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Dernières publications
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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⟩
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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
84
Publications avec texte intégral
Open Access
55 %
Mots clés
RNA interference
AAV8
Dynamin 2
Caveolin-3
Atrial heart defects
Satellite cell
Gene therapy
Becker muscular dystrophy BMD
Autosomal dominant centronuclear myopathy
Developmental biology
Dynamine
Cardiotoxin
Clathrine
Adult patients
Cytosquelette
Dynamin overexpression
Muscle
Adeno-associated virus
Duchenne muscular dystrophy DMD
Dynamin
AFM
Actin
Cancer
Outflow tract
Cellules de crête neurale
Amphiphysin
Cytoskeleton
BAR proteins
Biomarkers
Alpha-actinin-2
Caveolin
Adeno-Associated virus
Skeletal muscle
CAV-3 gene
AAV
Caveolins
Duchenne Muscular Dystrophy
Core myopathy
Congenital myopathy
Nesprin
Cell migration
Autophagy
Autophagosome maturation
DNM2
Endocytosis
Muscular dystrophy
BAF
Nuclear envelope
Dominant centronuclear myopathy
Cell signaling
Dullard
Adhesion
Cardiomyopathies
Ctdnep1
ACTN2
Cross-bridge kinetics
Migration
Disease modifiers
Myosin
Lamin
BMP signaling
Allele-specific silencing
Domaine LEM
Nucleus
Coeur
CAV3
Atrial cardiac defects
Cellular neuroscience
Antisense oligonucleotides
Duchenne muscular dystrophy
Autophagy cellular
Adeno-associated virus vector
Skin
Charcot-Marie-Tooth
Cavéoles
Neural crest cells
Animal models of human disease
Biophysics
Developmental myosin heavy chain
Cavins
Allele‐specific silencing therapy
Diaphragm
Autophagosome
Cell proliferation
CTL
A-type lamins
Allele specific RNA interference
Mechanotransduction
Correlative microscopy
Myopathie
Actin nucleus
Myopathy
Allele-specific silencing therapy
AD-CNM
DMyHC
Disease heterogeneity
Cross-presentation
Clathrin
Centronuclear myopathy
Caveolae