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 *

494 related articles for article (PubMed ID: 17697317)

  • 1. 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]  

  • 2. Gender-specific association of the PTPN22 C1858T polymorphism with achalasia.
    Santiago JL; Martínez A; Benito MS; Ruiz de León A; Mendoza JL; Fernández-Arquero M; Figueredo MA; de la Concha EG; Urcelay E
    Hum Immunol; 2007 Oct; 68(10):867-70. PubMed ID: 17961776
    [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. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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
    [TBL] [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; 56(2):522-6. PubMed ID: 17259401
    [TBL] [Abstract][Full Text] [Related]  

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

  • 11. 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]  

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

  • 13. Analysis of PTPN22 C1858T gene polymorphism in cases with type 1 diabetes of Azerbaijan, Northwest Iran.
    Almasi S; Aliparasti MR; Yazdchi-Marandi L; Aliasgarzadeh A; Sioofy-Khojine A; Mesri A; Zamani F
    Cell Immunol; 2014; 292(1-2):14-8. PubMed ID: 25243643
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 66(7):848-52. PubMed ID: 16112033
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

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

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 25.