Tang X - Search Results

1

A deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial function.

Wang M, Peng Y, Zheng J, Zheng B, Jin X, Liu H, Wang Y, Tang X, Huang T, Jiang P, Guan MX. Wang M, et al. Among authors: tang x. Nucleic Acids Res. 2016 Dec 15;44(22):10974-10985. doi: 10.1093/nar/gkw726. Epub 2016 Aug 17. Nucleic Acids Res. 2016. PMID: 27536005 Free PMC article.

2

[Mitochondrial DNA secondary mutation associated with deafness].

Tang XW, Guan MX. Tang XW, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012 Dec;47(12):1050-3. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012. PMID: 23328056 Review. Chinese. No abstract available.

3

[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.

4

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

Wu Y, Liang LZ, Xiao HL, Yang YL, Yu X, Zheng J, Fang F, Zheng BJ, Tang XW, Jin LJ, Guan MX. Wu Y, et al. Among authors: tang xw. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013 Dec;48(12):978-84. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013. PMID: 24506995 Chinese.

5

[Mitochondrial tRNA(Thr)T15943C mutation may be a new position that affects the phenotypic expression of deafness associated 12s rRNA A1555G mutation].

Xiao H, He Z, Gao Y, Yang Y, Zheng J, Cai Z, Zheng B, Tang X, Guan M. Xiao H, et al. Among authors: tang x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Apr;32(2):163-8. doi: 10.3760/cma.j.issn.1003-9406.2015.02.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 25863077 Chinese.

6

Contribution of the tRNA^Ile 4317A→G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A→G mutation.

Meng F, He Z, Tang X, Zheng J, Jin X, Zhu Y, Ren X, Zhou M, Wang M, Gong S, Mo JQ, Shu Q, Guan MX. Meng F, et al. Among authors: tang x. J Biol Chem. 2018 Mar 2;293(9):3321-3334. doi: 10.1074/jbc.RA117.000530. Epub 2018 Jan 18. J Biol Chem. 2018. PMID: 29348176 Free PMC article.

7

A deafness-associated mitochondrial DNA mutation altered the tRNA^Ser(UCN) metabolism and mitochondrial function.

Xue L, Chen Y, Tang X, Yao J, Huang H, Wang M, Ye S, Wang M, Guan MX. Xue L, et al. Among authors: tang x. Mitochondrion. 2019 May;46:370-379. doi: 10.1016/j.mito.2018.10.001. Epub 2018 Oct 15. Mitochondrion. 2019. PMID: 30336267

8

Contribution of a mitochondrial tyrosyl-tRNA synthetase mutation to the phenotypic expression of the deafness-associated tRNA^Ser(UCN) 7511A>G mutation.

Fan W, Zheng J, Kong W, Cui L, Aishanjiang M, Yi Q, Wang M, Cang X, Tang X, Chen Y, Mo JQ, Sondheimer N, Ge W, Guan MX. Fan W, et al. Among authors: tang x. J Biol Chem. 2019 Dec 13;294(50):19292-19305. doi: 10.1074/jbc.RA119.010598. Epub 2019 Nov 4. J Biol Chem. 2019. PMID: 31685661 Free PMC article.

9

[Spectrum of GJB6 variants in 318 pedigrees with non-syndromic hearing loss:one deafness pedigree carrying both GJB6 and GJB2 deletion variant].

Zheng BJ, Zhang T, Wang H, Tang XW, Zheng J, Lv JX, Guan MX. Zheng BJ, et al. Among authors: tang xw. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2016 Jun 20;30(12):933-937. doi: 10.13201/j.issn.1001-1781.2016.12.003. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2016. PMID: 29771057 Chinese.

10

[Mutation analysis of GJB2 gene in 1 822 patients with nonsyndromic hearing loss in Zhejiang Province].

Fan WL, Shi WW, Wang BB, Zheng BJ, Xue L, Tang XW, Guan MX. Fan WL, et al. Among authors: tang xw. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2017 Mar 5;31(5):352-355. doi: 10.13201/j.issn.1001-1781.2017.05.006. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2017. PMID: 29871260 Chinese.

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