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Journal Abstract Search

371 related items for PubMed ID: 28409662

  • 1. Association of Endothelial Nitric Oxide Synthase Gene Polymorphism with Susceptibility and Nephritis Development of Henoch-Schönlein Purpura in Chinese Han Children.
    Wang A, Wang A, Xiao Y, Wang J, Xu E.
    Genet Test Mol Biomarkers; 2017 Jun; 21(6):373-381. PubMed ID: 28409662
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  • 2. Association of endothelial nitric oxide synthase gene polymorphism with the risk of Henoch-Schönlein purpura/Henoch-Schönlein purpura nephritis.
    Zhong W, Zhou TB, Jiang Z.
    Ren Fail; 2015 Apr; 37(3):372-6. PubMed ID: 25585947
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  • 3. Inducible nitric oxide synthase gene polymorphisms are associated with a risk of nephritis in Henoch-Schönlein purpura children.
    Jiang J, Duan W, Shang X, Wang H, Gao Y, Tian P, Zhou Q.
    Eur J Pediatr; 2017 Aug; 176(8):1035-1045. PubMed ID: 28593405
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  • 4. Association study of ACE and eNOS single nucleotide polymorphisms with Henoch-Schönlein purpura nephritis.
    Di B, Li X, Song L, Wang Q, Liu S.
    Mol Med Rep; 2012 Nov; 6(5):1171-7. PubMed ID: 22895845
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  • 5. [Meta-analysis of the association between angiotension-converting enzyme I/D polymorphism and susceptibility to children with Henoch-Schönlein purpura or Henoch-Schölein purpura nephritis].
    Li H, Zhao D, Yang Q.
    Zhonghua Yi Xue Za Zhi; 2014 Jul 08; 94(26):2039-44. PubMed ID: 25312666
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  • 11. The association between genetic variation in interleukin-10 gene and susceptibility to Henoch-Schönlein purpura in Chinese children.
    Xu H, Jiang G, Shen H, Pan Y, Zhang J, Li W, Mao J.
    Clin Rheumatol; 2017 Dec 08; 36(12):2761-2767. PubMed ID: 28963667
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  • 12. Role of PAX2 gene polymorphisms in Henoch-Schonlein purpura nephritis.
    Yi ZW, Fang XL, Wu XC, He XJ, He QN, Dang XQ, Zhu CP, Mo SH.
    Nephrology (Carlton); 2006 Feb 08; 11(1):42-8. PubMed ID: 16509931
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  • 14. Chemokine MCP1/CCL2 and RANTES/CCL5 gene polymorphisms influence Henoch-Schönlein purpura susceptibility and severity.
    Yu HH, Liu PH, Yang YH, Lee JH, Wang LC, Chen WJ, Chiang BL.
    J Formos Med Assoc; 2015 Apr 08; 114(4):347-52. PubMed ID: 25839768
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  • 16. Association of the paired box 2 gene polymorphism with the susceptibility and pathogenesis of Henoch‑Schönlein purpura in children.
    Chen J, Fang X, Dang X, Wu X, Yi Z.
    Mol Med Rep; 2015 Mar 08; 11(3):1997-2003. PubMed ID: 25385517
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  • 17. Inducible nitric oxide synthase polymorphism is associated with susceptibility to Henoch-Schönlein purpura in northwestern Spain.
    Martin J, Paco L, Ruiz MP, Lopez-Nevot MA, Garcia-Porrua C, Amoli MM, Calviño MC, Ollier WE, Gonzalez-Gay MA.
    J Rheumatol; 2005 Jun 08; 32(6):1081-5. PubMed ID: 15940772
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  • 18. Lack of association between macrophage migration inhibitory factor gene promoter (-173 G/C) polymorphism and childhood Henoch-Schönlein purpura in Turkish patients.
    Nalbantoglu S, Tabel Y, Mir S, Berdeli A.
    Cytokine; 2013 Apr 08; 62(1):160-4. PubMed ID: 23523092
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  • 19. Effect of paraoxonase 1 gene polymorphisms on clinical course of Henoch-Schönlein purpura.
    Yilmaz A, Emre S, Agachan B, Bilge I, Yilmaz H, Ergen A, Isbir T, Sirin A.
    J Nephrol; 2009 Apr 08; 22(6):726-32. PubMed ID: 19967651
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