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