Zhang K - Search Results

1

Genetic association of LOXL1 gene variants and exfoliation glaucoma in a Utah cohort.

Yang X, Zabriskie NA, Hau VS, Chen H, Tong Z, Gibbs D, Farhi P, Katz BJ, Luo L, Pearson E, Goldsmith J, Ma X, Kaminoh Y, Chen Y, Yu B, Zeng J, Zhang K, Yang Z. Yang X, et al. Among authors: zhang k. Cell Cycle. 2008 Feb 15;7(4):521-4. doi: 10.4161/cc.7.4.5388. Cell Cycle. 2008. PMID: 18287813

2

Diverse macular dystrophy phenotype caused by a novel complex mutation in the ELOVL4 gene.

Bernstein PS, Tammur J, Singh N, Hutchinson A, Dixon M, Pappas CM, Zabriskie NA, Zhang K, Petrukhin K, Leppert M, Allikmets R. Bernstein PS, et al. Among authors: zhang k. Invest Ophthalmol Vis Sci. 2001 Dec;42(13):3331-6. Invest Ophthalmol Vis Sci. 2001. PMID: 11726641

3

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

4

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.

5

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.

6

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

7

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

8

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.

9

Examination of ELN as a candidate gene in the Utah intracranial aneurysm pedigrees.

Berthelemy-Okazaki N, Zhao Y, Yang Z, Camp NJ, Farnham J, Parker D, Tsuruda J, Macdonald J, Zhang K, Cannon-Albright LA. Berthelemy-Okazaki N, et al. Among authors: zhang k. Stroke. 2005 Jun;36(6):1283-4. doi: 10.1161/01.STR.0000166198.05439.f8. Epub 2005 May 12. Stroke. 2005. PMID: 15890991

10

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.

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