Cargando…

The SNP rs931794 in 15q25.1 Is Associated with Lung Cancer Risk: A Hospital-Based Case-Control Study and Meta-Analysis

BACKGROUND: Lung cancer is one of the most common human malignant diseases and the leading cause of cancer death worldwide. The rs931794, a SNP located in 15q25.1, has been suggested to be associated with lung cancer risk. Nevertheless, several genetic association studies yielded controversial resul...

Descripción completa

Detalles Bibliográficos
Autores principales:	Wang, Qi, Ke, Juntao, Song, Qibin, Hu, Weiguo, Lu, Xuzai, Wang, Zhenling, Gong, Hongyun, Xu, Tangpeng, Chen, Xueqin, Xu, Bin, Liu, Cheng, Sun, Yun, Gong, Yajie, Yang, Yang, Zhu, Ying
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2015
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4469418/ https://www.ncbi.nlm.nih.gov/pubmed/26079375 http://dx.doi.org/10.1371/journal.pone.0128201

Ejemplares similares

Quantitative Assessment of the Association between rs2046210 at 6q25.1 and Breast Cancer Risk
por: Wu, Xi, et al.
Publicado: (2013)

6q25.1-q25.3 Microdeletion in a Chinese Girl
por: Zhong, Mian-Ling, et al.
Publicado: (2021)

The SNP rs402710 in 5p15.33 Is Associated with Lung Cancer Risk: A Replication Study in Chinese Population and a Meta-Analysis
por: Lu, Xuzai, et al.
Publicado: (2013)

Association of a single nucleotide polymorphism at 6q25.1, rs2046210, with endometrial cancer risk among Chinese women
por: Li, Guoliang, et al.
Publicado: (2011)

Evidence that 6q25.1 variant rs6931104 confers susceptibility to chronic myeloid leukemia through RMND1 regulation
por: Woo, Young Min, et al.
Publicado: (2019)

Identification of two novel mammographic density loci at 6Q25.1
por: Brand, Judith S, et al.
Publicado: (2015)

Bioinformatic Evaluation of Features on Cis-regulatory Elements at 6q25.1
por: Sreekar, N, et al.
Publicado: (2023)

The 6q25.1 rs2046210 polymorphism is associated with an elevated susceptibility to breast cancer: A meta‐analysis of 261,703 subjects
por: Jin, Tie‐feng, et al.
Publicado: (2019)

Sequencing of Chromosomal Locus 6q25.1 Revealed Two Significant SNPs rs2046210 and rs2046211 Associated with Breast Cancer: A Case-Control Study in Egyptian Women
por: Saied, Marwa H, et al.
Publicado: (2022)

Identification of a Potential Regulatory Variant for Colorectal Cancer Risk Mapping to Chromosome 5q31.1: A Post-GWAS Study
por: Ke, Juntao, et al.
Publicado: (2015)

Evaluation of functional genetic variants at 6q25.1 and risk of breast cancer in a Chinese population
por: Wang, Yanru, et al.
Publicado: (2014)

Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk
por: Ji, Xuemei, et al.
Publicado: (2018)

Strong Association between Two Polymorphisms on 15q25.1 and Lung Cancer Risk: A Meta-Analysis
por: Gu, Mingliang, et al.
Publicado: (2012)

Genome-wide association study identifies variation at 6q25.1 associated with survival in multiple myeloma
por: Johnson, David C., et al.
Publicado: (2016)

Identification of a functional variant for colorectal cancer risk mapping to chromosome 5q31.1
por: Ke, Juntao, et al.
Publicado: (2016)

Genome-wide association study identifies a novel breast cancer susceptibility locus at 6q25.1
por: Zheng, Wei, et al.
Publicado: (2009)

25.1 OLIGODENDROCYTE PATHOLOGY IN PREFRONTAL WHITE MATTER IN SCHIZOPHRENIA
por: Uranova, Natalya, et al.
Publicado: (2018)

A Phosphorylation-Related Variant ADD1-rs4963 Modifies the Risk of Colorectal Cancer
por: Shen, Na, et al.
Publicado: (2015)

Prenatal diagnosis of a rare de novo 1q22‐q25.1 chromosomal deletion syndrome using oligo array CGH
por: Shariati, Gholamreza, et al.
Publicado: (2018)

A Functional p53 Responsive Polymorphism in KITLG, rs4590952, Does not Affect the Risk of Breast Cancer
por: Chen, Wei, et al.
Publicado: (2014)

Role of a Genetic Variant on the 15q25.1 Lung Cancer Susceptibility Locus in Smoking-Associated Nasopharyngeal Carcinoma
por: Ji, Xuemei, et al.
Publicado: (2014)

Evaluation of a newly discovered breast cancer susceptibility locus at 6q25.1 in Iranian Azari-Turkish women
por: Garehdaghchi, Ziba, et al.
Publicado: (2016)

The rs74794265 SNP of the SREK1 Gene is Associated with COPD in Kashi, China
por: Abudureheman, Zulipikaer, et al.
Publicado: (2021)

Variants Located Upstream of CHRNB4 on Chromosome 15q25.1 Are Associated with Age at Onset of Daily Smoking and Habitual Smoking
por: Kapoor, Manav, et al.
Publicado: (2012)

Clinical features and short-term outcomes of elderly patients with COVID-19
por: Li, Ping, et al.
Publicado: (2020)

Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer
por: Childs, Erica J, et al.
Publicado: (2015)

Rat Mammary carcinoma susceptibility 3 (Mcs3) pleiotropy, socioenvironmental interaction, and comparative genomics with orthologous human 15q25.1-25.2
por: Duderstadt, Emily L, et al.
Publicado: (2022)

Multiple Independent Loci at Chromosome 15q25.1 Affect Smoking Quantity: a Meta-Analysis and Comparison with Lung Cancer and COPD
por: Saccone, Nancy L., et al.
Publicado: (2010)

Rs2200733 and rs10033464 on chromosome 4q25 confer risk of cardioembolic stroke: an updated meta-analysis
por: Cao, Yan-yan, et al.
Publicado: (2013)

Genetic Variants at Chromosomes 2q35, 5p12, 6q25.1, 10q26.13, and 16q12.1 Influence the Risk of Breast Cancer in Men
por: Orr, Nick, et al.
Publicado: (2011)

ESR1 Is Co-Expressed with Closely Adjacent Uncharacterised Genes Spanning a Breast Cancer Susceptibility Locus at 6q25.1
por: Dunbier, Anita K., et al.
Publicado: (2011)

Down‐regulation in Multiple Human Cancers of a Novel Gene, DMHC, from 17q25.1 That Encodes an Integral Membrane Protein
por: Mikami, Iwao, et al.
Publicado: (2001)

6q25.1 (TAB2) microdeletion is a risk factor for hypoplastic left heart: a case report that expands the phenotype
por: Cheng, Andrew, et al.
Publicado: (2020)

Replication Study in Chinese Population and Meta-Analysis Supports Association of the 11q23 Locus with Colorectal Cancer
por: Zou, Li, et al.
Publicado: (2012)

Influences of UGT2B7 rs7439366 and rs12233719 Polymorphisms on Fentanyl Sensitivity in Chinese Gynecologic Patients
por: Yang, Zhenling, et al.
Publicado: (2020)

Suppressing H19 Modulates Tumorigenicity and Stemness in U251 and U87MG Glioma Cells
por: Li, Weiguo, et al.
Publicado: (2016)

SNP-SNP Interaction between TLR4 and MyD88 in Susceptibility to Coronary Artery Disease in the Chinese Han Population
por: Sun, Dandan, et al.
Publicado: (2016)

Anti-PD-1 Immunotherapy Combined With Stereotactic Body Radiation Therapy and GM-CSF as Salvage Therapy in a PD-L1-Positive Patient With Refractory Metastatic Thyroid Hürthle Cell Carcinoma: A Case Report and Literature Review
por: He, Haihua, et al.
Publicado: (2021)

Association of PTPN22 SNP1858 (rs2476601) and Gene SNP1123 (rs2488457) Polymorphism With Primary Immune Thrombocytopenia Susceptibility: A Meta-Analysis of Case-Control Studies and Trial Sequential Analysis
por: Tian, Haokun, et al.
Publicado: (2022)

25.1 IMPACT OF COVID-19 ON MENTAL AND PHYSICAL HEALTH OF INDIVIDUALS WITH INTELLECTUAL DEVELOPMENTAL DISORDERS
por: Verma, Shikha
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_hq96fjsogief5tncgtfb168kbb