Authors: Cong Lin, Xia Yiping, Dong Yanling, Cheng Jun DOI: 10.3760/cma.j.cn115989-20210107-00015 Published 2022-10-10 Cite asChin J Exp Ophthalmol, 2022, 40(10): 926-928. [View PDF] [Read Full Text] Contributor Information Cong Lin Qingdao Eye Hospital of Shandong First Medical University, State Key Laboratory Cultivation Base, Shandong Provincial Key Laboratory of Ophthalmology, Eye […]
Category: 2022, No. 10
Expert consensus on surgical technique for subretinal injection of gene therapy in China (2022)
Author: Fundus Disease Group of Chinese Medical Association Ophthalmology Branch, Fundus Disease Committee of Chinese Medical Doctor Association Ophthalmology Branch DOI: 10.3760/cma.j.cn115989-20220808-00366 Published 2022-10-10 Cite asChin J Exp Ophthalmol, 2022, 40(10): 887-893. Abstract [View PDF] [Read Full […]
Establishment of lens opacity model in Grx2 knockout mice based on CRISPR/cas9 system and the role of Grx2 in the pathogenesis of cataract
·Experimental Research· Establishment of a lens opacity model in Grx2 knockout mice based on the CRISPR/cas9 system and the role of Grx2 in cataract pathogenesis Guo Yong1, Guo Chenjun2, Zhang Jie2, Ning Xiaona2, Chen Xi3, Yan Hong1 1Department of Ophthalmology, Xi’an People’s Hospital, Xi’an Fourth Hospital, Shaanxi Eye Hospital, Xi’an 710004, China; 2Department of Ophthalmology, […]
Classification of adenoviral conjunctivitis based on sequencing and phylogenetic analysis of hexon and fiber
Authors: Wang Jing, Zhu Jianfeng, Lu Lina DOI: 10.3760/cma.j.cn115989-20200430-00300 Published 2022-10-10 Cite asChin J Exp Ophthalmol, 2022, 40(10): 902-907. Abstract [View PDF] [Read Full Text] Objective To classify human adenovirus (HAdV) of adenoviral conjunctivitis by sequencing and […]
Association between visual function and optic fiber layer thickness after gene therapy for Leber hereditary optic neuropathy
·Clinical Research· Association between visual function and optic fiber layer thickness after gene therapy for Leber hereditary optic neuropathy Yuan Jiajia1, Zhang Yong2, Chen Changzheng1, Yang Xueying1, Miao Qingmei1, Kai Yoon Fan3, Li Bin2,3 1Department of Ophthalmology, People’s Hospital of Wuhan University, Wuhan 430065, China; 2Department of Ophthalmology, Taihe Hospital, Hubei University of Medicine, Hubei, […]
Clinical and molecular genetics research of a Chinese Han family with Wagner syndrome
Authors: Cai Suping, Zhang Daren, Luo Xiaoling, Huang Longxiang, Wang Tingting, Xu Tingting, Liu Xuyang DOI: 10.3760/cma.j.cn115989-20210318-00184 Published 2022-10-10 Cite asChin J Exp Ophthalmol, 2022, 40(10): 914-919. Abstract [View PDF] [Read Full Text] Objective To explore the […]
Genotypes and clinical phenotypes of Hermansky-Pudlak syndrome
·Clinical Research· Genotypes and ocular and systemic clinical phenotypes of the Hermansky-Pudlak syndrome Yang Shangying1, Cheng Wanyu1, Zhang Yan2, Sheng Xunlun1,3 1Ningxia Eye Hospital, People’s Hospital of Ningxia Hui Autonomous Region, Yinchuan 750001, China; 2Electron Microscope Room, Science and Technology Center, Ningxia Medical University, Yinchuan 750001, China; 3Gansu Aier Optometry Hospital, Lanzhou 730000, China Corresponding […]
Screening of pathogenic mutation in a family with Axenfeld-Rieger syndrome by whole exome sequencing
·Clinical research· Pathogenic mutation screening in a family with Axenfeld-Rieger Syndrome by whole exome sequencing Wang Qi, Liu Xinna, Shao Zhengbo, Yuan Huiping Department of Ophthalmology, the Second Affiliated Hospital of Harbin Medical Universiiy, The Key Laboratory of Myocardial Ischemia, Harbin Medical University, Ministry Educatton, Future Medical Laboratory, the Second Affiilated Hospital of Harbin Medical […]
Identification of a COL2A1 mutation in a Chinese family with Stickler syndrome type 1 via whole exome sequencing
·Clinical Research· Identification of a COL2A1 mutation in a Chinese family with Stickler syndrome type 1 via whole exome sequencing Deng Fang, Cao Yingjie, Xie Lijing, Chen Shaowan, Xiao Xiaoqiang, Zhang Mingzhi Joint Shantou International Eye Center of Shantou University & The Chinese University of Hong Kong, Shantou 515041, China Corresponding author: Xiao Xiaoqiang, Email: […]
Clinical and genetic characteristics of a Han Chinese family with autosomal recessive enhanced S-cone syndrome
•Clinical Research• Clinical and genetic characteristics of a Han Chinese family with autosomal recessive enhanced S-cone syndrome Jiang Yongqiang, Chen Kang, Li Jie, Guo Haoyi Department of Ophthalmology, Henan Provincial People’s Hospital, Henan Eye Hospital, Henan Eye Institute, Zhengzhou 450003, China Corresponding […]