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