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