Use of Tag single nucleotide polymorphisms (SNPs) to screen PTPN21: no association with Graves' disease. (Q34558663)

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29 December 2019

title

Use of Tag single nucleotide polymorphisms (SNPs) to screen PTPN21: no association with Graves' disease (English)

1 reference

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single-nucleotide polymorphism

29 December 2019

main subject

1 reference

7

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29 December 2019

author name string

Zeitlin AA

1

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29 December 2019

Heward JM

2

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29 December 2019

Brand OJ

3

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29 December 2019

Newby PR

4

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29 December 2019

Franklyn JA

5

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29 December 2019

Gough SC

6

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publication date

1 September 2006

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29 December 2019

published in

Clinical Endocrinology

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29 December 2019

volume

65

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issue

3

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29 December 2019

page(s)

380-384

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A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes

29 December 2019

cites work

1 reference

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

21 January 2018

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

21 January 2018

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

21 January 2018

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HLA , CTLA-4 and PTPN22 : the shared genetic master-key to autoimmunity?

21 January 2018

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Protein-tyrosine phosphatase D1, a potential regulator and effector for Tec family kinases

21 January 2018

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New insights into the regulation and functions of Tec family tyrosine kinases in the immune system

21 January 2018

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Bruton tyrosine kinase is tyrosine phosphorylated and activated in pre-B lymphocytes and receptor-ligated B cells

21 January 2018

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Tec kinases: modulators of lymphocyte signaling and development

21 January 2018

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Activation of Bruton's tyrosine kinase (BTK) by a point mutation in its pleckstrin homology (PH) domain

21 January 2018

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Src kinase associates with a member of a distinct subfamily of protein-tyrosine phosphatases containing an ezrin-like domain

21 January 2018

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Common and unique susceptibility loci in Graves and Hashimoto diseases: results of whole-genome screening in a data set of 102 multiplex families

21 January 2018

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Contribution of single nucleotide polymorphisms within FCRL3 and MAP3K7IP2 to the pathogenesis of Graves' disease.

21 January 2018

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Haploview: analysis and visualization of LD and haplotype maps

21 January 2018

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Genome-wide association studies: theoretical and practical concerns

21 January 2018

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Regression mapping of association between the human leukocyte antigen region and Graves disease

21 January 2018

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Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

21 January 2018

1 reference

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Association of the TSHR gene with Graves' disease: the first disease specific locus.

21 January 2018

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A genome-wide screen in 1119 relative pairs with autoimmune thyroid disease.

21 January 2018

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Discovery, linkage disequilibrium and association analyses of polymorphisms of the immune complement inhibitor, decay-accelerating factor gene (DAF/CD55) in type 1 diabetes

21 January 2018

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Lymphoid tyrosine phosphatase (PTPN22/LYP) variant and Graves' disease in a Polish population: association and gene dose-dependent correlation with age of onset

21 January 2018

1 reference

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10.1111/J.1365-2265.2006.02608.X

21 January 2018

Identifiers

DOI

1 reference

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29 December 2019

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