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