Similar articles for PMID: 18386806

Year	Number of Results
1993	1
1994	2
1997	3
1998	3
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2000	1
2001	3
2002	4
2003	3
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2005	12
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2007	14
2008	21
2009	22
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2012	21
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2014	16
2015	14
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2017	7
2018	11
2019	7
2020	26
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2022	17
2023	1
2024	0

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. 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 modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families.

Wang X, Lu J, Zhu Y, Yang A, Yang L, Li R, Chen B, Qian Y, Tang X, Wang J, Zhang X, Guan MX. Wang X, et al. Pharmacogenet Genomics. 2008 Dec;18(12):1059-70. doi: 10.1097/FPC.0b013e3283131661. Pharmacogenet Genomics. 2008. PMID: 18820594 Free PMC article.

3

Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss.

Young WY, Zhao L, Qian Y, Li R, Chen J, Yuan H, Dai P, Zhai S, Han D, Guan MX. Young WY, et al. Am J Med Genet A. 2006 Oct 15;140(20):2188-97. doi: 10.1002/ajmg.a.31434. Am J Med Genet A. 2006. PMID: 16955413

4

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

5

Mitochondrial tRNA(Glu) A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family.

Ding Y, Li Y, You J, Yang L, Chen B, Lu J, Guan MX. Ding Y, et al. J Genet Genomics. 2009 Apr;36(4):241-50. doi: 10.1016/S1673-8527(08)60111-3. J Genet Genomics. 2009. PMID: 19376484

6

[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.

7

Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation.

Lu J, Qian Y, Li Z, Yang A, Zhu Y, Li R, Yang L, Tang X, Chen B, Ding Y, Li Y, You J, Zheng J, Tao Z, Zhao F, Wang J, Sun D, Zhao J, Meng Y, Guan MX. Lu J, et al. Mitochondrion. 2010 Jan;10(1):69-81. doi: 10.1016/j.mito.2009.09.007. Epub 2009 Oct 8. Mitochondrion. 2010. PMID: 19818876 Free PMC article.

8

Mitochondrial COX2 G7598A mutation may have a modifying role in the phenotypic manifestation of aminoglycoside antibiotic-induced deafness associated with 12S rRNA A1555G mutation in a Han Chinese pedigree.

Chen T, Liu Q, Jiang L, Liu C, Ou Q. Chen T, et al. Genet Test Mol Biomarkers. 2013 Feb;17(2):122-30. doi: 10.1089/gtmb.2012.0251. Epub 2012 Dec 20. Genet Test Mol Biomarkers. 2013. PMID: 23256547 Free PMC article.

9

Molecular and clinical characterization of the variable phenotype in Korean families with hearing loss associated with the mitochondrial A1555G mutation.

Bae JW, Kim DB, Choi JY, Park HJ, Lee JD, Hur DG, Bae SH, Jung DJ, Lee SH, Kim UK, Lee KY. Bae JW, et al. PLoS One. 2012;7(8):e42463. doi: 10.1371/journal.pone.0042463. Epub 2012 Aug 6. PLoS One. 2012. PMID: 22879993 Free PMC article.

10

Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss.

Yuan H, Chen J, Liu X, Cheng J, Wang X, Yang L, Yang S, Cao J, Kang D, Dai P, Zhai S, Han D, Young WY, Guan MX. Yuan H, et al. Biochem Biophys Res Commun. 2007 Oct 12;362(1):94-100. doi: 10.1016/j.bbrc.2007.07.161. Epub 2007 Aug 8. Biochem Biophys Res Commun. 2007. PMID: 17698030

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