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