Zhang K - Search Results

1

A genome-wide scan maps a novel autosomal dominant juvenile-onset open-angle glaucoma locus to 2p15-16.

Lin Y, Liu T, Li J, Yang J, Du Q, Wang J, Yang Y, Liu X, Fan Y, Lu F, Chen Y, Pu Y, Zhang K, He X, Yang Z. Lin Y, et al. Among authors: zhang k. Mol Vis. 2008 Apr 18;14:739-44. Mol Vis. 2008. PMID: 18432317 Free PMC article.

2

A new locus for autosomal dominant stargardt-like disease maps to chromosome 4.

Kniazeva M, Chiang MF, Morgan B, Anduze AL, Zack DJ, Han M, Zhang K. Kniazeva M, et al. Among authors: zhang k. Am J Hum Genet. 1999 May;64(5):1394-9. doi: 10.1086/302377. Am J Hum Genet. 1999. PMID: 10205271 Free PMC article.

3

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.

4

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.

5

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

6

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

7

Autosomal dominant cone dystrophy caused by a novel mutation in the GCAP1 gene (GUCA1A).

Jiang L, Katz BJ, Yang Z, Zhao Y, Faulkner N, Hu J, Baird J, Baehr W, Creel DJ, Zhang K. Jiang L, et al. Among authors: zhang k. Mol Vis. 2005 Feb 20;11:143-51. Mol Vis. 2005. PMID: 15735604 Free article.

8

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.

9

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.

10

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.

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