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