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