PTPN22 C1858T polymorphism in Colombian patients with autoimmune diseases (Q46703705)

24 December 2017

title

PTPN22 C1858T polymorphism in Colombian patients with autoimmune diseases (English)

1 reference

24 December 2017

2

Anaya JM

1 reference

24 December 2017

Gomez LM

1

1 reference

24 December 2017

Gonzalez CI

3

1 reference

24 December 2017

Pineda-Tamayo R

4

1 reference

24 December 2017

Otero W

5

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24 December 2017

Arango A

6

1 reference

24 December 2017

Martín J

7

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24 December 2017

publication date

1 October 2005

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24 December 2017

published in

Genes and Immunity

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24 December 2017

volume

6

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24 December 2017

issue

7

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24 December 2017

page(s)

628-631

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24 December 2017

Clustering of autoimmune disease in parents of siblings from the Type 1 diabetes Warren repository

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

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

21 January 2018

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

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

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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Association of the single nucleotide polymorphism C1858T of the PTPN22 gene with type 1 diabetes

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Confirmation of the association of the R620W polymorphism in the protein tyrosine phosphatase PTPN22 with type 1 diabetes in a family based study

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

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Differential association of the PTPN22 coding variant with autoimmune diseases in a Dutch population

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

21 January 2018

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The common variants/multiple disease hypothesis of common complex genetic disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364261

inferred from DOI database lookup

7 January 2021

based on heuristic

Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364261

inferred from DOI database lookup

7 January 2021

based on heuristic

Spontaneous development of multiple glandular and extraglandular lesions in aged IQI/Jic mice: a model for primary Sjogren's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364261

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.GENE.6364261

1 reference

24 December 2017

1 reference

24 December 2017