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