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

Polymorphisms in genes involved in the free-radical process in patients with sudden sensorineural hearing loss and Ménière's disease.

Free radical research - 1 Jul 2013

Teranishi M, Uchida Y, Nishio N, Kato K, Otake H, Yoshida T, Suzuki H, Sone M, Sugiura S, Ando F, Shimokata H, Nakashima T

Abstract excerpt

The etiologies of idiopathic sudden sensorineural hearing loss (SSNHL) and Ménière's disease remain unclear. Recently, accumulating evidence has demonstrated that free radicals are related to the pathology of inner ear disease. Because genetic factors may contribute partly to the etiologies of SSNHL and Ménière's disease, we investigated the association between genetic polymorphisms located in genes related to...

Read the complete abstract on PubMed

Topics

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

Share to Aged, 80 and over
Share to Free Radicals

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hearing Loss, Sensorineural

Share to Meniere Disease

Share to Nitric Oxide Synthase Type III

Share to Odds Ratio

Share to Risk Factors

Share to Young Adult

Source

Identifiers

PMID: 23560644
DOI: 10.3109/10715762.2013.793319

Genes

NOS3
MTR
MTRR

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Polymorphisms in genes involved in the free-radical process in patients with sudden sensorineural hearing loss and Ménière's disease.PMID 23560644Read ↗

Polymorphisms in Genes Involved in Oxidative Stress Response in Patients with Sudden Sensorineural Hearing Loss and Ménière's Disease in a Japanese PopulationSemantic proximity Read ↗

Genetic Polymorphisms in Sudden Sensorineural Hearing Loss: An Update.Semantic proximity Read ↗

Association of the C677T polymorphism in the methylenetetrahydrofolate reductase gene with sudden sensorineural hearing loss.Semantic proximity Read ↗

Mendelian Randomization Study Reveals a Predicted Relationship between Sensorineural Hearing Loss and Mitochondrial Proteins.Semantic proximity Read ↗

Association between polymorphisms in genes encoding methylenetetrahydrofolate reductase and the risk of Ménière's disease.Semantic proximity Read ↗

LINE-1 global DNA methylation, iron homeostasis genes, sex and age in sudden sensorineural hearing loss (SSNHL)Semantic proximity Read ↗

Genetically predicted cerebrospinal fluid metabolite levels and risk of sudden sensorineural hearing loss: A Mendelian randomization study.Semantic proximity Read ↗

SOD1 gene polymorphisms in sudden sensorineural hearing loss.Semantic proximity Read ↗

Functional variants in NOS1 and NOS2A are not associated with progressive hearing loss in Ménière's disease in a European Caucasian population.Semantic proximity Read ↗

Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74.Semantic proximity Read ↗

The Genetic Association of rs5746105 Polymorphism of SOD2 with the Susceptibility to Sudden Deafness.Semantic proximity Read ↗

Contribution of complement factor H Y402H polymorphism to sudden sensorineural hearing loss risk and possible interaction with diabetes.Semantic proximity Read ↗

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