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Molecular Vision
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October 10, 2009
Lack of association of two polymorphisms of IRF5 with Behcet's disease
Haijun Li, Peizeng Yang, Zhengxuan Jiang, et al.
Investigative Ophthalmology & Visual Science
|
December 30, 2011
JAK2 and STAT3 polymorphisms in a Han Chinese population with Behçet's disease
Ke Hu, Shengping Hou, Zhengxuan Jiang, et al.
Human Immunology
|
February 2, 2010
Polymorphisms of IL23R and Vogt-Koyanagi-Harada syndrome in a Chinese Han population
Zhengxuan Jiang, Peizeng Yang, Shengping Hou, et al.
Experimental Eye Research
|
November 1, 2019
Uveitis genetics
Shengping Hou, Na Li, Xingyun Liao, et al.
Frontiers in Cellular Neuroscience
|
January 3, 2022
Low Expression of YTH Domain-Containing 1 Promotes Microglial M1 Polarization by Reducing the Stability of Sirtuin 1 mRNA
Hongxiu Zhou, Zongren Xu, Xingyun Liao, et al.
Human Immunology
|
April 26, 2011
Behçet's disease exhibits an increased osteopontin serum level in active stage but no association with osteopontin and its receptor gene polymorphisms
Mingliang Chu, Peizeng Yang, Shengping Hou, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
November 10, 2010
Upregulation of interleukin 21 and promotion of interleukin 17 production in chronic or recurrent Vogt-Koyanagi-Harada disease
Fuzhen Li, Peizeng Yang, Xiaoli Liu, et al.
Investigative Ophthalmology & Visual Science
|
April 16, 2016
Association of T-Bet, GATA-3, RORC, and FOXP3 Copy Number Variations With Acute Anterior Uveitis With or Without Ankylosing Spondylitis in Chinese Han
Lin Bai, Yunjia Liu, Shengping Hou, et al.
Scientific Reports
|
August 14, 2015
Copy number variations and gene polymorphisms of complement components in ocular Behcet's disease and Vogt-Koyanagi-Harada syndrome
Dengfeng Xu, Shengping Hou, Jun Zhang, et al.
Molecular Vision
|
January 8, 2020
<i>PRKCQ</i> rs4750316 is associated with Vogt-Koyanagi-Harada syndrome in a Han Chinese population
Lei Xu, Tingting Zhao, Gangxiang Yuan, et al.
Page
of 15
Search research articles
Search
Showing results (11-20 of 147) with videos related to
Sort By:
Page
of 15
Molecular Vision
|
October 10, 2009
Lack of association of two polymorphisms of IRF5 with Behcet's disease
Haijun Li, Peizeng Yang, Zhengxuan Jiang, et al.
Investigative Ophthalmology & Visual Science
|
December 30, 2011
JAK2 and STAT3 polymorphisms in a Han Chinese population with Behçet's disease
Ke Hu, Shengping Hou, Zhengxuan Jiang, et al.
Human Immunology
|
February 2, 2010
Polymorphisms of IL23R and Vogt-Koyanagi-Harada syndrome in a Chinese Han population
Zhengxuan Jiang, Peizeng Yang, Shengping Hou, et al.
Experimental Eye Research
|
November 1, 2019
Uveitis genetics
Shengping Hou, Na Li, Xingyun Liao, et al.
Frontiers in Cellular Neuroscience
|
January 3, 2022
Low Expression of YTH Domain-Containing 1 Promotes Microglial M1 Polarization by Reducing the Stability of Sirtuin 1 mRNA
Hongxiu Zhou, Zongren Xu, Xingyun Liao, et al.
Human Immunology
|
April 26, 2011
Behçet's disease exhibits an increased osteopontin serum level in active stage but no association with osteopontin and its receptor gene polymorphisms
Mingliang Chu, Peizeng Yang, Shengping Hou, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
November 10, 2010
Upregulation of interleukin 21 and promotion of interleukin 17 production in chronic or recurrent Vogt-Koyanagi-Harada disease
Fuzhen Li, Peizeng Yang, Xiaoli Liu, et al.
Investigative Ophthalmology & Visual Science
|
April 16, 2016
Association of T-Bet, GATA-3, RORC, and FOXP3 Copy Number Variations With Acute Anterior Uveitis With or Without Ankylosing Spondylitis in Chinese Han
Lin Bai, Yunjia Liu, Shengping Hou, et al.
Scientific Reports
|
August 14, 2015
Copy number variations and gene polymorphisms of complement components in ocular Behcet's disease and Vogt-Koyanagi-Harada syndrome
Dengfeng Xu, Shengping Hou, Jun Zhang, et al.
Molecular Vision
|
January 8, 2020
<i>PRKCQ</i> rs4750316 is associated with Vogt-Koyanagi-Harada syndrome in a Han Chinese population
Lei Xu, Tingting Zhao, Gangxiang Yuan, et al.
Page
of 15