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