Advanced search
Publication Cover
Acta Oto-Laryngologica Volume 136, 2016 - Issue 8
Submit an article Journal homepage
254
Views
12
CrossRef citations to date
0
Altmetric
Research Article

GJB2, SLC26A4, and mitochondrial DNA12S rRNA hot-spots in 156 subjects with non-syndromic hearing loss in Tengzhou, China

Yalin MaDepartment of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, PR China; ;Shandong Provincial Key Laboratory of Otology, Jinan, PR China; ;Department of Otorhinolaryngology Head and Neck Surgery, Tengzhou Central People’s Hospital, Shandong, PR China
,
Yun XiaoDepartment of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, PR China; ;Shandong Provincial Key Laboratory of Otology, Jinan, PR China;
,
Xiaohui BaiDepartment of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, PR China; ;Shandong Provincial Key Laboratory of Otology, Jinan, PR China;
,
Fengguo ZhangDepartment of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, PR China; ;Shandong Provincial Key Laboratory of Otology, Jinan, PR China;
,
Daogong ZhangDepartment of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, PR China; ;Shandong Provincial Key Laboratory of Otology, Jinan, PR China;
,
Xinmao XuDepartment of Otorhinolaryngology Head and Neck Surgery, Tengzhou Central People’s Hospital, Shandong, PR China
,
Lei XuDepartment of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, PR China; ;Shandong Provincial Key Laboratory of Otology, Jinan, PR China;
&
Haibo WangDepartment of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, PR China; ;Shandong Provincial Key Laboratory of Otology, Jinan, PR China; Correspondence[email protected]
 show all
Pages 800-805 | Received 15 Jan 2016, Accepted 29 Feb 2016, Published online: 12 Apr 2016

References

  • Zhu Q, Liu X, Han D, Kang D, Zhang X, Jin Z, et al. [Molecular etiology of 573 patients with nonsyndromic hearing loss in 5 provinces of northwest region of China]. Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi 2007;21:460–2.
  • Xin F, Yuan Y, Deng X, Han M, Wang G, Zhao J, et al. Genetic mutations in nonsyndromic deafness patients of Chinese minority and Han ethnicities in Yunnan, China. J Transl Med 2013;11:312. DOI: 10.1186/1479-5876-11-312.
  • Chen J, Zheng H, Bei JX, Sun L, Jia WH, Li T, et al. Genetic structure of the Han Chinese population revealed by genome-wide SNP variation. Am J Hum Genet 2009;85:775–85.
  • Yi TM, Lander ES. Iterative template refinement: protein-fold prediction using iterative search and hybrid sequence/structure templates. Methods Enzymol 1996;266:322–39.
  • Du W, Cheng J, Ding H, Jiang Z, Guo Y, Yuan H. A rapid method for simultaneous multi-gene mutation screening in children with nonsyndromic hearing loss. Genomics 2014;104:264–70.
  • Chen X, Li S, Yang Y, Yang X, Liu Y, Liu Y, et al. Genome-wide association study validation identifies novel loci for atherosclerotic cardiovascular disease. J Thromb Haemost 2012;10:1508–14.
  • Wei J, Zheng L, Liu S, Yin J, Wang L, Wang X, et al. MiR-196a2 rs11614913 T > C polymorphism and risk of esophageal cancer in a Chinese population. Hum Immunol 2013;74:1199–205.
  • Zheng L, Yin J, Wang L, Wang X, Shi Y, Shao A, et al. Interleukin 1B rs16944 G > A polymorphism was associated with a decreased risk of esophageal cancer in a Chinese population. Clin Biochem 2013;46:1469–73.
  • Green GE, Scott DA, McDonald JM, Woodworth GG, Sheffield VC, Smith RJ. Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness. JAMA 1999;281:2211–16.
  • van der Zijl NJ, Hanemaaijer R, Tushuizen ME, Schindhelm RK, Boerop J, Rustemeijer C, et al. Urinary matrix metalloproteinase-8 and -9 activities in type 2 diabetic subjects: A marker of incipient diabetic nephropathy? Clin Biochem 2010;43:635–9.
  • Tsukamoto K, Suzuki H, Harada D, Namba A, Abe S, Usami S. Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged vestibular aqueduct: a unique spectrum of mutations in Japanese. Eur J Hum Genet 2003;11:916–22.
  • Wang Y, Su Y, Xu Y, Pan SH, Liu GD. Genetic polymorphism c. 1562C > T of the MMP-9 is associated with macroangiopathy in type 2 diabetes mellitus. Biochem Biophys Res Commun 2010;391:113–17.
  • Lewandowski KC, Banach E, Bienkiewicz M, Lewinski A. Matrix metalloproteinases in type 2 diabetes and non-diabetic controls: Effects of short-term and chronic hyperglycaemia. Arch Med Sci 2011;7:294–303.
  • Gharagozlian S, Svennevig K, Bangstad HJ, Winberg JO, Kolset SO. Matrix metalloproteinases in subjects with type 1 diabetes. BMC Clin Pathol 2009;9:7.
  • Dai P, Yu F, Han B, Liu X, Wang G, Li Q, et al. GJB2 mutation spectrum in 2,063 Chinese patients with nonsyndromic hearing impairment. J Transl Med 2009;7:26. DOI: 10.1186/1479-5876-7-26.
  • Jiang Y, Huang S, Deng T, Wu L, Chen J, Kang D, et al. Mutation spectrum of common deafness-causing genes in patients with non-syndromic deafness in the Xiamen area, China. PLoS One 2015;10:e0135088.
  • Dai P, Li Q, Huang D, Yuan Y, Kang D, Miller DT, et al. SLC26A4 c.919-2A > G varies among Chinese ethnic groups as a cause of hearing loss. Genet Med 2008;10:586–92.
  • Lee KY, Choi SY, Bae JW, Kim S, Chung KW, Drayna D, et al. Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patients. Int J Pediatr Otorhinolaryngol 2008;72:1301–9.
  • Lu J, Li Z, Zhu Y, Yang A, Li R, Zheng J, et al. Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss. Mitochondrion 2010;10:380–90.
  • Kupka S, Toth T, Wrobel M, Zeissler U, Szyfter W, Szyfter K, et al. Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients. Hum Mutat 2002;19:308–9.
  • Guo YF, Liu XW, Guan J, Han MK, Wang DY, Zhao YL, et al. GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects. Acta Otolaryngol 2008;128:297–303.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.