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 APE1 gene promoter is associated with noise-induced hearing loss in a Chinese population.

International archives of occupational and environmental health - 1 May 2016

Shen Huanxi, Dou Jianrui, Han Lei, Bai Ying, Li Qian, Hong Zhiqiang, Shi Jian, Zhang Hengdong, Zhang Feng, Du Cheng, Tong Zhimin, Zhu Baoli

Abstract excerpt

OBJECTIVE: To investigate whether the apurinic/apyrimidinic endonuclease 1 (APE1) 1349 T>G and -656 T>G polymorphisms were associated with the risk of noise-induced hearing loss (NIHL) in a Chinese population. METHODS: The two APE1 polymorphisms were analyzed among 613 NIHL workers and 613 normal hearing workers using the minor groove binder TaqMan probe assay. RESULTS: We found that the APE1 -656 TT genotype was...

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 China

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA-(Apurinic or Apyrimidinic Site) Lyase

Share to Gene Frequency

Share to Hearing Loss, Noise-Induced

Share to Occupational Diseases

Share to Promoter Regions, Genetic

Share to Risk Factors

Source

Identifiers

PMID: 26507517
DOI: 10.1007/s00420-015-1100-8

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic variation in APE1 gene promoter is associated with noise-induced hearing loss in a Chinese population.PMID 26507517Read ↗

Variations in the potassium voltage-gated channel subfamily E regulatory subunit 1 gene associated with noise-induced hearing loss in the Chinese population.Semantic proximity Read ↗

[Association between GPX-1 single nucleotide polymorphisms and susceptibility to noise-induced hearing loss among Chinese Han population].Semantic proximity Read ↗

Analysis of Polymorphisms Associated with Base Excision Repair in Patients Susceptible and Resistant to Noise-Induced Hearing Loss.Semantic proximity Read ↗

Genetic Variation in POU4F3 and GRHL2 Associated with Noise-Induced Hearing Loss in Chinese Population: A Case-Control Study.Semantic proximity Read ↗

A functional Ser326Cys polymorphism in hOGG1 is associated with noise-induced hearing loss in a Chinese population.Semantic proximity Read ↗

Polymorphisms of heat shock protein 70 genes (HSPA1A, HSPA1B and HSPA1L) and susceptibility of noise-induced hearing loss in a Chinese population: A case-control study.Semantic proximity Read ↗

Association between paraoxonase 2 gene polymorphisms and noise-induced hearing loss in the Chinese population.Semantic proximity Read ↗

Associations of genetic variations in EYA4, GRHL2 and DFNA5 with noise-induced hearing loss in Chinese population: a case- control study.Semantic proximity Read ↗

[Association between SNPs in DNMT1 and noise-induced hearing loss in Chinese Han population].Semantic proximity Read ↗

[Association between GSTP1 gene polymorphisms and susceptibility to noise-induced hearing loss].Semantic proximity Read ↗

Genetic Polymorphisms Associated with Hearing Threshold Shift in Subjects during First Encounter with Occupational Impulse Noise.Semantic proximity Read ↗

Interactions of genetic variations in FAS, GJB2 and PTPRN2 are associated with noise-induced hearing loss: a case-control study in China.Semantic proximity Read ↗

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