Authors: Liu Aihua, Gao Meizi, Huang Liangyu, Liu Xun, Su Ruihong, Zhao Jinzhi, Wang Liming, Zhang Xiaomin, Li Xiaorong, Dong Lijie DOI: 10.3760/cma.j.issn.2095-0160.2019.06.002 Published 2019-06-10 Cite as Chin J Exp Ophthalmol, 2019,37(6): 405-410. Abstract [View PDF] [Read Full Text] Objective To explore the role of forkhead box F2 (FoxF2) in the extracellular matrix of trabecular […]
Month: September 2019
Opportunities and challenges for glaucoma research
Author: Zhang Xiulan DOI: 10.3760/cma.j.issn.2095-0160.2019.06.001 Published 2019-06-10 Cite as Chin J Exp Ophthalmol, 2019,37(6): 401-404. Abstract [View PDF] [Read Full Text] Elevation of intraocular pressure (IOP) is the most eminent risk factor for the presence and progression of glaucoma, which leads to optic nerve damages ultimately.With […]
Analysis of GJA3 mutation associated with a Chinese family with autosomal dominant congenital cataract by whole-exome sequencing
Authors：Liu Yuying, Wan Wencui, Yang Ge, Pang Xuena, Yang Guoguo, Jin Xuemin DOI: 10.3760/cma.j.issn.2095-0160.2016.10.011 Published 2016-10-10 Cite as Chin J Exp Ophthalmol, 2016,34(10): 916-919. Abstract [Download PDF] [Read Full Text] Congenital cataract is one of the important reasons for the blindness of children, and most congenital […]
Association of Gly82Ser polymorphism of RAGE gene with diabetic retinopathy in Han people with type 2 diabetes of Wuxi region
Authors：Cao Jia, Yao Yong, Xie Tianhua, Gu Zheyao, Zou Jian DOI: 10.3760/cma.j.issn.2095-0160.2016.10.009 Published 2016-10-10 Cite as Chin J Exp Ophthalmol, 2016,34(10): 910-914. Abstract [Download PDF] [Read Full Text] Background Receptor for advanced glycation end products (RAGE) play an important role in the process of type 2 diabetes […]
Screening of TYR gene mutations and clinical classification in oculocutaneous albinism patients
Authors：Wang Liming, Han Ruifang, Ying Ming, Hao Peng, Li Ningdong DOI: 10.3760/cma.j.issn.2095-0160.2016.10.008 Published 2016-10-10 Cite as Chin J Exp Ophthalmol, 2016,34(10): 905-909. Abstract [Download PDF] [Read Full Text] Background Oculocutaneous albinism (OCA) is a hereditary disease of pigment absence in eyes, skin […]
Mutation analysis of Pax6 in Chinese patients with congenital aniridia
Authors：Hao Peng, Ying Ming, Han Ruifang, Wang Liming, Li Ningdong DOI: 10.3760/cma.j.issn.2095-0160.2016.10.007 Published 2016-10-10 Cite as Chin J Exp Ophthalmol, 2016,34(10): 900-904. Abstract [Download PDF] [Read Full Text] Background Congenital aniridia is a rare congenital autosomal dominant disease, which is shown as aniridia of double eyes, […]
Identification of genetic mutation in a Chinese pedigree with congenital cataract by whole-exome sequencing
Authors：Bu Juan, Liu Jing, Pang Honglei, Liu Feng, Wang Lejin DOI: 10.3760/cma.j.issn.2095-0160.2016.10.006 Published 2016-10-10 Cite as Chin J Exp Ophthalmol, 2016,34(10): 896-899. Abstract [Download PDF] [Read Full Text] Background Genetic mutation remains to be the most common cause of congenital cataract.Whole exon sequencing technology is an ideal […]
The efficiency and safety assessment of Entranster™ nanoparticle carrier for CD25 siRNA transfection in rat cornea
Authors：Qin Qin, Shi Yunjie, Zhao Min DOI: 10.3760/cma.j.issn.2095-0160.2016.10.005 Published 2016-10-10 Cite as Chin J Exp Ophthalmol, 2016,34(10): 888-895. Abstract [Download PDF] [Read Full Text] Background Gene transfection is an effective therapeutic avenue to target many kinds of eye diseases.Non-viral vectors with high transfection efficiency, long-term expression, […]
Identification of pathgenic bacteria in aqueous and vitreous of endophthalmitis by 16S rDNA sequencing technique
Authors: Yang Baoxia, Li Hong, Kong Fanfang, Huang Yusen DOI: 10.3760/cma.j.issn.2095-0160.2016.10.004 Published 2016-10-10 Cite as Chin J Exp Ophthalmol, 2016,34(10): 883-887. Abstract [Download PDF] [Read Full Text] Background Endophthalmitis is a serious complication of intraocular surgery.Conventional identification methods for bacteria are becterial culture and smear method, […]
Detection and analysis of differential gene expression between benign lymphoepithelial lesion of lacrimal gland and orbital cavernous hemangioma
Authors：Li Jing, Ge Xin, Ma Jianmin, Wang Xiaona, Liu Xiao DOI: 10.3760/cma.j.issn.2095-0160.2016.10.003 Published 2016-10-10 Cite as Chin J Exp Ophthalmol, 2016,34(10): 878-882. Abstract [Download PDF] [Read Full Text] Background Benign lymphoepithelial lesion of lacrimal gland is not a common orbital disease in clinic, which mainly presented as […]