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