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5. 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]
6. 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]
7. 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; 147(1-2):41-6. PubMed ID: 22743847 [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 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]
10. The R620W polymorphism in PTPN22 confers general susceptibility for the development of alopecia areata. Betz RC; König K; Flaquer A; Redler S; Eigelshoven S; Kortüm AK; Hanneken S; Hillmer A; Tüting T; Lambert J; De Weert J; Kruse R; Lutz G; Blaumeiser B; Nöthen MM Br J Dermatol; 2008 Feb; 158(2):389-91. PubMed ID: 18028494 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. PTPN22 is genetically associated with risk of generalized vitiligo, but CTLA4 is not. LaBerge GS; Bennett DC; Fain PR; Spritz RA J Invest Dermatol; 2008 Jul; 128(7):1757-62. PubMed ID: 18200060 [TBL] [Abstract][Full Text] [Related]
14. Association of PTPN22 1858C/T polymorphism with vitiligo susceptibility in Gujarat population. Laddha NC; Dwivedi M; Shajil EM; Prajapati H; Marfatia YS; Begum R J Dermatol Sci; 2008 Mar; 49(3):260-2. PubMed ID: 18037273 [No Abstract] [Full Text] [Related]
15. Clinical characteristics and PTPN22 1858C/T variant analysis in Jordanian Arab vitiligo patients. Alkhateeb A; Qarqaz F; Al-Sabah J; Al Rashaideh T Mol Diagn Ther; 2010 Jun; 14(3):179-84. PubMed ID: 20560680 [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. Protein tyrosine phosphatase PTPN22 in human autoimmunity. Vang T; Miletic AV; Bottini N; Mustelin T Autoimmunity; 2007 Sep; 40(6):453-61. PubMed ID: 17729039 [TBL] [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; 66(7):848-52. PubMed ID: 16112033 [TBL] [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; 54(12):3820-7. PubMed ID: 17133579 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]