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

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