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