R01 EY013132/EY/NEI NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2002	1
2004	1
2005	1
2006	2
2007	6
2008	2
2009	4
2010	5
2011	2
2012	2
2024	0

1

Genetic and phenotypic variations of inherited retinal diseases in dogs: the power of within- and across-breed studies.

Miyadera K, Acland GM, Aguirre GD. Miyadera K, et al. Mamm Genome. 2012 Feb;23(1-2):40-61. doi: 10.1007/s00335-011-9361-3. Epub 2011 Nov 8. Mamm Genome. 2012. PMID: 22065099 Free PMC article. Review.

2

Transcriptional profile analysis of RPGRORF15 frameshift mutation identifies novel genes associated with retinal degeneration.

Genini S, Zangerl B, Slavik J, Acland GM, Beltran WA, Aguirre GD. Genini S, et al. Invest Ophthalmol Vis Sci. 2010 Nov;51(11):6038-50. doi: 10.1167/iovs.10-5443. Epub 2010 Jun 23. Invest Ophthalmol Vis Sci. 2010. PMID: 20574030 Free PMC article.

3

Cloning and characterization of canine PAX6 and evaluation as a candidate gene in a canine model of aniridia.

Hunter LS, Sidjanin DJ, Hijar MV, Johnson JL, Kirkness E, Acland GM, Aguirre GD. Hunter LS, et al. Mol Vis. 2007 Mar 26;13:431-42. Mol Vis. 2007. PMID: 17417604 Free PMC article.

4

Development and validation of a canine-specific profiling array to examine expression of pro-apoptotic and pro-survival genes in retinal degenerative diseases.

Genini S, Beltran WA, Aguirre GD. Genini S, et al. Adv Exp Med Biol. 2012;723:353-63. doi: 10.1007/978-1-4614-0631-0_46. Adv Exp Med Biol. 2012. PMID: 22183353 Free PMC article.

5

Analysis of six candidate genes as potential modifiers of disease expression in canine XLPRA1, a model for human X-linked retinitis pigmentosa 3.

Guyon R, Pearce-Kelling SE, Zeiss CJ, Acland GM, Aguirre GD. Guyon R, et al. Mol Vis. 2007 Jul 11;13:1094-105. Mol Vis. 2007. PMID: 17653054 Free PMC article.

6

CREB1/ATF1 activation in photoreceptor degeneration and protection.

Beltran WA, Allore HG, Johnson E, Towle V, Tao W, Acland GM, Aguirre GD, Zeiss CJ. Beltran WA, et al. Invest Ophthalmol Vis Sci. 2009 Nov;50(11):5355-63. doi: 10.1167/iovs.09-3741. Epub 2009 Jul 30. Invest Ophthalmol Vis Sci. 2009. PMID: 19643965 Free PMC article.

7

Gene therapy rescues cone function in congenital achromatopsia.

Komáromy AM, Alexander JJ, Rowlan JS, Garcia MM, Chiodo VA, Kaya A, Tanaka JC, Acland GM, Hauswirth WW, Aguirre GD. Komáromy AM, et al. Hum Mol Genet. 2010 Jul 1;19(13):2581-93. doi: 10.1093/hmg/ddq136. Epub 2010 Apr 8. Hum Mol Genet. 2010. PMID: 20378608 Free PMC article.

8

Naturally occurring rhodopsin mutation in the dog causes retinal dysfunction and degeneration mimicking human dominant retinitis pigmentosa.

Kijas JW, Cideciyan AV, Aleman TS, Pianta MJ, Pearce-Kelling SE, Miller BJ, Jacobson SG, Aguirre GD, Acland GM. Kijas JW, et al. Proc Natl Acad Sci U S A. 2002 Apr 30;99(9):6328-33. doi: 10.1073/pnas.082714499. Epub 2002 Apr 23. Proc Natl Acad Sci U S A. 2002. PMID: 11972042 Free PMC article.

9

Bestrophin gene mutations cause canine multifocal retinopathy: a novel animal model for best disease.

Guziewicz KE, Zangerl B, Lindauer SJ, Mullins RF, Sandmeyer LS, Grahn BH, Stone EM, Acland GM, Aguirre GD. Guziewicz KE, et al. Invest Ophthalmol Vis Sci. 2007 May;48(5):1959-67. doi: 10.1167/iovs.06-1374. Invest Ophthalmol Vis Sci. 2007. PMID: 17460247 Free PMC article.

10

Targeting gene expression to cones with human cone opsin promoters in recombinant AAV.

Komáromy AM, Alexander JJ, Cooper AE, Chiodo VA, Glushakova LG, Acland GM, Hauswirth WW, Aguirre GD. Komáromy AM, et al. Gene Ther. 2008 Jul;15(14):1049-55. doi: 10.1038/gt.2008.32. Epub 2008 Mar 13. Gene Ther. 2008. PMID: 18337838 Free PMC article.

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