index - Organisation de la cellule musculaire et thérapie de la myopathie centronucléaire autosomique dominante

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