Authors: Cui Li, Jiang Yanrong, Zhao Mingwei, Li Xiaoxin DOI: 10.3760/cma.j.issn.2095-0160.2016.10.014 Published 2016-10-10 Cite as Chin J Exp Ophthalmol, 2016,34(10): 926-929. Abstract [Download PDF] [Read Full Text] Background The patients who have undergone successful surgery for retinal detachment (RD) cannot recover their vision quickly, and the reason […]
Category: 2016
A pilot study on indunction and differentiation of human fibroblasts to iPS cells and iPS-RPE cells mediated by retrovirus infection
Authors: Tian Yuanyuan, Jiang Chao, Chen Xue, Ding Sijia, Xu Min, Zhao Chen DOI: 10.3760/cma.j.issn.2095-0160.2016.09.006 Published 2016-09-10 Cite as Chin J Exp Ophthalmol, 2016,34(9): 793-798. Abstract [Download PDF] [Read Full Text] Background Retinal pigment epithelium (RPE) cell transplantation is the primary means of human trial for the treatment of retinal degeneration.Induced […]
Optimization of ultrastructure observation of human embryonic stem cell-derived retinal pigment epithelial cells
Authors: Wu Wei, Qu Ya, Wang Lei, Zeng Yuxiao, Xu Haiwei, Yin Zhengqin DOI: 10.3760/cma.j.issn.2095-0160.2016.09.004 Published 2016-09-10 Cite as Chin J Exp Ophthalmol, 2016,34(9): 786-790. Abstract [Download PDF] [Read Full Text] Background Normal ultrastructure is the anatomical basis of retinal pigment epithelial(RPE)cells to perform normal physiological function.At present the precipitation method […]
Therapeutic effect and mechanism of human umbilical cord mesenchymal stem cell transplantation for Sjögren syndrome in mice
Authors: Huang Shouqiang, Fu Yanxia, Mao Kejie, Zhang Xu, Zhang Cheng, Peng Xiujun DOI: 10.3760/cma.j.issn.2095-0160.2016.09.003 Published 2016-09-10 Cite as Chin J Exp Ophthalmol, 2016,34(9): 780-785. Abstract [Download PDF] [Read Full Text] Background The incidence of dry eye is gradually increased, and researches showed that inflammation participated in the pathogenesis and development […]
In vitro effects of bone marrow-derived mesenchymal stem cells on the biological behavior of lipopolysaccharide-activated retinal microglia
Authors: Huang Libin, Xu Guoxing, Xie Maosong, Lin Wen, Cui Yi, Li Jianbing DOI: 10.3760/cma.j.issn.2095-0160.2016.09.002 Published 2016-09-10 Cite as Chin J Exp Ophthalmol, 2016,34(9): 773-779. Abstract [Download PDF] [Read Full Text] Background Retinal microglia(RMG) plays an important role in the pathogenesis of retinal degenerative diseases, while chemokine CX3CL1 participates in the […]
To promote the development and translation of eye tissue engineering study in China
Authors: Liu Zuguo, Liu Jing DOI: 10.3760/cma.j.issn.2095-0160.2016.09.001 Published 2016-09-10 Cite as Chin J Exp Ophthalmol, 2016,34(9): 769-772. Abstract [Download PDF] [Read Full Text] Eye tissue engineering is a new direction of scientific research.It applies body tissues, cells or scaffolds with specific biological activities in vitro or in […]
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, […]