The CD40 Kozak SNP: a new susceptibility loci for Graves' disease?

The CD40 Kozak SNP: a new susceptibility loci for Graves' disease?

Bibliografiske detaljer
Main Authors:	Simmonds, M, Heward, J, Franklyn, J, Gough, S
Format:	Journal article
Sprog:	English
Udgivet:	2005

Lignende værker

Tag SNP screening of the PDCD1 gene for association with Graves' disease.
af: Newby, P, et al.
Udgivet: (2007)

A single nucleotide polymorphism in the CD40 gene on chromosome 20q (GD-2) provides no evidence for susceptibility to Graves' disease in UK Caucasians.
af: Heward, J, et al.
Udgivet: (2004)

Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study.
af: Newby, P, et al.
Udgivet: (2010)

Sharing of susceptibility loci between autoimmune diseases: lack of association of the insulin gene region with Graves' disease.
af: Allahabadia, A, et al.
Udgivet: (1999)

IL-13 and chromosome 5q31-q33: problems of identifying association within regions of linkage to Graves' disease.
af: Simmonds, M, et al.
Udgivet: (2005)

A systematic approach to the assessment of known TNF-alpha polymorphisms in Graves' disease.
af: Simmonds, M, et al.
Udgivet: (2004)

Association of PTPN22 haplotypes with Graves' disease.
af: Heward, J, et al.
Udgivet: (2007)

Association of the BTNL2 rs2076530 single nucleotide polymorphism with Graves' disease appears to be secondary to DRB1 exon 2 position beta74.
af: Simmonds, M, et al.
Udgivet: (2006)

Use of Tag single nucleotide polymorphisms (SNPs) to screen PTPN21: no association with Graves' disease.
af: Zeitlin, A, et al.
Udgivet: (2006)

Analysis of HLA class II genes in Hashimoto's thyroiditis reveals differences compared to Graves' disease.
af: Zeitlin, A, et al.
Udgivet: (2008)

No association of an interleukin 4 gene promoter polymorphism with Graves' disease in the United Kingdom.
af: Heward, J, et al.
Udgivet: (2001)

Association of FcGRIIa with Graves' disease: a potential role for dysregulated autoantibody clearance in disease onset/progression.
af: Yesmin, K, et al.
Udgivet: (2010)

Contribution of single nucleotide polymorphisms within FCRL3 and MAP3K7IP2 to the pathogenesis of Graves' disease.
af: Simmonds, M, et al.
Udgivet: (2006)

Preliminary evidence for interaction of PTPN12 polymorphism with TSHR genotype and association with Graves' ophthalmopathy.
af: Syed, A, et al.
Udgivet: (2007)

A novel and major association of HLA-C in Graves' disease that eclipses the classical HLA-DRB1 effect.
af: Simmonds, M, et al.
Udgivet: (2007)

Lack of association of the vitamin D receptor gene with Graves' disease in UK Caucasians.
af: Collins, J, et al.
Udgivet: (2004)

Polymorphisms of interleukin 4 receptor gene and interleukin 10 gene are not associated with Graves' disease in the UK.
af: Tait, K, et al.
Udgivet: (2004)

Regression mapping of association between the human leukocyte antigen region and Graves disease.
af: Simmonds, M, et al.
Udgivet: (2005)

MHC class II region, CTLA4 gene, and ophthalmopathy in patients with Graves' disease.
af: Allahabadia, A, et al.
Udgivet: (2001)

Association of the interleukin-2 receptor alpha (IL-2Ralpha)/CD25 gene region with Graves' disease using a multilocus test and tag SNPs.
af: Brand, O, et al.
Udgivet: (2007)

Propylthiouracil and carbimazole associated-antineutrophil cytoplasmic antibodies (ANCA) in patients with Graves' disease.
af: Harper, L, et al.
Udgivet: (2004)

The immunogenetics of Graves' disease
af: Gough, S
Udgivet: (1999)

The genetics of Graves' disease.
af: Gough, S
Udgivet: (2000)

Confirmation of association of chromosome 5q31-33 with United Kingdom Caucasian Graves' disease.
af: Simmonds, M, et al.
Udgivet: (2010)

Association of Fc receptor-like 5 (FCRL5) with Graves' disease is secondary to the effect of FCRL3.
af: Simmonds, M, et al.
Udgivet: (2010)

A nonsense mutation in exon 2 of the DNase I gene is not present in UK subjects with systemic lupus erythematosus and Graves' disease: Comment on the article by Rood et al.
af: Simmonds, M, et al.
Udgivet: (2002)

Genetic susceptibility to the development of autoimmune disease.
af: Heward, J, et al.
Udgivet: (1997)

Association of the thyroid stimulating hormone receptor gene (TSHR) with Graves' disease.
af: Brand, O, et al.
Udgivet: (2009)

Association of the large multifunctional proteasome (LMP2) gene with Graves' disease is a result of linkage disequilibrium with the HLA haplotype DRB1*0304-DQB1*02-DQA1*0501.
af: Heward, J, et al.
Udgivet: (1999)

The development of Graves' disease and the CTLA-4 gene on chromosome 2q33.
af: Heward, J, et al.
Udgivet: (1999)

High-density SNP association study of the autism susceptibility loci on chromosome 7q
af: Sykes, N, et al.
Udgivet: (2006)

Age and gender predict the outcome of treatment for Graves' hyperthyroidism.
af: Allahabadia, A, et al.
Udgivet: (2000)

Susceptibility loci in inflammatory bowel disease.
af: Parkes, M, et al.
Udgivet: (1996)

Association of the TSHR gene with Graves' disease: the first disease specific locus.
af: Dechairo, B, et al.
Udgivet: (2005)

Association of the TSHR gene with Graves' disease: The first disease specific locus
af: Dechairo, B, et al.
Udgivet: (2005)

Seven newly identified loci for autoimmune thyroid disease.
af: Cooper, J, et al.
Udgivet: (2012)

Lack of association between polymorphism of the thyrotropin receptor gene and Graves' disease in United Kingdom and Hong Kong Chinese patients: case control and family-based studies.
af: Allahabadia, A, et al.
Udgivet: (1998)

Thyroid stimulating hormone receptor (TSHR) intron 1 variants are major risk factors for Graves' disease in three European Caucasian cohorts.
af: Płoski, R, et al.
Udgivet: (2010)

Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function
af: Hancock, D, et al.
Udgivet: (2012)

Linkage disequilibrium between the human leukocyte antigen class II region of the major histocompatibility complex and Graves' disease: replication using a population case control and family-based study.
af: Heward, J, et al.
Udgivet: (1998)