Zheng J - 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: zheng b, zheng j. 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

[Modifier factors influencing the phenotypic manifestation of the deafness associated mitochondrial DNA mutations].

YANG AF, ZHENG J, LV JX, GUAN MX. YANG AF, et al. Among authors: zheng j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Apr;28(2):165-71. doi: 10.3760/cma.j.issn.1003-9406.2011.02.010. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 21462128 Review. Chinese.

3

Mitochondrial tRNA mutations associated with deafness.

Zheng J, Ji Y, Guan MX. Zheng J, et al. Mitochondrion. 2012 May;12(3):406-13. doi: 10.1016/j.mito.2012.04.001. Epub 2012 Apr 16. Mitochondrion. 2012. PMID: 22538251 Free article.

4

[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. Among authors: zheng bj, zheng j. Yi Chuan. 2013 Jun;35(6):752-60. doi: 10.3724/sp.j.1005.2013.00752. Yi Chuan. 2013. PMID: 23774020 Chinese.

5

[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: zheng bj, zheng j. 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.

6

Maternally inherited diabetes is associated with a homoplasmic T10003C mutation in the mitochondrial tRNA(Gly) gene.

Liu H, Li R, Li W, Wang M, Ji J, Zheng J, Mao Z, Mo JQ, Jiang P, Lu J, Guan MX. Liu H, et al. Among authors: zheng j. Mitochondrion. 2015 Mar;21:49-57. doi: 10.1016/j.mito.2015.01.004. Epub 2015 Jan 20. Mitochondrion. 2015. PMID: 25615420

7

[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: zheng b, zheng j. 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.

8

A Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNAGlu and Mitochondrial Dysfunction.

Wang M, Liu H, Zheng J, Chen B, Zhou M, Fan W, Wang H, Liang X, Zhou X, Eriani G, Jiang P, Guan MX. Wang M, et al. Among authors: zheng j. J Biol Chem. 2016 Sep 30;291(40):21029-21041. doi: 10.1074/jbc.M116.739482. Epub 2016 Aug 12. J Biol Chem. 2016. PMID: 27519417 Free PMC article.

9

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: zheng j. 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.

10

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: zheng j. 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.

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