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Items: 1 to 20 of 78

1.

Proteomic identification of unique photoreceptor disc components reveals the presence of PRCD, a protein linked to retinal degeneration.

Skiba NP, Spencer WJ, Salinas RY, Lieu EC, Thompson JW, Arshavsky VY.

J Proteome Res. 2013 Jun 7;12(6):3010-8. doi: 10.1021/pr4003678. Epub 2013 May 24.

2.

Progressive Rod-Cone Degeneration (PRCD) Protein Requires N-Terminal S-Acylation and Rhodopsin Binding for Photoreceptor Outer Segment Localization and Maintaining Intracellular Stability.

Spencer WJ, Pearring JN, Salinas RY, Loiselle DR, Skiba NP, Arshavsky VY.

Biochemistry. 2016 Sep 13;55(36):5028-37. doi: 10.1021/acs.biochem.6b00489. Epub 2016 Aug 30.

PMID:
27509380
3.
4.

Accumulation of non-outer segment proteins in the outer segment underlies photoreceptor degeneration in Bardet-Biedl syndrome.

Datta P, Allamargot C, Hudson JS, Andersen EK, Bhattarai S, Drack AV, Sheffield VC, Seo S.

Proc Natl Acad Sci U S A. 2015 Aug 11;112(32):E4400-9. doi: 10.1073/pnas.1510111112. Epub 2015 Jul 27.

5.

Ion-current-based proteomic profiling of the retina in a rat model of Smith-Lemli-Opitz syndrome.

Tu C, Li J, Jiang X, Sheflin LG, Pfeffer BA, Behringer M, Fliesler SJ, Qu J.

Mol Cell Proteomics. 2013 Dec;12(12):3583-98. doi: 10.1074/mcp.M113.027847. Epub 2013 Aug 26.

6.

A monogenic dominant mutation in Rom1 generated by N-ethyl-N-nitrosourea mutagenesis causes retinal degeneration in mice.

Sato H, Suzuki T, Ikeda K, Masuya H, Sezutsu H, Kaneda H, Kobayashi K, Miura I, Kurihara Y, Yokokura S, Nishida K, Tamai M, Gondo Y, Noda T, Wakana S.

Mol Vis. 2010 Mar 10;16:378-91.

7.
8.

Proteomic profiling of a layered tissue reveals unique glycolytic specializations of photoreceptor cells.

Reidel B, Thompson JW, Farsiu S, Moseley MA, Skiba NP, Arshavsky VY.

Mol Cell Proteomics. 2011 Mar;10(3):M110.002469. doi: 10.1074/mcp.M110.002469. Epub 2010 Dec 20.

9.

Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA).

Pang JJ, Chang B, Hawes NL, Hurd RE, Davisson MT, Li J, Noorwez SM, Malhotra R, McDowell JH, Kaushal S, Hauswirth WW, Nusinowitz S, Thompson DA, Heckenlively JR.

Mol Vis. 2005 Feb 28;11:152-62.

10.

Photoreceptor sensory cilia and inherited retinal degeneration.

Liu Q, Zhang Q, Pierce EA.

Adv Exp Med Biol. 2010;664:223-32. doi: 10.1007/978-1-4419-1399-9_26. Review.

11.
12.

Interphotoreceptor retinoid-binding protein (IRBP) in progressive rod-cone degeneration (prcd)--biochemical, immunocytochemical and immunologic studies.

Wiggert B, Kutty G, Long KO, Inouye L, Gery I, Chader GJ, Aguirre GD.

Exp Eye Res. 1991 Sep;53(3):389-98.

PMID:
1936175
13.

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.

Genomics. 2006 Nov;88(5):551-63. Epub 2006 Aug 30.

14.

Novel dominant rhodopsin mutation triggers two mechanisms of retinal degeneration and photoreceptor desensitization.

Iakhine R, Chorna-Ornan I, Zars T, Elia N, Cheng Y, Selinger Z, Minke B, Hyde DR.

J Neurosci. 2004 Mar 10;24(10):2516-26.

15.

Molecular cloning, membrane topology, and localization of bovine rom-1 in rod and cone photoreceptor cells.

Moritz OL, Molday RS.

Invest Ophthalmol Vis Sci. 1996 Feb;37(2):352-62.

PMID:
8603840
16.

Disruption of the retinitis pigmentosa 28 gene Fam161a in mice affects photoreceptor ciliary structure and leads to progressive retinal degeneration.

Karlstetter M, Sorusch N, Caramoy A, Dannhausen K, Aslanidis A, Fauser S, Boesl MR, Nagel-Wolfrum K, Tamm ER, J├Ągle H, Stoehr H, Wolfrum U, Langmann T.

Hum Mol Genet. 2014 Oct 1;23(19):5197-210. doi: 10.1093/hmg/ddu242. Epub 2014 May 15.

PMID:
24833722
17.

The Y141C knockin mutation in RDS leads to complex phenotypes in the mouse.

Stuck MW, Conley SM, Naash MI.

Hum Mol Genet. 2014 Dec 1;23(23):6260-74. doi: 10.1093/hmg/ddu345. Epub 2014 Jul 7.

18.

A murine RP1 missense mutation causes protein mislocalization and slowly progressive photoreceptor degeneration.

Song D, Grieco S, Li Y, Hunter A, Chu S, Zhao L, Song Y, DeAngelis RA, Shi LY, Liu Q, Pierce EA, Nishina PM, Lambris JD, Dunaief JL.

Am J Pathol. 2014 Oct;184(10):2721-9. doi: 10.1016/j.ajpath.2014.06.010. Epub 2014 Aug 1.

19.

Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouse.

Connell G, Bascom R, Molday L, Reid D, McInnes RR, Molday RS.

Proc Natl Acad Sci U S A. 1991 Feb 1;88(3):723-6.

20.

Downregulation of a unique photoreceptor protein correlates with improper outer segment assembly.

Wohabrebbi A, Umstot ES, Iannaccone A, Desiderio DM, Jablonski MM.

J Neurosci Res. 2002 Feb 1;67(3):298-308.

PMID:
11813234

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