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