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Journal Abstract Search

335 related items for PubMed ID: 17259401

  • 21. Confirmation of the association of the R620W polymorphism in the protein tyrosine phosphatase PTPN22 with type 1 diabetes in a family based study.
    Qu H, Tessier MC, Hudson TJ, Polychronakos C.
    J Med Genet; 2005 Mar; 42(3):266-70. PubMed ID: 15744042
    [No Abstract] [Full Text] [Related]

  • 22. The PTPN22 620W allele is a risk factor for Wegener's granulomatosis.
    Jagiello P, Aries P, Arning L, Wagenleiter SE, Csernok E, Hellmich B, Gross WL, Epplen JT.
    Arthritis Rheum; 2005 Dec; 52(12):4039-43. PubMed ID: 16320352
    [Abstract] [Full Text] [Related]

  • 23. Lymphoid tyrosine phosphatase (PTPN22/LYP) variant and Graves' disease in a Polish population: association and gene dose-dependent correlation with age of onset.
    Skórka A, Bednarczuk T, Bar-Andziak E, Nauman J, Ploski R.
    Clin Endocrinol (Oxf); 2005 Jun; 62(6):679-82. PubMed ID: 15943829
    [Abstract] [Full Text] [Related]

  • 24. Association of a functional single-nucleotide polymorphism of PTPN22, encoding lymphoid protein phosphatase, with rheumatoid arthritis and systemic lupus erythematosus.
    Orozco G, Sánchez E, González-Gay MA, López-Nevot MA, Torres B, Cáliz R, Ortego-Centeno N, Jiménez-Alonso J, Pascual-Salcedo D, Balsa A, de Pablo R, Nuñez-Roldan A, González-Escribano MF, Martín J.
    Arthritis Rheum; 2005 Jan; 52(1):219-24. PubMed ID: 15641066
    [Abstract] [Full Text] [Related]

  • 25. Interplay between PTPN22 C1858T polymorphism and cow's milk formula exposure in type 1 diabetes.
    Lempainen J, Vaarala O, Mäkelä M, Veijola R, Simell O, Knip M, Hermann R, Ilonen J.
    J Autoimmun; 2009 Sep; 33(2):155-64. PubMed ID: 19473815
    [Abstract] [Full Text] [Related]

  • 26. The PTPN22 promoter polymorphism -1123G>C association cannot be distinguished from the 1858C>T association in a Norwegian rheumatoid arthritis material.
    Viken MK, Olsson M, Flåm ST, Førre O, Kvien TK, Thorsby E, Lie BA.
    Tissue Antigens; 2007 Sep; 70(3):190-7. PubMed ID: 17661906
    [Abstract] [Full Text] [Related]

  • 27. The PTPN22 1858T variant is not associated with primary biliary cirrhosis.
    Milkiewicz P, Pache I, Buwaneswaran H, Liu X, Coltescu C, Heathcote EJ, Siminovitch KA.
    Tissue Antigens; 2006 May; 67(5):434-7. PubMed ID: 16671954
    [Abstract] [Full Text] [Related]

  • 28. Effects of PTPN22 C1858T polymorphism on susceptibility and clinical characteristics of British Caucasian rheumatoid arthritis patients.
    Harrison P, Pointon JJ, Farrar C, Brown MA, Wordsworth BP.
    Rheumatology (Oxford); 2006 Aug; 45(8):1009-11. PubMed ID: 16490755
    [Abstract] [Full Text] [Related]

  • 29. The functional R620W variant of the PTPN22 gene is associated with celiac disease.
    Santin I, Castellanos-Rubio A, Aransay AM, Castaño L, Vitoria JC, Bilbao JR.
    Tissue Antigens; 2008 Mar; 71(3):247-9. PubMed ID: 18194365
    [Abstract] [Full Text] [Related]

  • 30. Protein tyrosine phosphatase PTPN22 in human autoimmunity.
    Vang T, Miletic AV, Bottini N, Mustelin T.
    Autoimmunity; 2007 Sep; 40(6):453-61. PubMed ID: 17729039
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  • 32. The autoimmunity-related polymorphism PTPN22 1858C/T is associated with anti-titin antibody-positive myasthenia gravis.
    Greve B, Hoffmann P, Illes Z, Rozsa C, Berger K, Weissert R, Melms A.
    Hum Immunol; 2009 Jul; 70(7):540-2. PubMed ID: 19406179
    [Abstract] [Full Text] [Related]

  • 33. The non-synonymous C1858T substitution in the PTPN22 gene is associated with susceptibility to the severe forms of alopecia areata.
    Kemp EH, McDonagh AJ, Wengraf DA, Messenger AG, Gawkrodger DJ, Cork MJ, Tazi-Ahnini R.
    Hum Immunol; 2006 Jul; 67(7):535-9. PubMed ID: 16829308
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  • 37. Association analysis of the 1858C>T polymorphism in the PTPN22 gene in juvenile idiopathic arthritis and other autoimmune diseases.
    Viken MK, Amundsen SS, Kvien TK, Boberg KM, Gilboe IM, Lilleby V, Sollid LM, Førre OT, Thorsby E, Smerdel A, Lie BA.
    Genes Immun; 2005 May; 6(3):271-3. PubMed ID: 15759012
    [Abstract] [Full Text] [Related]

  • 38. Lack of association between the protein tyrosine phosphatase non-receptor 22 (PTPN22)*620W allele and systemic sclerosis in the French Caucasian population.
    Wipff J, Allanore Y, Kahan A, Meyer O, Mouthon L, Guillevin L, Pierlot C, Glikmans E, Bardin T, Boileau C, Cornélis F, Dieudé P.
    Ann Rheum Dis; 2006 Sep; 65(9):1230-2. PubMed ID: 16464986
    [Abstract] [Full Text] [Related]

  • 39. No evidence for association between 1858 C/T single-nucleotide polymorphism of PTPN22 gene and primary Sjögren's syndrome.
    Ittah M, Gottenberg JE, Proust A, Hachulla E, Puechal X, Loiseau P, Mariette X, Miceli-Richard C.
    Genes Immun; 2005 Aug; 6(5):457-8. PubMed ID: 15933742
    [Abstract] [Full Text] [Related]

  • 40. Association between the 1858T allele of the protein tyrosine phosphatase nonreceptor type 22 and type 1 diabetes in a Brazilian population.
    Chagastelles PC, Romitti M, Trein MR, Bandinelli E, Tschiedel B, Nardi NB.
    Tissue Antigens; 2010 Aug; 76(2):144-8. PubMed ID: 20331840
    [Abstract] [Full Text] [Related]

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