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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 with fulltext
Open Access
58 %
Mots clés
French Guiana
Physiopathologic mechanism muscular dystrophy
C9ORF72
Cardiology
Cellules souches
CMS
Cellules satellite
FTD frontotemporal dementia
Emery-Dreifuss muscular dystrophy
LMNA gene
Autophagy/lysosomal pathway
ALS HDAC motor neuron neuromuscular junction reinnervation
Emerin
Cardiomyopathie
CLS
ERK1/2 signaling
Dp71
Cellules musculaires lisses vasculaires
Acetyltransferase
Dental infection
CyTOF
Apoptosis
French West Indies
Hésitation vaccinale
Actin
Calcium handling
Confinement
HBV
Chromosome 1q
Antilles Françaises
Domestic
Cardiovascular disease
Cardiomyopathy
High-throughput screening
Lamin
Skeletal muscle
Deficiency
Fusion
Death
Emery–Dreifuss muscular dystrophy
Electrocardiography
Guyane Francaise
Microtubules
Animal model
ALS amyotrophic lateral sclerosis
Hutchinson-Gilford progeria syndrome
Electrophysiology
Connexin
Epidemiology
Muscle regeneration
Muscular dystrophy
Dystrophin
Cardiomyopathies
Covid 19
Bioingénierie
Genome organization
Biophysique
H-Adrenergic
Genetics research
Frank-Starling law
Defibrillators
Calcium
Dilated cardiomyopathy
Progeria
Agrin
Congenital myasthenic syndrome
Ethnobotany
Dilated Cardiomyopathy CMD1A
Ethnobotanique
Distal myopathy
Cardiac conduction system
France
Biomatériaux
LMNA
Development
Anthropology
DMD
A-type lamins
Aging
Emery-Dreifuss muscular dystrophy EDMD
Bioengineering
Channelopathies
Canine
Epizootic
Ca 2+ sensitivity
Satellite cells
Genetic background
Expression
Drug repurposing
Fibrin
HIV
Energy metabolism
Cofilin-1
Sarcolipin
Butyrylcholinesterase
Anthropologie
Emery-Dreifuss Muscular Dystrophy type 2 EDMD2
Neuromuscular disease
Dog
Nuclear envelope