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Journal Abstract Search

486 related items for PubMed ID: 25839768

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  • 4. Association of the polymorphisms of chemokine genes (IL8, RANTES, MIG, IP10, MCP1 and IL16) with the pathogenesis of autoimmune thyroid diseases.
    Akahane M, Watanabe M, Inoue N, Miyahara Y, Arakawa Y, Inoue Y, Katsumata Y, Hidaka Y, Iwatani Y.
    Autoimmunity; 2016 Aug; 49(5):312-9. PubMed ID: 27245471
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  • 5. Interleukin 8 gene polymorphism is associated with increased risk of nephritis in cutaneous vasculitis.
    Amoli MM, Thomson W, Hajeer AH, Calviño MC, Garcia-Porrua C, Ollier WE, Gonzalez-Gay MA.
    J Rheumatol; 2002 Nov; 29(11):2367-70. PubMed ID: 12415593
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  • 6. 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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  • 7. CCL2, CCL3 and CCL5 chemokines in systemic sclerosis: the correlation with SSc clinical features and the effect of prostaglandin E1 treatment.
    Bandinelli F, Del Rosso A, Gabrielli A, Giacomelli R, Bartoli F, Guiducci S, Matucci Cerinic M.
    Clin Exp Rheumatol; 2012 Jun; 30(2 Suppl 71):S44-9. PubMed ID: 22691208
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  • 8. 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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  • 12. Polymorphisms in the promoter region of RANTES and the regulatory region of monocyte chemoattractant protein-1 among Chinese children with systemic lupus erythematosus.
    Liao CH, Yao TC, Chung HT, See LC, Kuo ML, Huang JL.
    J Rheumatol; 2004 Oct; 31(10):2062-7. PubMed ID: 15468376
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  • 13. Polymorphisms of chemokine and chemokine receptor genes in idiopathic immune-mediated posterior segment uveitis.
    Ahad MA, Missotten T, Abdallah A, Lympany PA, Lightman S.
    Mol Vis; 2007 Mar 23; 13():388-96. PubMed ID: 17417600
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  • 16. Polymorphism at codon 469 of the intercellular adhesion molecule-1 locus is associated with protection against severe gastrointestinal complications in Henoch-Schönlein purpura.
    Amoli MM, Mattey DL, Calviño MC, Garcia-Porrua C, Thomson W, Hajeer AH, Ollier WE, Gonzalez-Gay MA.
    J Rheumatol; 2001 May 23; 28(5):1014-8. PubMed ID: 11361181
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  • 19. Interleukin 1 beta (IL1ß) rs16944 genetic variant as a genetic marker of severe renal manifestations and renal sequelae in Henoch-Schönlein purpura.
    López-Mejías R, Genre F, Remuzgo-Martínez S, Sevilla Pérez B, Castañeda S, Llorca J, Ortego-Centeno N, Ubilla B, Mijares V, Pina T, Calvo-Río V, Miranda-Filloy JA, Navas Parejo A, Argila D, Sánchez-Pérez J, Rubio E, Luque ML, Blanco-Madrigal JM, Galíndez-Aguirregoikoa E, Martín J, Blanco R, González-Gay MA.
    Clin Exp Rheumatol; 2016 May 23; 34(3 Suppl 97):S84-8. PubMed ID: 26842496
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