نتایج جستجو برای: ژن tox3

تعداد نتایج: 15841  

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2014
Katie M O'Brien Stephen R Cole Lawrence S Engel Jeannette T Bensen Charles Poole Amy H Herring Robert C Millikan

BACKGROUND Gene expression analyses indicate that breast cancer is a heterogeneous disease with at least five immunohistologic subtypes. Despite growing evidence that these subtypes are etiologically and prognostically distinct, few studies have investigated whether they have divergent genetic risk factors. To help fill in this gap in our understanding, we examined associations between breast c...

2009
Patricio Rivera Malin Melin Tara Biagi Tove Fall Jens Häggström Kerstin Lindblad-Toh Henrik von Euler

Breast cancer is a major contributor to overall morbidity and mortality in women. Several genes predisposing to breast cancer have been identified, but the majority of risk factors remain unknown. Even less is known about the inherited risk factors underlying canine mammary tumors (CMT). Clear breed predispositions exist, with 36% of English springer spaniels (ESS) in Sweden being affected. Her...

2013
Jingxuan Shan Shoba P. DSouza Sasha Bakhru Eman K. Al-Azwani Maria L. Ascierto Konduru S. Sastry Shahinaz Bedri Dhanya Kizhakayil Idil I. Aigha Joel Malek Issam Al-Bozom Salah Gehani Stacia Furtado Edith Mathiowitz Ena Wang Francesco M. Marincola Lotfi Chouchane

Although the linkage between germline mutations of BRCA1 and hereditary breast/ovarian cancers is well established, recent evidence suggests that altered expression ofwild-type BRCA1might contribute to the sporadic forms of breast cancer. The breast cancer gene trinucleotide-repeat-containing 9 (TNRC9; TOX3) has been associated with disease susceptibility but its function is undetermined. Here,...

Journal: :Journal of the National Cancer Institute 2008
Mitchell H Gail

One purpose for seeking common alleles that are associated with disease is to use them to improve models for projecting individualized disease risk. Two genome-wide association studies and a study of candidate genes recently identified seven common single-nucleotide polymorphisms (SNPs) that were associated with breast cancer risk in independent samples. These seven SNPs were located in FGFR2, ...

Journal: :Cancer research 2009
Patricio Rivera Malin Melin Tara Biagi Tove Fall Jens Häggström Kerstin Lindblad-Toh Henrik von Euler

Breast cancer is a major contributor to overall morbidity and mortality in women. Several genes predisposing to breast cancer have been identified, but the majority of risk factors remain unknown. Even less is known about the inherited risk factors underlying canine mammary tumors (CMT). Clear breed predispositions exist, with 36% of English springer spaniels (ESS) in Sweden being affected. Her...

2017
Li Chen Ling-Min Hu Yu-Feng Wang Hai-Yan Yang Xiao-Yang Huang Wei Zhou Hai-Xiang Sun

This study investigated the possible association between single nucleotide polymorphism (SNP) sites on a genome wide level and the presence of polycystic ovary syndrome (PCOS) in a local population. Patients treated for PCOS in the outpatient clinic of the reproductive medicine center of Changzhou Maternal and Child Health Care Hospital (affiliated to Nanjing Medical University) from January of...

Journal: :Cancer research 2013
Kristen N Stevens Celine M Vachon Fergus J Couch

Triple-negative breast cancers (TNBC), defined by the absence of estrogen receptor, progesterone receptor, and HER-2 expression, account for 12% to 24% of all breast cancers. TNBC is associated with early recurrence of disease and poor outcome. Germline mutations in the BRCA1 and BRCA2 breast cancer susceptibility genes have been associated with up to 15% of TNBC, and TNBC accounts for 70% of b...

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