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