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