R01EY14448/EY/NEI NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2004	5
2005	5
2006	5
2007	7
2008	7
2009	1
2010	2
2024	0

1

Genetic susceptibility of diabetic retinopathy.

Patel S, Chen H, Tinkham NH, Zhang K. Patel S, et al. Curr Diab Rep. 2008 Aug;8(4):257-62. doi: 10.1007/s11892-008-0046-6. Curr Diab Rep. 2008. PMID: 18631436 Review.

2

Slit-Robo signaling in ocular angiogenesis.

Chen H, Zhang M, Tang S, London NR, Li DY, Zhang K. Chen H, et al. Adv Exp Med Biol. 2010;664:457-63. doi: 10.1007/978-1-4419-1399-9_52. Adv Exp Med Biol. 2010. PMID: 20238047

3

Association of HTRA1 polymorphism and bilaterality in advanced age-related macular degeneration.

Chen H, Yang Z, Gibbs D, Yang X, Hau V, Zhao P, Ma X, Zeng J, Luo L, Pearson E, Constantine R, Kaminoh Y, Harmon J, Tong Z, Stratton CA, Cameron DJ, Tang S, Zhang K. Chen H, et al. Vision Res. 2008 Feb;48(5):690-4. doi: 10.1016/j.visres.2007.10.014. Vision Res. 2008. PMID: 18206206 Free article.

4

Mutant carbonic anhydrase 4 impairs pH regulation and causes retinal photoreceptor degeneration.

Yang Z, Alvarez BV, Chakarova C, Jiang L, Karan G, Frederick JM, Zhao Y, Sauvé Y, Li X, Zrenner E, Wissinger B, Hollander AI, Katz B, Baehr W, Cremers FP, Casey JR, Bhattacharya SS, Zhang K. Yang Z, et al. Hum Mol Genet. 2005 Jan 15;14(2):255-65. doi: 10.1093/hmg/ddi023. Epub 2004 Nov 24. Hum Mol Genet. 2005. PMID: 15563508

5

Mutation screen of the membrane-type frizzled-related protein (MFRP) gene in patients with inherited retinal degenerations.

Pauer GJ, Xi Q, Zhang K, Traboulsi EI, Hagstrom SA. Pauer GJ, et al. Ophthalmic Genet. 2005 Dec;26(4):157-61. doi: 10.1080/13816810500374425. Ophthalmic Genet. 2005. PMID: 16352475

6

A novel haplotype with the R345W mutation in the EFEMP1 gene associated with autosomal dominant drusen in a Japanese family.

Takeuchi T, Hayashi T, Bedell M, Zhang K, Yamada H, Tsuneoka H. Takeuchi T, et al. Invest Ophthalmol Vis Sci. 2010 Mar;51(3):1643-50. doi: 10.1167/iovs.09-4497. Epub 2009 Oct 22. Invest Ophthalmol Vis Sci. 2010. PMID: 19850834 Free PMC article.

7

Essential role of Elovl4 in very long chain fatty acid synthesis, skin permeability barrier function, and neonatal survival.

Cameron DJ, Tong Z, Yang Z, Kaminoh J, Kamiyah S, Chen H, Zeng J, Chen Y, Luo L, Zhang K. Cameron DJ, et al. Int J Biol Sci. 2007 Feb 6;3(2):111-9. doi: 10.7150/ijbs.3.111. Int J Biol Sci. 2007. PMID: 17304340 Free PMC article.

8

Biochemical analysis of a common human polymorphism associated with age-related macular degeneration.

Yu J, Wiita P, Kawaguchi R, Honda J, Jorgensen A, Zhang K, Fischetti VA, Sun H. Yu J, et al. Biochemistry. 2007 Jul 17;46(28):8451-61. doi: 10.1021/bi700459a. Epub 2007 Jun 20. Biochemistry. 2007. PMID: 17580967

9

A novel mutation in the ELOVL4 gene causes autosomal dominant Stargardt-like macular dystrophy.

Maugeri A, Meire F, Hoyng CB, Vink C, Van Regemorter N, Karan G, Yang Z, Cremers FP, Zhang K. Maugeri A, et al. Invest Ophthalmol Vis Sci. 2004 Dec;45(12):4263-7. doi: 10.1167/iovs.04-0078. Invest Ophthalmol Vis Sci. 2004. PMID: 15557430

10

10q26 is associated with increased risk of age-related macular degeneration in the Utah population.

Cameron DJ, Yang Z, Tong Z, Zhao Y, Praggastis A, Brinton E, Harmon J, Chen Y, Pearson E, Bernstein PS, Brinton G, Li X, Jorgensen A, Schneider S, Gibbs D, Chen H, Wang C, Howes K, Camp NJ, Zhang K. Cameron DJ, et al. Adv Exp Med Biol. 2008;613:253-8. doi: 10.1007/978-0-387-74904-4_29. Adv Exp Med Biol. 2008. PMID: 18188952 No abstract available.

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