(Q46819653)

25 December 2017

title

Association between PTPN22 C1858T and type 1 diabetes: a replication in continental Italy (English)

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25 December 2017

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10

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author name string

P Saccucci

1

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25 December 2017

E Del Duca

2

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25 December 2017

N Rapini

3

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25 December 2017

A Verrotti

4

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25 December 2017

S Piccinini

5

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25 December 2017

A Maccari

6

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25 December 2017

G Canu

7

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F Angelini

8

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25 December 2017

L Fontana

9

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25 December 2017

F Chiarelli

11

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25 December 2017

M L Manca Bitti

12

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25 December 2017

N Bottini

13

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25 December 2017

publication date

7 January 2008

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25 December 2017

published in

Tissue Antigens

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25 December 2017

volume

71

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25 December 2017

issue

3

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25 December 2017

page(s)

234-237

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25 December 2017

Role of PTPN22 in type 1 diabetes and other autoimmune diseases

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.00987.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.1399-0039.2007.00987.X

The PTPN22 C1858T functional polymorphism and autoimmune diseases--a meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.00987.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.1399-0039.2007.00987.X

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.00987.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.00987.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.00987.X

Ethnic differences in allele frequency of autoimmune-disease-associated SNPs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.00987.X

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.00987.X

Sex-specific association of PTPN22 1858T with type 1 diabetes but not with Hashimoto's thyroiditis or Addison's disease in the German population

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.00987.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.00987.X

No independent role of the -1123 G>C and+2740 A>G variants in the association of PTPN22 with type 1 diabetes and juvenile idiopathic arthritis in two Caucasian populations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.00987.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.1399-0039.2007.00987.X

The 1858T PTPN22 gene variant contributes to a genetic risk of type 1 diabetes in a Ukrainian population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.00987.X

PTPN22 C1858T polymorphism in Colombian patients with autoimmune diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.00987.X

Sex-specific association of the human PTPN22 1858T-allele with type 1 diabetes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.00987.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.00987.X

C1858T functional variant of PTPN22 gene is not associated with celiac disease genetic predisposition

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.00987.X

Lymphoid tyrosine phosphatase (LYP/PTPN22) Arg620Trp variant regulates insulin autoimmunity and progression to type 1 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.00987.X

A Haplotype-Based Analysis of the PTPN22 Locus in Type 1 Diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2007.00987.X

10.1111/J.1399-0039.2007.00987.X

21 January 2018

Identifiers

DOI

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25 December 2017

PubMed ID

18179648

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25 December 2017