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