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