Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease (Q46732649)

24 December 2017

title

Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease (English)

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24 December 2017

9

Dag E Undlien

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24 December 2017

2

Eystein S Husebye

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24 December 2017

Elizabeth Helen Kemp

7

E Helen Kemp

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24 December 2017

Beate Skinningsrud

1

Beate Skinningsrud

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24 December 2017

Kristian Løvås

4

Kristian Løvås

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24 December 2017

Anette Susanne Bøe Wolff

6

Anette B Wolff

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24 December 2017

Kristina Gervin

3

Kristina Gervin

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24 December 2017

Anne Blomhoff

5

Anne Blomhoff

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24 December 2017

author name string

Thore Egeland

8

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24 December 2017

publication date

27 February 2008

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24 December 2017

European Journal of Human Genetics

published in

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24 December 2017

volume

16

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24 December 2017

issue

8

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24 December 2017

page(s)

977-982

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24 December 2017

https://scigraph.springernature.com/pub.10.1038/ejhg.2008.33

exact match

0 references

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

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PTPN22 and autoimmune disease

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Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variant

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

21 January 2018

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A functional polymorphism (1858C/T) in the PTPN22 gene is linked and associated with type I diabetes in multiplex families

21 January 2018

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Replication of an association between the lymphoid tyrosine phosphatase locus (LYP/PTPN22) with type 1 diabetes, and evidence for its role as a general autoimmunity locus

21 January 2018

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

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

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Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE.

21 January 2018

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Association analysis of the 1858C>T polymorphism in the PTPN22 gene in juvenile idiopathic arthritis and other autoimmune diseases

21 January 2018

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The PTPN22 C1858T functional polymorphism and autoimmune diseases--a meta-analysis

21 January 2018

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Sex-specific association of PTPN22 1858T with type 1 diabetes but not with Hashimoto's thyroiditis or Addison's disease in the German population

21 January 2018

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Further evidence of a primary, causal association of the PTPN22 620W variant with type 1 diabetes.

21 January 2018

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Evidence for susceptibility determinant(s) to psoriasis vulgaris in or near PTPN22 in German patients

21 January 2018

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

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A haplotype map of the human genome

21 January 2018

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A Haplotype-Based Analysis of the PTPN22 Locus in Type 1 Diabetes

21 January 2018

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Autoimmune diseases: a leading cause of death among young and middle-aged women in the United States

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7 January 2021

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7 January 2021

The new genomics: global views of biology

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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

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7 January 2021

A cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism is associated with autoimmune Addison's disease in English patients

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7 January 2021

Identifiers

DOI

10.1038/EJHG.2008.33

1 reference

24 December 2017

release_fhbdkpggfbainaidsvfylfwmna

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/fhbdkpggfbainaidsvfylfwmna

24 November 2022

mapped directly with Wikidata item

PubMed ID

18301444

1 reference

24 December 2017