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