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Sökning: (WFRF:(Lund E Eiliv)) > Haplotypes of the e...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004749naa a2200793 4500
001oai:lup.lub.lu.se:66b2fb5f-cc51-4e91-88c2-221610dcc797
003SwePub
008160401s2008 | |||||||||||000 ||eng|
024a https://lup.lub.lu.se/record/11438472 URI
024a https://doi.org/10.1002/ijc.231272 DOI
040 a (SwePub)lu
041 a engb eng
042 9 SwePub
072 7a art2 swepub-publicationtype
072 7a ref2 swepub-contenttype
100a Cox, David G4 aut
2451 0a Haplotypes of the estrogen receptor beta gene and breast cancer risk
264 c 2007-10-12
264 1b Wiley,c 2008
520 a Exposure to exogenous (oral contraceptives, postmenopausal hormone therapy) and endogenous (number of ovulatory cycles, adiposity) steroid hormones is associated with breast cancer risk. Breast cancer risk associated with these exposures could hypothetically be modified by genes in the steroid hormone synthesis, metabolism and signaling pathways. Estrogen receptors are the first step along the path of signaling cell growth and development upon stimulation with estrogens. The National Cancer Institute Breast and Prostate Cancer Cohort Consortium has systematically selected haplotype tagging SNPs in genes along the steroid hormone synthesis, metabolism and binding pathways, including the estrogen receptor beta (ESR2) gene. Four htSNPs tag the 6 major (>5% frequency) haplotypes of the ESR2 gene. These polymorphisms have been genotyped in 5,789 breast cancer cases and 7,761 controls nested within the American Cancer Society Cancer Prevention Study II, European Prospective Investigation into Cancer and Nutrition, Multiethnic Cohort, Nurses' Health Study and Women's Health Study cohorts. None of the SNPs were independently associated with breast cancer risk. One haplotype of the ESR2 gene was associated with breast cancer risk before correction for multiple testing (OR 1.17, 95% CI 1.07-1.28, p = 0.0007). This haplotype remained associated with breast cancer risk after adjustment for multiple testing using a permutation procedure. There was no statistically significant heterogeneity in SNP or haplotype odds ratios across cohorts. These data suggest that inherited variants in ESR2 (while possibly conferring a small increased risk of breast cancer) are not associated with appreciable (OR > 1.2) changes in breast cancer risk among Caucasian women.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Cancer och onkologi0 (SwePub)302032 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Cancer and Oncology0 (SwePub)302032 hsv//eng
653 a risk
653 a haplotype
653 a polymorphism
653 a breast cancer
653 a estrogen receptor beta
700a Bretsky, Philip4 aut
700a Kraft, Peter4 aut
700a Pharoah, Paul4 aut
700a Albanes, Demetrius4 aut
700a Altshuler, David4 aut
700a Amiano, Pilar4 aut
700a Berglund, Göranu Lund University,Lunds universitet,Internmedicin - epidemiologi,Forskargrupper vid Lunds universitet,Internal Medicine - Epidemiology,Lund University Research Groups4 aut0 (Swepub:lu)medf-gbe
700a Boeing, Heiner4 aut
700a Buring, Julie4 aut
700a Burtt, Noel4 aut
700a Calle, Eugenia E4 aut
700a Canzian, Federico4 aut
700a Chanock, Stephen4 aut
700a Clavel-Chapelon, Françoise4 aut
700a Colditz, Graham A4 aut
700a Spencer Feigelson, Heather4 aut
700a Haiman, Christopher A4 aut
700a Hankinson, Susan E4 aut
700a Hirschhorn, Joel4 aut
700a Henderson, Brian E4 aut
700a Hoover, Robert4 aut
700a Hunter, David J4 aut
700a Kaaks, Rudolf4 aut
700a Kolonel, Laurence4 aut
700a LeMarchand, Loic4 aut
700a Lund, Eiliv4 aut
700a Palli, Domenico4 aut
700a Peeters, Petra H M4 aut
700a Pike, Malcolm C4 aut
700a Riboli, Elio4 aut
700a Stram, Daniel O4 aut
700a Thun, Michael4 aut
700a Tjonneland, Anne4 aut
700a Travis, Ruth C4 aut
700a Trichopoulos, Dimitrios4 aut
700a Yeager, Meredith4 aut
710a Internmedicin - epidemiologib Forskargrupper vid Lunds universitet4 org
773t International Journal of Cancerd : Wileyg 122:2, s. 387-392q 122:2<387-392x 0020-7136
856u http://dx.doi.org/10.1002/ijc.23127y FULLTEXT
856u https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ijc.23127
8564 8u https://lup.lub.lu.se/record/1143847
8564 8u https://doi.org/10.1002/ijc.23127

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