Authors: Liu Xiaochen, Wu Min DOI: 10.3760/cma.j.issn.2095-0160.2017.08.021 Published 2017-08-10 Cite as Chin J Exp Ophthalmol, 2017,35(8): 764-768. Abstract [Download PDF] [Read Full Text] MicroRNAs (miRNAs) are small, stable RNA molecules that post-transcriptionally regulate gene expression in plants and animals by base pairing to partially complementary sequences on […]
Category: 2017, No. 08
Research progress of miR-204 in the regulation of ophthalmic diseases
Authors: Xu Yanying, Mao Xinbang DOI: 10.3760/cma.j.issn.2095-0160.2017.08.020 Published 2017-08-10 Cite as Chin J Exp Ophthalmol, 2017,35(8): 761-763. Abstract [Download PDF] [Read Full Text] MicroRNAs (miRNAs) are endogenous short nucleotide non-coding RNAs which widely exist in eukaryotic organisms, involved in the body’s life process, including cell growth, differentiation, […]
Gene research progress of retinoblastoma
Authors: Yu Tian, Chen Changzheng, Xing Yiqiao DOI: 10.3760/cma.j.issn.2095-0160.2017.08.019 Published 2017-08-10 Cite as Chin J Exp Ophthalmol, 2017,35(8): 756-760. Abstract [Download PDF] [Read Full Text] Retinoblastoma (RB) is a common intraocular malignant tumor of infants.It not only seriously threats children’s eyesight, but also endangers their lives.RB develops from […]
Update on mutations of precursor mRNA splicing factor genes linked to retinitis pigmentosa
Authors: Xia Weiyi, Zhao Chen DOI: 10.3760/cma.j.issn.2095-0160.2017.08.018 Published 2017-08-10 Cite as Chin J Exp Ophthalmol, 2017,35(8): 752-755. Abstract [Download PDF] [Read Full Text] Retinitis pigmentosa (RP), one of the common forms of hereditary retinal dystrophies (HRD), is typified by significant genetic heterogeneities.Executed by the spliceosome, precursor mRNA […]
Research progress of DNA methylation in lens development and cataract
Authors: Wang Yong, Guan Huaijin DOI: 10.3760/cma.j.issn.2095-0160.2017.08.017 Published 2017-08-10 Cite as Chin J Exp Ophthalmol, 2017,35(8): 747-751. Abstract [Download PDF] [Read Full Text] Epigenetics is the study of genomic structural modifications that affects gene expression without DNA sequence change.Epigenetic mechanisms for the regulation of gene expression include […]
Survey of medical resources of eye care in Tibet autonomous region
Authors: Dan Zengrenqing, Li Xiaoxin, Tsedenyangkyi null DOI: 10.3760/cma.j.issn.2095-0160.2017.08.016 Published 2017-08-10 Cite as Chin J Exp Ophthalmol, 2017,35(8): 743-746. Abstract [Download PDF] [Read Full Text] Background The improvement of the eye care system has being a strong guarantee for blindness prevention.However, medical resources of eye care in Tibet autonomous […]
Associations of single nucleotide polymorphisms of UCP genes with diabetic retinopathy in Chinese Han population
Authors: Jin Peiyao, Li Zhiqiang, Xu Xian, He Jiangnan, Chen Jianhua, Xu Xun, Du Xuan, Bai Xuelin, Zhang Bo, He Xiangui, Lu Lina, Zhu Jianfeng, Shi Yongyong, Zou Haidong DOI: 10.3760/cma.j.issn.2095-0160.2017.08.015 Published 2017-08-10 Cite as Chin J Exp Ophthalmol, 2017,35(8): 737-742. Abstract [Download PDF] [Read Full Text] Background Researches showed that elevatory blood glucose level results in long-term damage […]
Affecting factors of corneal epithelial healing following de-epithelized corneal collagen cross linking in keratoconus patients
Authors: Huang Xiaojing, Shi Peiyan, Jiang Yin, Zhao Can, Sun Jijun, Wang Ting DOI: 10.3760/cma.j.issn.2095-0160.2017.08.014 Published 2017-08-10 Cite as Chin J Exp Ophthalmol, 2017,35(8): 732-736. Abstract [Download PDF] [Read Full Text] Background Corneal collagen cross-linking (CXL) shows good clinical effects for keratoconus, and de-epithelized CXL appears to be benefit to the […]
Clinical characteristic and management of Peters anomaly
Authors: Liang Tianwei, Zhang Chengyue, Zhang Yan, Li Cheng, Li Li, Wu Qian, Zhao Junyang DOI: 10.3760/cma.j.issn.2095-0160.2017.08.013 Published 2017-08-10 Cite as Chin J Exp Ophthalmol, 2017,35(8): 727-731. Abstract [Download PDF] [Read Full Text] Background Peters anomaly is a rare eye disease.Understanding the clinical features of Peters anomaly is helpful for us to […]
Genetic analysis of a Chinese family with congenital aniridia and detection of PAX6 mutation locus
Authors: Zhang Luxi, Yang Ge, Jia Jing, Wan Wencui, Yang Xin, Jin Xuemin DOI: 10.3760/cma.j.issn.2095-0160.2017.08.011 Published 2017-08-10 Cite as Chin J Exp Ophthalmol, 2017,35(8): 721-725. Abstract [Download PDF] [Read Full Text] Background Congenital aniridia is a rare bilateral hereditary ophthalmopathy which impact panocular.Researches showed that congenital aniridia can be caused by […]