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