index - Organisation de la cellule musculaire et thérapie de la myopathie centronucléaire autosomique dominante Accéder directement au contenu

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