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