(Q46525705)

22 December 2017

title

No evidence for association between 1858 C/T single-nucleotide polymorphism of PTPN22 gene and primary Sjögren's syndrome (English)

1 reference

22 December 2017

single-nucleotide polymorphism

main subject

1 reference

5

1 reference

22 December 2017

author name string

Ittah M

1

1 reference

22 December 2017

Gottenberg JE

2

1 reference

22 December 2017

Proust A

3

1 reference

22 December 2017

Hachulla E

4

1 reference

22 December 2017

Loiseau P

6

1 reference

22 December 2017

Mariette X

7

1 reference

22 December 2017

Miceli-Richard C

8

1 reference

22 December 2017

publication date

1 August 2005

1 reference

22 December 2017

published in

Genes and Immunity

1 reference

22 December 2017

volume

6

1 reference

22 December 2017

page(s)

457-458

1 reference

22 December 2017

issue

5

1 reference

22 December 2017

https://scigraph.springernature.com/pub.10.1038/sj.gene.6364229

exact match

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364229

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364229

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364229

Association of a functional single-nucleotide polymorphism of PTPN22, encoding lymphoid protein phosphatase, with rheumatoid arthritis and systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364229

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364229

Protein tyrosine phosphorylation in T cell signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364229

Primary Sjögren's syndrome and other autoimmune diseases in families. Prevalence and immunogenetic studies in six kindreds

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364229

The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364229

Association of transforming growth factor beta1 and tumor necrosis factor alpha polymorphisms with anti-SSB/La antibody secretion in patients with primary Sjögren's syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364229

In primary Sjögren's syndrome, HLA class II is associated exclusively with autoantibody production and spreading of the autoimmune response

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364229

Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364229

21 January 2018

Identifiers

DOI

10.1038/SJ.GENE.6364229

1 reference

22 December 2017

PubMed ID

15933742

1 reference

22 December 2017