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