Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Yang, Peizeng"'
Autor:
Zhou, Yan, Yu, Hongsong, Hou, Shengping, Fang, Jing, Qin, Jieying, Yuan, Gangxiang, Kijlstra, Aize, Yang, Peizeng
Publikováno v:
Molecular Vision
Molecular Vision, 22, 311-318. Molecular Vision
Molecular Vision, 22, 311-318. Molecular Vision
Purpose: Previous studies have identified that nitric oxide synthase (NOS) genes are associated with several immune-mediated diseases. This study aimed to investigate whether NOS2 and NOS3 gene polymorphisms are associated with Behcet's disease (BD)
Autor:
Sun, Min1,2, Yang, Peizeng2 peizengycmu@126.com, Du, Liping2, Yang, Yan2, Ye, Jian1 yejian1979@163.com
Publikováno v:
PLoS ONE. Apr2014, Vol. 9 Issue 4, p1-8. 8p.
Association of insulin-like growth factor-1 polymorphisms with high myopia in the Chinese population
Autor:
Zhuang, Wenjuan, Yang, Peizeng, Li, Zili, Sheng, Xunlun, Zhao, Jingjing, Li, Shanshan, Yang, Xueqiu, Xiang, Wei, Rong, Weining, Liu, Yani, Zhang, Fangxia
Publikováno v:
Molecular Vision
Purpose The purpose of this study was to determine whether genetic variants in the insulin-like growth factor-1 (IGF-1) gene were associated with high myopia in the Chinese population. Methods A case-control association study of 421 unrelated Chinese
Publikováno v:
Molecular Vision
Purpose To investigate the signaling pathways involved in interleukin (IL)-17A -mediated production of interleukin 8 (CXCL8), chemokine (C-C motif) ligand 2 (CCL2), and interleukin 6 (IL-6) by ARPE-19 cells, a spontaneously arisen cell line of retina
Publikováno v:
Molecular Vision
Purpose 1,25-Dihydroxyvitamin D3 [1,25(OH)2D3] has recently been found to be involved in the development of autoimmune diseases. This study was to investigate the expression and potential role of 1,25(OH)2D3 in the pathogenesis of Vogt-Koyanagi-Harad
Publikováno v:
Molecular Vision
Purpose Interferon regulation factor 5 (IRF5) is a member of the IRF family of transcription factors that control the transactivation of type I interferon system-related genes as well as the expression of several other genes involved in immune respon
Publikováno v:
Molecular Vision
Purpose The polymorphisms of the Fc receptor-like 3 gene (FCRL3), a novel immunoregulatory gene, have been shown to be associated with certain autoimmune diseases. This study was designed to examine whether the polymorphisms of FCRL3 are associated w
Autor:
Meng, Qianli, Liu, Xiaoli, Yang, Peizeng, Hou, Shengping, Du, Liping, Zhou, Hongyan, Kijlstra, Aize
Publikováno v:
Molecular Vision
Purpose To analyze the potential association of programmed cell death 1 (PDCD1) with Vogt-Koyanagi-Harada (VKH) syndrome in a Chinese Han population. Methods Three single nucleotide polymorphism (SNPs), PD-1.3G/A, PD-1.5C/T, and PD-1.6G/A, were genot
Autor:
Hou, Shengping, Yang, Peizeng, Du, Liping, Zhou, Hongyan, Lin, Xiaomin, Liu, Xiaoli, Kijlstra, Aize
Publikováno v:
Molecular Vision
Purpose To examine whether small ubiquitin-like modifier 4 (SUMO4) polymorphisms were associated with Vogt-Koyanagi-Harada (VKH) syndrome in the Chinese Han population. Methods Genotyping for SUMO4 polymorphisms at G-847A, A-504G, A+163G, and C+438T
Autor:
Zhao, Changlin, Yang, Peizeng, He, Hao, Lin, Xiaomin, Li, Bing, Zhou, Hongyan, Huang, Xiangkun, Kijlstra, Aize
Publikováno v:
Molecular Vision
Purpose To investigate the frequency and phenotypic and functional characteristics of S-antigen (S-Ag) specific T cells in patients with Behcet’s disease (BD). Methods Blood was taken from 23 active BD patients, 12 inactive BD patients, and 14 heal