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毒性弥漫性甲状腺肿与CTLA-4易感基因关系研究进展 被引量:2

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出处 《社区医学杂志》 2010年第21期21-23,共3页 Journal Of Community Medicine
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  • 1王巧宏,任跃忠.中国人CTLA-4基因外显子1多态性与Graves病的相关性[J].中华内分泌代谢杂志,2003,19(4):297-299. 被引量:11
  • 2Mustelin T, Alonso A, Bottini N, et al. Protein tyrosine phosphatases in T cell physiology[J].Mol lmmunol, 2004, 41(6 -7) : 687 -700.
  • 3Chelala C, Duchatelet S, Joffret ML, et al. PTPN22 R620W functional variant in type 1 diabetes and autoimmunity related traits[J].Diabetes, 2007, 56(2): 522-556.
  • 4Wesoly J, Hu X, Thabet MM, et al. The 620W allele is the PTPN22 genetic variant conferring susceptibility to RA in a Dutch population [ J ]. Rheumatology ( Oxford), 2007, 46 ( 4 ) : 617 - 621.
  • 5Heward JM, Brand OJ, Barrett JC, et al. Association of PTPN22 haplotypes with Graves' disease[ J ]. J Clin Endocrinol Metat, 2007, 92 (2) : 685 -690.
  • 6Kyogoku C, Langefeld CD, Ortmann WA, et al. Genetic assoCiation of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE[J]. Am JHum Genet, 2004, 75(3) : 504 -507.
  • 7Ikari K, Momohara S, Inoue E, et al. Haplotype analysis revealed no assoCiation between the PTPN22 gene and RA in a Japanese population [ J ]. Rheumatology ( Oxford), 2006, 45 ( 11 ) : 1345 - 1348.
  • 8Kawasaki E, Awata T, Ikegami H, et al. 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 [ J]. Am J Med Genet A, 2007, 143 (15): 1812-1813.
  • 9Ban Y, Tozaki T, Taniyama M, et al. The codon 620 single nucleotide polymorphism of the protein tyrosine phosphatase-22 gene does not contribute to autoimmune thyroid disease susceptibility in the Japanese [J]. Thyroid, 2005, 15(10): 1115-1118.
  • 10Juliger S, Bongartz M, Luty A J, et al. Functional analysis of a promoter variant of the gene encoding the interferon-gamma receptor chain Ⅰ[J]. Immunogenetics, 2003, 54( 10): 675 -680.

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