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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

177 related articles for article (PubMed ID: 17003357)

  • 1. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 8():54. PubMed ID: 17697317
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A functional polymorphism (1858C/T) in the PTPN22 gene is linked and associated with type I diabetes in multiplex families.
    Onengut-Gumuscu S; Ewens KG; Spielman RS; Concannon P
    Genes Immun; 2004 Dec; 5(8):678-80. PubMed ID: 15526003
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 56(2):522-6. PubMed ID: 17259401
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The 1858T PTPN22 gene variant contributes to a genetic risk of type 1 diabetes in a Ukrainian population.
    Fedetz M; Matesanz F; Caro-Maldonado A; Smirnov II; Chvorostinka VN; Moiseenko TA; Alcina A
    Tissue Antigens; 2006 May; 67(5):430-3. PubMed ID: 16671953
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The protein tyrosine phosphatase nonreceptor 22 (PTPN22) is associated with high GAD antibody titer in latent autoimmune diabetes in adults: Non Insulin Requiring Autoimmune Diabetes (NIRAD) Study 3.
    Petrone A; Suraci C; Capizzi M; Giaccari A; Bosi E; Tiberti C; Cossu E; Pozzilli P; Falorni A; Buzzetti R;
    Diabetes Care; 2008 Mar; 31(3):534-8. PubMed ID: 18056891
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Protein tyrosine phosphatase non-receptor type 22 gene variants at position 1858 are associated with type 1 and type 2 diabetes in Estonian population.
    Douroudis K; Prans E; Haller K; Nemvalts V; Rajasalu T; Tillmann V; Kisand K; Uibo R
    Tissue Antigens; 2008 Nov; 72(5):425-30. PubMed ID: 18764813
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Evidence for susceptibility determinant(s) to psoriasis vulgaris in or near PTPN22 in German patients.
    Hüffmeier U; Steffens M; Burkhardt H; Lascorz J; Schürmeier-Horst F; Ständer M; Kelsch R; Baumann C; Küster W; Mössner R; Reich K; Wienker TF; Traupe H; Reis A
    J Med Genet; 2006 Jun; 43(6):517-22. PubMed ID: 16339849
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association between PTPN22 C1858T and type 1 diabetes: a replication in continental Italy.
    Saccucci P; Del Duca E; Rapini N; Verrotti A; Piccinini S; Maccari A; Canu G; Angelini F; Fontana L; Giannini C; Chiarelli F; Manca Bitti ML; Bottini N
    Tissue Antigens; 2008 Mar; 71(3):234-7. PubMed ID: 18179648
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.