Acland GM - Search Results

1

Identical mutation in a novel retinal gene causes progressive rod-cone degeneration in dogs and retinitis pigmentosa in humans.

Zangerl B, Goldstein O, Philp AR, Lindauer SJ, Pearce-Kelling SE, Mullins RF, Graphodatsky AS, Ripoll D, Felix JS, Stone EM, Acland GM, Aguirre GD. Zangerl B, et al. Among authors: acland gm. Genomics. 2006 Nov;88(5):551-63. doi: 10.1016/j.ygeno.2006.07.007. Epub 2006 Aug 30. Genomics. 2006. PMID: 16938425 Free PMC article.

2

In vivo dynamics of retinal injury and repair in the rhodopsin mutant dog model of human retinitis pigmentosa.

Cideciyan AV, Jacobson SG, Aleman TS, Gu D, Pearce-Kelling SE, Sumaroka A, Acland GM, Aguirre GD. Cideciyan AV, et al. Among authors: acland gm. Proc Natl Acad Sci U S A. 2005 Apr 5;102(14):5233-8. doi: 10.1073/pnas.0408892102. Epub 2005 Mar 22. Proc Natl Acad Sci U S A. 2005. PMID: 15784735 Free PMC article.

3

Development and characterization of a normalized canine retinal cDNA library for genomic and expression studies.

Zangerl B, Sun Q, Pillardy J, Johnson JL, Schweitzer PA, Hernandez AG, Liu L, Acland GM, Aguirre GD. Zangerl B, et al. Among authors: acland gm. Invest Ophthalmol Vis Sci. 2006 Jun;47(6):2632-8. doi: 10.1167/iovs.05-1463. Invest Ophthalmol Vis Sci. 2006. PMID: 16723480

4

Linkage disequilibrium mapping in domestic dog breeds narrows the progressive rod-cone degeneration interval and identifies ancestral disease-transmitting chromosome.

Goldstein O, Zangerl B, Pearce-Kelling S, Sidjanin DJ, Kijas JW, Felix J, Acland GM, Aguirre GD. Goldstein O, et al. Among authors: acland gm. Genomics. 2006 Nov;88(5):541-50. doi: 10.1016/j.ygeno.2006.05.013. Epub 2006 Jul 20. Genomics. 2006. PMID: 16859891 Free PMC article.

5

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. Among authors: acland gm. 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.

6

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. Among authors: acland gm. Mol Vis. 2007 Jul 11;13:1094-105. Mol Vis. 2007. PMID: 17653054 Free PMC article.

7

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. Among authors: acland gm. 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.

8

Exonic SINE insertion in STK38L causes canine early retinal degeneration (erd).

Goldstein O, Kukekova AV, Aguirre GD, Acland GM. Goldstein O, et al. Among authors: acland gm. Genomics. 2010 Dec;96(6):362-8. doi: 10.1016/j.ygeno.2010.09.003. Epub 2010 Sep 29. Genomics. 2010. PMID: 20887780 Free PMC article.

9

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. Among authors: acland gm. 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.

10

Variation in retinal degeneration phenotype inherited at the prcd locus.

Aguirre GD, Acland GM. Aguirre GD, et al. Among authors: acland gm. Exp Eye Res. 1988 May;46(5):663-87. doi: 10.1016/s0014-4835(88)80055-1. Exp Eye Res. 1988. PMID: 3164273

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