Wang Q - Search Results

1

Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation.

Zhao L, Young WY, Li R, Wang Q, Qian Y, Guan MX. Zhao L, et al. Among authors: wang q. Biochem Biophys Res Commun. 2004 Dec 24;325(4):1503-8. doi: 10.1016/j.bbrc.2004.10.199. Biochem Biophys Res Commun. 2004. PMID: 15555598

2

[A report on a large family with X-linked recessive nonsyndromic hereditary low frequency neuropathic hearing impairment].

Wang Q, Cao J, Yu L, Guo W, Yu N, Yang W, Gu R. Wang Q, et al. Zhonghua Er Bi Yan Hou Ke Za Zhi. 2002 Aug;37(4):247-51. Zhonghua Er Bi Yan Hou Ke Za Zhi. 2002. PMID: 12772406 Chinese.

3

Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family.

Zhao H, Li R, Wang Q, Yan Q, Deng JH, Han D, Bai Y, Young WY, Guan MX. Zhao H, et al. Among authors: wang q. Am J Hum Genet. 2004 Jan;74(1):139-52. doi: 10.1086/381133. Epub 2003 Dec 12. Am J Hum Genet. 2004. PMID: 14681830 Free PMC article.

4

Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation.

Wang Q, Li R, Zhao H, Peters JL, Liu Q, Yang L, Han D, Greinwald JH Jr, Young WY, Guan MX. Wang Q, et al. Am J Med Genet A. 2005 Feb 15;133A(1):27-30. doi: 10.1002/ajmg.a.30424. Am J Med Genet A. 2005. PMID: 15637703 Free PMC article.

5

Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation.

Young WY, Zhao L, Qian Y, Wang Q, Li N, Greinwald JH Jr, Guan MX. Young WY, et al. Among authors: wang q. Biochem Biophys Res Commun. 2005 Mar 25;328(4):1244-51. doi: 10.1016/j.bbrc.2005.01.085. Biochem Biophys Res Commun. 2005. PMID: 15708009

6

Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss.

Zhao H, Young WY, Yan Q, Li R, Cao J, Wang Q, Li X, Peters JL, Han D, Guan MX. Zhao H, et al. Among authors: wang q. Nucleic Acids Res. 2005 Feb 18;33(3):1132-9. doi: 10.1093/nar/gki262. Print 2005. Nucleic Acids Res. 2005. PMID: 15722487 Free PMC article.

7

Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss.

Zhao L, Wang Q, Qian Y, Li R, Cao J, Hart LC, Zhai S, Han D, Young WY, Guan MX. Zhao L, et al. Among authors: wang q. Biochem Biophys Res Commun. 2005 Oct 28;336(3):967-73. doi: 10.1016/j.bbrc.2005.08.199. Biochem Biophys Res Commun. 2005. PMID: 16168391

8

Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation.

Wang Q, Li QZ, Han D, Zhao Y, Zhao L, Qian Y, Yuan H, Li R, Zhai S, Young WY, Guan MX. Wang Q, et al. Biochem Biophys Res Commun. 2006 Feb 10;340(2):583-8. doi: 10.1016/j.bbrc.2005.12.045. Epub 2005 Dec 19. Biochem Biophys Res Commun. 2006. PMID: 16380089

9

A novel mutation of POU3F4 causes congenital profound sensorineural hearing loss in a large Chinese family.

Wang QJ, Li QZ, Rao SQ, Zhao YL, Yuan H, Yang WY, Han DY, Shen Y. Wang QJ, et al. Laryngoscope. 2006 Jun;116(6):944-50. doi: 10.1097/01.MLG.0000215285.53045.24. Laryngoscope. 2006. PMID: 16735904

10

The large Chinese family with Y-linked hearing loss revisited: clinical investigation.

Wang QJ, Rao SQ, Zhao YL, Liu QJ, Zong L, Han MK, Han DY, Yang WY. Wang QJ, et al. Acta Otolaryngol. 2009 Jun;129(6):638-43. doi: 10.1080/00016480802216347. Acta Otolaryngol. 2009. PMID: 18720061

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