Qu J - Search Results

1

A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population.

Shi Y, Gong B, Chen L, Zuo X, Liu X, Tam PO, Zhou X, Zhao P, Lu F, Qu J, Sun L, Zhao F, Chen H, Zhang Y, Zhang D, Lin Y, Lin H, Ma S, Cheng J, Yang J, Huang L, Zhang M, Zhang X, Pang CP, Yang Z. Shi Y, et al. Among authors: qu j. Hum Mol Genet. 2013 Jun 1;22(11):2325-33. doi: 10.1093/hmg/ddt066. Epub 2013 Feb 12. Hum Mol Genet. 2013. PMID: 23406873

2

[Selection of animal model in myopia research].

Zhou XT, Qu J. Zhou XT, et al. Among authors: qu j. Zhonghua Yan Ke Za Zhi. 2005 Jun;41(6):486-7. Zhonghua Yan Ke Za Zhi. 2005. PMID: 16008905 Chinese.

3

Leber's hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese families.

Zhou X, Wei Q, Yang L, Tong Y, Zhao F, Lu C, Qian Y, Sun Y, Lu F, Qu J, Guan MX. Zhou X, et al. Among authors: qu j. Biochem Biophys Res Commun. 2006 Feb 3;340(1):69-75. doi: 10.1016/j.bbrc.2005.11.150. Epub 2005 Dec 6. Biochem Biophys Res Commun. 2006. PMID: 16364244 Clinical Trial.

4

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: qu j. Gene. 2006 Jul 5;376(1):79-86. doi: 10.1016/j.gene.2006.02.014. Epub 2006 Apr 19. Gene. 2006. PMID: 16624503

5

[Leber's hereditary optic neuropathy is associated with the mitochondrial G11696A mutation in two Chinese families].

Zhao FX, Zhou XT, Qu J, Wei QP, Tong Y, Yang L, Lv JX, Guan MX. Zhao FX, et al. Among authors: qu j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Oct;24(5):556-9. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007. PMID: 17922426 Chinese.

6

Expression of melanin-related genes in cultured adult human retinal pigment epithelium and uveal melanoma cells.

Lu F, Yan D, Zhou X, Hu DN, Qu J. Lu F, et al. Among authors: qu j. Mol Vis. 2007 Nov 3;13:2066-72. Mol Vis. 2007. PMID: 18079680

7

Mitochondrial variants may influence the phenotypic manifestation of Leber's hereditary optic neuropathy-associated ND4 G11778A mutation.

Cai W, Fu Q, Zhou X, Qu J, Tong Y, Guan MX. Cai W, et al. Among authors: qu j. J Genet Genomics. 2008 Nov;35(11):649-55. doi: 10.1016/S1673-8527(08)60086-7. J Genet Genomics. 2008. PMID: 19022198

8

[Dose the mice is ideal animal myopia model?].

Zhou XT, Qu J, Lü F. Zhou XT, et al. Among authors: qu j. Zhonghua Yan Ke Za Zhi. 2008 Jul;44(7):584-6. Zhonghua Yan Ke Za Zhi. 2008. PMID: 19040072 Chinese.

9

Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation.

Qu J, Zhou X, Zhang J, Zhao F, Sun YH, Tong Y, Wei QP, Cai W, Yang L, West CE, Guan MX. Qu J, et al. Ophthalmology. 2009 Mar;116(3):558-564.e3. doi: 10.1016/j.ophtha.2008.10.022. Epub 2009 Jan 22. Ophthalmology. 2009. PMID: 19167085 Free PMC article.

10

Leber's hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutation.

Zhao F, Guan M, Zhou X, Yuan M, Liang M, Liu Q, Liu Y, Zhang Y, Yang L, Tong Y, Wei QP, Sun YH, Qu J, Guan MX. Zhao F, et al. Among authors: qu j. Biochem Biophys Res Commun. 2009 Nov 20;389(3):466-72. doi: 10.1016/j.bbrc.2009.08.168. Epub 2009 Sep 2. Biochem Biophys Res Commun. 2009. PMID: 19732751 Free PMC article.

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