PTPN22 1858T is not a risk factor for North American pemphigus vulgaris (Q43883963)

27 November 2017

PTPN22 1858T is not a risk factor for North American pemphigus vulgaris (English)

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27 November 2017

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pemphigus vulgaris

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Amit Sachdev

1

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27 November 2017

Dhaval G Bhanusali

2

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27 November 2017

Kevin C Patterson

3

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27 November 2017

Matt B Zamora

4

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27 November 2017

Apram Ghuman

5

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27 November 2017

John A Gerlach

6

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27 November 2017

Animesh A Sinha

7

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27 November 2017

1 June 2011

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27 November 2017

Experimental Dermatology

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27 November 2017

20

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27 November 2017

514-519

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27 November 2017

6

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Desmoglein autoimmunity in the pathogenesis of pemphigus

27 November 2017

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https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

Targeting pemphigus autoantibodies through their heavy-chain variable region genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

Disease relevant HLA class II alleles isolated by genotypic, haplotypic, and sequence analysis in North American Caucasians with pemphigus vulgaris

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

A newly characterized HLA DQ beta allele associated with pemphigus vulgaris.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

Specific HLA-DQB and HLA-DRB1 alleles confer susceptibility to pemphigus vulgaris

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

Development and characterization of desmoglein-3 specific T cells from patients with pemphigus vulgaris.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

Linkage proof for PTPN22, a rheumatoid arthritis susceptibility gene and a human autoimmunity gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

Identification of substrates of human protein-tyrosine phosphatase PTPN22

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

Genetic variation in PTPN22 corresponds to altered function of T and B lymphocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

Protein tyrosine phosphatase gene C1858T allele confers risk for rheumatoid arthritis in Hungarian subjects

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

A type 1 diabetes subgroup with a female bias is characterised by failure in tolerance to thyroid peroxidase at an early age and a strong association with the cytotoxic T-lymphocyte-associated antigen-4 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

Protein tyrosine phosphatase non-receptor type 22 gene variants at position 1858 are associated with type 1 and type 2 diabetes in Estonian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

PTPN22: setting thresholds for autoimmunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

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/10.1111%2FJ.1600-0625.2011.01272.X

PTPN22 allele polymorphisms in 15 Chinese populations

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

The non-synonymous C1858T substitution in the PTPN22 gene is associated with susceptibility to the severe forms of alopecia areata.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

Consensus statement on definitions of disease, end points, and therapeutic response for pemphigus

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

Pemphigus vulgaris: incidence in Jews of different ethnic groups, according to age, sex, and initial lesion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

Association between the PTPN22 gene and rheumatoid arthritis and juvenile idiopathic arthritis in a UK population: further support that PTPN22 is an autoimmunity gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

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/10.1111%2FJ.1600-0625.2011.01272.X

Cytokine gene polymorphisms in endemic pemphigus foliaceus: a possible role for IL6 variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

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/10.1111%2FJ.1600-0625.2011.01272.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

Susceptibility to type 1 diabetes conferred by the PTPN22 C1858T polymorphism in the Spanish population

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

PTPN22 R620W Functional Variant in Type 1 Diabetes and Autoimmunity Related Traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0625.2011.01272.X

10.1111/J.1600-0625.2011.01272.X

21 January 2018

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DOI

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27 November 2017

1 reference