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