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