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