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