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