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Shengping Hou

Showing results (101-110 of 147) with videos related to

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Frontiers in Immunology|February 17, 2025
Identification and validation of diagnostic genes <i>IFI44</i> and <i>IRF9</i> in insomnia-associated autoimmune uveitisChao Wu, Hui Feng, Meng Tian, et al.
Investigative Ophthalmology & Visual Science|November 21, 2019
Replication of Genome-Wide Association Analysis Identifies New Susceptibility Loci at Long Noncoding RNA Regions for Vogt-Koyanagi-Harada DiseaseJian Qi, Liping Du, Jing Deng, et al.
Investigative Ophthalmology & Visual Science|July 27, 2022
LGALS3BP in Microglia Promotes Retinal Angiogenesis Through PI3K/AKT Pathway During HypoxiaChenyang Zhao, Yusen Liu, Jiayu Meng, et al.
The British Journal of Ophthalmology|March 5, 2018
Association of genetic variations in PTPN2 and CD122 with ocular Behcet's diseaseQi Zhang, Hua Li, Shengping Hou, et al.
Human Mutation|January 8, 2019
UVEOGENE: An SNP database for investigations on genetic factors associated with uveitis and their relationship with other systemic autoimmune diseasesQingfeng Wang, Guannan Su, Xiao Tan, et al.
Science Advances|January 1, 2026
Apolipoprotein E drives microglia activation in the development of autoimmune uveitis through up-regulation of peptidyl prolyl isomerase FShuhao Zeng, Yakun Wang, Xianyang Liu, et al.
Genes & Diseases|August 21, 2025
Integrated analysis of single-cell RNA-seq and ATAC-seq in lens epithelial cells: Unveiling the role of ATF6 as a key transcription factorHuiping Lu, Xianyang Liu, Qian Zhou, et al.
Investigative Ophthalmology & Visual Science|May 23, 2023
Apigenin Alleviates Autoimmune Uveitis by Inhibiting Microglia M1 Pro-Inflammatory PolarizationNan Shu, Zhi Zhang, Xiaotang Wang, et al.
Human Mutation|December 27, 2018
A novel mutation of PANK4 causes autosomal dominant congenital posterior cataractMin Sun, Chunlin Chen, Shengping Hou, et al.
Investigative Ophthalmology & Visual Science|March 1, 2018
Association of Long Noncoding RNAs Polymorphisms With Ankylosing Spondylitis, Vogt-Koyanagi-Harada Disease, and Behcet's DiseaseYingying Yue, Jun Zhang, Lu Yang, et al.
Pageof 15

Showing results (101-110 of 147) with videos related to

Sort By:
Pageof 15
Frontiers in Immunology|February 17, 2025
Identification and validation of diagnostic genes <i>IFI44</i> and <i>IRF9</i> in insomnia-associated autoimmune uveitisChao Wu, Hui Feng, Meng Tian, et al.
Investigative Ophthalmology & Visual Science|November 21, 2019
Replication of Genome-Wide Association Analysis Identifies New Susceptibility Loci at Long Noncoding RNA Regions for Vogt-Koyanagi-Harada DiseaseJian Qi, Liping Du, Jing Deng, et al.
Investigative Ophthalmology & Visual Science|July 27, 2022
LGALS3BP in Microglia Promotes Retinal Angiogenesis Through PI3K/AKT Pathway During HypoxiaChenyang Zhao, Yusen Liu, Jiayu Meng, et al.
The British Journal of Ophthalmology|March 5, 2018
Association of genetic variations in PTPN2 and CD122 with ocular Behcet's diseaseQi Zhang, Hua Li, Shengping Hou, et al.
Human Mutation|January 8, 2019
UVEOGENE: An SNP database for investigations on genetic factors associated with uveitis and their relationship with other systemic autoimmune diseasesQingfeng Wang, Guannan Su, Xiao Tan, et al.
Science Advances|January 1, 2026
Apolipoprotein E drives microglia activation in the development of autoimmune uveitis through up-regulation of peptidyl prolyl isomerase FShuhao Zeng, Yakun Wang, Xianyang Liu, et al.
Genes & Diseases|August 21, 2025
Integrated analysis of single-cell RNA-seq and ATAC-seq in lens epithelial cells: Unveiling the role of ATF6 as a key transcription factorHuiping Lu, Xianyang Liu, Qian Zhou, et al.
Investigative Ophthalmology & Visual Science|May 23, 2023
Apigenin Alleviates Autoimmune Uveitis by Inhibiting Microglia M1 Pro-Inflammatory PolarizationNan Shu, Zhi Zhang, Xiaotang Wang, et al.
Human Mutation|December 27, 2018
A novel mutation of PANK4 causes autosomal dominant congenital posterior cataractMin Sun, Chunlin Chen, Shengping Hou, et al.
Investigative Ophthalmology & Visual Science|March 1, 2018
Association of Long Noncoding RNAs Polymorphisms With Ankylosing Spondylitis, Vogt-Koyanagi-Harada Disease, and Behcet's DiseaseYingying Yue, Jun Zhang, Lu Yang, et al.
Pageof 15