Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genetic variations in base excision repair pathway and risk of bladder cancer: a case-control study in the United States.

Molecular carcinogenesis - 1 Jan 2015

Xie Hui, Gong Yilei, Dai Jingyao, Wu Xifeng, Gu Jian

Abstract excerpt

Base excision repair (BER) is one of the major cellular DNA repair pathways that repairs small isolated foci of DNA damage including reduced or oxidized single bases or fragments and small, non-bulky adducts. Genetic variations in BER genes may affect DNA repair capacity and increase susceptibility to bladder cancer. In a case-control study of 801 bladder cancer patients and 801 matched controls, we evaluated the...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Case-Control Studies
Share to DNA Repair
Share to Genetic Association Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Regression Analysis

Share to Signal Transduction

Share to United States

Share to Uracil-DNA Glycosidase

Share to Urinary Bladder Neoplasms

Source

Identifiers

PMID: 24038406
DOI: 10.1002/mc.22073

Genes

SMUG1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic variations in base excision repair pathway and risk of bladder cancer: a case-control study in the United States.PMID 24038406Read ↗

Genetic polymorphism in bladder cancer.Semantic proximity Read ↗

ERCC1 haplotypes modify bladder cancer risk: a case-control study.Semantic proximity Read ↗

High-order interactions among genetic variants in DNA base excision repair pathway genes and smoking in bladder cancer susceptibility.Semantic proximity Read ↗

Polymorphisms in DNA repair genes, smoking, and bladder cancer risk: findings from the international consortium of bladder cancer.Semantic proximity Read ↗

Complex association between ERCC2 gene polymorphisms, gender, smoking and the susceptibility to bladder cancer: a meta-analysis.Semantic proximity Read ↗

Genetic variation in the base excision repair pathway and bladder cancer risk.Semantic proximity Read ↗

Comprehensive pathway-based interrogation of genetic variations in the nucleotide excision DNA repair pathway and risk of bladder cancer.Semantic proximity Read ↗

DNA repair gene XRCC1 polymorphisms, smoking, and bladder cancer risk: a meta-analysis.Semantic proximity Read ↗

hOGG1 Ser326Cys polymorphism is associated with risk of bladder cancer in a Chinese population: a case-control study.Semantic proximity Read ↗

Bladder cancer epidemiology and genetic susceptibilitySemantic proximity Read ↗

Genetic risk scores based on risk-associated single nucleotide polymorphisms can reveal inherited risk of bladder cancer in Chinese population.Semantic proximity Read ↗

Genetic variants in 8-oxoguanine DNA glycosylase 1 (OGG1) and X-ray repair cross-complementing protein 1 (XRCC1) and non-genetic factors are associated with bladder cancer susceptibility and prognosis in a Brazilian population.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.