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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
49
Publications avec texte intégral
Open Access
59 %
Mots clés
Death
Electrophysiology
Dental infection
Electrocardiography
Endogeneous retrovirus
France
ALS HDAC motor neuron neuromuscular junction reinnervation
Cellules musculaires lisses vasculaires
Biomatériaux
Emerin
Emery-Dreifuss muscular dystrophy EDMD
Development
Ethnobotanique
CGAS-STING pathway
Genetics research
Emery-Dreifuss muscular dystrophy
ALS amyotrophic lateral sclerosis
Acetyltransferase
Confinement
Defibrillators
Emery-Dreifuss Muscular Dystrophy type 2 EDMD2
LMNA gene
Satellite cells
Domestic
GSE84016
H-Adrenergic
Progeria
Anthropology
Congenital myasthenic syndrome
Energy metabolism
Connexin
Distal myopathy
Biophysique
Animal model
Calcium handling
Lamin
HIV
Nuclear envelope
CLS
Cardiac conduction system
Dilated cardiomyopathy
Muscle regeneration
A-type lamins
Guyane Francaise
Epizootic
Genetic background
Dystrophin
Deficiency
Aging
Cardiovascular disease
C9ORF72
Dog
Drug repurposing
Fibrin
ERK1/2 signaling
Microtubules
DMD
Autophagy/lysosomal pathway
Canine
Actin
Ca 2+ sensitivity
Neuromuscular disease
Bioingénierie
Epidemiology
French West Indies
Skeletal muscle
Covid 19
Cardiomyopathies
LMNA
Cardiomyopathie
Dilated Cardiomyopathy CMD1A
HBV
Anthropologie
Channelopathies
Physiopathologic mechanism muscular dystrophy
Cellules satellite
Muscular dystrophy
Dp71
Fusion
French Guiana
Cellules souches
Agrin
Sarcolipin
Ethnobotany
Cofilin-1
Cardiology
Frank-Starling law
Chromosome 1q
CyTOF
Antilles Françaises
Calcium
Bioengineering
Expression
Cardiomyopathy
Butyrylcholinesterase
Apoptosis
CMS
Emery–Dreifuss muscular dystrophy
FTD frontotemporal dementia
Genome organization