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Journal of Cell Science|April 17, 2012
Role of triadin in the organization of reticulum membrane at the muscle triadAnne Fourest-Lieuvin, John Rendu, Alexis Osseni, et al.The Journal of Biological Chemistry|September 24, 2005
Triadin (Trisk 95) overexpression blocks excitation-contraction coupling in rat skeletal myotubesSophia Smida Rezgui, Stéphane Vassilopoulos, Julie Brocard, et al.The Journal of Biological Chemistry|October 22, 2009
Triadin deletion induces impaired skeletal muscle functionSarah Oddoux, Julie Brocard, Annie Schweitzer, et al.The Journal of General Physiology|November 21, 2022
Huntingtin regulates calcium fluxes in skeletal muscleMathilde Chivet, Maximilian McCluskey, Anne Sophie Nicot, et al.Molecular Therapy. Nucleic Acids|July 29, 2024
Functional benefit of CRISPR-Cas9-induced allele deletion for RYR1 dominant mutationMathilde Beaufils, Margaux Melka, Julie Brocard, et al.Human Mutation|October 30, 2016
Functional Characterization and Rescue of a Deep Intronic Mutation in OCRL Gene Responsible for Lowe SyndromeJohn Rendu, Rodrick Montjean, Charles Coutton, et al.Journal of Science and Medicine in Sport|May 31, 2020
Variations in the TRPV1 gene are associated to exertional heat strokeCaroline Bosson, John Rendu, Laurent Pelletier, et al.Skeletal Muscle|September 21, 2018
Deletion of the microtubule-associated protein 6 (MAP6) results in skeletal muscle dysfunctionMuriel Sébastien, Benoit Giannesini, Perrine Aubin, et al.Journal of Neuromuscular Diseases|November 19, 2016
Functional Characterization of a Central Core Disease RyR1 Mutation (p.Y4864H) Associated with Quantitative Defect in RyR1 ProteinMarine Cacheux, Ariane Blum, Muriel Sébastien, et al.Human Gene Therapy|June 29, 2013
Exon skipping as a therapeutic strategy applied to an RYR1 mutation with pseudo-exon inclusion causing a severe core myopathyJohn Rendu, Julie Brocard, Eric Denarier, et al.Pageof 3