Loading...
Dernières publications
-
-
-
-
-
Édouard Berling, Camille Verebi, Nadia Venturelli, Stéphane Vassilopoulos, Anthony Béhin, et al.. Caveolinopathy: Clinical, histological, and muscle imaging features and follow-up in a multicenter retrospective cohort. European Journal of Neurology, 2023, 30 (8), p.2506-2517. ⟨10.1111/ene.15832⟩. ⟨hal-04190879⟩
-
-
-
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⟩
-
-
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
84
Publications avec texte intégral
Open Access
55 %
Mots clés
Allele-specific silencing
Autophagy cellular
Dynamin overexpression
Atrial heart defects
Nesprin
Clathrine
RNA interference
Actin nucleus
Allele‐specific silencing therapy
Skin
Muscle
Correlative microscopy
Outflow tract
Antisense oligonucleotides
Cell proliferation
Myosin
Duchenne Muscular Dystrophy
Adeno-associated virus vector
Cellules de crête neurale
Migration
Muscular dystrophy
Dynamin
Actin
AD-CNM
AAV8
AAV
Domaine LEM
Neural crest cells
Skeletal muscle
Duchenne muscular dystrophy
Cross-presentation
Disease heterogeneity
Charcot-Marie-Tooth
AFM
Atrial cardiac defects
Caveolins
Mechanotransduction
Cardiomyopathies
Lamin
Congenital myopathy
Autophagosome maturation
Dominant centronuclear myopathy
Developmental biology
Nuclear envelope
BMP signaling
Cavins
Cytosquelette
Allele specific RNA interference
Ctdnep1
Cell signaling
Nucleus
Biomarkers
Dynamin 2
Autophagy
DMyHC
Diaphragm
Adult patients
Cell migration
Centronuclear myopathy
Gene therapy
BAR proteins
Developmental myosin heavy chain
CTL
Animal models of human disease
Cytoskeleton
Autosomal dominant centronuclear myopathy
Caveolae
Cavéoles
Allele-specific silencing therapy
Coeur
CAV3
Dullard
Satellite cell
Duchenne muscular dystrophy DMD
CAV-3 gene
Dynamine
Adhesion
Adeno-associated virus
Clathrin
A-type lamins
Core myopathy
Biophysics
Caveolin
Adeno-Associated virus
ACTN2
Amphiphysin
Myopathie
Autophagosome
Endocytosis
Becker muscular dystrophy BMD
Cardiotoxin
DNM2
BAF
Disease modifiers
Cancer
Myopathy
Caveolin-3
Cross-bridge kinetics
Cellular neuroscience
Alpha-actinin-2