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