Zhao C - Search Results

1

PRPF4 mutations cause autosomal dominant retinitis pigmentosa.

Chen X, Liu Y, Sheng X, Tam PO, Zhao K, Chen X, Rong W, Liu Y, Liu X, Pan X, Chen LJ, Zhao Q, Vollrath D, Pang CP, Zhao C. Chen X, et al. Among authors: zhao k, zhao c, zhao q. Hum Mol Genet. 2014 Jun 1;23(11):2926-39. doi: 10.1093/hmg/ddu005. Epub 2014 Jan 12. Hum Mol Genet. 2014. PMID: 24419317

2

[Novel splice-site mutation in the pre-mRNA splicing gene PRPF31 in a Chinese family with autosomal dominant retinitis pigmentosa].

Lu SS, Zhao C, Cui Y, Li ND, Zhang XM, Zhao KX. Lu SS, et al. Among authors: zhao c, zhao kx. Zhonghua Yan Ke Za Zhi. 2005 Apr;41(4):305-11. Zhonghua Yan Ke Za Zhi. 2005. PMID: 15924690 Chinese.

3

A novel locus (RP33) for autosomal dominant retinitis pigmentosa mapping to chromosomal region 2cen-q12.1.

Zhao C, Lu S, Zhou X, Zhang X, Zhao K, Larsson C. Zhao C, et al. Among authors: zhao k. Hum Genet. 2006 Jul;119(6):617-23. doi: 10.1007/s00439-006-0168-3. Epub 2006 Apr 13. Hum Genet. 2006. PMID: 16612614

4

An autosomal dominant progressive congenital zonular nuclear cataract linked to chromosome 20p12.2-p11.23.

Li N, Yang Y, Bu J, Zhao C, Lu S, Zhao J, Yan L, Cui L, Zheng R, Li J, Tang J, Zhao K. Li N, et al. Among authors: zhao j, zhao k, zhao c. Mol Vis. 2006 Dec 5;12:1506-10. Mol Vis. 2006. PMID: 17167408 Free article.

5

Two Chinese families with pulverulent congenital cataracts and deltaG91 CRYBA1 mutations.

Lu S, Zhao C, Jiao H, Kere J, Tang X, Zhao F, Zhang X, Zhao K, Larsson C. Lu S, et al. Among authors: zhao k, zhao f, zhao c. Mol Vis. 2007 Jul 13;13:1154-60. Mol Vis. 2007. PMID: 17653060

6

Novel and recurrent KIF21A mutations in congenital fibrosis of the extraocular muscles type 1 and 3.

Lu S, Zhao C, Zhao K, Li N, Larsson C. Lu S, et al. Among authors: zhao k, zhao c. Arch Ophthalmol. 2008 Mar;126(3):388-94. doi: 10.1001/archopht.126.3.388. Arch Ophthalmol. 2008. PMID: 18332320

7

Autosomal-dominant retinitis pigmentosa caused by a mutation in SNRNP200, a gene required for unwinding of U4/U6 snRNAs.

Zhao C, Bellur DL, Lu S, Zhao F, Grassi MA, Bowne SJ, Sullivan LS, Daiger SP, Chen LJ, Pang CP, Zhao K, Staley JP, Larsson C. Zhao C, et al. Among authors: zhao k, zhao f. Am J Hum Genet. 2009 Nov;85(5):617-27. doi: 10.1016/j.ajhg.2009.09.020. Epub 2009 Oct 29. Am J Hum Genet. 2009. PMID: 19878916 Free PMC article.

8

Generation of Cre transgenic mice with postnatal RPE-specific ocular expression.

Iacovelli J, Zhao C, Wolkow N, Veldman P, Gollomp K, Ojha P, Lukinova N, King A, Feiner L, Esumi N, Zack DJ, Pierce EA, Vollrath D, Dunaief JL. Iacovelli J, et al. Among authors: zhao c. Invest Ophthalmol Vis Sci. 2011 Mar 14;52(3):1378-83. doi: 10.1167/iovs.10-6347. Print 2011 Mar. Invest Ophthalmol Vis Sci. 2011. PMID: 21212186 Free PMC article.

9

mTOR pathway activation in age-related retinal disease.

Zhao C, Vollrath D. Zhao C, et al. Aging (Albany NY). 2011 Apr;3(4):346-7. doi: 10.18632/aging.100303. Aging (Albany NY). 2011. PMID: 21483039 Free PMC article. No abstract available.

10

Targeted sequencing of 179 genes associated with hereditary retinal dystrophies and 10 candidate genes identifies novel and known mutations in patients with various retinal diseases.

Chen X, Zhao K, Sheng X, Li Y, Gao X, Zhang X, Kang X, Pan X, Liu Y, Jiang C, Shi H, Chen X, Rong W, Chen LJ, Lai TY, Liu Y, Wang X, Yuan S, Liu Q, Vollrath D, Pang CP, Zhao C. Chen X, et al. Among authors: zhao k, zhao c. Invest Ophthalmol Vis Sci. 2013 Mar 1;54(3):2186-97. doi: 10.1167/iovs.12-10967. Invest Ophthalmol Vis Sci. 2013. PMID: 23462753

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