Karan G - Search Results

1

Recurrent 17 bp duplication in PITX3 is primarily associated with posterior polar cataract (CPP4).

Berry V, Yang Z, Addison PK, Francis PJ, Ionides A, Karan G, Jiang L, Lin W, Hu J, Yang R, Moore A, Zhang K, Bhattacharya SS. Berry V, et al. Among authors: karan g. J Med Genet. 2004 Aug;41(8):e109. doi: 10.1136/jmg.2004.020289. J Med Genet. 2004. PMID: 15286169 Free PMC article. No abstract available.

2

Expression of wild type and mutant ELOVL4 in cell culture: subcellular localization and cell viability.

Karan G, Yang Z, Zhang K. Karan G, et al. Mol Vis. 2004 Mar 31;10:248-53. Mol Vis. 2004. PMID: 15073583 Free article.

3

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. Among authors: karan g. 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

4

Treatment with carbonic anhydrase inhibitors depresses electroretinogram responsiveness in mice.

Sauvé Y, Karan G, Yang Z, Li C, Hu J, Zhang K. Sauvé Y, et al. Among authors: karan g. Adv Exp Med Biol. 2006;572:439-46. doi: 10.1007/0-387-32442-9_61. Adv Exp Med Biol. 2006. PMID: 17249607 No abstract available.

5

Loss of ER retention and sequestration of the wild-type ELOVL4 by Stargardt disease dominant negative mutants.

Karan G, Yang Z, Howes K, Zhao Y, Chen Y, Cameron DJ, Lin Y, Pearson E, Zhang K. Karan G, et al. Mol Vis. 2005 Aug 30;11:657-64. Mol Vis. 2005. PMID: 16145543 Free article.

6

Choroidal neovascularization in patients with adult-onset foveomacular dystrophy caused by mutations in the RDS/peripherin gene.

Moshfeghi DM, Yang Z, Faulkner ND, Karan G, Thirumalaichary S, Pearson E, Zhao Y, Tsai T, Zhang K. Moshfeghi DM, et al. Among authors: karan g. Adv Exp Med Biol. 2006;572:35-40. doi: 10.1007/0-387-32442-9_6. Adv Exp Med Biol. 2006. PMID: 17249552 No abstract available.

7

Elovl4 mRNA distribution in the developing mouse retina and phylogenetic conservation of Elovl4 genes.

Zhang XM, Yang Z, Karan G, Hashimoto T, Baehr W, Yang XJ, Zhang K. Zhang XM, et al. Among authors: karan g. Mol Vis. 2003 Jul 3;9:301-7. Mol Vis. 2003. PMID: 12847421 Free PMC article.

8

Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice.

Yang Z, Chen Y, Lillo C, Chien J, Yu Z, Michaelides M, Klein M, Howes KA, Li Y, Kaminoh Y, Chen H, Zhao C, Chen Y, Al-Sheikh YT, Karan G, Corbeil D, Escher P, Kamaya S, Li C, Johnson S, Frederick JM, Zhao Y, Wang C, Cameron DJ, Huttner WB, Schorderet DF, Munier FL, Moore AT, Birch DG, Baehr W, Hunt DM, Williams DS, Zhang K. Yang Z, et al. Among authors: karan g. J Clin Invest. 2008 Aug;118(8):2908-16. doi: 10.1172/JCI35891. J Clin Invest. 2008. PMID: 18654668 Free PMC article.

9

Lipofuscin accumulation, abnormal electrophysiology, and photoreceptor degeneration in mutant ELOVL4 transgenic mice: a model for macular degeneration.

Karan G, Lillo C, Yang Z, Cameron DJ, Locke KG, Zhao Y, Thirumalaichary S, Li C, Birch DG, Vollmer-Snarr HR, Williams DS, Zhang K. Karan G, et al. Proc Natl Acad Sci U S A. 2005 Mar 15;102(11):4164-9. doi: 10.1073/pnas.0407698102. Epub 2005 Mar 4. Proc Natl Acad Sci U S A. 2005. PMID: 15749821 Free PMC article.

10

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. Among authors: karan g. Invest Ophthalmol Vis Sci. 2004 Dec;45(12):4263-7. doi: 10.1167/iovs.04-0078. Invest Ophthalmol Vis Sci. 2004. PMID: 15557430

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