Get started
Author

Caroline Le Dour

Perilipin Deficiency and Autosomal Dominant Partial Lipodystrophy
2011 · Sheetal Gandotra, Caroline Le Dour, et al. · New England Journal of Medicine · 305
PDF
Molecular mechanisms of human lipodystrophies: From adipocyte lipid droplet to oxidative stress and lipotoxicity
2011 · Corinne Vigouroux, Martine Caron-Debarle, et al. · The International Journal of Biochemistry & Cell Biology · 147
ERK1/2 directly acts on CTGF/CCN2 expression to mediate myocardial fibrosis in cardiomyopathy caused by mutations in the lamin A/C gene
2016 · Maria Chatzifrangkeskou, Caroline Le Dour, et al. · Human Molecular Genetics · 103
PDF
LMNA Mutations Induce a Non-Inflammatory Fibrosis and a Brown Fat-Like Dystrophy of Enlarged Cervical Adipose Tissue
2011 · Véronique Béréziat, Pascale Cervera, et al. · American Journal Of Pathology · 74
PDF
Actin-microtubule cytoskeletal interplay mediated by MRTF-A/SRF signaling promotes dilated cardiomyopathy caused by LMNA mutations
2022 · Caroline Le Dour, Maria Chatzifrangkeskou, et al. · Nature Communications · 66
PDF
Decreased WNT/β-catenin signalling contributes to the pathogenesis of dilated cardiomyopathy caused by mutations in the lamin a/C gene
2016 · Caroline Le Dour, Coline Macquart, et al. · Human Molecular Genetics · 66
PDF
Microtubule cytoskeleton regulates Connexin 43 localization and cardiac conduction in cardiomyopathy caused by mutation in A-type lamins gene
2018 · Coline Macquart, Rene Jüttner, et al. · Human Molecular Genetics · 53
A Homozygous Mutation of Prelamin-A Preventing Its Farnesylation and Maturation Leads to a Severe Lipodystrophic Phenotype: New Insights into the Pathogenicity of Nonfarnesylated Prelamin-A
2011 · Caroline Le Dour, Stéphane Schneebeli, et al. · The Journal of Clinical Endocrinology & Metabolism · 48
Extracellular matrix remodeling and transforming growth factor-β signaling abnormalities induced by lamin A/C variants that cause lipodystrophy
2016 · Caroline Le Dour, Wei Wu, et al. · Journal of Lipid Research · 45
PDF
The R439C mutation in LMNA causes lamin oligomerization and susceptibility to oxidative stress
2009 · Valerie L.R.M. Verstraeten, Sandrine Caputo, et al. · Journal of Cellular and Molecular Medicine · 43
PDF
Lipodystrophic syndromes due toLMNAmutations: recent developments on biomolecular aspects, pathophysiological hypotheses and therapeutic perspectives
2018 · Corinne Vigouroux, Anne-Claire Guénantin, et al. · Nucleus · 41
PDF
Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria
2009 · S Dominici, V Fiori, et al. · European Journal of Histochemistry · 28
PDF
Depletion of lamina-associated polypeptide 1 from cardiomyocytes causes cardiac dysfunction in mice
2014 · Ji-Yeon Shin, Caroline Le Dour, et al. · Nucleus · 19
PDF
Modulation of cytoskeleton in cardiomyopathy caused by mutations in LMNA gene
2023 · Maria Chatzifrangkeskou, Caroline Le Dour, et al. · American Journal of Physiology-Cell Physiology · 17
The non-muscle ADF/cofilin-1 controls sarcomeric actin filament integrity and force production in striated muscle laminopathies
2021 · Nicolas Vignier, Maria Chatzifrangkeskou, et al. · Cell Reports · 15
PDF
Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria
2009 · S Dominici, V Fiori, et al. · European Journal of Histochemistry · 6
Les lipodystrophies génétiques
2011 · C. Vatier, G. Bidault, et al. · Médecine et Nutrition · 2
Une brève histoire des laminopathies
2008 · C. Vigouroux, O. Lascols, et al. · Médecine des Maladies Métaboliques · 1
011 Des mutations inactivatrices de la périlipine sont responsables d’un syndrome lipodystrophique de transmission autosomique dominante chez l’homme
2011 · C. Le Dour, S. Gandotra, et al. · Diabetes & Metabolism
PO24 L’expression d’une prélamine A non farnésylée est associée à un phénotype lipodystrophique avec insulino-résistance
2010 · C. Le Dour, S. Schneebeli, et al. · Diabetes & Metabolism
Liposdystrophies partielles liées à des mutations de la périlipine et des lamines A/C
2010 · Caroline Le Dour · OpenGrey (Institut de l'Information Scientifique et Technique)
O103 Le tissu adipeux des patients lipodystrophiques porteurs de mutations des lamines A/C présente des remaniements fibrotiques et des altérations mitochondriales en absence d’inflammation
2009 · V. Béréziat, P. Cervera, et al. · Diabetes & Metabolism
Works count: 24
Citation count: 1,079
H-index: 15
I10-index: 15
Year
Topic
Type