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