C
Christophe E. Pierreux
Researcher at Université catholique de Louvain
Publications - 74
Citations - 4166
Christophe E. Pierreux is an academic researcher from Université catholique de Louvain. The author has contributed to research in topics: Transcription factor & Cellular differentiation. The author has an hindex of 34, co-authored 60 publications receiving 3748 citations. Previous affiliations of Christophe E. Pierreux include Lincoln's Inn.
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Journal ArticleDOI
Intrahepatic Bile Ducts Develop According to a New Mode of Tubulogenesis Regulated by the Transcription Factor SOX9
Aline Antoniou,Peggy Raynaud,Sabine Cordi,Yiwei Zong,François Tronche,Ben Z. Stanger,Patrick Jacquemin,Christophe E. Pierreux,Frédéric Clotman,Frédéric P. Lemaigre +9 more
TL;DR: It is suggested that biliary development proceeds according to a new mode of tubulogenesis characterized by transient asymmetry and whose timing is controlled by SOX9.
Journal ArticleDOI
Control of liver cell fate decision by a gradient of TGFβ signaling modulated by Onecut transcription factors
Frédéric Clotman,Patrick Jacquemin,Nicolas Plumb-Rudewiez,Christophe E. Pierreux,Patrick Van Der Smissen,Harry C. Dietz,Pierre J. Courtoy,Guy G. Rousseau,Frédéric P. Lemaigre +8 more
TL;DR: A gradient of activin/TGFbeta signaling modulated by Onecut factors is required to segregate the hepatocytic and the biliary lineages.
Journal ArticleDOI
Raf induces TGFbeta production while blocking its apoptotic but not invasive responses: a mechanism leading to increased malignancy in epithelial cells.
Kerstin Lehmann,Elzbieta Janda,Christophe E. Pierreux,Marjatta Rytömaa,Almut Schulze,Martin McMahon,Caroline S. Hill,Hartmut Beug,Julian Downward +8 more
TL;DR: Using an inducible form of Raf in MDCK cells, it is shown that sustained activation of Raf alone is able to induce the transition from an epithelial to a mesenchymal phenotype, and the Raf-MAP kinase pathway thus synergizes with TGF beta in promoting malignancy but does not directly impair TGFbeta-induced Smad signaling.
Journal ArticleDOI
Transforming growth factor beta-independent shuttling of Smad4 between the cytoplasm and nucleus.
TL;DR: It is demonstrated that inhibition of CRM1-mediated nuclear export by treatment of cells with leptomycin B results in endogenous Smad4 accumulating very rapidly in the nucleus, indicating that the nucleocytoplasmic shuttling is specific for Smad 4.
Journal ArticleDOI
Hnf6 and Tcf2 (MODY5) are linked in a gene network operating in a precursor cell domain of the embryonic pancreas
Miguel A. Maestro,Sylvia F. Boj,Reini F. Luco,Christophe E. Pierreux,Judit Cabedo,Joan-Marc Servitja,Michael S. German,Guy G. Rousseau,Frédéric P. Lemaigre,Jorge Ferrer +9 more
TL;DR: It is shown that, at E13-E18, the embryonic stage during which the major burst of beta-cell neogenesis takes place, pancreatic duct cells express Hnf1beta, the product of the maturity-onset diabetes of the young type 5 (MODY5) gene, which is defined as a precursor cellular stage of the embryonic pancreas and placed in a genetic hierarchy that regulates the generation of pancreatic endocrine cells.