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