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