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

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