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