HuGE Literature Finder
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Records 1-14
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Association of genetic variations in PTPN2 and CD122 with ocular Behcet's disease.
The British journal of ophthalmology 2018 Mar . Zhang Qi, Li Hua, Hou Shengping, Yu Hongsong, Su Guannan, Deng Bolin, Qi Jian, Zhou Chunjiang, Kijlstra Aize, Yang Peize |
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Interleukin-17A gene polymorphism with the susceptibility of intestinal symptoms in patients with Behçet's disease.
The Journal of dermatology 2016 Jan . Nakamura Koichiro, Miyano Kyohei, Tsuchida Tetsuya, Meguro Akira, Mizuki Nobuhi |
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Complement C5 Gene Confers Risk for Acute Anterior Uveitis.
Investigative ophthalmology & visual science 2015 Jul 56 (8): 4954-60. Xu Dengfeng, Hou Shengping, Jiang Yanni, Zhang Jun, Cao Shuang, Zhang Dike, Luo Le, Kijlstra Aize, Yang Peize |
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Specific association of IL17A genetic variants with panuveitis.
The British journal of ophthalmology 2015 Apr 99 (4): 566-70. Mucientes Arkaitz, Márquez Ana, Cordero-Coma Miguel, Martín-Villa José Manuel, Gorroño-Echebarría Marina Begoña, Blanco Ricardo, Díaz Valle David, Benítez-del-Castillo José Manuel, del Rio María José, Blanco Ana, Olea Jose Luis, Cordero Yolanda, Capella María José, Gonzalez Jacobo, Díaz-Llopis Manuel, Ortego-Centeno Norberto, Adán Alfredo, Ruiz-Arruza Ioana, Llorenç Víctor, Fonollosa Alejandro, Martín Javi |
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Genetic variations of IL17F and IL23A show associations with Behçet's disease and Vogt-Koyanagi-Harada syndrome.
Ophthalmology 2015 Mar 122 (3): 518-23. Hou Shengping, Liao Dan, Zhang Jun, Fang Jing, Chen Lu, Qi Jian, Zhang Qi, Liu Yunjia, Bai Lin, Zhou Yan, Kijlstra Aize, Yang Peize |
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Copy number variations and gene polymorphisms of Complement components in ocular Behcet's disease and Vogt-Koyanagi-Harada syndrome.
Scientific reports 2015 5 12989. Xu Dengfeng, Hou Shengping, Zhang Jun, Jiang Yanni, Kijlstra Aize, Yang Peize |
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Interleukin-23 Receptor Gene Polymorphism May Enhance Expression of the IL-23 Receptor, IL-17, TNF-? and IL-6 in Behcet's Disease.
PloS one 2015 10 (7): e0134632. Jiang Zhengxuan, Hennein Lauren, Tao Yulin, Tao Limi |
Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study.
Arthritis and rheumatism 2012 Dec 64 (12): 4104-13. Hou Shengping, Yang Zhenglin, Du Liping, Jiang Zhengxuan, Shu Qinmeng, Chen Yuanyuan, Li Fuzhen, Zhou Qingyun, Ohno Shigeaki, Chen Rui, Kijlstra Aize, Rosenbaum James T, Yang Peize |
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The genetics of Behçet's disease in a Chinese population.
Frontiers of medicine 2012 Nov . Hou S, Kijlstra A, Yang P |
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Interactions between IL17A, IL23R, and STAT4 polymorphisms confer susceptibility to intestinal Behcet's disease in Korean population.
Life sciences 2012 May 90 (19-20): 740-6. Kim Eun Soo, Kim Seung Won, Moon Chang Mo, Park Jae Jun, Kim Tae Il, Kim Won Ho, Cheon Jae H |
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CFH 184G as a genetic risk marker for anterior uveitis in Chinese females.
Molecular vision 2011 17 2655-64. Yang Ming-ming, Lai Timothy Y Y, Tam Pancy O S, Chiang Sylvia W Y, Chan Carmen K M, Luk Fiona O J, Ng Tsz Kin, Pang Chi-P |
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Elevated serum osteopontin levels and genetic polymorphisms of osteopontin are associated with Vogt-Koyanagi-Harada disease.
Investigative ophthalmology & visual science 2011 52 (10): 7084-9. Chu Mingliang, Yang Peizeng, Hu Ranran, Hou Shengping, Li Fuzhen, Chen Yuanyuan, Kijlstra Ai |
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Interleukin-17 gene polymorphism is associated with Vogt-Koyanagi-Harada syndrome but not with Behçet's disease in a Chinese Han population.
Human immunology 2010 Oct 71 (10): 988-91. Shu Qinmeng, Yang Peizeng, Hou Shengping, Li Fuzhen, Chen Yuanyuan, Du Liping, Jiang Zhengxu |
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Interleukin-17F gene polymorphisms in Korean patients with Behçet's disease.
Rheumatology international 2008 Dec 29 (2): 173-8. Jang Won-Cheoul, Nam Yun-Hyoung, Ahn Young-Chang, Lee Sang-Hyun, Park Sung-Hoon, Choe Jung-Yoon, Lee Shin-Seok, Kim Seong-K |
- Page last reviewed:Mar 1, 2018
- Page last updated:Jun 13, 2019
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