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