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