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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 with fulltext
Open Access
58 %
Mots clés
Frank-Starling law
Actin
Bioengineering
Domestic
Dental infection
Muscle regeneration
Anthropology
Dystrophin
Genetic background
Dilated cardiomyopathy
CMS
ALS HDAC motor neuron neuromuscular junction reinnervation
Aging
Electrocardiography
Sarcolipin
Cellules satellite
Neuromuscular disease
Guyane Francaise
Drug repurposing
Dilated Cardiomyopathy CMD1A
Fibrin
Acetyltransferase
Antilles Françaises
Butyrylcholinesterase
Cardiovascular disease
Epizootic
Canine
Connexin
Animal model
Cardiomyopathies
Emery-Dreifuss muscular dystrophy
Ethnobotanique
Cofilin-1
Ca 2+ sensitivity
Biophysique
ALS amyotrophic lateral sclerosis
Anthropologie
H-Adrenergic
Genome organization
Congenital myasthenic syndrome
Fusion
Development
Ethnobotany
Bioingénierie
Cardiology
Microtubules
Physiopathologic mechanism muscular dystrophy
Dp71
Apoptosis
Emery-Dreifuss Muscular Dystrophy type 2 EDMD2
Cardiac conduction system
Epidemiology
Deficiency
Distal myopathy
Cardiomyopathie
Nuclear envelope
CyTOF
Cellules souches
DMD
Emerin
Emery–Dreifuss muscular dystrophy
ERK1/2 signaling
Hésitation vaccinale
Defibrillators
LMNA
A-type lamins
Skeletal muscle
LMNA gene
Agrin
Energy metabolism
French Guiana
Progeria
Cardiomyopathy
CLS
Muscular dystrophy
Expression
Satellite cells
Genetics research
Autophagy/lysosomal pathway
Calcium handling
Biomatériaux
France
Chromosome 1q
HBV
French West Indies
Hutchinson-Gilford progeria syndrome
Channelopathies
High-throughput screening
HIV
Electrophysiology
Lamin
FTD frontotemporal dementia
Calcium
Cellules musculaires lisses vasculaires
Dog
Confinement
C9ORF72
Emery-Dreifuss muscular dystrophy EDMD
Covid 19
Death