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