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