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

Detection of a 4-bp Insertion/deletion Polymorphism within the Promoter of EGLN2 Using Mismatch PCR-RFLP and Its Association with Susceptibility to Breast Cancer

Asian Pacific journal of cancer prevention : APJCP - 25 Apr 2018

Hashemi Mohammad, Danesh Hiva, Bizhani Fatemeh, Sattarifard Hedieh, Hashemi Seyed Mehdi, Bahari Gholamreza

Abstract excerpt

It has been shown that a 4-bp insertion/deletion (ins/del) polymorphism of EGLN2 influences the risk of several cancers. However, to date, no study has inspected the impact of the 4-bp ins/del polymorphism on breast cancer (BC) risk. A case-control study, including 134 breast cancer patients and 154 healthy women, was here conducted to examine the possible association between EGLN2 4-bp ins/del polymorphism and...

Read the complete abstract on PubMed

Topics

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

Share to Biomarkers, Tumor
Share to Breast Neoplasms

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Follow-Up Studies

Share to Hypoxia-Inducible Factor-Proline Dioxygenases

Share to INDEL Mutation

Share to Polymorphism, Restriction Fragment Length

Share to Prognosis

Share to Promoter Regions, Genetic

Source

Open in PubMed Open full text

Identifiers

PMID: 29693343
DOI: 10.22034/APJCP.2018.19.4.923
PMCID: PMC6031807

Genes

EGLN2

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

Detection of a 4-bp Insertion/deletion Polymorphism within the Promoter of EGLN2 Using Mismatch PCR-RFLP and Its Association with Susceptibility to Breast CancerPMID 29693343Read ↗

An insertion/deletion polymorphism within the promoter of EGLN2 is associated with susceptibility to colorectal cancer.Semantic proximity Read ↗

2q35-rs13387042 variant and the risk of breast cancer: a case-control study.Semantic proximity Read ↗

LncRNA MEG3 rs3087918 was associated with a decreased breast cancer risk in a Chinese population: a case-control studySemantic proximity Read ↗

Association between HLA-G 3'UTR 14-bp ins/del polymorphism and susceptibility to breast cancer.Semantic proximity Read ↗

Association of EGLN2 rs10680577 Polymorphism with the Risk and Clinicopathological Features of Patients with Prostate Cancer.Semantic proximity Read ↗

The functional 4-bp insertion/deletion ATTG polymorphism in the promoter region of NF-KB1 reduces the risk of BC.Semantic proximity Read ↗

Ile to Val polymorphism at codon 655 of HER-2 gene and breast cancer risk in Iranian women.Semantic proximity Read ↗

Her2 Ile655Val polymorphism and its association with breast cancer risk: an updated meta-analysis of case-control studies.Semantic proximity Read ↗

Genetic polymorphisms in the DNA repair enzyme ERCC2 and breast tumour risk in a Chinese population.Semantic proximity Read ↗

Association between human leukocyte antigen-G 14-bp insertion/deletion polymorphism and cancer risk: a meta-analysis and systematic review.Semantic proximity Read ↗

Genetic polymorphism in HLA-G 3'UTR 14-bp ins/del and risk of cancer: a meta-analysis of case-control study.Semantic proximity Read ↗

Association between Vascular Endothelial Growth Factor Gene Polymorphisms with Breast Cancer Risk in an Iranian PopulationSemantic proximity Read ↗

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