Mo JQ - Search Results

1

The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation.

Jiang P, Jin X, Peng Y, Wang M, Liu H, Liu X, Zhang Z, Ji Y, Zhang J, Liang M, Zhao F, Sun YH, Zhang M, Zhou X, Chen Y, Mo JQ, Huang T, Qu J, Guan MX. Jiang P, et al. Among authors: mo jq. Hum Mol Genet. 2016 Feb 1;25(3):584-96. doi: 10.1093/hmg/ddv498. Epub 2015 Dec 8. Hum Mol Genet. 2016. PMID: 26647310

2

Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber's hereditary optic neuropathy.

Qian Y, Zhou X, Hu Y, Tong Y, Li R, Lu F, Yang H, Mo JQ, Qu J, Guan MX. Qian Y, et al. Among authors: mo jq. Biochem Biophys Res Commun. 2005 Jul 1;332(2):614-21. doi: 10.1016/j.bbrc.2005.05.003. Biochem Biophys Res Commun. 2005. PMID: 15896721

3

Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss.

Yuan H, Qian Y, Xu Y, Cao J, Bai L, Shen W, Ji F, Zhang X, Kang D, Mo JQ, Greinwald JH, Han D, Zhai S, Young WY, Guan MX. Yuan H, et al. Among authors: mo jq. Am J Med Genet A. 2005 Oct 1;138A(2):133-40. doi: 10.1002/ajmg.a.30952. Am J Med Genet A. 2005. PMID: 16152638 Free PMC article.

4

The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation.

Qu J, Li R, Zhou X, Tong Y, Lu F, Qian Y, Hu Y, Mo JQ, West CE, Guan MX. Qu J, et al. Among authors: mo jq. Invest Ophthalmol Vis Sci. 2006 Feb;47(2):475-83. doi: 10.1167/iovs.05-0665. Invest Ophthalmol Vis Sci. 2006. PMID: 16431939

5

The mitochondrial tRNA(Thr) A15951G mutation may influence the phenotypic expression of the LHON-associated ND4 G11778A mutation in a Chinese family.

Li R, Qu J, Zhou X, Tong Y, Hu Y, Qian Y, Lu F, Mo JQ, West CE, Guan MX. Li R, et al. Among authors: mo jq. Gene. 2006 Jul 5;376(1):79-86. doi: 10.1016/j.gene.2006.02.014. Epub 2006 Apr 19. Gene. 2006. PMID: 16624503

6

Maternally inherited essential hypertension is associated with the novel 4263A>G mutation in the mitochondrial tRNAIle gene in a large Han Chinese family.

Wang S, Li R, Fettermann A, Li Z, Qian Y, Liu Y, Wang X, Zhou A, Mo JQ, Yang L, Jiang P, Taschner A, Rossmanith W, Guan MX. Wang S, et al. Among authors: mo jq. Circ Res. 2011 Apr 1;108(7):862-70. doi: 10.1161/CIRCRESAHA.110.231811. Circ Res. 2011. PMID: 21454794

7

The tRNAMet 4435A>G mutation in the mitochondrial haplogroup G2a1 is responsible for maternally inherited hypertension in a Chinese pedigree.

Lu Z, Chen H, Meng Y, Wang Y, Xue L, Zhi S, Qiu Q, Yang L, Mo JQ, Guan MX. Lu Z, et al. Among authors: mo jq. Eur J Hum Genet. 2011 Nov;19(11):1181-6. doi: 10.1038/ejhg.2011.111. Epub 2011 Jun 22. Eur J Hum Genet. 2011. PMID: 21694735 Free PMC article.

8

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. Among authors: mo jq. J Med Genet. 2011 Oct;48(10):682-90. doi: 10.1136/jmedgenet-2011-100219. J Med Genet. 2011. PMID: 21931169

9

The 12S rRNA A1555G mutation in the mitochondrial haplogroup D5a is responsible for maternally inherited hypertension and hearing loss in two Chinese pedigrees.

Chen H, Zheng J, Xue L, Meng Y, Wang Y, Zheng B, Fang F, Shi S, Qiu Q, Jiang P, Lu Z, Mo JQ, Lu J, Guan MX. Chen H, et al. Among authors: mo jq. Eur J Hum Genet. 2012 Jun;20(6):607-12. doi: 10.1038/ejhg.2011.259. Epub 2012 Feb 8. Eur J Hum Genet. 2012. PMID: 22317974 Free PMC article.

10

Mitochondrial tRNA mutations are associated with maternally inherited hypertension in two Han Chinese pedigrees.

Qiu Q, Li R, Jiang P, Xue L, Lu Y, Song Y, Han J, Lu Z, Zhi S, Mo JQ, Guan MX. Qiu Q, et al. Among authors: mo jq. Hum Mutat. 2012 Aug;33(8):1285-93. doi: 10.1002/humu.22109. Epub 2012 May 30. Hum Mutat. 2012. PMID: 22549939

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