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