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Aurore Coulomb
Researcher at University of Paris
Publications - 61
Citations - 1231
Aurore Coulomb is an academic researcher from University of Paris. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 17, co-authored 54 publications receiving 937 citations. Previous affiliations of Aurore Coulomb include Paris-Sorbonne University & Pierre-and-Marie-Curie University.
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Journal ArticleDOI
Gain of 1q As a Prognostic Biomarker in Wilms Tumors (WTs) Treated With Preoperative Chemotherapy in the International Society of Paediatric Oncology (SIOP) WT 2001 Trial: A SIOP Renal Tumours Biology Consortium Study
Tasnim Chagtai,Christina Zill,Linda Dainese,Jenny Wegert,Suvi Savola,Sergey Popov,William Mifsud,Gordan M. Vujanic,Neil J. Sebire,Yves Le Bouc,Peter F. Ambros,Leo Kager,Maureen J. O'Sullivan,Annick Blaise,Christophe Bergeron,Linda Holmquist Mengelbier,David Gisselsson,Marcel Kool,Godelieve A.M. Tytgat,Marry M. van den Heuvel-Eibrink,Norbert Graf,Harm van Tinteren,Aurore Coulomb,Manfred Gessler,Richard D. Williams,Kathy Pritchard-Jones +25 more
TL;DR: Gain of 1q is a potentially valuable prognostic biomarker in WT, in addition to histologic response to preoperative chemotherapy and tumor stage, and remained associated with poorer EFS in tumor subsets limited to either intermediate-risk localized disease or nonanaplastic localized disease.
Journal ArticleDOI
Clonally Expanded T Cells Reveal Immunogenicity of Rhabdoid Tumors
Amaury Leruste,Amaury Leruste,Jimena Tosello,Rodrigo Nalio Ramos,Arnault Tauziède-Espariat,Solene Brohard,Solene Brohard,Zhi-Yan Han,Zhi-Yan Han,Kevin Beccaria,Mamy Andrianteranagna,Pamela Caudana,Jovan Nikolic,Céline Chauvin,Céline Chauvin,Leticia Laura Niborski,Valeria Manriquez,Wilfrid Richer,Julien Masliah-Planchon,Sandrine Grossetête-Lalami,Sandrine Grossetête-Lalami,Mylène Bohec,Sonia Lameiras,Sylvain Baulande,Celio Pouponnot,Aurore Coulomb,Louise Galmiche,Didier Surdez,Didier Surdez,Nicolas Servant,Julie Helft,Christine Sedlik,Stéphanie Puget,Philippe Benaroch,Olivier Delattre,Olivier Delattre,Joshua J. Waterfall,Eliane Piaggio,Franck Bourdeaut,Franck Bourdeaut +39 more
TL;DR: It is shown that one mechanism mediating RTs immunogenicity involves SMARCB1-dependent re-expression of endogenous retroviruses and interferon-signaling activation.
Journal ArticleDOI
Renal Tubular Dysgenesis, a Not Uncommon Autosomal Recessive Disorder Leading to Oligohydramnios: Role of the Renin-Angiotensin System
Mireille Lacoste,Yi Cai,Liliane Guicharnaud,Françoise Mounier,Yves Dumez,Raymonde Bouvier,Frédérique Dijoud,Marie Gonzales,Jane Chatten,Anne-Lise Delezoide,Laurent Daniel,Madeleine Joubert,Nicole Laurent,Jacqueline Aziza,Tahya Sellami,Hatem Ben Amar,Catherine Jarnet,Anne Marie Frances,Farida Daïkha-Dahmane,Aurore Coulomb,Thomas Neuhaus,Bernard Foliguet,Pierre Chenal,Pascale Marcorelles,Jean Marie Gasc,Pierre Corvol,Marie Claire Gubler +26 more
TL;DR: The severity and the early onset of the clinical and pathologic expression of the disease underline the major importance of this system in fetal kidney function and development in humans.
Journal ArticleDOI
Molecular and cellular characteristics of ABCA3 mutations associated with diffuse parenchymal lung diseases in children
Florence Flamein,Laure Riffault,Céline Muselet-Charlier,Julie Pernelle,Delphine Feldmann,Laurence Jonard,Anne Marie Durand-Schneider,Aurore Coulomb,Michèle Maurice,Lawrence M. Nogee,Nobuya Inagaki,Serge Amselem,Jean Christophe Dubus,Virginie Rigourd,François Bremont,Christophe Marguet,Jacques Brouard,Jacques de Blic,Annick Clement,Ralph Epaud,Ralph Epaud,Loïc Guillot +21 more
TL;DR: New ABCA3 mutations in patients with life-threatening NRD and/or ILD were identified and two mutations associated with ILD acted via different pathophysiological mechanisms despite similar clinical phenotypes.
Journal ArticleDOI
Biallelic Mutations of Methionyl-tRNA Synthetase Cause a Specific Type of Pulmonary Alveolar Proteinosis Prevalent on Réunion Island
Alice Hadchouel,Thomas Wieland,Matthias Griese,Enrico Baruffini,Bettina Lorenz-Depiereux,Laurent Enaud,Elisabeth Graf,Jean Christophe Dubus,Sonia Halioui-Louhaichi,Aurore Coulomb,Christophe Delacourt,Christophe Delacourt,Christophe Delacourt,Gertrud Eckstein,Ralf Zarbock,Thomas Schwarzmayr,François Cartault,Thomas Meitinger,Tiziana Lodi,Jacques de Blic,Jacques de Blic,Tim M. Strom +21 more
TL;DR: In this article, biallelic missense mutations in MARS were identified in a specific form of pediatric pulmonary alveolar proteinosis (PAP), a severe lung disorder that is prevalent on the island of Reunion and the molecular basis of which is unresolved.