Authors:Liu Qing, Dong Yanling, Huang Yusen DOI: 10.3760/cma.j.issn.2095-0160.2019.09.003 Published 2019-09-10 Cite as Chin J Exp Ophthalmol, 2019,37(9): 701-706. Abstract [View PDF] [Read Full Text] Objective To investigate the possible pathogenesis of Staphylococcus aureus (S.aureus) corneal ulcer by analyzing the differentially expressed genes (DEGs) of S.aureus isolated from the patients with […]
Category: 2019
Proteomic research of human retinal microvascular pericytes stimulated with high glucose
Authors:Xiao Mengran, Zhang Xiaomin, Shao Xianfeng, Xiao Jing, Yang Fuhua, Zhang Hui, Ea Vicki L, Li Xiaorong DOI: 10.3760/cma.j.issn.2095-0160.2019.09.004 Published 2019-09-10 Cite as Chin J Exp Ophthalmol, 2019,37(9): 707-712. Abstract [View PDF] [Read Full Text] Objective To determine the changes of protein expressions in human retinal […]
Effect and potential signaling pathway of hedgehog protein on the function of human retinal microvascular endothelial cell
Authors:Li Yang, Hu Qinrui, Wang Bin, Xia Huika, Zhang Xiaohu DOI: 10.3760/cma.j.issn.2095-0160.2019.09.005 Published 2019-09-10 Cite as Chin J Exp Ophthalmol, 2019,37(9): 713-718. Abstract [View PDF] [Read Full Text] Objective To explore the impact of Hedgehog protein on human retinal microvascular endothelial cell(HRMEC)and its signaling pathway. Methods […]
Diagnosis of choroideremia in two Chinese families misdiagnosed as retinitis pigmentosa using next-generation sequencing
Authors:Wang Miaomiao, Wang Zhuoshi, Sun Yan, Xia Yang, He Wei DOI: 10.3760/cma.j.issn.2095-0160.2019.09.006 Published 2019-09-10 Cite as Chin J Exp Ophthalmol, 2019,37(9): 719-724. Abstract [View PDF] [Read Full Text] Objective To identify choroideremia and retinitis pigmentosa(RP)using next-generation sequencing(NGS)technology. Methods A cross-sectional study was adopted.The participants were two […]
Mutations analysis of FRMD7 gene in idiopathic congenital nystagmus families
Authors:Du Wei, Zhang Ye, Xie Zhenggao DOI: 10.3760/cma.j.issn.2095-0160.2019.09.008 Published 2019-09-10 Cite as Chin J Exp Ophthalmol, 2019,37(9): 726-729. Abstract [View PDF] [Read Full Text] Objective To reveal the pathogenic mutations in Chinese families with idiopathic congenital nystagmus(ICN) Methods Six families with ICN were recruited from Subei […]
Clinical manifestation and gene mutation of Bietti crystalline corneoretinal dystrophy
Authors:Guo Tong, Jia Ruixuan, Chen Ningning, Yang Liping DOI: 10.3760/cma.j.issn.2095-0160.2019.09.009 Published 2019-09-10 Cite as Chin J Exp Ophthalmol, 2019,37(9): 730-735. Abstract [View PDF] [Read Full Text] Objective To analyze the clinical manifestation and CYP4V2 mutations of Bietti crystalline corneoretinal dystrophy( BCD) families. Methods Total […]
Mutation screen of P4HA2 gene in Tujia high myopia patients
Authors:Yang Lin, Li Tuo, Cai Xiaojun, Ke Min, Chen Zhongshan DOI: 10.3760/cma.j.issn.2095-0160.2019.09.010 Published 2019-09-10 Cite as Chin J Exp Ophthalmol, 2019,37(9): 736-739. Abstract [View PDF] [Read Full Text] Objective To investigate the mutation of P4HA2 gene in Tujia high myopia patients. Methods Clinical data […]
Screening of pathogenic mutation in a Chinese family with congenital pulverulent cataract
Authors:Ji Kangkang, Gu Zhengyu, Wang Yaru, Bao Weili, Liao Rongfeng DOI: 10.3760/cma.j.issn.2095-0160.2019.09.011 Published 2019-09-10 Cite as Chin J Exp Ophthalmol, 2019,37(9): 740-744. Abstract [View PDF] [Read Full Text] Objective To analysis the pathogenic mutation and the clinical characteristics of a three generation family with congenital pulverulent […]
Measurement of biological parameters of nanophthalmos and its correlation with axial length
Authors:Wei Wei, Xiao Hui, Chen Liming, Luo Jingyi, Fang Lei, Lin Shufen, Liu Xing DOI: 10.3760/cma.j.issn.2095-0160.2019.09.012 Published 2019-09-10 Cite as Chin J Exp Ophthalmol, 2019,37(9): 745-749. Abstract [View PDF] [Read Full Text] Objective To quantitatively measure biological parameters of nanophthalmos and analyze the correlation between axial […]
Gene mutation spectrum analysis of retinitis pigmentosa patients in Ningxia Region of China
Authors:Rong Weining, Qi Rui, Wang Xiaoguang, Fang Xinhe, Sheng Xunlun DOI: 10.3760/cma.j.issn.2095-0160.2019.09.013 Published 2019-09-10 Cite as Chin J Exp Ophthalmol, 2019,37(9): 750-754. Abstract [View PDF] [Read Full Text] Objective To analysis the gene mutation spectrum of retinitis pigmentosa (RP) patients in Ningxia Region of China. Methods […]