(Q51807268)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16671953%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

title

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

1 reference

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20 January 2020

0 references

2

1 reference

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20 January 2020

Alfredo Caro-Maldonado

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16671953%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

Antonio Alcina

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16671953%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

author name string

Fedetz M

1

1 reference

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20 January 2020

Smirnov II

4

1 reference

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20 January 2020

Chvorostinka VN

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16671953%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

Moiseenko TA

6

1 reference

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20 January 2020

publication date

1 May 2006

1 reference

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20 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16671953%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

volume

67

1 reference

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20 January 2020

issue

5

1 reference

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20 January 2020

page(s)

430-433

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16671953%20AND%20SRC:MED&resulttype=core&format=json

A genome-wide search for human type 1 diabetes susceptibility genes

20 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00591.X

CTLA-4 in autoimmune diseases--a general susceptibility gene to autoimmunity?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00591.X

Confirmation of three susceptibility genes to insulin-dependent diabetes mellitus: IDDM4, IDDM5 and IDDM8

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00591.X

A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00591.X

Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00591.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.1399-0039.2006.00591.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.1399-0039.2006.00591.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00591.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.1399-0039.2006.00591.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.1399-0039.2006.00591.X

Protein tyrosine phosphatases in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00591.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.1399-0039.2006.00591.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00591.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.1399-0039.2006.00591.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.1399-0039.2006.00591.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00591.X

PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00591.X

Insulin-dependent diabetes mellitus (IDDM) is associated with CTLA4 polymorphisms in multiple ethnic groups

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00591.X

A search for type 1 diabetes susceptibility genes in families from the United Kingdom

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0039.2006.00591.X

10.1111/J.1399-0039.2006.00591.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16671953%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

1 reference