Article List

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

Volume: 37 Issue: 9

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