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Journal Abstract Search

240 related items for PubMed ID: 16015369

  • 1. 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]

  • 2. The PTPN22-1858C>T (R620W) functional polymorphism is associated with generalized vitiligo in the Romanian population.
    Laberge GS, Birlea SA, Fain PR, Spritz RA.
    Pigment Cell Melanoma Res; 2008 Apr; 21(2):206-8. PubMed ID: 18426414
    [Abstract] [Full Text] [Related]

  • 3. Association of the lymphoid tyrosine phosphatase R620W variant with rheumatoid arthritis, but not Crohn's disease, in Canadian populations.
    van Oene M, Wintle RF, Liu X, Yazdanpanah M, Gu X, Newman B, Kwan A, Johnson B, Owen J, Greer W, Mosher D, Maksymowych W, Keystone E, Rubin LA, Amos CI, Siminovitch KA.
    Arthritis Rheum; 2005 Jul; 52(7):1993-8. PubMed ID: 15986374
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. 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]

  • 6. Association of PTPN22 single nucleotide polymorphism with rheumatoid arthritis but not with allergic asthma.
    Majorczyk E, Jasek M, Płoski R, Wagner M, Kosior A, Pawlik A, Obojski A, Luszczek W, Nowak I, Wiśniewski A, Kuśnierczyk P.
    Eur J Hum Genet; 2007 Oct; 15(10):1043-8. PubMed ID: 17579671
    [Abstract] [Full Text] [Related]

  • 7. Analysis of allelic variants in the catalase gene in patients with the skin depigmenting disorder vitiligo.
    Gavalas NG, Akhtar S, Gawkrodger DJ, Watson PF, Weetman AP, Kemp EH.
    Biochem Biophys Res Commun; 2006 Jul 14; 345(4):1586-91. PubMed ID: 16729966
    [Abstract] [Full Text] [Related]

  • 8. Susceptibility to type 1 diabetes conferred by the PTPN22 C1858T polymorphism in the Spanish population.
    Santiago JL, Martínez A, de la Calle H, Fernández-Arquero M, Figueredo MA, de la Concha EG, Urcelay E.
    BMC Med Genet; 2007 Aug 13; 8():54. PubMed ID: 17697317
    [Abstract] [Full Text] [Related]

  • 9. PTPN22 R620W functional variant in type 1 diabetes and autoimmunity related traits.
    Chelala C, Duchatelet S, Joffret ML, Bergholdt R, Dubois-Laforgue D, Ghandil P, Pociot F, Caillat-Zucman S, Timsit J, Julier C.
    Diabetes; 2007 Feb 13; 56(2):522-6. PubMed ID: 17259401
    [Abstract] [Full Text] [Related]

  • 10. 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 13; 66(4):314-7. PubMed ID: 16185327
    [Abstract] [Full Text] [Related]

  • 11. The R620W C/T polymorphism of the gene PTPN22 is associated with SLE independently of the association of PDCD1.
    Reddy MV, Johansson M, Sturfelt G, Jönsen A, Gunnarsson I, Svenungsson E, Rantapää-Dahlqvist S, Alarcón-Riquelme ME.
    Genes Immun; 2005 Dec 13; 6(8):658-62. PubMed ID: 16052172
    [Abstract] [Full Text] [Related]

  • 12. Genetic influence of PTPN22 R620W polymorphism in tuberculosis.
    Gomez LM, Anaya JM, Martin J.
    Hum Immunol; 2005 Dec 13; 66(12):1242-7. PubMed ID: 16690411
    [Abstract] [Full Text] [Related]

  • 13. 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 13; 52(1):219-24. PubMed ID: 15641066
    [Abstract] [Full Text] [Related]

  • 14. Association of PTPN22 gene functional variants with development of pulmonary tuberculosis in Moroccan population.
    Lamsyah H, Rueda B, Baassi L, Elaouad R, Bottini N, Sadki K, Martin J.
    Tissue Antigens; 2009 Sep 13; 74(3):228-32. PubMed ID: 19563523
    [Abstract] [Full Text] [Related]

  • 15. 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 13; 147(1-2):41-6. PubMed ID: 22743847
    [Abstract] [Full Text] [Related]

  • 16. 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 13; 62(6):679-82. PubMed ID: 15943829
    [Abstract] [Full Text] [Related]

  • 17. Protein tyrosine phosphatase PTPN22 in human autoimmunity.
    Vang T, Miletic AV, Bottini N, Mustelin T.
    Autoimmunity; 2007 Sep 13; 40(6):453-61. PubMed ID: 17729039
    [Abstract] [Full Text] [Related]

  • 18. C1858T functional variant of PTPN22 gene is not associated with celiac disease genetic predisposition.
    Rueda B, Núñez C, Orozco G, López-Nevot MA, de la Concha EG, Martin J, Urcelay E.
    Hum Immunol; 2005 Jul 13; 66(7):848-52. PubMed ID: 16112033
    [Abstract] [Full Text] [Related]

  • 19. 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 13; 54(12):3820-7. PubMed ID: 17133579
    [Abstract] [Full Text] [Related]

  • 20. The PTPN22 1858C/T polymorphism is associated with anti-cyclic citrullinated peptide antibody-positive early rheumatoid arthritis in northern Sweden.
    Kokkonen H, Johansson M, Innala L, Jidell E, Rantapää-Dahlqvist S.
    Arthritis Res Ther; 2007 Dec 13; 9(3):R56. PubMed ID: 17553139
    [Abstract] [Full Text] [Related]

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