Zhao X - Search Results

1

Exclusion of the human collagen type XVII (COL17A1) gene as the cause of Thiel-Behnke corneal dystrophy (CDB2) on chromosome 10q23-q25.

Sullivan LS, Zhao X, Bowne SJ, Xu X, Daiger SP, Yee SB, Yee RW. Sullivan LS, et al. Among authors: zhao x. Curr Eye Res. 2003 Oct;27(4):223-6. doi: 10.1076/ceyr.27.4.223.16595. Curr Eye Res. 2003. PMID: 14562173

2

Recurrence of chromosome 10 Thiel-Behnke corneal dystrophy (CDB2) after excimer laser phototherapeutic keratectomy or penetrating keratoplasty.

Sorour HM, Yee SB, Peterson NJ, Li FT, Macsai MS, Zhao XC, Yee RW. Sorour HM, et al. Cornea. 2005 Jan;24(1):45-50. doi: 10.1097/01.ico.0000126442.61088.a8. Cornea. 2005. PMID: 15604866

3

A novel mutation of the Keratin 12 gene responsible for a severe phenotype of Meesmann's corneal dystrophy.

Sullivan LS, Baylin EB, Font R, Daiger SP, Pepose JS, Clinch TE, Nakamura H, Zhao XC, Yee RW. Sullivan LS, et al. Mol Vis. 2007 Jun 21;13:975-80. Mol Vis. 2007. PMID: 17653038 Free PMC article.

4

Individual phenotypic variances in a family with Thiel-Behnke corneal dystrophy.

Nakamura H, Li FT, Foltermann MO, Macsai M, Ma X, Zhao XC, Flaherty K, Yee RW. Nakamura H, et al. Among authors: zhao xc. Cornea. 2012 Nov;31(11):1217-22. doi: 10.1097/ICO.0b013e3181c32efd. Cornea. 2012. PMID: 22965308

5

Spontaneous and inheritable R555Q mutation in the TGFBI/BIGH3 gene in two unrelated families exhibiting Bowman's layer corneal dystrophy.

Zhao XC, Nakamura H, Subramanyam S, Stock LE, Gillette TE, Yoshikawa S, Ma X, Yee RW. Zhao XC, et al. Ophthalmology. 2007 Nov;114(11):e39-46. doi: 10.1016/j.ophtha.2007.07.029. Ophthalmology. 2007. PMID: 17980739

6

Comparison of the relative toxicity of travoprost 0.004% without benzalkonium chloride and latanoprost 0.005% in an immortalized human cornea epithelial cell culture system.

Yee RW, Norcom EG, Zhao XC. Yee RW, et al. Adv Ther. 2006 Jul-Aug;23(4):511-9. doi: 10.1007/BF02850039. Adv Ther. 2006. PMID: 17050493

7

The zebrafish cornea: structure and development.

Zhao XC, Yee RW, Norcom E, Burgess H, Avanesov AS, Barrish JP, Malicki J. Zhao XC, et al. Invest Ophthalmol Vis Sci. 2006 Oct;47(10):4341-8. doi: 10.1167/iovs.05-1611. Invest Ophthalmol Vis Sci. 2006. PMID: 17003424

8

Transgenic analysis of the anterior eye-specific enhancers of the zebrafish gelsolin-like 1 (gsnl1) gene.

Yoshikawa S, Norcom E, Nakamura H, Yee RW, Zhao XC. Yoshikawa S, et al. Dev Dyn. 2007 Jul;236(7):1929-38. doi: 10.1002/dvdy.21197. Dev Dyn. 2007. PMID: 17576137 Free article.

9

Excimer laser exacerbation of Avellino corneal dystrophy.

Lee WB, Himmel KS, Hamilton SM, Zhao XC, Yee RW, Kang SJ, Grossniklaus HE. Lee WB, et al. J Cataract Refract Surg. 2007 Jan;33(1):133-8. doi: 10.1016/j.jcrs.2006.09.024. J Cataract Refract Surg. 2007. PMID: 17189809

10

CRB1 gene mutations are associated with keratoconus in patients with leber congenital amaurosis.

McMahon TT, Kim LS, Fishman GA, Stone EM, Zhao XC, Yee RW, Malicki J. McMahon TT, et al. Invest Ophthalmol Vis Sci. 2009 Jul;50(7):3185-7. doi: 10.1167/iovs.08-2886. Epub 2009 Apr 30. Invest Ophthalmol Vis Sci. 2009. PMID: 19407021

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