Li R - Search Results

1

Cosegregation of the ND4 G11696A mutation with the LHON-associated ND4 G11778A mutation in a four generation Chinese family.

Qu J, Li R, Zhou X, Tong Y, Yang L, Chen J, Zhao F, Lu C, Qian Y, Lu F, Guan MX. Qu J, et al. Among authors: li r. Mitochondrion. 2007 Feb-Apr;7(1-2):140-6. doi: 10.1016/j.mito.2006.11.015. Epub 2006 Dec 8. Mitochondrion. 2007. PMID: 17300996 Free PMC article.

2

Only male matrilineal relatives with Leber's hereditary optic neuropathy in a large Chinese family carrying the mitochondrial DNA G11778A mutation.

Qu J, Li R, Tong Y, Hu Y, Zhou X, Qian Y, Lu F, Guan MX. Qu J, et al. Among authors: li r. Biochem Biophys Res Commun. 2005 Mar 25;328(4):1139-45. doi: 10.1016/j.bbrc.2005.01.062. Biochem Biophys Res Commun. 2005. PMID: 15707996 Clinical Trial.

3

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: li r. Invest Ophthalmol Vis Sci. 2006 Feb;47(2):475-83. doi: 10.1167/iovs.05-0665. Invest Ophthalmol Vis Sci. 2006. PMID: 16431939

4

Aminoglycoside-induced and non-syndromic hearing loss is associated with the G7444A mutation in the mitochondrial COI/tRNASer(UCN) genes in two Chinese families.

Zhu Y, Qian Y, Tang X, Wang J, Yang L, Liao Z, Li R, Ji J, Li Z, Chen J, Choo DI, Lu J, Guan MX. Zhu Y, et al. Among authors: li z, li r. Biochem Biophys Res Commun. 2006 Apr 14;342(3):843-50. doi: 10.1016/j.bbrc.2006.02.027. Epub 2006 Feb 17. Biochem Biophys Res Commun. 2006. PMID: 16500624

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. 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 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. Among authors: li w, li r. 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

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. Among authors: li y, li z, li r. 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 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss.

Lu J, Li Z, Zhu Y, Yang A, Li R, Zheng J, Cai Q, Peng G, Zheng W, Tang X, Chen B, Chen J, Liao Z, Yang L, Li Y, You J, Ding Y, Yu H, Wang J, Sun D, Zhao J, Xue L, Wang J, Guan MX. Lu J, et al. Among authors: li y, li z, li r. Mitochondrion. 2010 Jun;10(4):380-90. doi: 10.1016/j.mito.2010.01.007. Epub 2010 Jan 25. Mitochondrion. 2010. PMID: 20100600 Free PMC article.

9

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: li w, li r. Mitochondrion. 2015 Mar;21:49-57. doi: 10.1016/j.mito.2015.01.004. Epub 2015 Jan 20. Mitochondrion. 2015. PMID: 25615420

10

[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.

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