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Dernières publications
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Caroline Le Dour, Maria Chatzifrangkeskou, Coline Macquart, Maria M Magiera, Cécile Peccate, et al.. Actin-microtubule cytoskeletal interplay mediated by MRTF-A/SRF signaling promotes dilated cardiomyopathy caused by LMNA mutations. Nature Communications, 2022, 13 (1), pp.7886. ⟨10.1038/s41467-022-35639-x⟩. ⟨hal-03921784⟩
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Clémence Labasse, Guy Brochier, Ana-Lia Taratuto, Bruno Cadot, John Rendu, et al.. Severe ACTA1-related nemaline myopathy: intranuclear rods, cytoplasmic bodies, and enlarged perinuclear space as characteristic pathological features on muscle biopsies. Acta Neuropathologica Communications, 2022, 10 (1), pp.101. ⟨10.1186/s40478-022-01400-0⟩. ⟨hal-03820052⟩
Chiffres clés
83
Publications avec texte intégral
Open Access
55 %
Mots clés
Caveolin
Cell proliferation
Autosomal dominant centronuclear myopathy
Clathrin
AAV
Autophagosome maturation
Autophagy
Allele specific RNA interference
Satellite cell
RNA interference
Duchenne Muscular Dystrophy
Cell migration
Autophagy cellular
Ctdnep1
Charcot-Marie-Tooth
A-type lamins
Biomarkers
Cellules de crête neurale
Myopathie
ACTN2
Neural crest cells
CTL
Cross-bridge kinetics
Cardiotoxin
Animal models of human disease
Endocytosis
Caveolins
Mechanotransduction
Dullard
Dominant centronuclear myopathy
Dynamine
Dynamin
Cardiomyopathies
Skin
Adeno-associated virus
Correlative microscopy
Amphiphysin
Diaphragm
Myosin
Outflow tract
Lamin
Disease modifiers
BAR proteins
Cancer
Allele‐specific silencing therapy
Dystrophie musculaire de Duchenne
Cell signaling
Nesprin
Developmental myosin heavy chain
Adeno-associated virus vector
Caveolae
Duchenne muscular dystrophy
Dynamin 2
Nuclear envelope
Myopathy
Cross-presentation
Allele-specific silencing
Cytoskeleton
Cavins
Cavéoles
CAV-3 gene
AAV8
Skeletal muscle
Dystrophie musculaire d'Emery Dreifuss
BAF
Actin nucleus
Disease heterogeneity
Antisense oligonucleotides
Allele-specific silencing therapy
Atrial heart defects
Cytosquelette
Domaine LEM
Biophysics
Alpha-actinin-2
Atrial cardiac defects
Core myopathy
DMyHC
Muscular dystrophy
Gene therapy
Clathrine
Centronuclear myopathy
DNM2
Dynamin overexpression
Adult patients
Actin
Cellular neuroscience
BMP signaling
AFM
AD-CNM
Developmental biology
Muscle
Coeur
Duchenne muscular dystrophy DMD
Becker muscular dystrophy BMD
Adeno-Associated virus
Adhesion
Migration
Congenital myopathy
Nucleus
Autophagosome