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Circulation|July 19, 2019
Allele-Specific Silencing Ameliorates Restrictive Cardiomyopathy Attributable to a Human Myosin Regulatory Light Chain MutationKathia Zaleta-Rivera, Alexandra Dainis, Alexandre J S Ribeiro, et al.Cell|December 17, 2016
Disease Model of GATA4 Mutation Reveals Transcription Factor Cooperativity in Human CardiogenesisYen-Sin Ang, Renee N Rivas, Alexandre J S Ribeiro, et al.Stem Cell Reports|May 21, 2021
Increased tissue stiffness triggers contractile dysfunction and telomere shortening in dystrophic cardiomyocytesAlex C Y Chang, Gaspard Pardon, Andrew C H Chang, et al.Biorxiv : the Preprint Server for Biology|June 19, 2023
Multi-scale models reveal hypertrophic cardiomyopathy MYH7 G256E mutation drives hypercontractility and elevated mitochondrial respirationSoah Lee, Alison S Vander Roest, Cheavar A Blair, et al.Proceedings of the National Academy of Sciences of the United States of America|April 29, 2024
Incomplete-penetrant hypertrophic cardiomyopathy MYH7 G256E mutation causes hypercontractility and elevated mitochondrial respirationSoah Lee, Alison S Vander Roest, Cheavar A Blair, et al.Pageof 9