Home
|
Help
|
Contact
Sign in
WPRIM Management System>
DCMS
>
Chinese Journal of Experimental Ophthalmology
>
2015
>
33
>
8
Volume:
33
Issue:
8
1. Promoting effect of connective tissue growth factor on expression of E-cadherin in human Tenon capsule fibroblasts
Page:695—698
2. Association of MCP-1-2518A/G polymorphism with uveitis susceptibility: a Meta-analysis
Page:739—744
3. Association analysis of accommodative microfluctuations and wavefront aberration in emmetropia and myopia in teenagers
Page:745—750
4. Regulation roles of COUP transcription factors in the development of embryonic eye
Page:751—754
5. Research progress of Leber hereditary optic neuropathy
Page:755—759
6. Advances in molecular genetics of exfoliation syndrome
Page:760—763
7. Advances in genetic study of achromatopsia
Page:764—767
8. Epigenetics,diseases and therapy in ophthalmology
Page:673—677
9. Next generation sequencing based molecular genetic analysis of a Chinese Han family with autosomal retinitis pigmentosa
Page:699—703
10. Modulation of MEK/ERK and PI3K/Akt pathways to the expression of DDR2 and MMP-13 in choroidal neovascularization
Page:678—685
11. Construction and assessment of recombinant plasmid pRNAT-U6.1/CFB siRNA and its inhibitory effect on proliferation of human umbilical vein endothelial cells
Page:686—690
12. Change of serum response factor expression in eyelid of different embryo development stages of B6-Co mice
Page:691—694
13. Detection of disease-causing gene in a Hui congential cataract pedigree by exon combined target region capture sequencing chip
Page:711—715
14. Dynamic changes of retinal nerve fiber layer thickness and visual contrast sensitivity in young population with type 2 diabetes mellitus
Page:716—721
15. A recurrent mutation of CRYGD gene in a northern Chinese family with autosomal dominant congenital nuclear cataract
Page:722—726
16. Application of computer-aided designing and manufacturing technology in the reconstruction of orbital blow-out fracture
Page:727—732
17. Association between single nucleotide polymorphisms at LOXL1 promoter and Uygur patients with exfoliation syndrome
Page:733—738