Article List

WPRIM Management System> DCMS> Chinese Journal of Experimental Ophthalmology> 2019> 37> 9

Volume: 37 Issue: 9

1. Focus on the treatment of inherited retinal diseases	Page:689—693
2. Differentially expressed genes analysis of retinal vascular endothelial cells under hyperglycemia and hyperlipidemia induced by α-melanocyte-stimulating hormone	Page:694—700
3. Analysis of differentially expressed genes of Staphylococcus aureus isolated from corneal ulcer and healthy conjunctival sac	Page:701—706
4. Proteomic research of human retinal microvascular pericytes stimulated with high glucose	Page:707—712
5. Effect and potential signaling pathway of hedgehog protein on the function of human retinal microvascular endothelial cell	Page:713—718
6. Diagnosis of choroideremia in two Chinese families misdiagnosed as retinitis pigmentosa using next-generation sequencing	Page:719—724
7. Mutations analysis of FRMD7 gene in idiopathic congenital nystagmus families	Page:726—729
8. Clinical manifestation and gene mutation of Bietti crystalline corneoretinal dystrophy	Page:730—735
9. Mutation screen of P4HA2 gene in Tujia high myopia patients	Page:736—739
10. Screening of pathogenic mutation in a Chinese family with congenital pulverulent cataract	Page:740—744
11. Measurement of biological parameters of nanophthalmos and its correlation with axial length	Page:745—749
12. Gene mutation spectrum analysis of retinitis pigmentosa patients in Ningxia Region of China	Page:750—754
13. Research progress of FYCO1 gene mutation	Page:755—758
14. Research progress of Cre/LoxP system in the eyes of animal model	Page:759—763
15. Advances in vitreous proteomics of vitreoretinal diseases	Page:764—768
16. Focus on the treatment of inherited retinal diseases	Page:689—693
17. Differentially expressed genes analysis of retinal vascular endothelial cells under hyperglycemia and hyperlipidemia induced by α-melanocyte-stimulating hormone	Page:694—700
18. Analysis of differentially expressed genes of Staphylococcus aureus isolated from corneal ulcer and healthy conjunctival sac	Page:701—706
19. Proteomic research of human retinal microvascular pericytes stimulated with high glucose	Page:707—712
20. Effect and potential signaling pathway of hedgehog protein on the function of human retinal microvascular endothelial cell	Page:713—718
21. Diagnosis of choroideremia in two Chinese families misdiagnosed as retinitis pigmentosa using next-generation sequencing	Page:719—724
22. Mutations analysis of FRMD7 gene in idiopathic congenital nystagmus families	Page:726—729
23. Clinical manifestation and gene mutation of Bietti crystalline corneoretinal dystrophy	Page:730—735
24. Mutation screen of P4HA2 gene in Tujia high myopia patients	Page:736—739
25. Screening of pathogenic mutation in a Chinese family with congenital pulverulent cataract	Page:740—744
26. Measurement of biological parameters of nanophthalmos and its correlation with axial length	Page:745—749
27. Gene mutation spectrum analysis of retinitis pigmentosa patients in Ningxia Region of China	Page:750—754
28. Research progress of FYCO1 gene mutation	Page:755—758
29. Research progress of Cre/LoxP system in the eyes of animal model	Page:759—763
30. Advances in vitreous proteomics of vitreoretinal diseases	Page:764—768