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