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.
167 related articles for article (PubMed ID: 24117662)
1. A novel single nucleotide polymorphism in the protein tyrosine phosphatase N22 gene (PTPN22) is associated with Type 1 diabetes in a Chinese population. Pei Z; Chen X; Sun C; Du H; Wei H; Song W; Yang Y; Zhang M; Lu W; Cheng R; Luo F Diabet Med; 2014 Feb; 31(2):219-26. PubMed ID: 24117662 [TBL] [Abstract][Full Text] [Related]
2. Systematic search for single nucleotide polymorphisms in a lymphoid tyrosine phosphatase gene (PTPN22): association between a promoter polymorphism and type 1 diabetes in Asian populations. Kawasaki E; Awata T; Ikegami H; Kobayashi T; Maruyama T; Nakanishi K; Shimada A; Uga M; Kurihara S; Kawabata Y; Tanaka S; Kanazawa Y; Lee I; Eguchi K Am J Med Genet A; 2006 Mar; 140(6):586-93. PubMed ID: 16470599 [TBL] [Abstract][Full Text] [Related]
3. The -1123G>C variant of PTPN22 gene promoter is associated with latent autoimmune diabetes in adult Chinese Hans. Liu F; Liu J; Zheng TS; Li Q; Wang C; Pan XP; Lu H; Zhao YW Cell Biochem Biophys; 2012 Mar; 62(2):273-9. PubMed ID: 21956362 [TBL] [Abstract][Full Text] [Related]
4. Associations of protein tyrosine phosphatase nonreceptor 22 (PTPN22) gene polymorphisms with susceptibility to Graves' disease in a Japanese population. Ichimura M; Kaku H; Fukutani T; Koga H; Mukai T; Miyake I; Yamada K; Koda Y; Hiromatsu Y Thyroid; 2008 Jun; 18(6):625-30. PubMed ID: 18578611 [TBL] [Abstract][Full Text] [Related]
5. Association of the PTPN22 gene (+1858C/T, -1123G/C) polymorphisms with type 1 diabetes mellitus: a systematic review and meta-analysis. Tang S; Peng W; Wang C; Tang H; Zhang Q Diabetes Res Clin Pract; 2012 Sep; 97(3):446-52. PubMed ID: 22572103 [TBL] [Abstract][Full Text] [Related]
6. A PTPN22 promoter polymorphism -1123G>C is associated with RA pathogenesis in Chinese. Huang JJ; Qiu YR; Li HX; Sun DH; Yang J; Yang CL Rheumatol Int; 2012 Mar; 32(3):767-71. PubMed ID: 21193990 [TBL] [Abstract][Full Text] [Related]
7. Distribution of PTPN22 polymorphisms in SLE from western Mexico: correlation with mRNA expression and disease activity. Machado-Contreras JR; Muñoz-Valle JF; Cruz A; Salazar-Camarena DC; Marín-Rosales M; Palafox-Sánchez CA Clin Exp Med; 2016 Aug; 16(3):399-406. PubMed ID: 26013387 [TBL] [Abstract][Full Text] [Related]
8. PTPN22 -1123G > C polymorphism is associated with susceptibility to primary immune thrombocytopenia in Chinese population. Ge J; Li H; Gu D; Du W; Xue F; Sui T; Xu J; Yang R Platelets; 2013; 24(6):448-53. PubMed ID: 23098231 [TBL] [Abstract][Full Text] [Related]
9. No independent role of the -1123 G>C and+2740 A>G variants in the association of PTPN22 with type 1 diabetes and juvenile idiopathic arthritis in two Caucasian populations. Cinek O; Hradsky O; Ahmedov G; Slavcev A; Kolouskova S; Kulich M; Sumnik Z Diabetes Res Clin Pract; 2007 May; 76(2):297-303. PubMed ID: 17000021 [TBL] [Abstract][Full Text] [Related]
10. Association of PTPN22 gene polymorphism with type 1 diabetes mellitus in Chinese children and adolescents. Liu HW; Xu RY; Sun RP; Wang Q; Liu JL; Ge W; Yu Z Genet Mol Res; 2015 Jan; 14(1):63-8. PubMed ID: 25729936 [TBL] [Abstract][Full Text] [Related]
11. Further evidence of a primary, causal association of the PTPN22 620W variant with type 1 diabetes. Zoledziewska M; Perra C; Orrù V; Moi L; Frongia P; Congia M; Bottini N; Cucca F Diabetes; 2008 Jan; 57(1):229-34. PubMed ID: 17934143 [TBL] [Abstract][Full Text] [Related]
12. Association Between Protein Tyrosine Phosphatase Non-Receptor Type 22 (PTPN22) Polymorphisms and Risk of Ankylosing Spondylitis: A Meta-analysis. Wang W; Meng X; Liu Y; Ma X; Zhang Q; Li C; Li C; Ren L Med Sci Monit; 2017 May; 23():2619-2624. PubMed ID: 28555069 [TBL] [Abstract][Full Text] [Related]
13. A variant within intron 1 of the PTPN22 gene decreases the genetic susceptibility of ankylosing spondylitis in a central south Chinese Han population. Tang L; Wang Y; Chen BF Scand J Rheumatol; 2014; 43(5):380-4. PubMed ID: 24749936 [TBL] [Abstract][Full Text] [Related]
14. PTPN22 Trp620 explains the association of chromosome 1p13 with type 1 diabetes and shows a statistical interaction with HLA class II genotypes. Smyth DJ; Cooper JD; Howson JM; Walker NM; Plagnol V; Stevens H; Clayton DG; Todd JA Diabetes; 2008 Jun; 57(6):1730-7. PubMed ID: 18305142 [TBL] [Abstract][Full Text] [Related]
15. Meta-analysis reveals PTPN22 1858C/T polymorphism confers susceptibility to rheumatoid arthritis in Caucasian but not in Asian population. Nabi G; Akhter N; Wahid M; Bhatia K; Mandal RK; Dar SA; Jawed A; Haque S Autoimmunity; 2016; 49(3):197-210. PubMed ID: 26763276 [TBL] [Abstract][Full Text] [Related]
16. Association of PTPN22 gene (rs2488457) polymorphism with ulcerative colitis and high levels of PTPN22 mRNA in ulcerative colitis. Chen Z; Zhang H; Xia B; Wang P; Jiang T; Song M; Wu J Int J Colorectal Dis; 2013 Oct; 28(10):1351-8. PubMed ID: 23456301 [TBL] [Abstract][Full Text] [Related]
17. Association of PTPN22+1858C/T polymorphism with Type 1 diabetes in the North Indian population. Kumar N; Kaur G; Kanga U; Tandon N; Caillat-Zucman S; Mehra NK Int J Immunogenet; 2014 Aug; 41(4):318-23. PubMed ID: 24913133 [TBL] [Abstract][Full Text] [Related]
18. Association of polymorphism of NLRP3, ICAM-1, PTPN22, INS genes in childhood onset type 1 diabetes in a Pakistani population. Jabeen A; Riaz S; Usman M; Parveen A; Mukhtar M; Wajid A; Hanif A; Batool A Mol Biol Rep; 2024 Oct; 51(1):1070. PubMed ID: 39425874 [TBL] [Abstract][Full Text] [Related]
19. Role of the C1858T polymorphism of protein tyrosine phosphatase non-receptor type 22 (PTPN22) in children and adolescents with type 1 diabetes. Blasetti A; Di Giulio C; Tumini S; Provenzano M; Rapino D; Comegna L; Prezioso G; Chiuri R; Franchini S; Chiarelli F; Stuppia L Pharmacogenomics J; 2017 Mar; 17(2):186-191. PubMed ID: 26902538 [TBL] [Abstract][Full Text] [Related]
20. STAT4 rs7574865 G/T and PTPN22 rs2488457 G/C polymorphisms influence the risk of developing juvenile idiopathic arthritis in Han Chinese patients. Fan ZD; Wang FF; Huang H; Huang N; Ma HH; Guo YH; Zhang YY; Qian XQ; Yu HG PLoS One; 2015; 10(3):e0117389. PubMed ID: 25781893 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]