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