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