Qu C - Search Results

1

A genetic variant in the SKIV2L gene is significantly associated with age-related macular degeneration in a Han Chinese population.

Lu F, Shi Y, Qu C, Zhao P, Liu X, Gong B, Ma S, Zhou Y, Zhang Q, Fei P, Xu Y, Hu J, Fan Y, Lin Y, Zhu X, Yang Z. Lu F, et al. Among authors: qu c. Invest Ophthalmol Vis Sci. 2013 Apr 26;54(4):2911-7. doi: 10.1167/iovs.12-11381. Invest Ophthalmol Vis Sci. 2013. PMID: 23557739

2

Protamine sulfate downregulates vascular endothelial growth factor (VEGF) expression and inhibits VEGF and its receptor binding in vitro.

Hu J, Qu C, Yu Y, Ping M, Wei D, Dandan D. Hu J, et al. Among authors: qu c. Adv Exp Med Biol. 2010;664:341-7. doi: 10.1007/978-1-4419-1399-9_39. Adv Exp Med Biol. 2010. PMID: 20238034

3

Near-infrared light protect the photoreceptor from light-induced damage in rats.

Qu C, Cao W, Fan Y, Lin Y. Qu C, et al. Adv Exp Med Biol. 2010;664:365-74. doi: 10.1007/978-1-4419-1399-9_42. Adv Exp Med Biol. 2010. PMID: 20238037

4

Genetic association study between INSULIN pathway related genes and high myopia in a Han Chinese population.

Liu X, Wang P, Qu C, Zheng H, Gong B, Ma S, Lin H, Cheng J, Yang Z, Lu F, Shi Y. Liu X, et al. Among authors: qu c. Mol Biol Rep. 2015 Jan;42(1):303-10. doi: 10.1007/s11033-014-3773-6. Epub 2014 Sep 30. Mol Biol Rep. 2015. PMID: 25266237

5

A new method using xenogeneicacellular dermal matrix in the reconstruction of lacrimal drainage.

Chen L, Gong B, Wu Z, Jetton J, Chen R, Qu C. Chen L, et al. Among authors: qu c. Br J Ophthalmol. 2014 Nov;98(11):1583-7. doi: 10.1136/bjophthalmol-2014-304932. Epub 2014 Jun 11. Br J Ophthalmol. 2014. PMID: 25271909 Free PMC article.

6

Mutation spectrum of CYP1B1 in Chinese patients with primary open-angle glaucoma.

Gong B, Qu C, Li X, Shi Y, Lin Y, Zhou Y, Shuai P, Yang Y, Liu X, Zhang D, Yang Z. Gong B, et al. Among authors: qu c. Br J Ophthalmol. 2015 Mar;99(3):425-30. doi: 10.1136/bjophthalmol-2014-306054. Epub 2014 Dec 19. Br J Ophthalmol. 2015. PMID: 25527694

7

Identification of a novel MYOC mutation in a Chinese family with primary open-angle glaucoma.

Yang Y, Shi Y, Huang X, Li X, Ye Z, Shuai P, Qu C, Chen R, Xu J, Yang Z, Lu F, Gong B. Yang Y, et al. Among authors: qu c. Gene. 2015 Oct 25;571(2):188-93. doi: 10.1016/j.gene.2015.06.042. Epub 2015 Jun 19. Gene. 2015. PMID: 26095806

8

Whole-exome sequencing reveals a novel frameshift mutation in the FAM161A gene causing autosomal recessive retinitis pigmentosa in the Indian population.

Zhou Y, Saikia BB, Jiang Z, Zhu X, Liu Y, Huang L, Kim R, Yang Y, Qu C, Hao F, Gong B, Tai Z, Niu L, Yang Z, Sundaresan P, Zhu X. Zhou Y, et al. Among authors: qu c. J Hum Genet. 2015 Oct;60(10):625-30. doi: 10.1038/jhg.2015.92. Epub 2015 Aug 6. J Hum Genet. 2015. PMID: 26246154

9

Novel Compound Heterozygous CBS Mutations Cause Homocystinuria in a Han Chinese Family.

Gong B, Liu L, Li Z, Ye Z, Xiao Y, Zeng G, Shi Y, Wang Y, Feng X, Li X, Hao F, Liu X, Qu C, Li Y, Mu G, Yang Z. Gong B, et al. Among authors: qu c. Sci Rep. 2015 Dec 15;5:17947. doi: 10.1038/srep17947. Sci Rep. 2015. PMID: 26667307 Free PMC article.

10

Whole-exome Sequencing Analysis Identifies Mutations in the EYS Gene in Retinitis Pigmentosa in the Indian Population.

Di Y, Huang L, Sundaresan P, Li S, Kim R, Ballav Saikia B, Qu C, Zhu X, Zhou Y, Jiang Z, Zhang L, Lin Y, Zhang D, Li Y, Zhang H, Yin Y, Lu F, Zhu X, Yang Z. Di Y, et al. Among authors: qu c. Sci Rep. 2016 Jan 20;6:19432. doi: 10.1038/srep19432. Sci Rep. 2016. PMID: 26787102 Free PMC article.

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