237 related articles for article (PubMed ID: 16320352)
1. The PTPN22 620W allele is a risk factor for Wegener's granulomatosis.
Jagiello P; Aries P; Arning L; Wagenleiter SE; Csernok E; Hellmich B; Gross WL; Epplen JT
Arthritis Rheum; 2005 Dec; 52(12):4039-43. PubMed ID: 16320352
[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. Lack of association between the protein tyrosine phosphatase non-receptor 22 (PTPN22)*620W allele and systemic sclerosis in the French Caucasian population.
Wipff J; Allanore Y; Kahan A; Meyer O; Mouthon L; Guillevin L; Pierlot C; Glikmans E; Bardin T; Boileau C; Cornélis F; Dieudé P
Ann Rheum Dis; 2006 Sep; 65(9):1230-2. PubMed ID: 16464986
[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. 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]
6. PTPN22 R620W polymorphism in the ANCA-associated vasculitides.
Martorana D; Maritati F; Malerba G; Bonatti F; Alberici F; Oliva E; Sebastio P; Manenti L; Brugnano R; Catanoso MG; Fraticelli P; Guida G; Gregorini G; Possenti S; Moroni G; Leoni A; Pavone L; Pesci A; Sinico RA; Di Toma L; D'Amico M; Tumiati B; D'Ippolito R; Buzio C; Neri TM; Vaglio A
Rheumatology (Oxford); 2012 May; 51(5):805-12. PubMed ID: 22237046
[TBL] [Abstract][Full Text] [Related]
7. Relative importance of CCR5 and antineutrophil cytoplasmic antibodies in patients with Wegener's granulomatosis.
Zhou Y; Huang D; Farver C; Hoffman GS
J Rheumatol; 2003 Jul; 30(7):1541-7. PubMed ID: 12858455
[TBL] [Abstract][Full Text] [Related]
8. The PTPN22 R620W polymorphism associates with RF positive rheumatoid arthritis in a dose-dependent manner but not with HLA-SE status.
Lee AT; Li W; Liew A; Bombardier C; Weisman M; Massarotti EM; Kent J; Wolfe F; Begovich AB; Gregersen PK
Genes Immun; 2005 Mar; 6(2):129-33. PubMed ID: 15674368
[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. 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. 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]
12. 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]
13. 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]
14. 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]
15. Risk of progression from undifferentiated arthritis to rheumatoid arthritis: the effect of the PTPN22 1858T-allele in anti-citrullinated peptide antibody positive patients.
Feitsma AL; Toes RE; Begovich AB; Chokkalingam AP; de Vries RR; Huizinga TW; van der Helm-van Mil AH
Rheumatology (Oxford); 2007 Jul; 46(7):1092-5. PubMed ID: 17341507
[TBL] [Abstract][Full Text] [Related]
16. Association of the PTPN22*R620W polymorphism with autoimmune myasthenia gravis.
Vandiedonck C; Capdevielle C; Giraud M; Krumeich S; Jais JP; Eymard B; Tranchant C; Gajdos P; Garchon HJ
Ann Neurol; 2006 Feb; 59(2):404-7. PubMed ID: 16437561
[TBL] [Abstract][Full Text] [Related]
17. No evidence for association between 1858 C/T single-nucleotide polymorphism of PTPN22 gene and primary Sjögren's syndrome.
Ittah M; Gottenberg JE; Proust A; Hachulla E; Puechal X; Loiseau P; Mariette X; Miceli-Richard C
Genes Immun; 2005 Aug; 6(5):457-8. PubMed ID: 15933742
[TBL] [Abstract][Full Text] [Related]
18. Pathways to gene identification in rheumatoid arthritis: PTPN22 and beyond.
Gregersen PK
Immunol Rev; 2005 Apr; 204():74-86. PubMed ID: 15790351
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
