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Dernières publications
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Pauline Garcia, William Jarassier, Caroline Brun, Lorenzo Giordani, Fany Agostini, et al.. Setdb1 protects genome integrity in murine muscle stem cells to allow for regenerative myogenesis and inflammation. Developmental Cell, 2024, 59 (17), pp.2375-2392.e8. ⟨10.1016/j.devcel.2024.05.012⟩. ⟨hal-04747691⟩
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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⟩
Chiffres clés
48
Publications avec texte intégral
Open Access
59 %
Mots clés
Epizootic
Butyrylcholinesterase
Muscular dystrophy
Biomatériaux
Electrophysiology
Development
Autophagy/lysosomal pathway
Guyane Francaise
Actin
Connexin
Genome organization
Bioingénierie
French Guiana
Fusion
High-throughput screening
Antilles Françaises
ERK1/2 signaling
Physiopathologic mechanism muscular dystrophy
HBV
Biophysique
CLS
CMS
C9ORF72
Cellules souches
Fibrin
Dystrophin
Hésitation vaccinale
Ethnobotanique
Congenital myasthenic syndrome
Ethnobotany
Dog
Defibrillators
Muscle regeneration
DMD
Cellules musculaires lisses vasculaires
Satellite cells
H-Adrenergic
Neuromuscular disease
Skeletal muscle
Calcium handling
Cardiomyopathie
Anthropologie
Cardiomyopathies
FTD frontotemporal dementia
Epidemiology
Frank-Starling law
Channelopathies
Drug repurposing
Ca 2+ sensitivity
ALS amyotrophic lateral sclerosis
LMNA gene
Emery-Dreifuss muscular dystrophy
Distal myopathy
A-type lamins
Confinement
Calcium
Cardiology
Energy metabolism
Expression
Cardiomyopathy
Bioengineering
Canine
Genetics research
Hutchinson-Gilford progeria syndrome
Acetyltransferase
Cofilin-1
Emery–Dreifuss muscular dystrophy
Animal model
Sarcolipin
Death
Apoptosis
Genetic background
French West Indies
Cardiac conduction system
Dp71
LMNA
CyTOF
Dilated cardiomyopathy
HIV
Dental infection
Emerin
Cardiovascular disease
France
Deficiency
Lamin
ALS HDAC motor neuron neuromuscular junction reinnervation
Progeria
Emery-Dreifuss muscular dystrophy EDMD
Aging
Dilated Cardiomyopathy CMD1A
Cellules satellite
Domestic
Covid 19
Agrin
Anthropology
Chromosome 1q
Emery-Dreifuss Muscular Dystrophy type 2 EDMD2
Electrocardiography
Microtubules
Nuclear envelope