Liu X - 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: liu h, liu x. 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

Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation.

Qu J, Zhou X, Zhao F, Liu X, Zhang M, Sun YH, Liang M, Yuan M, Liu Q, Tong Y, Wei QP, Yang L, Guan MX. Qu J, et al. Among authors: liu x, liu q. Biochim Biophys Acta. 2010 Mar;1800(3):305-12. doi: 10.1016/j.bbagen.2009.08.010. Epub 2009 Sep 3. Biochim Biophys Acta. 2010. PMID: 19733221 Free PMC article.

3

[Leber's hereditary optic neuropathy may be associated with the mitochondrial tRNAGlu A14693G mutation in three Chinese families].

Zhang YM, Ji YC, Liu XL, Zhou XT, Zhao FX, Sun YH, Wei QP, Zhang JJ, Liu Y, Qu J, Guan MX. Zhang YM, et al. Yi Chuan. 2010 Apr;32(4):353-9. doi: 10.3724/sp.j.1005.2010.00353. Yi Chuan. 2010. PMID: 20423889 Chinese.

4

Leber's hereditary optic neuropathy is associated with the T12338C mutation in mitochondrial ND5 gene in six Han Chinese families.

Liu XL, Zhou X, Zhou J, Zhao F, Zhang J, Li C, Ji Y, Zhang Y, Wei QP, Sun YH, Yang L, Lin B, Yuan Y, Li Y, Qu J, Guan MX. Liu XL, et al. Ophthalmology. 2011 May;118(5):978-85. doi: 10.1016/j.ophtha.2010.09.003. Epub 2010 Dec 4. Ophthalmology. 2011. PMID: 21131053

5

[The mitochondrial ND5 T12338C mutation may be associated with Leber's hereditary optic neuropathy in two Chinese families].

Ji YC, Liu XL, Zhao FX, Zhang JJ, Zhang Y, Zhou XT, Qu J, Guan MX. Ji YC, et al. Yi Chuan. 2011 Apr;33(4):322-8. doi: 10.3724/sp.j.1005.2011.00322. Yi Chuan. 2011. PMID: 21482521 Chinese.

6

A novel OPA1 mutation in a Chinese family with autosomal dominant optic atrophy.

Zhang J, Yuan Y, Lin B, Feng H, Li Y, Dai X, Zhou H, Dong X, Liu XL, Guan MX. Zhang J, et al. Among authors: liu xl. Biochem Biophys Res Commun. 2012 Mar 23;419(4):670-5. doi: 10.1016/j.bbrc.2012.02.073. Epub 2012 Feb 20. Biochem Biophys Res Commun. 2012. PMID: 22382025

7

[The analysis of Leber's hereditary optic neuropathy associated with mitochondrial tRNAAla C5601T mutation in seven Han Chinese families].

Zhou HH, Dai XN, Lin B, Mi H, Liu XL, Zhao FX, Zhang JJ, Zhou XT, Sun YH, Wei QP, Qu J, Guan MX. Zhou HH, et al. Yi Chuan. 2012 Aug;34(8):1031-42. doi: 10.3724/sp.j.1005.2012.01031. Yi Chuan. 2012. PMID: 22917908 Chinese.

8

Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese families.

Zhang J, Zhao F, Fu Q, Liang M, Tong Y, Liu X, Lin B, Mi H, Zhang M, Wei QP, Xue L, Jiang P, Zhou X, Mo JQ, Huang T, Qu J, Guan MX. Zhang J, et al. Among authors: liu x. Mitochondrion. 2013 Nov;13(6):772-81. doi: 10.1016/j.mito.2013.05.002. Epub 2013 May 9. Mitochondrion. 2013. PMID: 23665487

9

Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathy.

Liang M, Jiang P, Li F, Zhang J, Ji Y, He Y, Xu M, Zhu J, Meng X, Zhao F, Tong Y, Liu X, Sun Y, Zhou X, Mo JQ, Qu J, Guan MX. Liang M, et al. Among authors: liu x. Invest Ophthalmol Vis Sci. 2014 Mar 6;55(3):1321-31. doi: 10.1167/iovs.13-13011. Invest Ophthalmol Vis Sci. 2014. PMID: 24398099

10

Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated ND1 G3460A mutation in Chinese families.

Ji Y, Liang M, Zhang J, Zhang M, Zhu J, Meng X, Zhang S, Gao M, Zhao F, Wei QP, Jiang P, Tong Y, Liu X, Qin Mo J, Guan MX. Ji Y, et al. Among authors: liu x. J Hum Genet. 2014 Mar;59(3):134-40. doi: 10.1038/jhg.2013.134. Epub 2014 Jan 16. J Hum Genet. 2014. PMID: 24430572

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