Zhang K - Search Results

1

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: zhang k. J Clin Invest. 2008 Aug;118(8):2908-16. doi: 10.1172/JCI35891. J Clin Invest. 2008. PMID: 18654668 Free PMC article.

2

Evaluation of the ELOVL4 gene in patients with age-related macular degeneration.

Ayyagari R, Zhang K, Hutchinson A, Yu Z, Swaroop A, Kakuk LE, Seddon JM, Bernstein PS, Lewis RA, Tammur J, Yang Z, Li Y, Zhang H, Yashar BM, Liu J, Petrukhin K, Sieving PA, Allikmets R. Ayyagari R, et al. Among authors: zhang k, zhang h. Ophthalmic Genet. 2001 Dec;22(4):233-9. doi: 10.1076/opge.22.4.233.2219. Ophthalmic Genet. 2001. PMID: 11803489

3

Butterfly-shaped pattern dystrophy: a genetic, clinical, and histopathological report.

Zhang K, Garibaldi DC, Li Y, Green WR, Zack DJ. Zhang K, et al. Arch Ophthalmol. 2002 Apr;120(4):485-90. doi: 10.1001/archopht.120.4.485. Arch Ophthalmol. 2002. PMID: 11934323

4

Genomic organisation and alternative splicing of human RIM1, a gene implicated in autosomal dominant cone-rod dystrophy (CORD7).

Johnson S, Halford S, Morris AG, Patel RJ, Wilkie SE, Hardcastle AJ, Moore AT, Zhang K, Hunt DM. Johnson S, et al. Among authors: zhang k. Genomics. 2003 Mar;81(3):304-14. doi: 10.1016/s0888-7543(03)00010-7. Genomics. 2003. PMID: 12659814

5

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: zhang k. Mol Vis. 2003 Jul 3;9:301-7. Mol Vis. 2003. PMID: 12847421 Free PMC article.

6

Dominant cone and cone-rod dystrophies: functional analysis of mutations in retGC1 and GCAP1.

Hunt DM, Wilkie SE, Newbold R, Deery E, Warren MJ, Bhattacharya SS, Zhang K. Hunt DM, et al. Among authors: zhang k. Novartis Found Symp. 2004;255:37-49; discussion 49-50, 177-8. doi: 10.1002/0470092645.ch4. Novartis Found Symp. 2004. PMID: 14750595

7

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.

8

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: zhang k. 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.

9

A novel RDS/peripherin gene mutation associated with diverse macular phenotypes.

Yang Z, Li Y, Jiang L, Karan G, Moshfeghi D, O'Connor S, Li X, Yu Z, Lewis H, Zack D, Jacobson S, Zhang K. Yang Z, et al. Among authors: zhang k. Ophthalmic Genet. 2004 Jun;25(2):133-45. doi: 10.1080/13816810490514388. Ophthalmic Genet. 2004. PMID: 15370544

10

Dominant optic atrophy, sensorineural hearing loss, ptosis, and ophthalmoplegia: a syndrome caused by a missense mutation in OPA1.

Payne M, Yang Z, Katz BJ, Warner JE, Weight CJ, Zhao Y, Pearson ED, Treft RL, Hillman T, Kennedy RJ, Meire FM, Zhang K. Payne M, et al. Among authors: zhang k. Am J Ophthalmol. 2004 Nov;138(5):749-55. doi: 10.1016/j.ajo.2004.06.011. Am J Ophthalmol. 2004. PMID: 15531309

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