Alternative splicing CRISPR/Cas9 Becker muscular dystrophy RNA interference Exon Skipping CDNA synthesis Gene therapy Canine X-linked muscular dystrophy in Japan CXMD J Neuromuscular disease Human muscle stem/progenitor cells Human Gel electrophoresis Cell Therapy Flavonoid Adeno-associated viral vector Antisense oligonucleotide Muscle Myotonic dystrophy Culture platform Immortalized dystrophic canine myoblast Clinical trial candidate screening Immortalisation Laminographie Allele-specific silencing therapy Autophagosome Dynamin 2 Emerin Biomimetism Lamin A/C nuclei Motor neuron Allele-specific silencing Adhesion KLF15 DsDNA break repair 3D co-culture Autophagy Neuromuscular junction Drisapersen Fibroblast Coculture DiPRO1 CMS DM1 myoblasts Dystrophin Developmental biology Eteplirsen Folding-defective proteins LRP4 Cell-penetrating peptide Fibrosis Bioinformatics Gut microbiota ICU-acquired weakness Exon-skipping HDMD/Dmd-null mice BMD Centronuclear myopathy Genetics Exon skipping Duchenne muscular dystrophy Glucose Differentiation CTG⋅CAGn repeat Gene network analysis Myotube Myogenesis Endocytosis Human artificial chromosomes BAF Chromatin FoxO Acetylcholine receptor subunit epsilon Actin Insulin Glucocorticoid-induced muscle atrophy CLS Conjugation Gene Therapy Exondys 51 Cell biology DNM2 LTβR Lamina-associated domain Dominant centronuclear myopathy Fear response CXCL12 Migration Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS Antisense morpholino DMD CXCR4 FSHD ITSN1 Atrial cardiac defects Expanded repeats Computer software CFTR correctors Duchenne Muscular Dystrophy Skeletal muscle Bile acid