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

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