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