Ray K - Search Results

1

Canine rod photoreceptor cGMP-gated channel protein alpha-subunit: studies on the expression of the gene and characterization of the cDNA.

Zhang Q, Pearce-kelling S, Acland GM, Aguirre GD, Ray K. Zhang Q, et al. Among authors: ray k. Exp Eye Res. 1997 Aug;65(2):301-9. doi: 10.1006/exer.1997.0342. Exp Eye Res. 1997. PMID: 9268598 Free article.

2

Cloning and characterization of the cDNA and gene encoding the gamma-subunit of cGMP-phosphodiesterase in canine retinal rod photoreceptor cells.

Wang W, Acland GM, Aguirre GD, Ray K. Wang W, et al. Among authors: ray k. Gene. 1996 Nov 28;181(1-2):1-5. doi: 10.1016/s0378-1119(96)00319-8. Gene. 1996. PMID: 8973300 Free article.

3

Canine rod transducin alpha-1: cloning of the cDNA and evaluation of the gene as a candidate for progressive retinal atrophy.

Ray K, Baldwin VJ, Zeiss C, Acland GM, Aguirre GD. Ray K, et al. Curr Eye Res. 1997 Jan;16(1):71-7. doi: 10.1076/ceyr.16.1.71.5122. Curr Eye Res. 1997. PMID: 9043826

4

Cloning and characterization of the cDNA encoding the alpha-subunit of cGMP-phosphodiesterase in canine retinal rod photoreceptor cells.

Wang W, Acland GM, Aguirre GD, Ray K. Wang W, et al. Among authors: ray k. Mol Vis. 1996 May 9;2:3. Mol Vis. 1996. PMID: 9233984 Free article. No abstract available.

5

Characterization of canine photoreceptor phosducin cDNA and identification of a sequence variant in dogs with photoreceptor dysplasia.

Zhang Q, Acland GM, Parshall CJ, Haskell J, Ray K, Aguirre GD. Zhang Q, et al. Among authors: ray k. Gene. 1998 Jul 30;215(2):231-9. doi: 10.1016/s0378-1119(98)00310-2. Gene. 1998. PMID: 9714819 Free article.

6

Congenital stationary night blindness in the dog: common mutation in the RPE65 gene indicates founder effect.

Aguirre GD, Baldwin V, Pearce-Kelling S, Narfström K, Ray K, Acland GM. Aguirre GD, et al. Among authors: ray k. Mol Vis. 1998 Oct 30;4:23. Mol Vis. 1998. PMID: 9808841 Free article.

7

Photoreceptor dysplasia (pd) in miniature schnauzer dogs: evaluation of candidate genes by molecular genetic analysis.

Zhang Q, Baldwin VJ, Acland GM, Parshall CJ, Haskel J, Aguirre GD, Ray K. Zhang Q, et al. Among authors: ray k. J Hered. 1999 Jan-Feb;90(1):57-61. doi: 10.1093/jhered/90.1.57. J Hered. 1999. PMID: 9987905

8

Strategies for identification of mutations causing hereditary retinal diseases in dogs: evaluation of opsin as a candidate gene.

Ray K, Wang W, Czarnecki J, Zhang Q, Acland GM, Aguirre GD. Ray K, et al. J Hered. 1999 Jan-Feb;90(1):133-7. doi: 10.1093/jhered/90.1.133. J Hered. 1999. PMID: 9987920

9

Frequency of the codon 807 mutation in the cGMP phosphodiesterase beta-subunit gene in Irish setters and other dog breeds with hereditary retinal degeneration.

Aguirre GD, Baldwin V, Weeks KM, Acland GM, Ray K. Aguirre GD, et al. Among authors: ray k. J Hered. 1999 Jan-Feb;90(1):143-7. doi: 10.1093/jhered/90.1.143. J Hered. 1999. PMID: 9987922

10

Evaluation of the APOH gene as a positional candidate for prcd in dogs.

Gu W, Ray K, Pearce-Kelling S, Baldwin VJ, Langston AA, Ray J, Ostrander EA, Acland GM, Aguirre GD. Gu W, et al. Among authors: ray j, ray k. Invest Ophthalmol Vis Sci. 1999 May;40(6):1229-37. Invest Ophthalmol Vis Sci. 1999. PMID: 10235557

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