(Q43013127)

12 November 2017

title

Clinical characteristics and PTPN22 1858C/T variant analysis in Jordanian Arab vitiligo patients (English)

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12 November 2017

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Asem Alkhateeb

1

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12 November 2017

Firas Qarqaz

series ordinal

2

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12 November 2017

Jude Al-Sabah

series ordinal

3

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12 November 2017

Tasnim Al Rashaideh

series ordinal

4

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12 November 2017

publication date

1 June 2010

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Molecular Diagnosis and Therapy

12 November 2017

published in

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12 November 2017

volume

14

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12 November 2017

issue

3

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12 November 2017

page(s)

179-184

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Frontiers and controversies in the pathobiology of vitiligo: separating the wheat from the chaff

12 November 2017

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1 reference

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21 January 2018

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CTLA4 and generalized vitiligo: two genetic association studies and a meta-analysis of published data

21 January 2018

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Autoimmune etiology of generalized vitiligo.

21 January 2018

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NALP1 in vitiligo-associated multiple autoimmune disease

21 January 2018

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Genetic variations in NALP1 are associated with generalized vitiligo in a Romanian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

Association of PTPN22 1858C/T polymorphism with vitiligo susceptibility in Gujarat population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

PTPN22 is genetically associated with risk of generalized vitiligo, but CTLA4 is not.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

The PTPN22-1858C>T (R620W) functional polymorphism is associated with generalized vitiligo in the Romanian population

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03256371

The genetics of generalized vitiligo

21 January 2018

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Cooperative inhibition of T-cell antigen receptor signaling by a complex between a kinase and a phosphatase

21 January 2018

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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/10.1007%2FBF03256371

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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https://api.crossref.org/works/10.1007%2FBF03256371

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

Association of the PTPN22*R620W polymorphism with autoimmune myasthenia gravis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03256371

The definition and assessment of vitiligo: a consensus report of the Vitiligo European Task Force

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

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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https://api.crossref.org/works/10.1007%2FBF03256371

Cutting edge: the PTPN22 allelic variant associated with autoimmunity impairs B cell signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

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/10.1007%2FBF03256371

Association of PTPN22 C1858T and CTLA-4 A49G polymorphisms with Type 1 Diabetes in Croatians

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03256371

The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22) gene predisposes to autoimmune Addison's disease.

21 January 2018

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

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03256371

Effects of PTPN22 C1858T polymorphism on susceptibility and clinical characteristics of British Caucasian rheumatoid arthritis patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

The functional R620W variant of the PTPN22 gene is associated with celiac disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

PTPN22 C1858T polymorphism and human brucellosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

The protein tyrosine phosphatase non-receptor type 22 C1858T polymorphism is a joint susceptibility locus for immunthyroiditis and autoimmune diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

PTPN22 C1858T polymorphism in Colombian patients with autoimmune diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

Association of PTPN22 gene functional variants with development of pulmonary tuberculosis in Moroccan population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

The R620W polymorphism of the protein tyrosine phosphatase 22 gene in autoimmune thyroid diseases and rheumatoid arthritis in the Tunisian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

PTPN22 gene polymorphism in Takayasu's arteritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

Protein tyrosine phosphatase non-receptor type 22 (PTPN22) gene R620W variant and sporadic idiopathic hypoparathyroidism in Asian Indians.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

PTPN22 allele polymorphisms in 15 Chinese populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

Associations of protein tyrosine phosphatase nonreceptor 22 (PTPN22) gene polymorphisms with susceptibility to Graves' disease in a Japanese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

The association of the PTPN22 620W polymorphism with Behcet's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

CTLA4 polymorphisms are associated with vitiligo, in patients with concomitant autoimmune diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

The 620W allele is the PTPN22 genetic variant conferring susceptibility to RA in a Dutch population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03256371

Note on an exact treatment of contingency, goodness of fit and other problems of significance

21 January 2018

1 reference

12 December 2020

Genetic epidemiology and heritability of vitiligo in the Qassim region of Saudi Arabia.

1 reference

12 December 2020

Clinical characteristics in 113 Turkish vitiligo patients.

1 reference

12 December 2020

Epidemiology of vitiligo and associated autoimmune diseases in Caucasian probands and their families

1 reference

12 December 2020

Primer3 on the WWW for general users and for biologist programmers

1 reference

12 December 2020

Association of the PTPN22/LYP gene with type 1 diabetes

1 reference

12 December 2020

The PTPN22 1858T variant is not associated with primary biliary cirrhosis

1 reference

12 December 2020

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

1 reference

12 December 2020

Early disease onset and increased risk of other autoimmune diseases in familial generalized vitiligo

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF03256371

1 reference

12 November 2017

1 reference