Category: Highlights

Interaction mechanism between gut-retina axis and eye diseases

Authors: Huang Yinhua, Chen Jiansu, Tang Shibo DOI: 10.3760/cma.j.cn115989-20210201-00083 Published: 2024-11-10 Citation Huang Yinhua, Chen Jiansu, Tang Shibo. Interaction mechanism between gut-retina axis and eye diseases[J]. Chin J Exp Ophthalmol, 2024, 42(11):1053-1059. DOI: 10.3760/cma.j.cn115989-20210201-00083. ABSTRACT                     [Download PDF] [Read Full Text]  Gut microbiome is an important part of […]

Role of intercellular communication involving microglia in retinal neurovascular unit

Authors: Lei Linyi, Cao Yuan, Yao Jin DOI: 10.3760/cma.j.cn115989-20230627-00025 Published: 2024-11-10 Citation Lei Linyi, Cao Yuan, Yao Jin. Role of intercellular communication involving microglia in retinal neurovascular unit[J]. Chin J Exp Ophthalmol, 2024, 42(11):1060-1064. DOI: 10.3760/cma.j.cn115989-20230627-00025 . ABSTRACT                                [Download PDF] [Read […]

Influencing factors and research progress in the mouse model of myopia

Authors: Liu Susu, Shi Menghai, Zhang Hongmin DOI: 10.3760/cma.j.cn115989-20240108-00011 Published:  2024 -11 -10 Citation Liu Susu, Shi Menghai, Zhang Hongmin. Influencing factors and research progress in the mouse model of myopia[J]. Chin J Exp Ophthalmol, 2024, 42(11):1065-1072. DOI: 10.3760/cma.j.cn115989-20240108-00011. ABSTRACT                                    […]

Expert recommendation on the management of perioperative hyphema and intraocular pressure spike following goniotomy

Authors: Zhang Xiulan, Pan Xiaojing, Ke Min, Tang Li, Xie Lin, Tao Liming, Fan Sujie, Tang Guangxian, Duan Xuanchu, Yuan Huiping, Glaucoma Society of Ophthalmology, Guangdong Medical Association DOI: 10.3760/cma.j.cn115989-20240602-00141 Published: 2024 -10 -10 · Citation: Zhang Xiulan, Pan Xiaojing, Ke Min, et al. Expert recommendation on the management of perioperative hyphema and intraocular pressure spike following goniotomy[J]. Chin J […]

Identification of key genes involved in the inhibition of inflammation by overexpression of PEDF adenovirus in THP1 cells

Authors: Zhang Yuanyuan, Wu Honglian, Xu Manhong, Li Xiaorong, Shao Yan DOI: 10.3760/cma.j.cn115989-20230607-00219 Published: 2024 -10 -10 · Citation: Zhang Yuanyuan, Wu Honglian, Xu Manhong, et al. Identification of key genes involved in the inhibition of inflammation by overexpression of PEDF adenovirus in THP1 cells[J]. Chin J Exp Ophthalmol, 2024, 42(10): 887-897. DOI: 10.3760/cma.j.cn115989-20230607-00219. ABSTRACT            […]

Effect and mechanism of VSIG4 gene mutation on the function of microglia in retinitis pigmentosa

Authors: Xu Chunlong, Zhang Guowei, Du Jun, Jia Zhen, Wang Jingping, Wang Ziwen, Li Yang Lu Hong DOI: 10.3760/cma.j.cn115989-20240304-00063 Published: 2024 -10 -10 Citation: Xu Chunlong, Zhang Guowei, Du Jun, et al. Effect and mechanism of VSIG4 gene mutation on the function of microglia in retinitis pigmentosa[J]. Chin J Exp Ophthalmol, 2024, 42(10): 898-908. DOI: 10.3760/cma.j.cn115989-20240304-00063. ABSTRACT      […]

Genetic characteristics of 51 retinitis pigmentosa families

Authors: Zhou Lingling, Zhou Menghan, Shen Yin DOI: 10.3760/cma.j.cn115989-20230221-00058 Published: 2024 -10 -10 Citation: Zhou Lingling, Zhou Menghan, Shen Yin. Genetic characteristics of 51 retinitis pigmentosa families[J]. Chin J Exp Ophthalmol, 2024, 42(10):909-918. DOI: 10.3760/cma.j.cn115989-20230221-00058. ABSTRACT                                        […]

Genetic analysis of a family with posterior segment microphthalmia-retinoschisis and drusen syndrome

Authors: Xie Ting, Chen Qingshan, Liang Jia, Fang Dong, Chen Lu, Zhang Shaochong DOI: 10.3760/cma.j.cn115989-20230626-00023 Published: 2024 -10 -10 Citation: Xie Ting, Chen Qingshan, Liang Jia, et al. Genetic analysis of a family with posterior segment microphthalmia-retinoschisis and drusen syndrome[J]. Chin J Exp Ophthalmol, 2024, 42(10): 919-925. DOI:  10.3760/cma.j.cn115989-20230626-00023. ABSTRACT                    […]

Clinical phenotype and genotype analysis of a Chinese family with congenital aniridia caused by a novel frameshift and nonsense variant in PAX6

Authors: Wang Dongdong, Du Jiao, Huang Zixu, Dan Handong, Lin Zuopeng, Song Zongming DOI: 10.3760/cma.j.cn115989-20240613-00151 Published: 2024 -10 -10 · Citation: Wang Dongdong, Du Jiao, Huang Zixu,et al. Clinical phenotype and genotype analysis of a Chinese family with congenital aniridia caused by a novel frameshift and nonsense variant in PAX6[J]. Chin J Exp Ophthalmol, 2024, 42(10): 927-931. DOI: 10.3760/cma.j.cn115989-20240613-00151. ABSTRACT  […]

Clinical phenotype and genotype analysis of a family with autosomal dominant optic atrophy caused by a novel nonsense variant in OPA1

Authors: Wang Lihong, Wang Zhili, Chen Xiao, Wei Jia, Chen Kang, Cui Longjiang DOI: 10.3760/cma.j.cn115989-20231227-00224 Published: 2024 -10 -10 · Citation: Wang Lihong, Wang Zhili, Chen Xiao,et al. Clinical phenotype and genotype analysis of a family with autosomal dominant optic atrophy caused by a novel nonsense variant in OPA1[J]. Chin J Exp Ophthalmol, 2024, 42(10):932-937. DOI: 10.3760/cma.j.cn115989-20231227-00224. ABSTRACT      […]