharrofi, et al.Biorxiv : the Preprint Server for Biology|June 12, 2025
Multi-Omic Profiling Identifies Conserved Metabolic Pathways Critical for SARS-CoV-2 Variants InfectionScotland E Farley, Jennifer E Kyle, Helene Jahn, et al.Elife|March 26, 2025
AI-based discovery and cryoEM structural elucidation of a KATP channel pharmacochaperoneAssmaa Elsheikh, Camden M Driggers, Ha H Truong, et al.The Journal of Biological Chemistry|February 6, 2008
Destabilization of ATP-sensitive potassium channel activity by novel KCNJ11 mutations identified in congenital hyperinsulinismYu-Wen Lin, Jeremy D Bushman, Fei-Fei Yan, et al.American Journal of Medical Genetics. Part A|August 30, 2019
Novel dominant KATP channel mutations in infants with congenital hyperinsulinism: Validation by in vitro expression studies and in vivo carrier phenotypingKara E Boodhansingh, Balamurugan Kandasamy, Lauren Mitteer, et al.Elife|July 26, 2019
Mechanism of pharmacochaperoning in a mammalian KATP channel revealed by cryo-EMGregory M Martin, Min Woo Sung, Zhongying Yang, et al.Proceedings of the National Academy of Sciences of the United States of America|October 29, 2021
Vascular KATP channel structural dynamics reveal regulatory mechanism by Mg-nucleotidesMin Woo Sung, Zhongying Yang, Camden M Driggers, et al.Methods in Enzymology|March 1, 2026
Tracing sphingolipid metabolism kinetics using radioactive and non-radioactive labelsAlec Griffith, Helene Jahn, Fikadu G TafesseElife|January 17, 2017
Cryo-EM structure of the ATP-sensitive potassium channel illuminates mechanisms of assembly and gatingGregory M Martin, Craig Yoshioka, Emily A Rex, et al.The Journal of Clinical Investigation|July 4, 2008
Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutationsSara E Pinney, Courtney MacMullen, Susan Becker, et al.Pageof 31