Human muscle stem/progenitor cells KLF15 Developmental biology Insulin Mitochondrial ROS Actin Duchenne muscular dystrophy Coculture Acetylcholine receptor subunit epsilon Bile acid CLS Immortalized dystrophic canine myoblast Lamin A/C nuclei RNA interference Lamina-associated domain Differentiation Myogenesis Mechano-transduction Antisense morpholino Centronuclear myopathy Muscle Gel electrophoresis DNM2 Clinical trial candidate screening 3D co-culture BMD DsDNA break repair Eteplirsen Endocytosis Dominant centronuclear myopathy Autophagy Exondys 51 LTβR Microarray Dystrophin Lymphotoxin-β-receptor Autophagosome Cell-penetrating peptide Chromatin Motor neuron Human FoxO Conjugation ICU-acquired weakness Becker muscular dystrophy CRISPR/Cas9 Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS Fibroblast Exon-skipping Dynamin 2 HDMD/Dmd-null mice Migration BAF Adeno-associated viral vector Computer software Mdx52 mice LRP4 DMD CFTR correctors CTG⋅CAGn repeat Fibrosis Mechanisms of disease Allele-specific silencing Drisapersen Expanded repeats Myotonic dystrophy Gut microbiota Myotube Glucocorticoid-induced muscle atrophy Antisense oligonucleotide MSCs FSHD Machine learning Cell biology Immortalisation CXCL12 Glucose Emerin Laminographie CXCR4 DM1 myoblasts Neuromuscular junction Allele-specific silencing therapy CMS Human artificial chromosomes Flavonoid Mdx MT RNA/DNA Editing Alternative splicing Gene therapy Gene network analysis ITSN1 Fear response Atrial cardiac defects Skeletal muscle Folding-defective proteins Canine X-linked muscular dystrophy in Japan CXMD J Exon skipping Adhesion CDNA synthesis