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