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