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