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