Similar articles for PMID: 21931169

Year	Number of Results
1989	1
1990	1
1991	1
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1994	2
1995	4
1996	3
1997	3
1998	4
1999	4
2000	4
2001	3
2002	5
2003	3
2004	9
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2006	13
2007	10
2008	10
2009	11
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2012	22
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2014	13
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2018	19
2019	16
2020	16
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2024	0

1

Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis gene.

Yan X, Wang X, Wang Z, Sun S, Chen G, He Y, Mo JQ, Li R, Jiang P, Lin Q, Sun M, Li W, Bai Y, Zhang J, Zhu Y, Lu J, Yan Q, Li H, Guan MX. Yan X, et al. J Med Genet. 2011 Oct;48(10):682-90. doi: 10.1136/jmedgenet-2011-100219. J Med Genet. 2011. PMID: 21931169

2

Maternally transmitted diabetes mellitus associated with the mitochondrial tRNA(Leu(UUR)) A3243G mutation in a four-generation Han Chinese family.

Lu J, Wang D, Li R, Li W, Ji J, Zhao J, Ye W, Yang L, Qian Y, Zhu Y, Guan MX. Lu J, et al. Biochem Biophys Res Commun. 2006 Sep 15;348(1):115-9. doi: 10.1016/j.bbrc.2006.07.010. Epub 2006 Jul 13. Biochem Biophys Res Commun. 2006. PMID: 16876129

3

The Mitochondrial tRNAHis G12192A Mutation May Modulate the Clinical Expression of Deafness-Associated tRNAThr G15927A Mutation in a Chinese Pedigree.

Ding Y, Teng YS, Zhuo GC, Xia BH, Leng JH. Ding Y, et al. Curr Mol Med. 2019;19(2):136-146. doi: 10.2174/1566524019666190308121552. Curr Mol Med. 2019. PMID: 30854964

4

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

5

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. 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

6

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.

7

Late onset nonsyndromic hearing loss in a Dongxiang Chinese family is associated with the 593T>C variant in the mitochondrial tRNA^Phe gene.

Chen X, Nie Z, Wang F, Wang J, Liu XW, Zheng J, Guo YF, Guan MX. Chen X, et al. Mitochondrion. 2017 Jul;35:111-118. doi: 10.1016/j.mito.2017.05.013. Epub 2017 Jun 1. Mitochondrion. 2017. PMID: 28579530

8

[Audiological findings and mitochondrial DNA mutation in a large family with matrilineal sensorineural hearing loss].

Xing G, Bu X, Yan M, Lu L, Yang S. Xing G, et al. Zhonghua Er Bi Yan Hou Ke Za Zhi. 2000 Apr;35(2):98-101. Zhonghua Er Bi Yan Hou Ke Za Zhi. 2000. PMID: 12768662 Chinese.

9

Mitochondrial 12S rRNA A827G mutation is involved in the genetic susceptibility to aminoglycoside ototoxicity.

Xing G, Chen Z, Wei Q, Tian H, Li X, Zhou A, Bu X, Cao X. Xing G, et al. Biochem Biophys Res Commun. 2006 Aug 11;346(4):1131-5. doi: 10.1016/j.bbrc.2006.05.208. Epub 2006 Jun 12. Biochem Biophys Res Commun. 2006. PMID: 16782057

10

Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families.

Dai P, Yuan Y, Huang D, Qian Y, Liu X, Han D, Yuan H, Wang X, Young WY, Guan MX. Dai P, et al. Biochem Biophys Res Commun. 2006 Sep 15;348(1):200-5. doi: 10.1016/j.bbrc.2006.07.031. Epub 2006 Jul 17. Biochem Biophys Res Commun. 2006. PMID: 16875663

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