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

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