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