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Journal Abstract Search

142 related items for PubMed ID: 24480412

  • 1. PTPN2 rs1893217 single-nucleotide polymorphism is associated with risk of Behçet's disease in a Chinese Han population.
    Wu Z, Chen H, Sun F, Xu J, Zheng W, Li P, Chen S, Shen M, Zhang W, Li M, You X, Wu Q, Zhang F, Li Y.
    Clin Exp Rheumatol; 2014; 32(4 Suppl 84):S20-6. PubMed ID: 24480412
    [Abstract] [Full Text] [Related]

  • 2. Protein tyrosine phosphatase non-receptor type 2 (PTPN2) gene polymorphisms (rs2542151, rs7234029) in Egyptian Behçet's disease patients: a preliminary report.
    Attia DHS, Alkaffas M, Eissa M, Rashed L, Khattab RAM, Elzanaty R, Khattab RA, Samy LA.
    Clin Rheumatol; 2024 Nov; 43(11):3439-3448. PubMed ID: 39320556
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  • 3. Association of genetic variations in PTPN2 and CD122 with ocular Behcet's disease.
    Zhang Q, Li H, Hou S, Yu H, Su G, Deng B, Qi J, Zhou C, Kijlstra A, Yang P.
    Br J Ophthalmol; 2018 Jul; 102(7):996-1002. PubMed ID: 29502070
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  • 4. Replication study confirms the association between UBAC2 and Behçet's disease in two independent Chinese sets of patients and controls.
    Hou S, Shu Q, Jiang Z, Chen Y, Li F, Chen F, Kijlstra A, Yang P.
    Arthritis Res Ther; 2012 Mar 29; 14(2):R70. PubMed ID: 22455605
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  • 6. 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 29; 99(8):1150-4. PubMed ID: 25873652
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  • 11. Genetic variants in the JAK1 gene confer higher risk of Behcet's disease with ocular involvement in Han Chinese.
    Hou S, Qi J, Zhang Q, Liao D, Li Q, Hu K, Zhou Y, Kijlstra A, Yang P.
    Hum Genet; 2013 Sep 29; 132(9):1049-58. PubMed ID: 23674219
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  • 12. Weak association of a TNFRSF1A polymorphism with Behcet's disease in Chinese Han.
    Hu L, Tan H, Cao Q, Yuan G, Huang C, Su G, Kijlstra A, Yang P.
    Exp Eye Res; 2020 Jul 29; 196():108045. PubMed ID: 32389622
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  • 13. 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 29; 132():225-30. PubMed ID: 25576669
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  • 14. Association study of rs924080 and rs11209032 polymorphisms of IL23R-IL12RB2 in a Northern Chinese Han population with Behcet's disease.
    Qin X, Xu J, Wu Z, Sun F, Chen H, Zheng W, Li S, Li P, Chen S, Shen M, Zhang W, You X, Wu Q, Zhang F, Li YZ.
    Hum Immunol; 2016 Dec 29; 77(12):1284-1290. PubMed ID: 27660093
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  • 15. Crohn's disease-associated polymorphism within the PTPN2 gene affects muramyl-dipeptide-induced cytokine secretion and autophagy.
    Scharl M, Mwinyi J, Fischbeck A, Leucht K, Eloranta JJ, Arikkat J, Pesch T, Kellermeier S, Mair A, Kullak-Ublick GA, Truninger K, Noreen F, Regula J, Gaj P, Pittet V, Mueller C, Hofmann C, Fried M, McCole DF, Rogler G.
    Inflamm Bowel Dis; 2012 May 29; 18(5):900-12. PubMed ID: 22021207
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  • 20. Association between the PTPN2 gene and Crohn's disease: dissection of potential causal variants.
    Marcil V, Mack DR, Kumar V, Faure C, Carlson CS, Beaulieu P, Israel D, Krupoves A, Costea I, Lambrette P, Grimard G, Dong J, Seidman EG, Amre DK, Levy E.
    Inflamm Bowel Dis; 2013 May 29; 19(6):1149-55. PubMed ID: 23518806
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