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