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