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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⟩
Chiffres clés
82
Publications avec texte intégral
Open Access
55 %
Mots clés
Amphiphysin
Dystrophie musculaire de Duchenne
Adeno-associated virus
Antisense oligonucleotides
Cell signaling
Skeletal muscle
AAV
Cavins
Dullard
Neural crest cells
Adeno-Associated virus
Cellules de crête neurale
Core myopathy
Dynamin overexpression
Cytosquelette
Autophagosome
Dynamine
Domaine LEM
Developmental myosin heavy chain
Nesprin
Allele specific RNA interference
Cross-presentation
Atrial cardiac defects
Cellular neuroscience
RNA interference
Cardiotoxin
Nucleus
Clathrine
Nuclear envelope
Muscular dystrophy
Endocytosis
Alpha-actinin-2
A-type lamins
AAV8
Autophagosome maturation
Migration
DMyHC
Caveolae
Diaphragm
Adeno-associated virus vector
Actin nucleus
Dynamin 2
Cavéoles
Coeur
Biophysics
Biomarkers
Charcot-Marie-Tooth
Satellite cell
Autophagy
Clathrin
BMP signaling
Duchenne Muscular Dystrophy
Allele‐specific silencing therapy
Cardiomyopathies
Animal models of human disease
DNM2
Cancer
Ctdnep1
Autosomal dominant centronuclear myopathy
Dystrophie musculaire d'Emery Dreifuss
AFM
Adhesion
Allele-specific silencing
Caveolin
BAR proteins
AD-CNM
Caveolins
Myopathy
CAV-3 gene
Dynamin
Duchenne muscular dystrophy
Myosin
Outflow tract
Cytoskeleton
Cell proliferation
BAF
Cell migration
Correlative microscopy
Disease heterogeneity
Lamin
Muscle
Myopathie
Actin
Allele-specific silencing therapy
Duchenne muscular dystrophy DMD
Dominant centronuclear myopathy
Disease modifiers
CTL
Skin
Mechanotransduction
Adult patients
Cross-bridge kinetics
Congenital myopathy
ACTN2
Atrial heart defects
Developmental biology
Gene therapy
Becker muscular dystrophy BMD
Centronuclear myopathy
Autophagy cellular