检索结果 - Odile Cabaret
- Showing 1 - 6 results of 6
-
1
-
2
Combined Tumor-Based BRCA1/2 and TP53 Mutation Testing in Ovarian Cancer 由 Édith Borcoman, Elizabeth Santana Dos Santos, Catherine Genestie, Patricia Pautier, Ludovic Lacroix, Sandrine M. Caputo, Odile Cabaret, Marine Guillaud-Bataille, Judith Michels, Aurélie Auguste, Alexandra Léary, Étienne Rouleau
出版 2023Artigo -
3
Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium “Care for CMMR-D” (C4CMMR-D) 由 Hans F. A. Vasen, Zeinab Ghorbanoghli, Franck Bourdeaut, Odile Cabaret, Olivier Caron, Alex Duval, Natacha Entz‐Werlé, Yael Goldberg, Denisa Ilenčíková, Christian P. Kratz, Noémie Lavoine, Jan Loeffen, F. H. Menko, Martine Muleris, G. Sébille, Chrystelle Colas, B Burkhardt, Laurence Brugières, Katharina Wimmer
出版 2014Artigo -
4
Germline BAP1 Mutations Predispose to Renal Cell Carcinomas 由 Tatiana Popova, Lucie Hebert, Virginie Jacquemin, Sophie Gad, Virginie Caux-Moncoutier, C. Dubois-d’Enghien, Bénédicte Richaudeau, Xavier Renaudin, Jason Sellers, Nicolás André, Xavier Sastre‐Garau, Laurence Desjardins, Gàbor Gyapay, Virginie Raynal, Olga M. Sinilnikova, Nadine Andrieu, Élodie Manié, Antoine De Pauw, Paul Gesta, Valérie Bonadona, Christine M. Maugard, Clotilde Penet, Marie‐Françoise Avril, Emmanuel Barillot, Odile Cabaret, Olivier Delattre, Richard J. Kahnoski, Olivier Caron, M. Benfodda, Hui-Han Hu, Nadem Soufir, Brigitte Bressac–de Paillerets, Dominique Stoppa-Lyonnet, Marc‐Henri Stern
出版 2013Artigo -
5
Diagnosis of Constitutional Mismatch Repair-Deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents 由 Sahra Bodo, Chrystelle Colas, Olivier Buhard, Ada Collura, Julie Tinat, Noémie Lavoine, Agathe Guilloux, Alexandra Chalastanis, Philippe Lafitte, Florence Coulet, Marie‐Pierre Buisine, Denisa Ilenčíková, Clara Ruíz-Ponte, Miriam Kinzel, S Grandjouan, Hilde Brems, Sophie Lejeune, Hélène Blanché, Qing Wang, Olivier Caron, Odile Cabaret, Magali Svrcek, Dominique Vidaud, Béatrice Parfait, Alain Verloès, Ulrich J. Knappe, Florent Soubrier, Isabelle Mortemousque, Alexander Leis, Jessie Auclair‐Perrossier, Thierry Frébourg, Jean–François Fléjou, Natacha Entz‐Werlé, Julie Leclerc, David Malka, Odile Cohen‐Haguenauer, Yael Goldberg, Anne‐Marie Gerdes, Faten Fedhila, Michèle Mathieu‐Dramard, Richard Hamelin, Wafaa Badre, Marion Gauthier‐Villars, Franck Bourdeaut, Eamonn Sheridan, Hans F. A. Vasen, Laurence Brugières, Katharina Wimmer, Martine Muleris, Alex Duval
出版 2015Artigo -
6
Comprehensive Study of the Clinical Phenotype of Germline<i>BAP1</i>Variant-Carrying Families Worldwide 由 Sebastian Walpole, Antonia L. Pritchard, Colleen M. Cebulla, Robert Pilarski, Meredith Stautberg, Frederick H. Davidorf, Arnaud de la Fouchardière, Odile Cabaret, Lisa Golmard, Dominique Stoppa‐Lyonnet, Erin M. Garfield, Ching-Ni Jenny Njauw, Mitchell Cheung, Joni A. Turunen, Pauliina Repo, Reetta-Stiina Järvinen, Remco van Doorn, Martine J. Jager, Gregorius P. M. Luyten, Marina Marinkovic, Cindy Chau, Míriam Potrony, Veronica Höiom, Hildur Helgadóttir, Lorenza Pastorino, William Bruno, Virginia Andreotti, Bruna Dalmasso, Giulia Ciccarese, Paola Queirolo, Luca Mastracci, Karin Wadt, Jens Folke Kiilgaard, Michael R. Speicher, Natasha van Poppelen, Emine Kılıç, Rana’a T. Al‐Jamal, Irma Dianzani, Marta Betti, Carsten Bergmann, Sandro Santagata, Sonika Dahiya, Saleem Taibjee, Jo Burke, Nicola Poplawski, Sally J. O’Shea, Julia Newton‐Bishop, Julian Adlard, David J. Adams, Anne-Marie Lane, Ivana K. Kim, Sonja Klebe, Hilary Racher, J. William Harbour, Michael L. Nickerson, Rajmohan Murali, Jane M. Palmer, Madeleine Howlie, Judith Symmons, Hayley R. Hamilton, Sunil Warrier, William Glasson, Peter A. Johansson, Carla Daniela Robles‐Espinoza, Raúl Ossio, Annelies de Klein, Susana Puig, Paola Ghiorzo, Maartje Nielsen, Tero Kivelä, Hensin Tsao, Joseph R. Testa, Pedram Gerami, Marc‐Henri Stern, Brigitte Bressac–de Paillerets, Mohamed H. Abdel‐Rahman, Nicholas K. Hayward
出版 2018Revisão
相关主题
Biology
Gene
Medicine
Genetics
Germline
Germline mutation
Internal medicine
Mutation
Oncology
Allele
BAP1
Cancer
Cancer research
DNA mismatch repair
Biochemistry
Bronchoalveolar lavage
Cancer syndrome
Carcinogenesis
Colorectal cancer
Computational biology
DNA
DNA extraction
DNA repair
Exome sequencing
Genetic predisposition
Human immunodeficiency virus (HIV)
Immunology
Loss of heterozygosity
Lung
Lymphocyte