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.
174 related articles for article (PubMed ID: 28809090)
1. The association between P selectin glycoprotein ligand 1 gene variable number of tandem repeats polymorphism and risk of thrombosis in Behçet's disease. Cosan F; Oku B; Gedar Totuk OM; Abaci N; Ustek D; Diz Kucukkaya R; Gul A Int J Rheum Dis; 2018 Dec; 21(12):2175-2179. PubMed ID: 28809090 [TBL] [Abstract][Full Text] [Related]
2. Association of IL-4 gene VNTR variant with deep venous thrombosis in Behçet's disease and its effect on ocular involvement. Inanir A; Tural S; Yigit S; Kalkan G; Pancar GS; Demir HD; Ates O Mol Vis; 2013; 19():675-83. PubMed ID: 23559861 [TBL] [Abstract][Full Text] [Related]
3. P-selectin glycoprotein ligand-1 VNTR polymorphisms and risk of thrombosis in the antiphospholipid syndrome. Diz-Kucukkaya R; Inanc M; Afshar-Kharghan V; Zhang QE; López JA; Pekcelen Y Ann Rheum Dis; 2007 Oct; 66(10):1378-80. PubMed ID: 17545190 [TBL] [Abstract][Full Text] [Related]
4. Endothelial nitric oxide synthase gene polymorphisms in Behçet's disease and rheumatic diseases with vasculitis. Kim JU; Chang HK; Lee SS; Kim JW; Kim KT; Lee SW; Chung WT Ann Rheum Dis; 2003 Nov; 62(11):1083-7. PubMed ID: 14583572 [TBL] [Abstract][Full Text] [Related]
5. The association of P-selectin glycoprotein ligand-1 VNTR polymorphisms with coronary stent restenosis. Ozben B; Diz-Kucukkaya R; Bilge AK; Hancer VS; Oncul A J Thromb Thrombolysis; 2007 Jun; 23(3):181-7. PubMed ID: 17221329 [TBL] [Abstract][Full Text] [Related]
6. The variable number of tandem repeat polymorphism in the P-selectin glycoprotein ligand-1 gene is not associated with coronary heart disease. Bugert P; Hoffmann MM; Winkelmann BR; Vosberg M; Jahn J; Entelmann M; Katus HA; März W; Mansmann U; Boehm BO; Goerg S; Klüter H J Mol Med (Berl); 2003 Aug; 81(8):495-501. PubMed ID: 12879153 [TBL] [Abstract][Full Text] [Related]
7. The role of immune checkpoint inhibitors: Variable number of tandem repeat (VNTR) polymorphism in the second exon of the P-selectin glycoprotein ligand-1 (PSGL-1) gene polymorphism in multiple myeloma. Oyaci Y; Pehlivan M; Pehlivan S; Cinli TA; Tuncel FC; Ertas E; Serin I Mol Carcinog; 2024 Oct; 63(10):1980-1987. PubMed ID: 38953715 [TBL] [Abstract][Full Text] [Related]
8. Polymorphisms of the NOS3 gene in Tunisian patients with Behçet's disease. Kallel A; Sbaï MH; Houman MH; Sediri Y; Ouertani D; Smiti Khanfir M; Ben Ghorbel I; Jemaa R; Kaabachi N Int J Immunogenet; 2015 Apr; 42(2):87-92. PubMed ID: 25639851 [TBL] [Abstract][Full Text] [Related]
9. Polymorphisms in the endothelial nitric oxide synthase gene are associated with Behçet's disease. Karasneh JA; Hajeer AH; Silman A; Worthington J; Ollier WE; Gul A Rheumatology (Oxford); 2005 May; 44(5):614-7. PubMed ID: 15705632 [TBL] [Abstract][Full Text] [Related]
10. P-selectin glycoprotein ligand-1 variable number of tandem repeats (VNTR) polymorphism in patients with multiple sclerosis. Scalabrini D; Galimberti D; Fenoglio C; Comi C; De Riz M; Venturelli E; Castelli L; Piccio L; Ronzoni M; Lovati C; Mariani C; Monaco F; Bresolin N; Scarpini E Neurosci Lett; 2005 Nov; 388(3):149-52. PubMed ID: 16039046 [TBL] [Abstract][Full Text] [Related]
11. Association of MMP-9 gene polymorphisms with Behçet's disease risk. Naouali A; Kaabachi W; Tizaoui K; Amor AB; Hamzaoui A; Hamzaoui K Immunol Lett; 2015 Mar; 164(1):18-24. PubMed ID: 25639450 [TBL] [Abstract][Full Text] [Related]
12. Correlations of PSGL-1 VNTR polymorphism with the susceptibility to severe HFMD associated with EV-71 and the immune status after infection. Wang X; Qian J; Mi Y; Li Y; Cao Y; Qiao K Virol J; 2024 Aug; 21(1):187. PubMed ID: 39148126 [TBL] [Abstract][Full Text] [Related]
13. Factor V gene (1691A and 4070G) and prothrombin gene 20210A mutations in patients with Behçet's disease. Ateş A; Düzgün N; Ulu A; Tiryaki AO; Akar N Pathophysiol Haemost Thromb; 2003; 33(3):157-63. PubMed ID: 15170396 [TBL] [Abstract][Full Text] [Related]
14. Could be serum uric acid a risk factor for thrombosis and/or uveitis in Behcet's disease? Atıl A; Deniz A Vascular; 2018 Aug; 26(4):378-386. PubMed ID: 29360007 [TBL] [Abstract][Full Text] [Related]
15. Mevalonate kinase gene mutations and their clinical correlations in Behçet's disease. Arslan Taş D; Erken E; Yildiz F; Dinkçi S; Sakalli H Int J Rheum Dis; 2014 May; 17(4):435-43. PubMed ID: 24411001 [TBL] [Abstract][Full Text] [Related]
16. Associations between interferon regulatory factor-1 polymorphisms and Behçet's disease. Lee YJ; Kang SW; Song JK; Baek HJ; Choi HJ; Bae YD; Ryu HJ; Lee EY; Lee EB; Song YW Hum Immunol; 2007 Sep; 68(9):770-8. PubMed ID: 17869652 [TBL] [Abstract][Full Text] [Related]
17. No association of the TLR2 gene Arg753Gln polymorphism with rheumatic heart disease and Behçet's disease. Coşan F; Oku B; Cakiris A; Duymaz-Tozkir J; Mercanoğlu F; Saruhan-Direskeneli G; Ustek D; Gül A Clin Rheumatol; 2009 Dec; 28(12):1385-8. PubMed ID: 19693643 [TBL] [Abstract][Full Text] [Related]
18. Why are male patients with Behçet's disease prone to thrombosis? A rotational thromboelastographic analysis. Kara Kivanc B; Gönüllü E; Akay OM; Ertürk A; Bal C; Cansu DÜ; Korkmaz C Clin Exp Rheumatol; 2018; 36(6 Suppl 115):63-67. PubMed ID: 29998845 [TBL] [Abstract][Full Text] [Related]