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 […]
Category: Highlights
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 […]
Diagnosis and treatment of corneal ulcer perforation in a patient with alkali burn caused by Achromobacter xylosoxidans: a case report
Authors: Liu Yan, Xiao Gege, Peng Rongmei, Hong Jing DOI: 10.3760/cma.j.cn115989-20201218-00850 Published： 2024 -10 -10 · Citation: Liu Yan, Xiao Gege, Peng Rongmei,et al. Diagnosis and treatment of corneal ulcer perforation in a patient with alkali burn caused by Achromobacter xylosoxidans: a case report[J]. Chin J Exp Ophthalmol, 2024, 42(10):925-926. DOI: 10.3760/cma.j.cn115989-20201218-00850. [Download PDF] [Read Full Text] Authors Info & […]
Research progress on pathogenic gene and molecular mechanism of congenital cranial dysinnervation disorders
Authors: Zhao Andi, Liu Hu DOI: 10.3760/cma.j.cn115989-20210508-00298 Published： 2024 -10 -10 Citation: Zhao Andi, Liu Hu. Research progress on pathogenic gene and molecular mechanism of congenital cranial dysinnervation disorders[J].Chin J Exp Ophthalmol, 2024, 42(10):938-944. DOI: 10.3760/cma.j.cn115989-20210508-00298. ABSTRACT […]
Genetic etiology and clinical strategies of congenital anophthalmia and microphthalmia
Authors: Liao Keren, Shen Yin DOI:10.3760/cma.j.cn115989-20220212-00053 Published: 2024 -10 -10 Citation: Liao Keren, Shen Yin. Genetic etiology and clinical strategies of congenital anophthalmia and microphthalmia[J]. Chin J Exp Ophthalmol, 2024, 42(10):945-951. DOI: 10.3760/cma.j.cn115989-20220212-00053. ABSTRACT […]
Advances in genetic research on complications of pathological myopia
Authors: Lu Qiang, Zhu Xiangjia, Lu Yi DOI:10.3760/cma.j.cn115989-20210429C-00288 Published： 2024 -10 -10 · Citation: Lu Qiang, Zhu Xiangjia, Lu Yi. Advances in genetic research on complications of pathological myopia[J]. Chin J Exp Ophthalmol,2024,42(10): 952-957. DOI: 10.3760/cma.j.cn115989-20210429-00288. ABSTRACT […]