TITLE

Notch1 single nucleotide polymorphism rs3124591 is associated with the risk of development of invasive ductal breast carcinoma in a Chinese population

AUTHOR(S)
Yu-Wen Cao; Guo-XingWan; Chun-Xia Zhao; Jian-MingHu; Li Li; Wei-Hua Liang; Wen-Qin Li; Yu-Cong Li; Yi-Xiao Li; Xiao-Ming Du; Shi-Ying Yu; Feng Li
PUB. DATE
July 2014
SOURCE
International Journal of Clinical & Experimental Pathology;2014, Vol. 7 Issue 7, p4286
SOURCE TYPE
Academic Journal
DOC. TYPE
Article
ABSTRACT
No abstract available.
ACCESSION #
97436073

 

Related Articles

  • Genetic variants of fibroblast growth factor receptor 2 ( FGFR2) are associated with breast cancer risk in Chinese women of the Han nationality. Chen, Fan; Lv, Min; Xue, Yun; Zhou, Jing; Hu, Feifei; Chen, Xin; Zhao, Zhanqin; Li, Yang; Wang, XingGuo // Immunogenetics;Jan2012, Vol. 64 Issue 1, p71 

    Fibroblast growth factor receptor 2 ( FGFR2), a recently described risk factor for breast cancer, plays important roles in cell growth, invasiveness, motility, and angiogenesis. In attempt to investigate whether FGFR2 polymorphisms are associated with a risk of breast cancer in Chinese women of...

  • Lack of association between rs7566605 and obesity in a Chinese population. Yan Feng; Hongxing Dong; Qingyun Xiang; Xiumei Hong; Wilker, Elissa; Yan Zhang; Xiping Xu; Xin Xu // Human Genetics;Dec2006, Vol. 120 Issue 5, p743 

    A letter to the editor about the lack of association between a common single nucleotide polymorphism (rs7566605) and obesity in Chinese population is presented.

  • Genetic variants at 5p12 and risk of breast cancer in Han Chinese. Liu, Xiao'an; Qin, Zhenzhen; Shen, Hao; Xue, Jialei; Jiang, Yue; Hu, Zhibin; Shen, Hongbing; Wang, Shui // Journal of Human Genetics;Oct2012, Vol. 57 Issue 10, p638 

    A genome-wide association study, conducted among women of European ancestry, has identified two single-nucleotide polymorphisms (SNPs) rs4415084 (T>C) and rs10941679 (A>G) at chromosome 5p12 were associated with risk of breast cancer, suggesting that genetic variants in this region may have a...

  • Genetic polymorphisms in centrobin and Nek2 are associated with breast cancer susceptibility in a Chinese Han population. Wang, Hui; Xie, Yun-Tao; Han, Ji-Yuan; Ruan, Yuan; Song, Ai-Ping; Zheng, Li-Yuan; Zhang, Wei-Zao; Sajdik, Constantin; Li, Yan; Tian, Xin-Xia; Fang, Wei-Gang // Breast Cancer Research & Treatment;Nov2012, Vol. 136 Issue 1, p241 

    Centrosome aberrations have been suggested to cause chromosomal instability and aneuploidy, and eventually promote cancer development. The Centrobin and Nek2 proteins interact with each other and both are involved in centrosome duplication and chromosome segregation. This study aimed to...

  • Different Effects of Three Polymorphisms in MicroRNAs on Cancer Risk in Asian Population: Evidence from Published Literatures. Xu, Yeqiong; Gu, Ling; Pan, Yuqin; Li, Rui; Gao, Tianyi; Song, Guoqi; Nie, Zhenlin; Chen, Liping; Wang, Shukui; He, Bangshun // PLoS ONE;Jun2013, Vol. 8 Issue 6, p1 

    MicroRNAs (miRNAs) are a class of small non-protein-coding RNAs, which have emerged as integrated and important post-transcriptional regulators of gene expression. It has been demonstrated that single nucleotide polymorphisms (SNPs) exist in protein-coding genes. Accumulated studies have...

  • Research Highlights.  // Nature Reviews Cancer;Apr2008, Vol. 8 Issue 4, p248 

    The article highlights two clinical researches in cancer. A study on risk perception and among 374 women in Eastern Massachusetts who had been diagnosed with ductal carcinoma in situ (DCIS) reveals that 54% of the women perceived a moderate risk for DCIS recurrence, and 39% perceived a moderate...

  • Polymorphisms in Second Intron of the FGFR2 Gene Are Associated with the Risk of Early-Onset Breast Cancer in Chinese Han Women. Fangmeng Fu; Chuan Wang; Meng Huang; Chuangui Song; Shunguo Lin; Heguang Huang // Tohoku Journal of Experimental Medicine;Mar2012, Vol. 226 Issue 3, p221 

    Fibroblast growth factor receptor 2 (FGFR2) plays an important role in tumor cell growth, invasiveness, motility, and angiogenesis. Several single-nucleotide polymorphisms (SNPs) in the second intron of the FGFR2 gene are associated with the risk of breast cancer. In this study, we determined...

  • Replication of results of genome-wide association studies on esophageal squamous cell carcinoma susceptibility loci in a Korean population. Piao, J.-M.; Shin, M.-H.; Kim, H. N.; Song, H.-R.; Kweon, S.-S.; Choi, J.-S.; Shim, H.-J.; Hwang, J.-E.; Bae, W.-K.; Kim, S.-H.; Choi, Y.-D.; Cui, L.-H. // Diseases of the Esophagus;Nov2014, Vol. 27 Issue 8, p798 

    Two recent genome-wide association studies have identified that the rs2274223 single-nucleotide polymorphism inphospholipase C epsilon 1 and the single-nucleotide polymorphism rs13042395 in C 20orf54 are involved in esophageal squamous cell carcinoma ( ESCC) in Chinese populations. We...

  • NOTCH2 in breast cancer: association of SNP rs11249433 with gene expression in ER-positive breast tumors without TP53 mutations. Yi-Ping Fu; Edvardsen, Hege; Kaushiva, Alpana; Arhancet, Juan P.; Howe, Tiffany M.; Kohaar, Indu; Porter-Gill, Patricia; Shah, Anushi; Landmark-Høyvik, Hege; Fosså, Sophie D.; Ambs, Stefan; Naume, Bjørn; Børresen-Dale, Anne-Lise; Kristensen, Vessela N.; Prokunina-Olsson, Ludmila // Molecular Cancer;2010, Vol. 9, p113 

    Background: A recent genome-wide association study (GWAS) has identified a single nucleotide polymorphism (SNP) rs11249433 in the 1p11.2 region as a novel genetic risk factor for breast cancer, and this association was stronger in patients with estrogen receptor (ER)+ versus ER- cancer. Results:...

  • Genetic variation in TP53 and risk of breast cancer in a population-based case–control study. Sprague, Brian L.; Trentham-Dietz, Amy; Garcia-Closas, Montserrat; Newcomb, Polly A.; Titus-Ernstoff, Linda; Hampton, John M.; Chanock, Stephen J.; Haines, Jonathan L.; Egan, Kathleen M. // Carcinogenesis;Aug2007, Vol. 28 Issue 8, p1680 

    Whereas germ line missense mutations in the tumor suppressor gene TP53 are associated with a marked predisposition to breast cancer, single-nucleotide polymorphisms (SNPs) may play a more modest role in breast cancer susceptibility. We examined genetic variation in TP53 in relation to breast...

Share

Read the Article

Courtesy of THE LIBRARY OF VIRGINIA

Sorry, but this item is not currently available from your library.

Try another library?
Sign out of this library

Other Topics