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