Zhang K - Search Results

1

Identification and characterization of a novel mutation in the carbonic anhydrase IV gene that causes retinitis pigmentosa.

Alvarez BV, Vithana EN, Yang Z, Koh AH, Yeung K, Yong V, Shandro HJ, Chen Y, Kolatkar P, Palasingam P, Zhang K, Aung T, Casey JR. Alvarez BV, et al. Among authors: zhang k. Invest Ophthalmol Vis Sci. 2007 Aug;48(8):3459-68. doi: 10.1167/iovs.06-1515. Invest Ophthalmol Vis Sci. 2007. PMID: 17652713

2

A novel mutation in the RDS/Peripherin gene causes adult-onset foveomacular dystrophy.

Yang Z, Lin W, Moshfeghi DM, Thirumalaichary S, Li X, Jiang L, Zhang H, Zhang S, Kaiser PK, Traboulsi EI, Zhang K. Yang Z, et al. Among authors: zhang s, zhang k, zhang h. Am J Ophthalmol. 2003 Feb;135(2):213-8. doi: 10.1016/s0002-9394(02)01815-9. Am J Ophthalmol. 2003. PMID: 12566026

3

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. Among authors: zhang k. Mol Vis. 2004 Mar 31;10:248-53. Mol Vis. 2004. PMID: 15073583 Free article.

4

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

5

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: zhang k. 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

6

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. Among authors: zhang k. Mol Vis. 2005 Aug 30;11:657-64. Mol Vis. 2005. PMID: 16145543 Free article.

7

Clinical features of autosomal dominant retinitis pigmentosa associated with a Rhodopsin mutation.

Chen H, Chen Y, Horn R, Yang Z, Wang C, Turner MJ, Zhang K. Chen H, et al. Among authors: zhang k. Ann Acad Med Singap. 2006 Jun;35(6):411-5. Ann Acad Med Singap. 2006. PMID: 16865192 Free article.

8

A novel locus for X-linked retinitis pigmentosa.

Tong Z, Yang Z, Meyer JJ, McInnes AW, Xue L, Azimi AM, Baird J, Zhao Y, Pearson E, Wang C, Chen Y, Zhang K. Tong Z, et al. Among authors: zhang k. Ann Acad Med Singap. 2006 Jul;35(7):476-8. Ann Acad Med Singap. 2006. PMID: 16902723 Free article.

9

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: zhang k. 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.

10

The R345W mutation in EFEMP1 is pathogenic and causes AMD-like deposits in mice.

Fu L, Garland D, Yang Z, Shukla D, Rajendran A, Pearson E, Stone EM, Zhang K, Pierce EA. Fu L, et al. Among authors: zhang k. Hum Mol Genet. 2007 Oct 15;16(20):2411-22. doi: 10.1093/hmg/ddm198. Epub 2007 Jul 30. Hum Mol Genet. 2007. PMID: 17666404

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