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