Tang X - Search Results

1

Mitochondrial ND5 T12338C, tRNA(Cys) T5802C, and tRNA(Thr) G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees.

Chen B, Sun D, Yang L, Zhang C, Yang A, Zhu Y, Zhao J, Chen Y, Guan M, Wang X, Li R, Tang X, Wang J, Tao Z, Lu J, Guan MX. Chen B, et al. Among authors: tang x. Am J Med Genet A. 2008 May 15;146A(10):1248-58. doi: 10.1002/ajmg.a.32285. Am J Med Genet A. 2008. PMID: 18386806

2

[Mitochondrial tRNAThr G15927A mutation may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation.].

Tang XW, Li ZY, Lu JX, Zhu Y, Li RH, Wang JD, Guan MX. Tang XW, et al. Yi Chuan. 2008 Oct;30(10):1287-94. doi: 10.3724/sp.j.1005.2008.01287. Yi Chuan. 2008. PMID: 18930888 Chinese.

3

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

Zhao JY, Tang XW, Lan JS, Lv JX, Yang L, Li ZY, Zhu Y, Sun DM, Yang AF, Wang JD, Xu J, Guan MX. Zhao JY, et al. Yi Chuan. 2008 Dec;30(12):1557-62. doi: 10.3724/sp.j.1005.2008.01557. Yi Chuan. 2008. PMID: 19073569 Chinese.

4

[Spectrum and frequency of mitochondrial 12S rRNA variants in the Chinese subjects with nonsynrdomic hearing loss in Zhejiang Province].

Zheng BJ, Peng GH, Chen BB, Fang F, Zheng J, Wu Y, Liang LZ, Nan BY, Tang XW, Zhu Y, Lu JX, Guan MX. Zheng BJ, et al. Yi Chuan. 2012 Jun;34(6):695-704. doi: 10.3724/sp.j.1005.2012.00695. Yi Chuan. 2012. PMID: 22698740 Chinese.

5

[Mitochondrial 12S rRNA A1555G mutation associated with nonsyndromic hearing loss in twenty-five Han Chinese pedigrees].

Peng GH, Zheng BJ, Fang F, Wu Y, Liang LZ, Zheng J, Nan BY, Yu X, Tang XW, Zhu Y, Lu JX, Chen BB, Guan MX. Peng GH, et al. Among authors: tang xw. Yi Chuan. 2013 Jan;35(1):62-72. doi: 10.3724/sp.j.1005.2013.00062. Yi Chuan. 2013. PMID: 23357266 Chinese.

6

[Mitochondrial tRNAIle A4317G mutation may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation].

Liang LZ, Wu Y, Yang YL, Cai Q, Xiao HL, Zheng J, Zheng BJ, Tang XW, Zhu Y, Lu JX, Guan MX. Liang LZ, et al. Yi Chuan. 2013 Jun;35(6):752-60. doi: 10.3724/sp.j.1005.2013.00752. Yi Chuan. 2013. PMID: 23774020 Chinese.

7

Aminoglycoside-induced and non-syndromic hearing loss is associated with the G7444A mutation in the mitochondrial COI/tRNASer(UCN) genes in two Chinese families.

Zhu Y, Qian Y, Tang X, Wang J, Yang L, Liao Z, Li R, Ji J, Li Z, Chen J, Choo DI, Lu J, Guan MX. Zhu Y, et al. Among authors: tang x. Biochem Biophys Res Commun. 2006 Apr 14;342(3):843-50. doi: 10.1016/j.bbrc.2006.02.027. Epub 2006 Feb 17. Biochem Biophys Res Commun. 2006. PMID: 16500624

8

Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutation.

Tang X, Yang L, Zhu Y, Liao Z, Wang J, Qian Y, Tao Z, Hu L, Wu G, Lan J, Wang X, Ji J, Wu J, Ji Y, Feng J, Chen J, Li Z, Zhang X, Lu J, Guan MX. Tang X, et al. Gene. 2007 May 15;393(1-2):11-9. doi: 10.1016/j.gene.2007.01.001. Epub 2007 Jan 24. Gene. 2007. PMID: 17341440

9

Mitochondrial tRNASer(UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing loss.

Jin L, Yang A, Zhu Y, Zhao J, Wang X, Yang L, Sun D, Tao Z, Tsushima A, Wu G, Xu L, Chen C, Yi B, Cai J, Tang X, Wang J, Li D, Yuan Q, Liao Z, Chen J, Li Z, Lu J, Guan MX. Jin L, et al. Among authors: tang x. Biochem Biophys Res Commun. 2007 Sep 14;361(1):133-9. doi: 10.1016/j.bbrc.2007.06.171. Epub 2007 Jul 10. Biochem Biophys Res Commun. 2007. PMID: 17659260

10

Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees.

Chen J, Yang L, Yang A, Zhu Y, Zhao J, Sun D, Tao Z, Tang X, Wang J, Wang X, Tsushima A, Lan J, Li W, Wu F, Yuan Q, Ji J, Feng J, Wu C, Liao Z, Li Z, Greinwald JH, Lu J, Guan MX. Chen J, et al. Among authors: tang x. Gene. 2007 Oct 15;401(1-2):4-11. doi: 10.1016/j.gene.2007.06.009. Epub 2007 Jun 20. Gene. 2007. PMID: 17698299 Free PMC article.

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