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 variation in CXCL12 and risk of cervical carcinoma: a population-based case-control study.

International journal of immunogenetics - 1 Dec 2009

Maley S N, Schwartz S M, Johnson L G, Malkki M, Du Q, Daling J R, Li S S, Zhao L P, Petersdorf E W, Madeleine M M

Abstract excerpt

CXCL12 provides a chemotactic signal-directing leucocyte migration and regulates metastatic behaviour of tumour cells. We conducted a population-based case-control study to test the hypothesis that common genetic variation in CXCL12 individual single nucleotide polymorphism (SNP) alleles and haplotypes] is associated with the risk of cervical carcinoma. Cases (n = 917) were residents of western Washington State...

Read the complete abstract on PubMed

Topics

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

Share to 3' Untranslated Regions
Share to Carcinoma

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Case-Control Studies

Share to Chemokine CXCL12

Share to Gene Expression Regulation, Neoplastic

Share to Haplotypes

Share to Neoplasm Invasiveness

Share to Uterine Cervical Neoplasms

Source

Open in PubMed Open full text

Identifiers

PMID: 19788587
DOI: 10.1111/j.1744-313X.2009.00877.x
PMCID: PMC2784202

Genes

CXCL12

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic variation in CXCL12 and risk of cervical carcinoma: a population-based case-control study.PMID 19788587Read ↗

CXCL12/CXCR4 axis gene variants contribute to an increased vulnerability to HPV infection and cervical oncogenesis.Semantic proximity Read ↗

CXCL12 rs266085 and TNF-α rs1799724 polymorphisms and susceptibility to cervical cancer in a Chinese population.Semantic proximity Read ↗

Nucleotide variation in IL-10 and IL-12 and their receptors and cervical and vulvar cancer risk: a hybrid case-parent triad and case-control study.Semantic proximity Read ↗

Genetic Variants of Interleukin-8 and Interleukin-16 and Their Association with Cervical Cancer RiskSemantic proximity Read ↗

The CXCL12 G801A polymorphism and cancer risk: evidence from 17 case-control studies.Semantic proximity Read ↗

Genomic Risk Factors for Cervical CancerSemantic proximity Read ↗

The G801A polymorphism in the CXCL12 gene and risk of breast carcinoma: evidence from a meta-analysis including 2,931 subjects.Semantic proximity Read ↗

Association of the CXCL12 rs1801157 Polymorphism with Breast Cancer Risk: A Meta-Analysis.Semantic proximity Read ↗

A population-based case-control study of genetic variation in cytokine genes associated with risk of cervical and vulvar cancers.Semantic proximity Read ↗

Genome-wide association study of susceptibility loci for cervical cancer.Semantic proximity Read ↗

Associations of CXCL12 polymorphisms with clinicopathological features in breast cancer: a case-control study.Semantic proximity Read ↗

Meta-analyses of the relationship between five CXCL8 gene polymorphisms and overall cancer risk, and a case-control study of oral cancer.Semantic proximity Read ↗

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