Cancer Nesprin Animal models of human disease Centronuclear myopathy Domaine LEM CTL Lamin RNA interference Allele‐specific silencing therapy Endocytosis Actin nucleus Adeno-Associated virus Dystrophie musculaire de Duchenne Adhesion Dystrophin Congenital myopathy Diaphragm Outflow tract Alpha-actinin-2 Duchenne muscular dystrophy CAV-3 gene Dullard Myopathy Clathrine Charcot-Marie-Tooth Cellular neuroscience Mechanotransduction Myopathie BMP signaling Dominant centronuclear myopathy Skeletal muscle Dynamin overexpression Skin Dynamin 2 Muscle Cross-bridge kinetics Cardiomyopathies Neural crest cells Nucleus Myosin DNM2 Cell migration Gene therapy Clathrin Caveolins Amphiphysin A-type lamins Biophysics BAF Cytoskeleton Actin Allele specific RNA interference Adult patients Autophagosome AD-CNM Adeno-associated virus vector ACTN2 Atrial cardiac defects Core myopathy Developmental myosin heavy chain Autosomal dominant centronuclear myopathy Atrial heart defects Cardiotoxin Antisense oligonucleotides Adeno-associated virus Cytosquelette Allele-specific silencing therapy AAV8 Biomarkers Dystrophie musculaire d'Emery Dreifuss Correlative microscopy DMyHC Ctdnep1 Autophagosome maturation AFM BAR proteins AAV Migration Coeur Disease heterogeneity Disease modifiers Muscular dystrophy Satellite cell Cross-presentation Nuclear envelope Cell proliferation Caveolae Becker muscular dystrophy BMD Allele-specific silencing Dynamine Dynamin Cavins Developmental biology Cellules de crête neurale Caveolin Cell signaling Cavéoles Autophagy Duchenne Muscular Dystrophy Duchenne muscular dystrophy DMD