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