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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
51
Publications avec texte intégral
Open Access
60 %
Mots clés
Aging
Epidemiology
Dilated Cardiomyopathy CMD1A
Endogeneous retrovirus
Drug repurposing
Bioingénierie
ERK1/2 signaling
Genome organization
Ca 2+ sensitivity
Epizootic
Biomatériaux
Apoptosis
Frank-Starling law
Actin
Congenital myasthenic syndrome
Energy metabolism
Progeria
Defibrillators
Dystrophin
Guyane Francaise
Dental infection
Cardiomyopathie
Cardiomyopathy
Ethnobotany
HBV
CGAS-STING pathway
Death
Nuclear envelope
Fibrin
Microtubules
Satellite cells
Cardiomyopathies
Biophysique
Acetyltransferase
Dilated cardiomyopathy
Agrin
Anthropologie
DMD
Confinement
Cofilin-1
Bioengineering
Expression
Cellules souches
Butyrylcholinesterase
Distal myopathy
Development
Dp71
France
Channelopathies
Domestic
Skeletal muscle
Muscle regeneration
C9ORF72
Genetic background
Deficiency
French Guiana
French West Indies
Covid 19
Muscular dystrophy
Cellules musculaires lisses vasculaires
Neuromuscular disease
Ethnobotanique
Calcium
Chromosome 1q
Electrophysiology
Autophagy/lysosomal pathway
Physiopathologic mechanism muscular dystrophy
Cellules satellite
Cardiovascular disease
Genetics research
Connexin
CLS
HIV
Calcium handling
LMNA
Emery-Dreifuss Muscular Dystrophy type 2 EDMD2
Lamin
FTD frontotemporal dementia
Antilles Françaises
Emery-Dreifuss muscular dystrophy
Electrocardiography
ALS amyotrophic lateral sclerosis
CyTOF
H-Adrenergic
LMNA gene
CMS
Dog
A-type lamins
Canine
Emerin
Sarcolipin
Emery–Dreifuss muscular dystrophy
Anthropology
Cardiology
ALS HDAC motor neuron neuromuscular junction reinnervation
GSE84016
Animal model
Cardiac conduction system
Emery-Dreifuss muscular dystrophy EDMD
Fusion