Sophie Gad

Sophie Gad

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Sophie Gad

Sophie Gad

Publications by authors named "Sophie Gad"

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31Publications

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Renal Cell Carcinoma Programmed Death-ligand 1, a New Direct Target of Hypoxia-inducible Factor-2 Alpha, is Regulated by von Hippel-Lindau Gene Mutation Status.

Eur Urol 2016 10 23;70(4):623-632. Epub 2015 Dec 23.

INSERM (Institut National de la Santé et de la Recherche Médicale) UMR1186, Laboratory Integrative Tumor Immunology and Genetic Oncology, Villejuif, France; INSERM, Gustave Roussy, Univ. Paris-Sud, Université Paris-Saclay, Villejuif, F-94805, France. Electronic address:

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http://dx.doi.org/10.1016/j.eururo.2015.11.029DOI Listing
October 2016

Fumarate Hydratase-deficient Cell Line NCCFH1 as a New In Vitro Model of Hereditary Papillary Renal Cell Carcinoma Type 2.

Anticancer Res 2015 Dec;35(12):6639-53

Division of Medical Sciences, National Cancer Centre Singapore, Singapore, Republic of Singapore Division of Cancer and Stem Cell Biology, Duke-NUS Graduate Medical School, Singapore, Republic of Singapore

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December 2015

A germline mutation in PBRM1 predisposes to renal cell carcinoma.

J Med Genet 2015 Jun 24;52(6):426-30. Epub 2015 Apr 24.

Ecole Pratique des Hautes Etudes, Paris, France Laboratoire de Génétique Oncologique EPHE, INSERM U753, Villejuif, France Faculté de Médecine Université Paris-Sud, Le Kremlin-Bicêtre, France.

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http://dx.doi.org/10.1136/jmedgenet-2014-102912DOI Listing
June 2015

Von Hippel-Lindau: how a rare disease illuminates cancer biology.

Semin Cancer Biol 2013 Feb 30;23(1):26-37. Epub 2012 May 30.

Laboratoire de Génétique Oncologique EPHE, INSERM U743, Faculté de Médecine Paris-Sud, 94276 Le Kremlin-Bicêtre et Institut de cancérologie Gustave Roussy, 94800 Villejuif, France.

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http://dx.doi.org/10.1016/j.semcancer.2012.05.005DOI Listing
February 2013

A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma.

Authors:
Corine Bertolotto Fabienne Lesueur Sandy Giuliano Thomas Strub Mahaut de Lichy Karine Bille Philippe Dessen Benoit d'Hayer Hamida Mohamdi Audrey Remenieras Eve Maubec Arnaud de la Fouchardière Vincent Molinié Pierre Vabres Stéphane Dalle Nicolas Poulalhon Tanguy Martin-Denavit Luc Thomas Pascale Andry-Benzaquen Nicolas Dupin Françoise Boitier Annick Rossi Jean-Luc Perrot Bruno Labeille Caroline Robert Bernard Escudier Olivier Caron Laurence Brugières Simon Saule Betty Gardie Sophie Gad Stéphane Richard Jérôme Couturier Bin Tean Teh Paola Ghiorzo Lorenza Pastorino Susana Puig Celia Badenas Hakan Olsson Christian Ingvar Etienne Rouleau Rosette Lidereau Philippe Bahadoran Philippe Vielh Eve Corda Hélène Blanché Diana Zelenika Pilar Galan François Aubin Bertrand Bachollet Céline Becuwe Pascaline Berthet Yves Jean Bignon Valérie Bonadona Jean-Louis Bonafe Marie-Noëlle Bonnet-Dupeyron Fréderic Cambazard Jacqueline Chevrant-Breton Isabelle Coupier Sophie Dalac Liliane Demange Michel d'Incan Catherine Dugast Laurence Faivre Lynda Vincent-Fétita Marion Gauthier-Villars Brigitte Gilbert Florent Grange Jean-Jacques Grob Philippe Humbert Nicolas Janin Pascal Joly Delphine Kerob Christine Lasset Dominique Leroux Julien Levang Jean-Marc Limacher Cristina Livideanu Michel Longy Alain Lortholary Dominique Stoppa-Lyonnet Sandrine Mansard Ludovic Mansuy Karine Marrou Christine Matéus Christine Maugard Nicolas Meyer Catherine Nogues Pierre Souteyrand Laurence Venat-Bouvet Hélène Zattara Valérie Chaudru Gilbert M Lenoir Mark Lathrop Irwin Davidson Marie-Françoise Avril Florence Demenais Robert Ballotti Brigitte Bressac-de Paillerets

Nature 2011 Oct 19;480(7375):94-8. Epub 2011 Oct 19.

1] INSERM, U895 (équipe 1), Equipe labélisée Ligue Contre le Cancer, C3M, 06204 Nice, France [2] Université of Nice Sophia-Antipolis, UFR Médecine, 06204 Nice, France [3] Centre Hospitalier Universitaire de Nice, Service de Dermatologie, 06204 Nice, France [4].

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http://dx.doi.org/10.1038/nature10539DOI Listing
October 2011

PHD2 mutation and congenital erythrocytosis with paraganglioma.

N Engl J Med 2008 Dec;359(25):2685-92

Génétique Oncologique, Ecole Pratique des Hautes Etudes and Centre National de la Recherche Scientifique (FRE 2939), Institut de Cancérologie Gustave Roussy, Villejuif, France.

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http://dx.doi.org/10.1056/NEJMoa0806277DOI Listing
December 2008

Familial non-VHL clear cell (conventional) renal cell carcinoma: clinical features, segregation analysis, and mutation analysis of FLCN.

Clin Cancer Res 2008 Sep;14(18):5925-30

Cancer Research UK Renal Molecular Oncology Group and Department of Medical and Molecular Genetics, University of Birmingham and West Midlands Regional Genetics Service, Birmingham Women's Hospital, United Kingdom.

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http://dx.doi.org/10.1158/1078-0432.CCR-08-0608DOI Listing
September 2008

Trichloroethylene exposure and somatic mutations of the VHL gene in patients with Renal Cell Carcinoma.

J Occup Med Toxicol 2007 Nov 12;2:13. Epub 2007 Nov 12.

Laboratoire de Génétique Oncologique EPHE, Faculté de Médecine Paris-Sud, Le Kremlin-Bicêtre 94275 Le Kremlin-Bicêtre Cedex, France.

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http://dx.doi.org/10.1186/1745-6673-2-13DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2211482PMC
November 2007

[Genetics and angiogenesis: the example of von Hippel-Lindau disease].

Bull Cancer 2007 Jul;94 Spec No:S170-9

Laboratoire de génétique oncologique Ephe, CNRS FRE 2939, Faculté de Médecine Paris-Sud, 94276 Le Kremlin-Bicêtre et Institut de cancérologie Gustave Roussy, 94800 Villejuif.

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July 2007

Crypt-restricted proliferation and commitment to the Paneth cell lineage following Apc loss in the mouse intestine.

Development 2005 Mar 16;132(6):1443-51. Epub 2005 Feb 16.

Institut Cochin, INSERM U567, CNRS UMR8104, Université Paris V, 24 rue du Fb St-Jacques, 75014 Paris, France.

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http://dev.biologists.org/cgi/doi/10.1242/dev.01700
Publisher Site
http://dx.doi.org/10.1242/dev.01700DOI Listing
March 2005

Is the gene encoding Chibby implicated as a tumour suppressor in colorectal cancer ?

BMC Cancer 2004 Jul 9;4:31. Epub 2004 Jul 9.

UMR-S Inserm 490, Laboratoire de Toxicologie Moléculaire, Université René Descartes-Paris V, 75006 Paris, France.

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http://dx.doi.org/10.1186/1471-2407-4-31DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC471554PMC
July 2004

Distinct BRCA1 rearrangements involving the BRCA1 pseudogene suggest the existence of a recombination hot spot.

Am J Hum Genet 2002 Apr 5;70(4):858-65. Epub 2002 Mar 5.

Laboratoire de Génétique, Unité Mixte de Recherche 5641 CNRS, Université Claude Bernard, 8 avenue Rockefeller, 69373 Lyon cedex 08, France.

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http://linkinghub.elsevier.com/retrieve/pii/S000292970760293
Publisher Site
http://dx.doi.org/10.1086/339434DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC379114PMC
April 2002