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