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

[Research on mitochondrial DNA T1095C gene variation in military noise-induced hearing loss].

Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery - 1 May 2010

Qu Li, Xue Xijun, Dai Pu, Han Dongyi, Cao Xianbao, Yang Xiaodong, Shao Fuyin, Zhang Bo, Ma Tao, Yu Ruili, Zhong Ling

Abstract excerpt

OBJECTIVE: To study the clinical and sequence character of the entire mitochondrial genome in five subjects with mitochondrial 12SrRNA T1095C mutation, and to analyze its relationship with the military noise-induced hearing loss (NIHL). METHOD: Three hundreds and four soldiers exposed to military noise were selected in Yunan and Beijing, including susceptible (experimental) and tolerance (control) groups....

Read the complete abstract on PubMed

Topics

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

Share to Base Sequence
Share to DNA, Mitochondrial

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hearing Loss, Noise-Induced

Share to Military Personnel

Share to Mutation

Share to Young Adult

Source

Identifiers

PMID: 20669660

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

[Research on mitochondrial DNA T1095C gene variation in military noise-induced hearing loss].PMID 20669660Read ↗

[Investigation into the relationship between mitochondrial 12 S rRNA gene, tRNA gene and cytochrome oxidase Ⅱ gene variations and the risk of noise-induced hearing loss].Semantic proximity Read ↗

[Mitochondrial 12S rRNA variants studies in 456 subjects with hearing loss in seven schools for deaf and mutes in Zhejiang province].Semantic proximity Read ↗

[Study of mtDNA 12S rRNA A1555G, GJB2, GJB3 gene mutation in Uighur and Han people with hereditary nonsyndromic hearing loss in Xinjiang].Semantic proximity Read ↗

Co-segregation of the T1095C with the A1555G mutation of the mitochondrial 12S rRNA gene in a patient with non-syndromic hearing loss.Semantic proximity Read ↗

Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families.Semantic proximity Read ↗

Increased Risk of Hearing Loss Associated with MT-RNR1 Gene Mutations: A Real-World Investigation Among Han Taiwanese PopulationSemantic proximity Read ↗

[Mitochondrial 12S rRNA gene A827G in two pedigrees with nonsyndromic deafness].Semantic proximity Read ↗

[Hearing loss may be associated with the novel mitochondrial tRNA(Asp) A7551G mutation in a Chinese family].Semantic proximity Read ↗

Novel nucleotide changes in mutational analysis of mitochondrial 12SrRNA gene in patients with nonsyndromic and aminoglycoside-induced hearing loss.Semantic proximity Read ↗

[Mitochondrial DNA A1555G mutation analysis in 802 nonsyndromic hearing impairment patients].Semantic proximity Read ↗

[Modification factors associated with maternally inherited non-syndromic hearing loss].Semantic proximity Read ↗

[Hearing loss and epilepsy may be associated with the novel mitochondrial tRNASer(UCN) 7472delC mutation in a Chinese family].Semantic proximity Read ↗

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