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