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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

291 related items for PubMed ID: 26747760

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Association analysis of TGFBR3 gene with Vogt-Koyanagi-Harada disease and Behcet's disease in the Chinese Han population.
    Chen Y, Yang P, Li F, Hou S, Jiang Z, Shu Q, Kijlstra A.
    Curr Eye Res; 2012 Apr; 37(4):312-7. PubMed ID: 22440163
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Association of ERAP1 Gene Polymorphisms With Behçet's Disease in Han Chinese.
    Zhang L, Yu H, Zheng M, Li H, Liu Y, Kijlstra A, Yang P.
    Invest Ophthalmol Vis Sci; 2015 Sep; 56(10):6029-35. PubMed ID: 26393469
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Interleukin-17 gene polymorphism is associated with Vogt-Koyanagi-Harada syndrome but not with Behçet's disease in a Chinese Han population.
    Shu Q, Yang P, Hou S, Li F, Chen Y, Du L, Jiang Z.
    Hum Immunol; 2010 Oct; 71(10):988-91. PubMed ID: 20620187
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. The Association of Chemokine Gene Polymorphisms with VKH and Behcet's Disease in a Chinese Han Population.
    Huang Y, Yu H, Cao Q, Deng J, Huang X, Kijlstra A, Yang P.
    Biomed Res Int; 2017 Oct; 2017():1274960. PubMed ID: 28589131
    [Abstract] [Full Text] [Related]

  • 11. 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 Oct; 9(5):e98373. PubMed ID: 24859272
    [Abstract] [Full Text] [Related]

  • 12. Association of TLR2 gene polymorphisms with ocular Behcet's disease in a Chinese Han population.
    Fang J, Hu R, Hou S, Ye Z, Xiang Q, Qi J, Zhou Y, Kijlstra A, Yang P.
    Invest Ophthalmol Vis Sci; 2013 Dec 30; 54(13):8384-92. PubMed ID: 24255044
    [Abstract] [Full Text] [Related]

  • 13. MIF gene polymorphisms confer susceptibility to Vogt-Koyanagi-Harada syndrome in a Han Chinese population.
    Zhang C, Liu S, Hou S, Lei B, Zheng X, Xiao X, Kijlstra A, Yang P.
    Invest Ophthalmol Vis Sci; 2013 Nov 21; 54(12):7734-8. PubMed ID: 24194192
    [Abstract] [Full Text] [Related]

  • 14. Association of Long Noncoding RNAs Polymorphisms With Ankylosing Spondylitis, Vogt-Koyanagi-Harada Disease, and Behcet's Disease.
    Yue Y, Zhang J, Yang L, Liu S, Qi J, Cao Q, Zhou C, Wang Y, Kijlstra A, Yang P, Hou S.
    Invest Ophthalmol Vis Sci; 2018 Feb 01; 59(2):1158-1166. PubMed ID: 29490353
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No 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 01; 51(1):47-51. PubMed ID: 22087016
    [Abstract] [Full Text] [Related]

  • 17. 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 Jan 01; 9(5):e95573. PubMed ID: 24788730
    [Abstract] [Full Text] [Related]

  • 18. 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 Jan 01; 9(1):e84214. PubMed ID: 24416204
    [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 01; 71(7):723-6. PubMed ID: 20438790
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 15.