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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
59 %
Mots clés
Autophagy/lysosomal pathway
Dog
Emery-Dreifuss Muscular Dystrophy type 2 EDMD2
Cellules satellite
Deficiency
Actin
Anthropologie
Calcium
Expression
A-type lamins
Genome organization
Biophysique
Butyrylcholinesterase
DMD
Cardiomyopathie
H-Adrenergic
Neuromuscular disease
Frank-Starling law
Energy metabolism
Ca 2+ sensitivity
Canine
French West Indies
Epizootic
Covid 19
Genetic background
CyTOF
Genetics research
Death
CMS
CLS
Cofilin-1
Physiopathologic mechanism muscular dystrophy
Bioingénierie
Dp71
Dystrophin
Electrophysiology
Hésitation vaccinale
HIV
Cardiac conduction system
Muscle regeneration
Ethnobotanique
Confinement
C9ORF72
Fusion
Bioengineering
Congenital myasthenic syndrome
Cardiomyopathy
Emery-Dreifuss muscular dystrophy
Drug repurposing
ERK1/2 signaling
Fibrin
ALS amyotrophic lateral sclerosis
Ethnobotany
Emerin
Nuclear envelope
Dilated cardiomyopathy
Anthropology
Animal model
HBV
Cellules musculaires lisses vasculaires
Emery–Dreifuss muscular dystrophy
Guyane Francaise
Microtubules
Chromosome 1q
Distal myopathy
Agrin
Aging
Sarcolipin
Cellules souches
FTD frontotemporal dementia
Skeletal muscle
Epidemiology
Biomatériaux
Acetyltransferase
Development
Satellite cells
Emery-Dreifuss muscular dystrophy EDMD
Cardiology
Channelopathies
Defibrillators
ALS HDAC motor neuron neuromuscular junction reinnervation
Domestic
Electrocardiography
LMNA gene
Lamin
Antilles Françaises
High-throughput screening
LMNA
Progeria
Cardiovascular disease
Calcium handling
Dental infection
Hutchinson-Gilford progeria syndrome
Dilated Cardiomyopathy CMD1A
Apoptosis
France
Cardiomyopathies
Connexin
Muscular dystrophy
French Guiana