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 *

196 related articles for article (PubMed ID: 16893384)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. The R620W polymorphism of the protein tyrosine phosphatase 22 gene in autoimmune thyroid diseases and rheumatoid arthritis in the Tunisian population.
    Chabchoub G; Teixiera EP; Maalej A; Ben Hamad M; Bahloul Z; Cornelis F; Ayadi H
    Ann Hum Biol; 2009; 36(3):342-9. PubMed ID: 19343596
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 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. 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]  

  • 8. 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]  

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

  • 10. 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]  

  • 11. 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; 9(3):R56. PubMed ID: 17553139
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Multiplex family-based study in systemic lupus erythematosus: association between the R620W polymorphism of PTPN22 and the FcgammaRIIa (CD32A) R131 allele.
    Balada E; Villarreal-Tolchinsky J; Ordi-Ros J; Labrador M; Serrano-Acedo S; Martinez-Lostao L; Vilardell-Tarrés M
    Tissue Antigens; 2006 Nov; 68(5):432-8. PubMed ID: 17092257
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.