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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

412 related items for PubMed ID: 18764813

  • 21. The +1858C/T PTPN22 gene polymorphism confers genetic susceptibility to rheumatoid arthritis in Mexican population from the Western Mexico.
    Torres-Carrillo NM, Ruiz-Noa Y, Martínez-Bonilla GE, Leyva-Torres SD, Torres-Carrillo N, Palafox-Sánchez CA, Navarro-Hernández RE, Rangel-Villalobos H, Oregón-Romero E, Muñoz-Valle JF.
    Immunol Lett; 2012 Sep; 147(1-2):41-6. PubMed ID: 22743847
    [Abstract] [Full Text] [Related]

  • 22. PTPN22 1858T allele is associated with younger age at onset of type 1 diabetes and is not related to subsequent thyroid autoimmunity.
    Kordonouri O, Hartmann R, Badenhoop K, Kahles H, Ilonen J.
    Hum Immunol; 2010 Jul; 71(7):731-2. PubMed ID: 20438787
    [Abstract] [Full Text] [Related]

  • 23. Protein tyrosine phosphatase non-receptor type 22 (PTPN22) gene R620W variant and sporadic idiopathic hypoparathyroidism in Asian Indians.
    Ray D, Tomar N, Gupta N, Goswami R.
    Int J Immunogenet; 2006 Aug; 33(4):237-40. PubMed ID: 16893384
    [Abstract] [Full Text] [Related]

  • 24. Cytotoxic T-lymphocyte antigen 4 gene polymorphisms are associated with latent autoimmune diabetes in adults.
    Douroudis K, Prans E, Kisand K, Nemvalts V, Uibo R.
    Clin Chim Acta; 2009 May; 403(1-2):226-8. PubMed ID: 19332045
    [Abstract] [Full Text] [Related]

  • 25. The functional genetic variation in the PTPN22 gene has a negligible effect on the susceptibility to develop inflammatory bowel disease.
    Martín MC, Oliver J, Urcelay E, Orozco G, Gómez-Garcia M, López-Nevot MA, Piñero A, Brieva JA, de la Concha EG, Nieto A, Martín J.
    Tissue Antigens; 2005 Oct; 66(4):314-7. PubMed ID: 16185327
    [Abstract] [Full Text] [Related]

  • 26. 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
    [Abstract] [Full Text] [Related]

  • 27. A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes.
    Bottini N, Musumeci L, Alonso A, Rahmouni S, Nika K, Rostamkhani M, MacMurray J, Meloni GF, Lucarelli P, Pellecchia M, Eisenbarth GS, Comings D, Mustelin T.
    Nat Genet; 2004 Apr; 36(4):337-8. PubMed ID: 15004560
    [Abstract] [Full Text] [Related]

  • 28. 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
    [Abstract] [Full Text] [Related]

  • 29. Association of PTPN22 C1858T polymorphism and type 1 diabetes: a meta-analysis.
    Peng H, Zhou M, Xu WD, Xu K, Zhai Y, Li R, Wang W, Zhang YJ, Liu SS, Pan HF, Ye DQ.
    Immunol Invest; 2012 Jul; 41(5):484-96. PubMed ID: 22429252
    [Abstract] [Full Text] [Related]

  • 30. The protein tyrosine phosphatase non-receptor type 22 C1858T polymorphism is a joint susceptibility locus for immunthyroiditis and autoimmune diabetes.
    Dultz G, Matheis N, Dittmar M, Röhrig B, Bender K, Kahaly GJ.
    Thyroid; 2009 Feb; 19(2):143-8. PubMed ID: 19090780
    [Abstract] [Full Text] [Related]

  • 31. The 620W allele is the PTPN22 genetic variant conferring susceptibility to RA in a Dutch population.
    Wesoly J, Hu X, Thabet MM, Chang M, Uh H, Allaart CF, Toes RE, Houwing-Duistermaat JJ, Begovich AB, Huizinga TW.
    Rheumatology (Oxford); 2007 Apr; 46(4):617-21. PubMed ID: 17135225
    [Abstract] [Full Text] [Related]

  • 32. PTPN22 gene polymorphism in Behçet's disease.
    Sahin N, Bicakcigil M, Atagunduz P, Direskeneli H, Saruhan-Direskeneli G.
    Tissue Antigens; 2007 Nov; 70(5):432-4. PubMed ID: 17868256
    [Abstract] [Full Text] [Related]

  • 33. Rheumatoid arthritis association with the FCRL3 -169C polymorphism is restricted to PTPN22 1858T-homozygous individuals in a Canadian population.
    Newman WG, Zhang Q, Liu X, Walker E, Ternan H, Owen J, Johnson B, Greer W, Mosher DP, Maksymowych WP, Bykerk VP, Keystone EC, Amos CI, Siminovitch KA.
    Arthritis Rheum; 2006 Dec; 54(12):3820-7. PubMed ID: 17133579
    [Abstract] [Full Text] [Related]

  • 34. PTPN22 polymorphism is related to autoimmune disease risk in patients with Turner syndrome.
    Bianco B, Verreschi IT, Oliveira KC, Guedes AD, Galera BB, Galera MF, Barbosa CP, Lipay MV.
    Scand J Immunol; 2010 Sep; 72(3):256-9. PubMed ID: 20696024
    [Abstract] [Full Text] [Related]

  • 35. PTPN22/LYP 1858C>T gene polymorphism and susceptibility to endometriosis in a Polish population.
    Płoski R, Dziunycz P, Kostrzewa G, Roszkowski PI, Barcz E, Zabek J, Milewski Ł, Kamiński P, Malejczyk J.
    J Reprod Immunol; 2009 Jan; 79(2):196-200. PubMed ID: 19237203
    [Abstract] [Full Text] [Related]

  • 36. A single-nucleotide polymorphism in the gene encoding lymphoid protein tyrosine phosphatase (PTPN22) confers susceptibility to generalised vitiligo.
    Cantón I, Akhtar S, Gavalas NG, Gawkrodger DJ, Blomhoff A, Watson PF, Weetman AP, Kemp EH.
    Genes Immun; 2005 Oct; 6(7):584-7. PubMed ID: 16015369
    [Abstract] [Full Text] [Related]

  • 37. 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]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. A haplotype-based analysis of the PTPN22 locus in type 1 diabetes.
    Onengut-Gumuscu S, Buckner JH, Concannon P.
    Diabetes; 2006 Oct; 55(10):2883-9. PubMed ID: 17003357
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 21.