Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Olga, Sinilnikova"'
Autor:
Francisco Javier Gracia-Aznarez, Victoria Fernandez, Guillermo Pita, Paolo Peterlongo, Orlando Dominguez, Miguel de la Hoya, Mercedes Duran, Ana Osorio, Leticia Moreno, Anna Gonzalez-Neira, Juan Manuel Rosa-Rosa, Olga Sinilnikova, Sylvie Mazoyer, John Hopper, Conchi Lazaro, Melissa Southey, Fabrice Odefrey, Siranoush Manoukian, Irene Catucci, Trinidad Caldes, Henry T Lynch, Florentine S M Hilbers, Christi J van Asperen, Hans F A Vasen, David Goldgar, Paolo Radice, Peter Devilee, Javier Benitez
Publikováno v:
PLoS ONE, Vol 8, Iss 2, p e55681 (2013)
The identification of the two most prevalent susceptibility genes in breast cancer, BRCA1 and BRCA2, was the beginning of a sustained effort to uncover new genes explaining the missing heritability in this disease. Today, additional high, moderate an
Externí odkaz:
https://doaj.org/article/8d2de2f1da8b4285a404e7b32bbfc2f0
Autor:
Marie Plourde, Alexandra Ferland, Penny Soucy, Yosr Hamdi, Martine Tranchant, Francine Durocher, Olga Sinilnikova, Van Luu The, Jacques Simard
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 116:134-153
A family history and estrogen exposure are well-known risk factors for breast cancer. Members of the 17beta-hydroxysteroid dehydrogenase family are responsible for important steps in the metabolism of androgens and estrogens in peripheral tissues, in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::daa1a26ac038285835dd85cd825b0afb
https://doi.org/10.1016/j.jsbmb.2009.05.005
https://doi.org/10.1016/j.jsbmb.2009.05.005
Autor:
Kelly L, Bolton, Georgia, Chenevix-Trench, Cindy, Goh, Siegal, Sadetzki, Susan J, Ramus, Beth Y, Karlan, Diether, Lambrechts, Evelyn, Despierre, Daniel, Barrowdale, Lesley, McGuffog, Sue, Healey, Douglas F, Easton, Olga, Sinilnikova, Javier, Benítez, María J, García, Susan, Neuhausen, Mitchell H, Gail, Patricia, Hartge, Susan, Peock, Debra, Frost, D Gareth, Evans, Rosalind, Eeles, Andrew K, Godwin, Mary B, Daly, Ava, Kwong, Edmond S K, Ma, Conxi, Lázaro, Ignacio, Blanco, Marco, Montagna, Emma, D'Andrea, Maria Ornella, Nicoletto, Sharon E, Johnatty, Susanne Krüger, Kjær, Allan, Jensen, Estrid, Høgdall, Ellen L, Goode, Brooke L, Fridley, Jennifer T, Loud, Mark H, Greene, Phuong L, Mai, Angela, Chetrit, Flora, Lubin, Galit, Hirsh-Yechezkel, Gord, Glendon, Irene L, Andrulis, Amanda E, Toland, Leigha, Senter, Martin E, Gore, Charlie, Gourley, Caroline O, Michie, Honglin, Song, Jonathan, Tyrer, Alice S, Whittemore, Valerie, McGuire, Weiva, Sieh, Ulf, Kristoffersson, Håkan, Olsson, Åke, Borg, Douglas A, Levine, Linda, Steele, Mary S, Beattie, Salina, Chan, Robert L, Nussbaum, Kirsten B, Moysich, Jenny, Gross, Ilana, Cass, Christine, Walsh, Andrew J, Li, Ronald, Leuchter, Ora, Gordon, Montserrat, Garcia-Closas, Simon A, Gayther, Stephen J, Chanock, Antonis C, Antoniou, Paul D P, Pharoah, Roger, Milne
Publikováno v:
JAMA. 307(4)
Approximately 10% of women with invasive epithelial ovarian cancer (EOC) carry deleterious germline mutations in BRCA1 or BRCA2. A recent article suggested that BRCA2-related EOC was associated with an improved prognosis, but the effect of BRCA1 rema
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e7dfa048c5e8364a35feb267a5618bfe
https://pubmed.ncbi.nlm.nih.gov/23053156
https://pubmed.ncbi.nlm.nih.gov/23053156
Autor:
Vaclav Hana, Arnaud Murat, Jean-François Vanbellinghen, Guido Tamburrano, Bin Tean Teh, Sok Kean Khoo, Armando Basso, Vincent Bours, Adriana Oneto, Anne Barlier, Olivier Chabre, Annamaria Colao, Natalia Garcia Basavilbaso, Maria Isabel Sabaté, Albert Beckers, Graciela Stalldecker, Alfred Penfornis, P. Lecomte, Francesco Cavagnini, Thierry Brue, Gérald Raverot, Blandine Gatta, Vincent Rohmer, F. Archambeaud, Dreanina Delettieres, Luciana Ansaneli Naves, Philippe Emy, Jean-Louis Sadoul, Douglas C. Luccio-Camelo, Piero Ferolla, Philippe Caron, Anne-Paule Gimenez-Roqueplo, Olga Sinilnikova, Wouter W. de Herder, Mirtha Guitelman, Marie Lise Jaffrain-Rea, Enrica Ciccarelli, Jean-Louis Wémeau, Angela R. Solano, Xavier Bertagna, Bruno Estour, Carmen Fajardo Montañana, Adrian Daly, Alain Calender
Publikováno v:
J. Clin. Endocrinol. Metab.
J. Clin. Endocrinol. Metab., 2007, sous presse
Journal of Clinical Endocrinology and Metabolism, 92(5), 1891-1896. Endocrine Society
J. Clin. Endocrinol. Metab., 2007, sous presse
Journal of Clinical Endocrinology and Metabolism, 92(5), 1891-1896. Endocrine Society
Context: An association between germline aryl hydrocarbon receptor-interacting protein (AIP) gene mutations and pituitary adenomas was recently shown. Objective: The objective of the study was to assess the frequency of AIP gene mutations in a large
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce49037866ef0967bea3b0aa1161f22b
http://hdl.handle.net/11588/339692
http://hdl.handle.net/11588/339692
Autor:
Valérie, Bonadona, Pierre, Saltel, Françoise, Desseigne, Hervé, Mignotte, Jean-Christophe, Saurin, Qing, Wang, Olga, Sinilnikova, Sophie, Giraud, Gilles, Freyer, Henri, Plauchu, Alain, Puisieux, Christine, Lasset
Publikováno v:
Cancer epidemiology, biomarkersprevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 11(1)
The aim of this prospective study was to evaluate the consequences of the disclosure of a positive genetic test result to patients affected with cancer. Personal repercussions and patients' behavior with the transmission of their results to relatives
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7d134404511ae2d8aba49e2c5f9ec0f3
https://pubmed.ncbi.nlm.nih.gov/11815406
https://pubmed.ncbi.nlm.nih.gov/11815406
Autor:
Isabelle Coupier, Pierre-Yves Cousin, David Hughes, Patricia Legoix-Né, Alexandra Trehin, Olga Sinilnikova, Dominique Stoppa-Lyonnet
Publikováno v:
Familial Cancer; Nov2005, Vol. 4 Issue 4, p273-277, 5p