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