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Dernières publications
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Marion Masingue, Olivia Cattaneo, Nicolas Wolff, Céline Buon, Damien Sternberg, et al.. New mutation in the β1 propeller domain of LRP4 responsible for congenital myasthenic syndrome associated with Cenani–Lenz syndrome. Scientific Reports, 2023, 13 (1), pp.14054. ⟨10.1038/s41598-023-41008-5⟩. ⟨hal-04191765⟩
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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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Nicolas Vignier, Maria Chatzifrangkeskou, Luca Pinton, Hugo Wioland, Thibaut Marais, et al.. The non-muscle ADF/cofilin-1 controls sarcomeric actin filament integrity and force production in striated muscle laminopathies. Cell Reports, 2021, 36 (8), pp.109601. ⟨10.1016/j.celrep.2021.109601⟩. ⟨hal-03350074⟩
Chiffres clés
46
Publications avec texte intégral
Open Access
58 %
Mots clés
LMNA gene
H-Adrenergic
Distal myopathy
Dilated Cardiomyopathy CMD1A
Deficiency
Dystrophin
CMS
Dilated cardiomyopathy
Epizootic
Animal model
Cellules musculaires lisses vasculaires
French West Indies
Bioengineering
Actin
Cardiomyopathy
Apoptosis
Energy metabolism
Cardiovascular disease
Cardiology
ERK1/2 signaling
Physiopathologic mechanism muscular dystrophy
C9ORF72
Anthropology
ALS amyotrophic lateral sclerosis
Expression
Hésitation vaccinale
French Guiana
CyTOF
Fibrin
Microtubules
Emery-Dreifuss muscular dystrophy
Hutchinson-Gilford progeria syndrome
Agrin
Covid 19
Autophagy/lysosomal pathway
Biophysique
Chromosome 1q
Genetics research
Dental infection
Genetic background
Satellite cells
DMD
Dog
Guyane Francaise
A-type lamins
Progeria
Ca 2+ sensitivity
Nuclear envelope
CLS
Frank-Starling law
Emery-Dreifuss muscular dystrophy EDMD
Development
Lamin
Emerin
Dp71
Death
FTD frontotemporal dementia
Electrophysiology
Cardiac conduction system
Cardiomyopathie
Canine
Muscular dystrophy
Connexin
Confinement
Acetyltransferase
Channelopathies
Defibrillators
Drug repurposing
Genome organization
Sarcolipin
Cardiomyopathies
Emery–Dreifuss muscular dystrophy
Bioingénierie
Epidemiology
ALS HDAC motor neuron neuromuscular junction reinnervation
Cofilin-1
Emery-Dreifuss Muscular Dystrophy type 2 EDMD2
HIV
Muscle regeneration
Calcium
HBV
Calcium handling
Domestic
Aging
Ethnobotanique
France
Biomatériaux
Skeletal muscle
High-throughput screening
Cellules souches
Fusion
Neuromuscular disease
Butyrylcholinesterase
Ethnobotany
Anthropologie
Cellules satellite
Antilles Françaises
Congenital myasthenic syndrome
Electrocardiography
LMNA