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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
47
Publications avec texte intégral
Open Access
58 %
Mots clés
HIV
Skeletal muscle
Electrocardiography
Muscle regeneration
Muscular dystrophy
Hutchinson-Gilford progeria syndrome
CMS
Ethnobotany
Distal myopathy
Genetics research
Calcium
Cardiomyopathies
Emery-Dreifuss muscular dystrophy
Dilated cardiomyopathy
Cellules musculaires lisses vasculaires
Development
Animal model
C9ORF72
Fusion
Emerin
Fibrin
Agrin
Acetyltransferase
CLS
Bioengineering
ALS amyotrophic lateral sclerosis
FTD frontotemporal dementia
Apoptosis
Anthropology
Congenital myasthenic syndrome
Emery-Dreifuss Muscular Dystrophy type 2 EDMD2
Cardiovascular disease
Ethnobotanique
H-Adrenergic
Lamin
Canine
Guyane Francaise
CyTOF
Expression
High-throughput screening
Deficiency
Aging
Electrophysiology
Cardiac conduction system
Chromosome 1q
France
ALS HDAC motor neuron neuromuscular junction reinnervation
HBV
Cellules satellite
Emery-Dreifuss muscular dystrophy EDMD
Emery–Dreifuss muscular dystrophy
Genetic background
Epizootic
Ca 2+ sensitivity
Satellite cells
A-type lamins
Dp71
ERK1/2 signaling
Physiopathologic mechanism muscular dystrophy
Sarcolipin
Cardiomyopathy
Frank-Starling law
Cofilin-1
Calcium handling
Cardiology
Biophysique
Nuclear envelope
LMNA gene
Autophagy/lysosomal pathway
Energy metabolism
Neuromuscular disease
LMNA
Anthropologie
Bioingénierie
Butyrylcholinesterase
Drug repurposing
Dog
Cardiomyopathie
Epidemiology
Progeria
Actin
Domestic
Connexin
Covid 19
Defibrillators
Hésitation vaccinale
Dental infection
DMD
Dystrophin
Genome organization
Cellules souches
French Guiana
Antilles Françaises
Biomatériaux
Dilated Cardiomyopathy CMD1A
French West Indies
Death
Confinement
Channelopathies
Microtubules