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