Yuan S - Search Results

1

Suppression of experimental choroidal neovascularization by curcumin in mice.

Xie P, Zhang W, Yuan S, Chen Z, Yang Q, Yuan D, Wang F, Liu Q. Xie P, et al. Among authors: yuan s, yuan d. PLoS One. 2012;7(12):e53329. doi: 10.1371/journal.pone.0053329. Epub 2012 Dec 28. PLoS One. 2012. PMID: 23285282 Free PMC article.

2

Mechanism of corneal endothelial cells lesion during phacoemulsification and aspiration.

Yuan S, Xie L, Liu Q, Yuan N. Yuan S, et al. Among authors: yuan n. Yan Ke Xue Bao. 2003 Mar;19(1):10-4. Yan Ke Xue Bao. 2003. PMID: 12852081

3

Application of foldable intraocular lens in multiple types of cataract.

Yuan S, Liu Q, Jiang Q, Yuan N. Yuan S, et al. Among authors: yuan n. Yan Ke Xue Bao. 2002 Mar;18(1):23-6. Yan Ke Xue Bao. 2002. PMID: 15510670

4

Complement factor H Val62Ile variant and risk of age-related macular degeneration: a meta-analysis.

Yuan D, Yang Q, Liu X, Yuan D, Yuan S, Xie P, Liu Q. Yuan D, et al. Among authors: yuan s. Mol Vis. 2013;19:374-83. Epub 2013 Feb 13. Mol Vis. 2013. PMID: 23441108 Free PMC article.

5

Targeted sequencing of 179 genes associated with hereditary retinal dystrophies and 10 candidate genes identifies novel and known mutations in patients with various retinal diseases.

Chen X, Zhao K, Sheng X, Li Y, Gao X, Zhang X, Kang X, Pan X, Liu Y, Jiang C, Shi H, Chen X, Rong W, Chen LJ, Lai TY, Liu Y, Wang X, Yuan S, Liu Q, Vollrath D, Pang CP, Zhao C. Chen X, et al. Among authors: yuan s. Invest Ophthalmol Vis Sci. 2013 Mar 1;54(3):2186-97. doi: 10.1167/iovs.12-10967. Invest Ophthalmol Vis Sci. 2013. PMID: 23462753

6

Yuan D, Yuan D, Yuan S, Liu Q. Yuan D, et al. Among authors: yuan s. Ophthalmology. 2013 Oct;120(10):2051-7. doi: 10.1016/j.ophtha.2013.03.026. Epub 2013 May 19. Ophthalmology. 2013. PMID: 23697955 Review.

7

Genetic association with response to intravitreal ranibizumab for neovascular age-related macular degeneration in the Han Chinese population.

Yuan D, Yuan D, Liu X, Yuan S, Xie P, Liu Q. Yuan D, et al. Among authors: yuan s. Ophthalmologica. 2013;230(4):227-32. doi: 10.1159/000355068. Epub 2013 Sep 25. Ophthalmologica. 2013. PMID: 24080590

8

Interleukin-6 prevents NMDA-induced neuronal death via Gp130 signaling-dependent IP3R inhibition.

Qiu AW, Yang Q, Yuan ST, Xie P, Liu QH. Qiu AW, et al. Neuro Endocrinol Lett. 2013;34(6):529-38. Neuro Endocrinol Lett. 2013. PMID: 24378454

9

Maternal germline mosaicism of kinesin family member 21A (KIF21A) mutation causes complex phenotypes in a Chinese family with congenital fibrosis of the extraocular muscles.

Liu G, Chen X, Sun X, Liu H, Zhao K, Chang Q, Pan X, Wang X, Yuan S, Liu Q, Zhao C. Liu G, et al. Among authors: yuan s. Mol Vis. 2014 Jan 6;20:15-23. eCollection 2014. Mol Vis. 2014. PMID: 24426772 Free PMC article.

10

[Targeted sequencing identifies a hotspot mutation SNRNP200 p.S1087L correlates with novel phenotypes in retinitis pigmentosa].

Chen X, Gao X, Zhao KX, Pan XY, Zhang XM, Wang XY, Yuan ST, Liu QH, Zhao C. Chen X, et al. Zhonghua Yan Ke Za Zhi. 2013 Dec;49(12):1104-10. Zhonghua Yan Ke Za Zhi. 2013. PMID: 24499697 Chinese.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

8,621 results

Search Page

Filters