Authors: Hu Shanshan, Qi Yanhua DOI: 10.3760/cma.j.issn.2095-0160.2015.06.019 Published 2015-06-10 Cite as Chin J Exp Ophthalmol, 2015,33(6): 568-572. Abstract [Download PDF] [Read Full Text] Congenital cataract is one of the leading causes of children vision impairment and blindness.Among the many causative factors, inheritance […]
Category: Review
Cyclic nucleotide-gated channels and retinal cone photoreceptor cells function
Authors: Xu Jianhua, Zhang Zhaofeng, Du Jing DOI: 10.3760/cma.j.issn.2095-0160.2015.06.020 Published 2015-06-10 Cite as Chin J Exp Ophthalmol, 2015,33(6): 573-576. Abstract [Download PDF] [Read Full Text] Cyclic nucleotide-gated (CNG) channels are ion channels which are activated by the binding of cyclic guanosine monophosphate […]
Signal pathways related to retinopathy of prematurity
Authors: Zhang Tongmei, Han Mei DOI: 10.3760/cma.j.issn.2095-0160.2015.07.021 Published 2015-07-10 Cite as Chin J Exp Ophthalmol, 2015,33(7): 664-668. Abstract [Download PDF] [Read Full Text] Retinopathy of prematurity (ROP) is a kind of vasoproliferative disorders, which leads to vision loss even blindness in premature […]
Current research of acute zonal occult outer retinopathy
Authors: Yin Lu, Ma Xiang DOI: 10.3760/cma.j.issn.2095-0160.2015.07.022 Published 2015-07-10 Cite as Chin J Exp Ophthalmol, 2015,33(7): 669-672. Abstract [Download PDF] [Read Full Text] Acute zonal occult outer retinopathy (AZOOR) is a relatively rare ocular disease that is characterized by the rapid loss […]
Regulation roles of COUP transcription factors in the development of embryonic eye
Authors: Du Yaru, Yu Jing DOI: 10.3760/cma.j.issn.2095-0160.2015.08.017 Published 2015-08-10 Cite as Chin J Exp Ophthalmol, 2015,33(8): 751-754. Abstract [Download PDF] [Read Full Text] Chicken ovalbumin upstream promoter-transcription factors (COUP-TFs) are the orphan receptors of the steroid/thyroid hormone receptor superfamily. These factors include COUP-TFⅠ […]
Research progress of Leber hereditary optic neuropathy
Authors: Zhang Yangyang, Pang Jijing DOI: 10.3760/cma.j.issn.2095-0160.2015.08.018 Published 2015-08-10 Cite as Chin J Exp Ophthalmol, 2015,33(8): 755-759. Abstract [Download PDF] [Read Full Text] Leber hereditary optic neuropathy (LHON) is one of the most common maternally transmitted hereditary retinal diseases, which is […]
Advances in molecular genetics of exfoliation syndrome
Authors: Yin Yan, Fan Ning, Liu Xuyang DOI: 10.3760/cma.j.issn.2095-0160.2015.08.019 Published 2015-08-10 Cite as Chin J Exp Ophthalmol, 2015,33(8): 760-763. Abstract [Download PDF] [Read Full Text] Exfoliation syndrome (XFS), one of the most common causes of glaucoma, represents an age related, complex, multifactorial and […]
Advances in genetic study of achromatopsia
Authors: Liang Xiaofang, Sui Ruifang, Dong Fangtian DOI: 10.3760/cma.j.issn.2095-0160.2015.08.020 Published 2015-08-10 Cite as Chin J Exp Ophthalmol, 2015,33(8): 764-767. Abstract [Download PDF] [Read Full Text] Achromatopsia is a kind of autosomal recessive cone disorder. It occurs with nystagmus, photophobia, inability of color […]
Research progress in conjunctival epithelial stem cells
Authors: Yao Qinke, Fu Yao DOI: 10.3760/cma.j.issn.2095-0160.2015.09.016 Published 2015-09-10 Cite as Chin J Exp Ophthalmol, 2015,33(9): 840-843. Abstract [Download PDF] [Read Full Text] Conjunctival epithelial stem cells are the common progenitor cells of both conjunctival epithelial cells and goblet cells, having the […]
Advances in differentiation of human embryonic stem cells into corneal endothelial cells under the mimical microenvironment
Authors: Sun Lin, Wu Xinyi DOI: 10.3760/cma.j.issn.2095-0160.2015.09.017 Published 2015-09-10 Cite as Chin J Exp Ophthalmol, 2015,33(9): 844-847. Abstract [Download PDF] [Read Full Text] The lack of donor corneal endothelium is a serious impediment to the development of corneal endothelial transplantation, whereas the […]