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