Cargando…

Assessing Interactions between the Association of Common Genetic Variant at 1p11 (rs11249433) and Hormone Receptor Status with Breast Cancer Risk

BACKGROUND: The association between rs11249433 polymorphism on 1p11 and breast cancer (BC) has been widely evaluated since it was first identified through genome-wide association approach. However, the results have been inconclusive. To investigate this inconsistency, we performed a meta-analysis of...

Descripción completa

Detalles Bibliográficos
Autores principales:	Chen, Qian, Shi, Rongliang, Liu, Weiyan, Jiang, Daowen
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2013
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3745461/ https://www.ncbi.nlm.nih.gov/pubmed/23977306 http://dx.doi.org/10.1371/journal.pone.0072487

Ejemplares similares

Association between 1p11-rs11249433 Polymorphism and Breast Cancer Susceptibility: Evidence from 15 Case-Control Studies
por: Wu, Sheng, et al.
Publicado: (2013)

NOTCH2 in breast cancer: association of SNP rs11249433 with gene expression in ER-positive breast tumors without TP53 mutations
por: Fu, Yi-Ping, et al.
Publicado: (2010)

Quantitative Assessment of Common Genetic Variants on Chromosome 5p12 and Hormone Receptor Status with Breast Cancer Risk
por: Yu, Yanmin, et al.
Publicado: (2013)

Assessing Interactions between Common Genetic Variant on 2q35 and Hormone Receptor Status with Breast Cancer Risk: Evidence Based on 26 Studies
por: Huang, Tao, et al.
Publicado: (2013)

Common genetic variant rs3802842 in 11q23 contributes to colorectal cancer risk in Chinese population
por: Zhang, Chunze, et al.
Publicado: (2017)

The interplay of common genetic variants NRG1 rs2439302 and RET rs2435357 increases the risk of developing Hirschsprung’s disease
por: Chi, Shuiqing, et al.
Publicado: (2023)

Quantitative Assessment of 2q35-rs13387042 Polymorphism and Hormone Receptor Status with Breast Cancer Risk
por: Gu, Chao, et al.
Publicado: (2013)

Interleukin-21 rs2055979 and Interleukin-21 receptor rs3093390 genetic variants and hepatitis C virus chronic infection
por: Shoraka, Shahrzad, et al.
Publicado: (2017)

CTLA-4 Genetic Variants (rs11571317 and rs3087243): Role in Susceptibility and Progression of Breast Cancer
por: Goske, Maruthi, et al.
Publicado: (2017)

Common Genetic Variant of INSIG2 Gene rs7566605 Polymorphism Is Associated with Severe Obesity in North India
por: Prakash, Jai, et al.
Publicado: (2017)

Is the β Common Receptor the Key Molecule for the Protective Effect of Erythropoietin?
por: Yang, Zhenhong, et al.
Publicado: (2023)

The Common Variant rs11646213 Is Associated with Preeclampsia in Han Chinese Women
por: Wan, Ji-peng, et al.
Publicado: (2013)

Common rs7138803 variant of FAIM2 and obesity in Han Chinese
por: Li, Cong, et al.
Publicado: (2013)

Common Variant of FTO Gene, rs9939609, and Obesity in Pakistani Females
por: Shahid, Adeela, et al.
Publicado: (2013)

Association of the genetic variants of luteinizing hormone, luteinizing hormone receptor and polycystic ovary syndrome
por: Liu, Nana, et al.
Publicado: (2012)

Association of the Lipoprotein Receptor SCARB1 Common Missense Variant rs4238001 with Incident Coronary Heart Disease
por: Manichaikul, Ani, et al.
Publicado: (2015)

Association of BCL11A genetic variant (rs11886868) with severity in β-thalassaemia major & sickle cell anaemia
por: Dadheech, Sneha, et al.
Publicado: (2016)

Common FTO rs9939609 variant and risk of type 2 diabetes in Palestine
por: Sabarneh, Anas, et al.
Publicado: (2018)

Association of FTO common variant (rs9939609) with body fat in Turkish individuals
por: AĞAGÜNDÜZ, Duygu, et al.
Publicado: (2019)

Association between genetic variants (rs920778, rs4759314, and rs217727) in LncRNAs and cervical cancer susceptibility in Chinese population: A systematic review and meta-analysis
por: Liu, Yi, et al.
Publicado: (2022)

Effects of interactions between common genetic variants and smoking on colorectal cancer
por: Song, Nan, et al.
Publicado: (2017)

Genetic Variants of the Gsr Gene (rs2978663) and the Progression of Osteoporosis
por: Abdulabbas, Hadi Sajid, et al.
Publicado: (2023)

Interaction of two functional genetic variants LOXL1 rs1048661 and VEGFA rs3025039 on the risk of age-related macular degeneration in Chinese women
por: Chen, Han, et al.
Publicado: (2020)

The NOD2 Single Nucleotide Polymorphisms rs2066843 and rs2076756 Are Novel and Common Crohn's Disease Susceptibility Gene Variants
por: Glas, Jürgen, et al.
Publicado: (2010)

Association between ANKK1 (rs1800497) and LTA (rs909253) Genetic Variants and Risk of Schizophrenia
por: Arab, Arwa H., et al.
Publicado: (2015)

Common Variant rs9939609 in Gene FTO Confers Risk to Polycystic Ovary Syndrome
por: Li, Tao, et al.
Publicado: (2013)

Common variant rs356182 near SNCA defines a Parkinson's disease endophenotype
por: Cooper, Christine A., et al.
Publicado: (2016)

A common variant rs2054564 in ADAMTS17 is associated with susceptibility to lumbar spondylosis
por: Taniguchi, Yuki, et al.
Publicado: (2023)

The Association between Five Genetic Variants in MicroRNAs (rs2910164, rs11614913, rs3746444, rs11134527, and rs531564) and Cervical Cancer Risk: A Meta-Analysis
por: Liu, Jia, et al.
Publicado: (2021)

Marital status independently predicts gastric cancer survival after surgical resection--an analysis of the SEER database
por: Shi, Rong-liang, et al.
Publicado: (2016)

The Association between Four Genetic Variants in MicroRNAs (rs11614913, rs2910164, rs3746444, rs2292832) and Cancer Risk: Evidence from Published Studies
por: He, Bangshun, et al.
Publicado: (2012)

The FGF-21 genetic variants rs838133 and rs838145 are associated with high salt intake in the Emirati population
por: Saber-Ayad, Maha, et al.
Publicado: (2020)

MIR149 rs2292832 and MIR499 rs3746444 Genetic Variants Associated with the Risk of Rheumatoid Arthritis
por: Ali, Yasir, et al.
Publicado: (2023)

3127 The effect of common genetic variants in the oxytocin receptor gene on oxytocin response.
por: Malik, Manasi, et al.
Publicado: (2019)

AURKA Gene Variants rs1047972, and rs8173 Are Associated With Breast Cancer
por: Maciel-Cruz, Eric Jonathan, et al.
Publicado: (2023)

MON-092 Role of Genetic Variants of NNMT rs694539 and rs1941404, FTO rs1421085 and Irx3 rs3751723 Polymorphisms on Resting Energy Expenditure and BMI
por: Bañales Luna, Maciel, et al.
Publicado: (2019)

DNA methylation and hormone receptor status in breast cancer
por: Benevolenskaya, Elizaveta V., et al.
Publicado: (2016)

Identification of rs671, a common variant of ALDH2, as a gout susceptibility locus
por: Sakiyama, Masayuki, et al.
Publicado: (2016)

Common variants in P2RY11 are associated with narcolepsy
por: Kornum, Birgitte R, et al.
Publicado: (2010)

ESR2 gene variants (rs1256049, rs4986938, and rs1256030) and their association with breast cancer risk
por: Gallegos-Arreola, Martha Patricia, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_ordqd4durkngtqmuoblsil04je