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