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