These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (PubMed ID: 25439430)

  • 1. Genetic variations of IL17F and IL23A show associations with Behçet's disease and Vogt-Koyanagi-Harada syndrome.
    Hou S; Liao D; Zhang J; Fang J; Chen L; Qi J; Zhang Q; Liu Y; Bai L; Zhou Y; Kijlstra A; Yang P
    Ophthalmology; 2015 Mar; 122(3):518-23. PubMed ID: 25439430
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Copy number variations and gene polymorphisms of complement components in ocular Behcet's disease and Vogt-Koyanagi-Harada syndrome.
    Xu D; Hou S; Zhang J; Jiang Y; Kijlstra A; Yang P
    Sci Rep; 2015 Aug; 5():12989. PubMed ID: 26269006
    [TBL] [Abstract][Full Text] [Related]  

  • 3. miR-23a, miR-146a and miR-301a confer predisposition to Vogt-Koyanagi-Harada syndrome but not to Behcet's disease.
    Hou S; Ye Z; Liao D; Bai L; Liu Y; Zhang J; Kijlstra A; Yang P
    Sci Rep; 2016 Jan; 6():20057. PubMed ID: 26818976
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Copy number variants and genetic polymorphisms in TBX21, GATA3, Rorc, Foxp3 and susceptibility to Behcet's disease and Vogt-Koyanagi-Harada syndrome.
    Liao D; Hou S; Zhang J; Fang J; Liu Y; Bai L; Cao Q; Kijlstra A; Yang P
    Sci Rep; 2015 Apr; 5():9511. PubMed ID: 25873156
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A variant of CLEC16A gene confers protection for Vogt-Koyanagi-Harada syndrome but not for Behcet's disease in a Chinese Han population.
    Li K; Hou S; Qi J; Kijlstra A; Yang P
    Exp Eye Res; 2015 Mar; 132():225-30. PubMed ID: 25576669
    [TBL] [Abstract][Full Text] [Related]  

  • 6. FAS Gene Copy Numbers are Associated with Susceptibility to Behçet Disease and VKH Syndrome in Han Chinese.
    Yu H; Luo L; Wu L; Zheng M; Zhang L; Liu Y; Li H; Cao Q; Kijlstra A; Yang P
    Hum Mutat; 2015 Nov; 36(11):1064-9. PubMed ID: 26136352
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Interleukin-10 gene polymorphisms are associated with Behcet's disease but not with Vogt-Koyanagi-Harada syndrome in the Chinese Han population.
    Hu J; Hou S; Zhu X; Fang J; Zhou Y; Liu Y; Bai L; Kijlstra A; Yang P
    Mol Vis; 2015; 21():589-603. PubMed ID: 26015771
    [TBL] [Abstract][Full Text] [Related]  

  • 8. No association between Bach2 gene polymorphisms with Vogt-Koyanagi-Harada syndrome (VKH) and Behcet's disease (BD) in a Chinese Han population.
    Gao X; Tan X; Qin J; Lv S; Hou S; Kijlstra A; Yang P
    Br J Ophthalmol; 2015 Aug; 99(8):1150-4. PubMed ID: 25873652
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Association Between Copy Number Variations of TLR7 and Ocular Behçet's Disease in a Chinese Han Population.
    Fang J; Chen L; Tang J; Hou S; Liao D; Ye Z; Wang C; Cao Q; Kijlstra A; Yang P
    Invest Ophthalmol Vis Sci; 2015 Feb; 56(3):1517-23. PubMed ID: 25650422
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Decreased expression of A20 is associated with ocular Behcet's disease (BD) but not with Vogt-Koyanagi-Harada (VKH) disease.
    He Y; Wang C; Su G; Deng B; Ye Z; Huang Y; Yuan G; Aize K; Li H; Yang P
    Br J Ophthalmol; 2018 Aug; 102(8):1167-1172. PubMed ID: 29699987
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Association of ATG5 Gene Polymorphisms With Behçet's Disease and ATG10 Gene Polymorphisms With VKH Syndrome in a Chinese Han Population.
    Zheng M; Yu H; Zhang L; Li H; Liu Y; Kijlstra A; Yang P
    Invest Ophthalmol Vis Sci; 2015 Dec; 56(13):8280-7. PubMed ID: 26747760
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic variations of IL-12B, IL-12Rβ1, IL-12Rβ2 in Behcet's disease and VKH syndrome.
    Li X; Bai L; Fang J; Hou S; Zhou Q; Yu H; Kijlstra A; Yang P
    PLoS One; 2014; 9(5):e98373. PubMed ID: 24859272
    [TBL] [Abstract][Full Text] [Related]  

  • 13. TRAF5 and TRAF3IP2 gene polymorphisms are associated with Behçet's disease and Vogt-Koyanagi-Harada syndrome: a case-control study.
    Xiang Q; Chen L; Hou S; Fang J; Zhou Y; Bai L; Liu Y; Kijlstra A; Yang P
    PLoS One; 2014; 9(1):e84214. PubMed ID: 24416204
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Predisposition to Behçet's disease and VKH syndrome by genetic variants of miR-182.
    Yu H; Liu Y; Bai L; Kijlstra A; Yang P
    J Mol Med (Berl); 2014 Sep; 92(9):961-7. PubMed ID: 24801147
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association of a TNIP1 polymorphism with Vogt-Koyanagi-Harada syndrome but not with ocular Behcet's disease in Han Chinese.
    Shi Y; Jia Y; Hou S; Fang J; Zhou Y; Kijlstra A; Yang P
    PLoS One; 2014; 9(5):e95573. PubMed ID: 24788730
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CD40 gene polymorphisms confer risk of Behcet's disease but not of Vogt-Koyanagi-Harada syndrome in a Han Chinese population.
    Chen F; Hou S; Jiang Z; Chen Y; Kijlstra A; Rosenbaum JT; Yang P
    Rheumatology (Oxford); 2012 Jan; 51(1):47-51. PubMed ID: 22087016
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Association of a NOS3 gene polymorphism with Behçet's disease but not with Vogt-Koyanagi-Harada syndrome in Han Chinese.
    Zhou Y; Yu H; Hou S; Fang J; Qin J; Yuan G; Kijlstra A; Yang P
    Mol Vis; 2016; 22():311-8. PubMed ID: 27114698
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Uveitis genetics.
    Hou S; Li N; Liao X; Kijlstra A; Yang P
    Exp Eye Res; 2020 Jan; 190():107853. PubMed ID: 31669406
    [TBL] [Abstract][Full Text] [Related]  

  • 19. STAT4 polymorphism in a Chinese Han population with Vogt-Koyanagi-Harada syndrome and Behçet's disease.
    Hu K; Yang P; Jiang Z; Hou S; Du L; Li F
    Hum Immunol; 2010 Jul; 71(7):723-6. PubMed ID: 20438790
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A functional variant of pre-miRNA-196a2 confers risk for Behcet's disease but not for Vogt-Koyanagi-Harada syndrome or AAU in ankylosing spondylitis.
    Qi J; Hou S; Zhang Q; Liao D; Wei L; Fang J; Zhou Y; Kijlstra A; Yang P
    Hum Genet; 2013 Dec; 132(12):1395-404. PubMed ID: 23928854
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.