Clinical associations of the genetic variants of CTLA-4, Tg, TSHR, PTPN22, PTPN12 and FCRL3 in patients with Graves' disease.
about
Current concepts in the molecular pathogenesis of thyroid-associated ophthalmopathy.Association of the CTLA4 gene with Graves' disease in the Chinese Han population.CTLA4 variants and haplotype contribute genetic susceptibility to myasthenia gravis in northern Chinese population.Human FcR polymorphism and disease.An epistatic interaction between the PAX8 and STK17B genes in papillary thyroid cancer susceptibility.Genetic heterogeneity of susceptibility gene in different ethnic populations: refining association study of PTPN22 for Graves' disease in a Chinese Han population.Association of TLR7 and TSHR copy number variation with Graves' disease and Graves' ophthalmopathy in Chinese population in TaiwanPolymorphisms of the TNFAIP3 region and Graves' disease.The genetic basis of graves' disease.Genetic profiling in Graves' disease: further evidence for lack of a distinct genetic contribution to Graves' ophthalmopathy.Correlation between single nucleotide polymorphism of FCRL-3 gene and Graves' disease in Han population of northern Anhui province, ChinaAssociation between CTLA-4 rs231775 polymorphism and hepatocellular carcinoma susceptibility.The new perspectives on genetic studies of type 2 diabetes and thyroid diseasesCTLA-4 gene polymorphisms and susceptibility to chronic obstructive pulmonary diseaseThe Emerging Role of Epigenetics in Autoimmune Thyroid Diseases.The soluble CTLA-4 receptor and its role in autoimmune diseases: an updateAssociation study between polymorphisms of CD28, CTLA4 and ICOS and non-segmental vitiligo in a Korean population.Variants in PTPN22 and SMOC2 genes and the risk of thyroid disease in the Jordanian Arab population.Functional assessment of the BMPR2 gene in lymphoblastoid cell lines from Graves' disease patients.RNASET2, GPR174, and PTPN22 gene polymorphisms are related to the risk of liver damage associated with the hyperthyroidism in patients with Graves' disease.Association between C1q gene polymorphisms and autoimmune thyroid diseases.Association of polymorphisms of rs179247 and rs12101255 in thyroid stimulating hormone receptor intron 1 with an increased risk of Graves' disease: A meta-analysis.The Fc receptor-like 3 gene polymorphisms and susceptibility to autoimmune diseases: an updated meta-analysis.Correlation between CTLA-4 and CD40 gene polymorphisms and their interaction in graves' disease in a Chinese Han populationAssociation of Hashimoto's thyroiditis with cytotoxic T lymphocyte-associated antigen-4 (CTLA-4) and inducible co-stimulator (ICOS) genes in a Kuwaiti populationAssociations between autoimmune thyroid disease prognosis and functional polymorphisms of susceptibility genes, CTLA4, PTPN22, CD40, FCRL3, and ZFAT, previously revealed in genome-wide association studiesNovel missense mutation in PTPN22 in a Chinese pedigree with Hashimoto's thyroiditis
P2860
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P2860
Clinical associations of the genetic variants of CTLA-4, Tg, TSHR, PTPN22, PTPN12 and FCRL3 in patients with Graves' disease.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
2009年论文
@zh
2009年论文
@zh-cn
name
Clinical associations of the g ...... patients with Graves' disease.
@en
Clinical associations of the g ...... patients with Graves' disease.
@nl
type
label
Clinical associations of the g ...... patients with Graves' disease.
@en
Clinical associations of the g ...... patients with Graves' disease.
@nl
prefLabel
Clinical associations of the g ...... patients with Graves' disease.
@en
Clinical associations of the g ...... patients with Graves' disease.
@nl
P2093
P1476
Clinical associations of the g ...... patients with Graves' disease.
@en
P2093
Guang Ning
Huai-dong Song
Min-jia Zhang
Shuang-xia Zhao
Yong-ju Zhao
P304
P356
10.1111/J.1365-2265.2009.03617.X
P577
2009-04-27T00:00:00Z