MT RNA/DNA Editing CLS Skeletal muscle ITSN1 Exondys 51 Adeno-associated viral vector Immortalisation Glucose FSHD Coculture Computer software Myotonic dystrophy Mechanisms of disease LTβR LRP4 FoxO Acetylcholine receptor subunit epsilon HDMD/Dmd-null mice CFTR correctors Fibrosis Laminographie Allele-specific silencing ICU-acquired weakness Expanded repeats Differentiation DNM2 Autophagosome Canine X-linked muscular dystrophy in Japan CXMD J Clinical trial candidate screening Flavonoid Lymphotoxin-β-receptor CTG⋅CAGn repeat Immortalized dystrophic canine myoblast Atrial cardiac defects Migration Glucocorticoid-induced muscle atrophy Becker muscular dystrophy CRISPR/Cas9 Gene network analysis Emerin Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS Antisense oligonucleotide Alternative splicing Gel electrophoresis Myotube Exon-skipping CMS Lamina-associated domain CDNA synthesis Adhesion RNA interference Endocytosis Duchenne muscular dystrophy Neuromuscular junction Mdx Antisense morpholino MSCs DM1 myoblasts Cell-penetrating peptide Drisapersen Human artificial chromosomes Human muscle stem/progenitor cells DsDNA break repair Muscle CXCR4 Microarray Folding-defective proteins Dominant centronuclear myopathy Machine learning Dystrophin BMD Myogenesis CXCL12 Chromatin Gene therapy Allele-specific silencing therapy Lamin A/C nuclei Actin Fear response KLF15 Eteplirsen Mechano-transduction 3D co-culture Cell biology Mitochondrial ROS Bile acid Autophagy Motor neuron Human Gut microbiota Conjugation Exon skipping Developmental biology Mdx52 mice Insulin Fibroblast Dynamin 2 BAF DMD Centronuclear myopathy