WPRIM Management System> DCMS> Chinese Journal of Experimental Ophthalmology> 2017> 35> 8

Volume: 35 Issue: 8

1. Research progress of miR-204 in the regulation of ophthalmic diseases Page:761—763
2. Associations of single nucleotide polymorphisms of UCP genes with diabetic retinopathy in Chinese Han population Page:737—742
3. Clinical characteristic and management of Peters anomaly Page:727—731
4. Genetic analysis of a Chinese family with congenital aniridia and detection of PAX6 mutation locus Page:721—725
5. Mutation analysis of a Chinese pedigree of Leber hereditary optic neuropathy with only male patients Page:710—715
6. Pedigree and clinical characteristics in a Chinese family with lattice corneal dystrophy Page:704—708
7. Aggravation effects of JAK-STAT signaling pathway in retinal ischemia reperfusion injury Page:690—694
8. Construction of combined lentiviral vectors for rat Slit2 gene RNA interfering and its down-regulation effects on Slit2 gene in rat retinal pigment epithelial cells Page:683—689
9. Inhibition of adenovirus-mediated recombinant Tum5 gene overexpression on human umbilical vein endothelial cells in physiological status Page:677—682
10. Update on mutations of precursor mRNA splicing factor genes linked to retinitis pigmentosa Page:752—755
11. Survey of medical resources of eye care in Tibet autonomous region Page:743—746
12. Gene research progress of retinoblastoma Page:756—760
13. Research progress of DNA methylation in lens development and cataract Page:747—751
14. Research progress on correlation between microRNA and retinal development Page:764—768
15. Affecting factors of corneal epithelial healing following de-epithelized corneal collagen cross linking in keratoconus patients Page:732—736
16. Genetic association between corneal curvature-related genes and high myopia in Chinese Han population Page:716—720
17. Inhibitory effects of microRNA-375 on biological behaviour of human retinal capillary endothelial cells induced by hypoxia Page:695—702
18. Clinical phenotype assessment is very important in mutation analysis for patients with hereditary eye disease Page:673—676

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