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Diseases Jonction neuromusculaire JNM Dystrophie Musculaire de Becker BMD Dystrophin central domain Connexins Calcium Channels Human Umbilical Vein Endothelial Cells Dilated Cardiomyopathy CaVβs Hepatocellular carcinoma Becker muscular dystrophy MiARN Dystrophie Musculaire de Duchenne DMD Multi exon skipping Mitochondrial fission Immunoglobulin Fc Fragments/pharmacology Autophagy Long noncoding RNA Inbred mdx Ex-vivo Adult muscle stem cells Isoformes Cardiomyopathy Isoforms Cells Becker BMD muscular dystrophy Animals Epigenetics Inhibitors Hear Liver Cachexia Gene Expression Regulation/drug effects Multi resolution modeling Metabolism Duchenne DMD dystrophy L-Type Dystrophine Activin Receptors Cell Biology LKB1 Morphogenesis Allele‐specific silencing therapy Becker muscular dystrophy BMD Base Sequence Muscle Biology Cell homeostasis DHPR α1S Knockout LncARN Molecular docking Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS Mdx mouse Male Drp1 LncRNA Delivery Dystrophin-EGFP Genomic Energy Metabolism/drug effects CaVβ1 Modificateurs de gènes Duchenne muscular dystrophy DMD Becker Muscular Dystrophy Skeletal muscle Long QT DMD Heart Failure Dynamin 2 Dystrophie myotonique de type 1 DM1 Animal/physiopathology Antisense oligonucleotides Duchenne muscular dystrophy Humans Calcium Invivo Génomique Gene expression Centronuclear myopathy Gene modifiers Cultured Dystrophie musculaire de Becker Cardiomyopathie Multiresolution modeling DMO Dystrophin Cell Line CD38 Exon skipping Clinical trials Inbred C57BL BMD CaV subunits Homeostasis Mice Dystrophy Muscle CTNNB1 MES Molecular Sequence Data