Caroline Le Dour

Perilipin Deficiency and Autosomal Dominant Partial Lipodystrophy

Sheetal Gandotra, Caroline Le Dour, William Bottomley et al. · New England Journal of Medicine · 2011 · 307 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

ERK1/2 directly acts on CTGF/CCN2 expression to mediate myocardial fibrosis in cardiomyopathy caused by mutations in the lamin A/C gene

Maria Chatzifrangkeskou, Caroline Le Dour, Wei Wu et al. · Human Molecular Genetics · 2016 · 104 citations · Full text

Life Sciences, Cardiology, Molecular Biology +15

LMNA Mutations Induce a Non-Inflammatory Fibrosis and a Brown Fat-Like Dystrophy of Enlarged Cervical Adipose Tissue

Véronique Béréziat, Pascale Cervera, Caroline Le Dour et al. · American Journal Of Pathology · 2011 · 72 citations · Full text

Medicine, Pathobiology, Pathology +17

Decreased WNT/β-catenin signalling contributes to the pathogenesis of dilated cardiomyopathy caused by mutations in the lamin a/C gene

Caroline Le Dour, Coline Macquart, Fusako Sera et al. · Human Molecular Genetics · 2016 · 65 citations · Full text

Life Sciences, Cardiology, Molecular Biology +15

Actin-microtubule cytoskeletal interplay mediated by MRTF-A/SRF signaling promotes dilated cardiomyopathy caused by LMNA mutations

Caroline Le Dour, Maria Chatzifrangkeskou, Coline Macquart et al. · Nature Communications · 2022 · 62 citations · Full text

Life Sciences, Cardiology, Cell Biology +13