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