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