Multiplex family-based study in systemic lupus erythematosus: association between the R620W polymorphism of PTPN22 and the FcgammaRIIa (CD32A) R131 allele. (Q54572337)

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English	Multiplex family-based study in systemic lupus erythematosus: association between the R620W polymorphism of PTPN22 and the FcgammaRIIa (CD32A) R131 allele.	scientific article

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scholarly article

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17092257%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

Multiplex family-based study in systemic lupus erythematosus: association between the R620W polymorphism of PTPN22 and the FcgammaRIIa (CD32A) R131 allele (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17092257%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

systemic lupus erythematosus

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based on heuristic

inferred from title

Luis Martinez-Lostao

6

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17092257%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

Moises Labrador-Horrillo

4

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21 December 2019

author name string

Balada E

1

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21 December 2019

Villarreal-Tolchinsky J

2

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21 December 2019

Ordi-Ros J

3

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21 December 2019

Serrano-Acedo S

5

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21 December 2019

Vilardell-Tarrés M

7

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21 December 2019

publication date

1 November 2006

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21 December 2019

Tissue Antigens

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21 December 2019

68

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21 December 2019

5

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21 December 2019

432-438

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21 December 2019

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00695.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00695.X

21 January 2018

PEST domain-enriched tyrosine phosphatase (PEP) regulation of effector/memory T cells

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00695.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00695.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00695.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00695.X

21 January 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://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00695.X

21 January 2018

A single-nucleotide polymorphism in the gene encoding lymphoid protein tyrosine phosphatase (PTPN22) confers susceptibility to generalised vitiligo

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00695.X

21 January 2018

Informed consent in human experimentation before the Nuremberg code

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00695.X

21 January 2018

Mannose binding lectin (MBL) genotype distributions with relation to serum levels in UK Caucasoids

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00695.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00695.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00695.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00695.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00695.X

21 January 2018

Association of the lymphoid tyrosine phosphatase R620W variant with rheumatoid arthritis, but not Crohn's disease, in Canadian populations

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00695.X

21 January 2018

Association analysis of the R620W polymorphism of protein tyrosine phosphatase PTPN22 in systemic lupus erythematosus families: increased T allele frequency in systemic lupus erythematosus patients with autoimmune thyroid disease

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00695.X

21 January 2018

Association of mannose-binding lectin gene variation with disease severity and infections in a population-based cohort of systemic lupus erythematosus patients.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00695.X

21 January 2018

Mannose binding lectin and FcgammaRIIa (CD32) polymorphism in Spanish systemic lupus erythematosus patients.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00695.X

21 January 2018

The genetics of complex autoimmune diseases: non-MHC susceptibility genes

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00695.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00695.X

21 January 2018

Identifiers

10.1111/J.1399-0039.2006.00695.X

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17092257%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17092257%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

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