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