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