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Items: 1 to 20 of 112

1.

A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis.

Begovich AB, Carlton VE, Honigberg LA, Schrodi SJ, Chokkalingam AP, Alexander HC, Ardlie KG, Huang Q, Smith AM, Spoerke JM, Conn MT, Chang M, Chang SY, Saiki RK, Catanese JJ, Leong DU, Garcia VE, McAllister LB, Jeffery DA, Lee AT, Batliwalla F, Remmers E, Criswell LA, Seldin MF, Kastner DL, Amos CI, Sninsky JJ, Gregersen PK.

Am J Hum Genet. 2004 Aug;75(2):330-7. Epub 2004 Jun 18.

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.

3.

Association between the PTPN22 gene and rheumatoid arthritis and juvenile idiopathic arthritis in a UK population: further support that PTPN22 is an autoimmunity gene.

Hinks A, Barton A, John S, Bruce I, Hawkins C, Griffiths CE, Donn R, Thomson W, Silman A, Worthington J.

Arthritis Rheum. 2005 Jun;52(6):1694-9.

4.

PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis.

Carlton VE, Hu X, Chokkalingam AP, Schrodi SJ, Brandon R, Alexander HC, Chang M, Catanese JJ, Leong DU, Ardlie KG, Kastner DL, Seldin MF, Criswell LA, Gregersen PK, Beasley E, Thomson G, Amos CI, Begovich AB.

Am J Hum Genet. 2005 Oct;77(4):567-81. Epub 2005 Aug 10.

5.

The PTPN22 620W allele confers susceptibility to systemic sclerosis: findings of a large case-control study of European Caucasians and a meta-analysis.

Dieudé P, Guedj M, Wipff J, Avouac J, Hachulla E, Diot E, Granel B, Sibilia J, Cabane J, Meyer O, Mouthon L, Kahan A, Boileau C, Allanore Y.

Arthritis Rheum. 2008 Jul;58(7):2183-8. doi: 10.1002/art.23601.

6.

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.

PMID:
17092257
7.

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. doi: 10.1111/j.1399-0039.2007.00987.x. Epub 2008 Jan 7.

PMID:
18179648
8.

Association of protein tyrosine phosphatase 1B gene polymorphisms with type 2 diabetes.

Bento JL, Palmer ND, Mychaleckyj JC, Lange LA, Langefeld CD, Rich SS, Freedman BI, Bowden DW.

Diabetes. 2004 Nov;53(11):3007-12.

9.

A functional haplotype of the PADI4 gene associated with increased rheumatoid arthritis susceptibility in Koreans.

Kang CP, Lee HS, Ju H, Cho H, Kang C, Bae SC.

Arthritis Rheum. 2006 Jan;54(1):90-6.

10.

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.

PMID:
15526003
11.

PTPN22 C1858T polymorphism and human brucellosis.

Bravo MJ, Colmenero JD, Queipo-Ortuño MI, Morata P, Orozco G, Martin J, Alonso A, Caballero A.

Scand J Infect Dis. 2009;41(2):109-12. doi: 10.1080/00365540802641864.

PMID:
19107641
12.

Association of PTPN22 gene functional variants with development of pulmonary tuberculosis in Moroccan population.

Lamsyah H, Rueda B, Baassi L, Elaouad R, Bottini N, Sadki K, Martin J.

Tissue Antigens. 2009 Sep;74(3):228-32. doi: 10.1111/j.1399-0039.2009.01304.x. Epub 2009 Jun 25.

PMID:
19563523
13.

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. Epub 2006 Nov 29.

PMID:
17135225
14.

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.

PMID:
16112033
15.

Protein tyrosine phosphatase PTPN22 in human autoimmunity.

Vang T, Miletic AV, Bottini N, Mustelin T.

Autoimmunity. 2007 Sep;40(6):453-61. Review.

PMID:
17729039
16.

PTPN22 allele polymorphisms in 15 Chinese populations.

Zhang ZH, Chen F, Zhang XL, Jin Y, Bai J, Fu SB.

Int J Immunogenet. 2008 Dec;35(6):433-7. doi: 10.1111/j.1744-313X.2008.00803.x.

PMID:
19046301
17.

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.

18.

Association of a functional polymorphism of PTPN22 encoding a lymphoid protein phosphatase in bilateral Meniere's disease.

Lopez-Escamez JA, Saenz-Lopez P, Acosta L, Moreno A, Gazquez I, Perez-Garrigues H, Lopez-Nevot A, Lopez-Nevot MA.

Laryngoscope. 2010 Jan;120(1):103-7. doi: 10.1002/lary.20650.

PMID:
19780033
19.

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. Epub 2007 Sep 16.

PMID:
17868256
20.

The FCRL3 -169T>C polymorphism is associated with rheumatoid arthritis and shows suggestive evidence of involvement with juvenile idiopathic arthritis in a Scandinavian panel of autoimmune diseases.

Eike MC, Nordang GB, Karlsen TH, Boberg KM, Vatn MH; IBSEN study group, Dahl-Jørgensen K, Rønningen KS, Joner G, Flatø B, Bergquist A, Thorsby E, Førre O, Kvien TK, Undlien DE, Lie BA.

Ann Rheum Dis. 2008 Sep;67(9):1287-91. Epub 2007 Dec 7.

PMID:
18065500

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