(Q33236610)

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A functional PTPN22 polymorphism associated with several autoimmune diseases is not associated with IgA deficiency in the Spanish population

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scholarly article

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Europe PubMed Central

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24 July 2017

A functional PTPN22 polymorphism associated with several autoimmune diseases is not associated with IgA deficiency in the Spanish population (English)

1 reference

Europe PubMed Central

PubMed publication ID

24 July 2017

object named as

Elena Urcelay

7

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author name string

Concepción Núñez

1

1 reference

Europe PubMed Central

PubMed publication ID

24 July 2017

Raquel López-Mejías

2

1 reference

Europe PubMed Central

PubMed publication ID

24 July 2017

Alfonso Martínez

3

1 reference

Europe PubMed Central

PubMed publication ID

24 July 2017

M Cruz García-Rodríguez

4

1 reference

Europe PubMed Central

PubMed publication ID

24 July 2017

Miguel Fernández-Arquero

5

1 reference

Europe PubMed Central

PubMed publication ID

24 July 2017

Emilio G de la Concha

6

1 reference

Europe PubMed Central

PubMed publication ID

24 July 2017

publication date

15 March 2006

1 reference

Europe PubMed Central

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24 July 2017

BMC Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

24 July 2017

7

1 reference

Europe PubMed Central

PubMed publication ID

24 July 2017

25

1 reference

Europe PubMed Central

PubMed publication ID

24 July 2017

https://scigraph.springernature.com/pub.10.1186/1471-2350-7-25

0 references

TACI is mutant in common variable immunodeficiency and IgA deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1431514

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1431514

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1431514

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1431514

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1431514

21 June 2018

Fine-scale mapping at IGAD1 and genome-wide genetic linkage analysis implicate HLA-DQ/DR as a major susceptibility locus in selective IgA deficiency and common variable immunodeficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1431514

21 June 2018

Autoimmunity in human primary immunodeficiency diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1431514

21 June 2018

IgA deficiency.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1431514

21 June 2018

The transmission/disequilibrium test: history, subdivision, and admixture

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1431514

21 June 2018

Competition for follicular niches excludes self-reactive cells from the recirculating B-cell repertoire.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1431514

21 June 2018

PTPN22 and autoimmune disease

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-25

21 January 2018

Power and sample size calculations for studies involving linear regression

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-25

21 January 2018

MHC susceptibility genes to IgA deficiency are located in different regions on different HLA haplotypes

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-25

21 January 2018

Primary immunodeficiency diseases. Report of a WHO scientific group

1 reference

https://pubmed.ncbi.nlm.nih.gov/16539704

12 December 2020

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10.1186/1471-2350-7-25

1 reference

Europe PubMed Central

PubMed publication ID

24 July 2017

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release_dk7aafmsvfc3dmmvcnpvtfpvly

1 reference

https://api.fatcat.wiki/v0/release/dk7aafmsvfc3dmmvcnpvtfpvly

24 November 2022

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PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

24 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

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24 July 2017

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