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Journal of Molecular and Cellular Cardiology|April 3, 2012
Increased myofilament Ca2+ sensitivity and diastolic dysfunction as early consequences of Mybpc3 mutation in heterozygous knock-in miceBodvaël Fraysse, Florian Weinberger, Sonya C Bardswell, et al.Journal of Cell Science|May 9, 2014
Cellular microenvironments reveal defective mechanosensing responses and elevated YAP signaling in LMNA-mutated muscle precursorsAnne T Bertrand, Simindokht Ziaei, Camille Ehret, et al.Cells|April 28, 2016
A Heterozygous ZMPSTE24 Mutation Associated with Severe Metabolic Syndrome, Ectopic Fat Accumulation, and Dilated CardiomyopathyDamien Galant, Bénédicte Gaborit, Camille Desgrouas, et al.The FEBS Journal|December 14, 2016
Emerin self-assembly mechanism: role of the LEM domainCamille Samson, Florian Celli, Kitty Hendriks, et al.The Journal of Cell Biology|October 24, 2018
EHD2 is a mechanotransducer connecting caveolae dynamics with gene transcriptionStéphanie Torrino, Wei-Wei Shen, Cédric M Blouin, et al.Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|April 20, 2010
Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practiceVeronique Fressart, Guillaume Duthoit, Erwan Donal, et al.Pageof 5