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