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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⟩
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Mark R Viggars, Daniel Owens, Claire Stewart, Catherine Coirault, Abigail L Mackey, et al.. PCM1 labelling reveals myonuclear and nuclear dynamics in skeletal muscle across species. American Journal of Physiology - Cell Physiology, 2022, Online ahead of print. ⟨10.1152/ajpcell.00285.2022⟩. ⟨inserm-03852473⟩
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Chiffres clés
80
Publications with fulltext
Open Access
55 %
Mots clés
Adeno-associated virus vector
Atrial cardiac defects
Dominant centronuclear myopathy
Alpha-actinin-2
Cellular neuroscience
Allele-specific silencing therapy
Antisense oligonucleotides
RNA interference
Adhesion
BAR proteins
Adult patients
Cell proliferation
Dystrophie musculaire d'Emery Dreifuss
Adeno-associated virus
Gene therapy
Amphiphysin
Caveolin
Congenital myopathy
Mechanotransduction
DMyHC
Cancer
Cavins
CTL
Myopathie
Disease modifiers
Adeno-Associated virus
Cytoskeleton
Allele specific RNA interference
Cytosquelette
Biophysics
Cell migration
Cross-presentation
Duchenne muscular dystrophy
Dynamine
Atrial heart defects
Cellules de crête neurale
Duchenne muscular dystrophy DMD
AAV
Developmental myosin heavy chain
BMP signaling
A-type lamins
Muscular dystrophy
Disease heterogeneity
BAF
Coeur
AFM
Nucleus
CAV-3 gene
Animal models of human disease
Neural crest cells
Diaphragm
Skin
Autophagosome
Clathrine
Outflow tract
Ctdnep1
Actin nucleus
Nuclear envelope
Charcot-Marie-Tooth
AAV8
Satellite cell
Dynamin 2
Nesprin
Allele‐specific silencing therapy
AD-CNM
Biomarkers
Dynamin
Allele-specific silencing
Migration
Dystrophie musculaire de Duchenne
Core myopathy
Becker muscular dystrophy BMD
Correlative microscopy
Caveolae
Cardiotoxin
Caveolins
Cell signaling
DNM2
ACTN2
Cardiomyopathies
Autophagy
Muscle
Lamin
Endocytosis
Cross-bridge kinetics
Autophagosome maturation
Developmental biology
Clathrin
Dullard
Domaine LEM
Autophagy cellular
Autosomal dominant centronuclear myopathy
Actin
Cavéoles
Dynamin overexpression
Myopathy
Skeletal muscle
Myosin
Duchenne Muscular Dystrophy
Centronuclear myopathy