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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
47
Publications avec texte intégral
Open Access
58 %
Mots clés
Lamin
Hutchinson-Gilford progeria syndrome
Anthropologie
FTD frontotemporal dementia
France
LMNA
CMS
Cardiac conduction system
Dilated Cardiomyopathy CMD1A
Cardiomyopathie
Dystrophin
Anthropology
Apoptosis
Drug repurposing
HBV
Domestic
CLS
Cellules souches
Cellules satellite
Muscle regeneration
High-throughput screening
Fibrin
Progeria
Biomatériaux
Emery-Dreifuss muscular dystrophy EDMD
Cofilin-1
Bioengineering
Muscular dystrophy
Death
Covid 19
Fusion
Guyane Francaise
CyTOF
Biophysique
Ethnobotany
Congenital myasthenic syndrome
Nuclear envelope
Emery-Dreifuss muscular dystrophy
Dp71
Chromosome 1q
Antilles Françaises
Hésitation vaccinale
Defibrillators
Deficiency
Emery-Dreifuss Muscular Dystrophy type 2 EDMD2
Cellules musculaires lisses vasculaires
Animal model
Ethnobotanique
Physiopathologic mechanism muscular dystrophy
Sarcolipin
Actin
Confinement
Genome organization
Dilated cardiomyopathy
Skeletal muscle
Aging
Expression
Canine
Epizootic
Neuromuscular disease
Frank-Starling law
Cardiovascular disease
Microtubules
H-Adrenergic
Energy metabolism
Bioingénierie
Dog
Electrophysiology
Cardiomyopathies
Epidemiology
Agrin
Calcium handling
French Guiana
Butyrylcholinesterase
ALS HDAC motor neuron neuromuscular junction reinnervation
ALS amyotrophic lateral sclerosis
ERK1/2 signaling
C9ORF72
LMNA gene
Genetic background
Development
Autophagy/lysosomal pathway
Emerin
A-type lamins
Emery–Dreifuss muscular dystrophy
Dental infection
French West Indies
Genetics research
Cardiology
Connexin
Ca 2+ sensitivity
Electrocardiography
Satellite cells
Cardiomyopathy
Channelopathies
DMD
HIV
Distal myopathy
Calcium
Acetyltransferase