Single-Nucleotide Polymorphisms in Are Associated with Noise-Induced Hearing Loss in a Chinese Population

Overview

Journal Biochem Res Int

Publisher Wiley

Specialty Biochemistry

Date 2020 Mar 10

PMID 32148964

Citations 4

Authors

Ning Wang

Boshen Wang

Jiadi Guo

Suhao Zhang

Lei Han

Juan Zhang

Baoli Zhu

Affiliations

Soon will be listed here.

Abstract

Objectives: The purpose of this study was to investigate the correlation between single-nucleotide polymorphism (SNP) in 3'UTR of gene and the occurrence of noise-induced hearing loss (NIHL), and to further explore the regulatory mechanism of miRNAs in NIHL on gene and the occurrence of noise-induced hearing loss (NIHL), and to further explore the regulatory mechanism of miRNAs in NIHL on.

Methods: We conducted a case-control study involving 1040 cases and 1060 controls. The effects of SNPs on gene and the occurrence of noise-induced hearing loss (NIHL), and to further explore the regulatory mechanism of miRNAs in NIHL on.

Results: We genotyped four SNPs (rs2257082, rs11077, rs7755135, and rs1106841) in the gene and the occurrence of noise-induced hearing loss (NIHL), and to further explore the regulatory mechanism of miRNAs in NIHL on gene and the occurrence of noise-induced hearing loss (NIHL), and to further explore the regulatory mechanism of miRNAs in NIHL on gene and the occurrence of noise-induced hearing loss (NIHL), and to further explore the regulatory mechanism of miRNAs in NIHL on . The genetic polymorphism, rs11077, within is associated with the risk of noise-induced hearing loss in a Chinese population. gene and the occurrence of noise-induced hearing loss (NIHL), and to further explore the regulatory mechanism of miRNAs in NIHL on.

Citing Articles

Relationship Between the Occurrence of Depression and (rs6877842, rs10719) and (rs11077) Single-Nucleotide Polymorphisms in the Polish Population: A Case-Control Study.

Kowalczyk M, Kowalczyk E, Talarowska M, Majsterek I, Skrzypek M, Poplawski T Int J Mol Sci. 2024; 25(22).

PMID: 39596271 PMC: 11594337. DOI: 10.3390/ijms252212204.

The Role of Genetic Variants in the Susceptibility of Noise-Induced Hearing Loss.

Chen X, Xue X, Yu N, Guo W, Yuan S, Jiang Q Front Cell Neurosci. 2022; 16:946206.

PMID: 35903368 PMC: 9315435. DOI: 10.3389/fncel.2022.946206.

Genetic association study between TAB2 polymorphisms and noise-induced-hearing-loss in a Han Chinese population.

Yang G, Wang B, Sun D, Wang H, Chen M, Chen H PLoS One. 2021; 16(5):e0251090.

PMID: 33974633 PMC: 8112696. DOI: 10.1371/journal.pone.0251090.

Erratum to "Single-Nucleotide Polymorphisms in XPO5 are Associated with Noise-Induced Hearing Loss in a Chinese Population".

Wang N, Wang B, Guo J, Zhang S, Han L, Zhang J Biochem Res Int. 2021; 2020:9649346.

PMID: 33457014 PMC: 7787785. DOI: 10.1155/2020/9649346.

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