Gu YS - Search Results

1

Genotype-phenotype correlations in Chinese patients with TGFBI gene-linked corneal dystrophy.

Long Y, Gu YS, Han W, Li XY, Yu P, Qi M. Long Y, et al. Among authors: gu ys. J Zhejiang Univ Sci B. 2011 Apr;12(4):287-92. doi: 10.1631/jzus.B1000154. J Zhejiang Univ Sci B. 2011. PMID: 21462384 Free PMC article.

2

MGB probe assay for rapid detection of mtDNA11778 mutation in the Chinese LHON patients by real-time PCR.

Wang JY, Gu YS, Wang J, Tong Y, Wang Y, Shao JB, Qi M. Wang JY, et al. Among authors: gu ys. J Zhejiang Univ Sci B. 2008 Aug;9(8):610-5. doi: 10.1631/jzus.B0820058. J Zhejiang Univ Sci B. 2008. PMID: 18763310 Free PMC article.

3

Identification of a novel mutation in a Chinese family with Nance-Horan syndrome by whole exome sequencing.

Hong N, Chen YH, Xie C, Xu BS, Huang H, Li X, Yang YQ, Huang YP, Deng JL, Qi M, Gu YS. Hong N, et al. Among authors: gu ys. J Zhejiang Univ Sci B. 2014 Aug;15(8):727-34. doi: 10.1631/jzus.B1300321. J Zhejiang Univ Sci B. 2014. PMID: 25091991 Free PMC article.

4

A clinical and molecular-genetic analysis of Chinese patients with lattice corneal dystrophy and novel Thr538Pro mutation in the TGFBI (BIGH3) gene.

Yu P, Gu Y, Yang Y, Yan X, Chen L, Ge Z, Qi M, Si J, Guo L. Yu P, et al. J Genet. 2006 Apr;85(1):73-6. doi: 10.1007/BF02728974. J Genet. 2006. PMID: 16809844 No abstract available.

5

p.Ala546 > Asp and p.Arg555 > Trp mutations of TGFBI gene and their clinical manifestations in two large Chinese families with granular corneal dystrophy type I.

Yu P, Gu Y, Jin F, Hu R, Chen L, Yan X, Yang Y, Qi M. Yu P, et al. Genet Test. 2008 Sep;12(3):421-5. doi: 10.1089/gte.2008.0005. Genet Test. 2008. PMID: 18752451

6

Clinical investigation of surgery for intermittent exotropia.

Yang CQ, Shen Y, Gu YS, Han W. Yang CQ, et al. Among authors: gu ys. J Zhejiang Univ Sci B. 2008 Jun;9(6):470-3. doi: 10.1631/jzus.B0720007. J Zhejiang Univ Sci B. 2008. PMID: 18543400 Free PMC article.

7

Investigation of the influence of Arg555Trp and Thr538Pro TGFBI mutations on C-terminal cleavage and cell endoplasmic reticulum stress.

Zhu M, Yu P, Jiang B, Gu Y. Zhu M, et al. Mol Vis. 2012;18:1156-64. Epub 2012 May 3. Mol Vis. 2012. PMID: 22605926 Free PMC article.

8

Indications and outcomes of penetrating keratoplasty in a tertiary hospital in the developing world.

Pan Q, Li X, Gu Y. Pan Q, et al. Clin Exp Ophthalmol. 2012 Apr;40(3):232-8. doi: 10.1111/j.1442-9071.2011.02598.x. Epub 2011 Sep 2. Clin Exp Ophthalmol. 2012. PMID: 21575124

9

Phenotype-genotype correlation with Sanger sequencing identified retinol dehydrogenase 12 (RDH12) compound heterozygous variants in a Chinese family with Leber congenital amaurosis.

Li Y, Pan Q, Gu YS. Li Y, et al. Among authors: gu ys. J Zhejiang Univ Sci B. 2017 May;18(5):421-429. doi: 10.1631/jzus.B1600156. J Zhejiang Univ Sci B. 2017. PMID: 28471114 Free PMC article.

10

Outcomes of 4 surgical adjuvants used for internal limiting membrane peeling in macular hole surgery: a systematic review and network Meta-analysis.

Wang XW, Long Y, Gu YS, Guo DY. Wang XW, et al. Among authors: gu ys. Int J Ophthalmol. 2020 Mar 18;13(3):481-487. doi: 10.18240/ijo.2020.03.17. eCollection 2020. Int J Ophthalmol. 2020. PMID: 32309187 Free PMC article.

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