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Items: 5

1.

The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease.

Velaga MR, Wilson V, Jennings CE, Owen CJ, Herington S, Donaldson PT, Ball SG, James RA, Quinton R, Perros P, Pearce SH.

J Clin Endocrinol Metab. 2004 Nov;89(11):5862-5.

PMID:
15531553
2.

Role of PTPN22 in type 1 diabetes and other autoimmune diseases.

Bottini N, Vang T, Cucca F, Mustelin T.

Semin Immunol. 2006 Aug;18(4):207-13. Epub 2006 May 11. Review.

PMID:
16697661
3.

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
4.

The putative role of the C1858T polymorphism of protein tyrosine phosphatase PTPN22 gene in autoimmunity.

Gianchecchi E, Palombi M, Fierabracci A.

Autoimmun Rev. 2013 May;12(7):717-25. doi: 10.1016/j.autrev.2012.12.003. Epub 2012 Dec 20. Review.

PMID:
23261816
5.

Lymphoid-specific tyrosine phosphatase (Lyp): a potential drug target for treatment of autoimmune diseases.

Du J, Qiao Y, Sun L, Wang X.

Curr Drug Targets. 2014 Mar;15(3):335-46. Review.

PMID:
24188455

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