Yu Y - Search Results

1

Gallium-Based Nanoplatform for Combating Multidrug-Resistant Pseudomonas aeruginosa and Postoperative Inflammation in Endophthalmitis Secondary to Cataract Surgery.

Qiao Y, Li Y, Ye Y, Yu Y, Wang W, Yao K, Zhou M. Qiao Y, et al. Among authors: yu y. ACS Appl Mater Interfaces. 2022 Nov 23;14(46):51763-51775. doi: 10.1021/acsami.2c15834. Epub 2022 Nov 14. ACS Appl Mater Interfaces. 2022. PMID: 36373472

2

New applications of femtosecond laser in cataract surgery.

Yu Y, Yao K. Yu Y, et al. Eye Sci. 2012 Mar;27(1):50-6. doi: 10.3969/j.issn.1000-4432.2012.01.012. Eye Sci. 2012. PMID: 22447555 Review.

3

Congenital polymorphic cataract associated with a G to A splice site mutation in the human beta-crystallin gene CRYβA3/A1.

Yu Y, Li J, Xu J, Wang Q, Yu Y, Yao K. Yu Y, et al. Mol Vis. 2012;18:2213-20. Epub 2012 Aug 8. Mol Vis. 2012. PMID: 22919269 Free PMC article.

4

Bromfenac sodium 0.1%, fluorometholone 0.1% and dexamethasone 0.1% for control of ocular inflammation and prevention of cystoid macular edema after phacoemulsification.

Wang QW, Yao K, Xu W, Chen PQ, Shentu XC, Xie X, Weng Y, Zhang L, Jin CF, Wu W, Zhu YN, Yu YH. Wang QW, et al. Among authors: yu yh. Ophthalmologica. 2013;229(4):187-94. doi: 10.1159/000346847. Epub 2013 Feb 14. Ophthalmologica. 2013. PMID: 23429038 Clinical Trial.

5

A novel connexin 50 gene (gap junction protein, alpha 8) mutation associated with congenital nuclear and zonular pulverulent cataract.

Li J, Wang Q, Fu Q, Zhu Y, Zhai Y, Yu Y, Zhang K, Yao K. Li J, et al. Among authors: yu y. Mol Vis. 2013 Apr 5;19:767-74. Print 2013. Mol Vis. 2013. PMID: 23592913 Free PMC article.

6

[Recent advances in femtosecond laser-assisted cataract surgery].

Yu YH, Yao K. Yu YH, et al. Zhonghua Yan Ke Za Zhi. 2013 May;49(5):464-7. Zhonghua Yan Ke Za Zhi. 2013. PMID: 24021187 Review. Chinese.

7

A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family.

Yu Y, Yu Y, Chen P, Li J, Zhu Y, Zhai Y, Yao K. Yu Y, et al. BMC Med Genet. 2014 Jan 9;15:6. doi: 10.1186/1471-2350-15-6. BMC Med Genet. 2014. PMID: 24405844 Free PMC article.

8

A nonsense mutation of γD-crystallin associated with congenital nuclear and posterior polar cataract in a Chinese family.

Zhai Y, Li J, Zhu Y, Xia Y, Wang W, Yu Y, Yao K. Zhai Y, et al. Among authors: yu y. Int J Med Sci. 2014 Jan 5;11(2):158-63. doi: 10.7150/ijms.7567. eCollection 2014. Int J Med Sci. 2014. PMID: 24465161 Free PMC article.

9

A novel phenotype-genotype correlation with an Arg555Trp mutation of TGFBI gene in Thiel-Behnke corneal dystrophy in a Chinese pedigree.

Yu Y, Qiu P, Zhu Y, Li J, Wu M, Zhang B, Yao K. Yu Y, et al. BMC Ophthalmol. 2015 Oct 13;15:131. doi: 10.1186/s12886-015-0121-0. BMC Ophthalmol. 2015. PMID: 26464103 Free PMC article.

10

A novel FBN1 missense mutation (p.C102Y) associated with ectopia lentis syndrome in a Chinese family.

Zhai Y, Wang W, Zhu YN, Li JY, Yu YH, Lai KR, Yao K. Zhai Y, et al. Among authors: yu yh. Int J Ophthalmol. 2015 Oct 18;8(5):855-9. doi: 10.3980/j.issn.2222-3959.2015.05.01. eCollection 2015. Int J Ophthalmol. 2015. PMID: 26558191 Free PMC article.

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