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

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