Coincidence of PTPN22 c.1858CC and FCRL3 -169CC genotypes as a biomarker of preserved residual β-cell function in children with type 1 diabetes.

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Association of protein tyrosine phosphatase non-receptor type 22 gene functional variant C1858T, HLA-DQ/DR genotypes and autoantibodies with susceptibility to type-1 diabetes mellitus in Kuwaiti Arabs.

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Q55429854-784A6A18-47DB-40D6-BCA2-10AD633F4935

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Coincidence of PTPN22 c.1858CC and FCRL3 -169CC genotypes as a biomarker of preserved residual β-cell function in children with type 1 diabetes.

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http://www.wikidata.org/entity/Q48004863

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年學術文章

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2016年學術文章

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Coincidence of PTPN22 c.1858CC ...... children with type 1 diabetes.

@en

Coincidence of PTPN22 c.1858CC ...... children with type 1 diabetes.

@nl

type

Item

label

Coincidence of PTPN22 c.1858CC ...... children with type 1 diabetes.

@en

Coincidence of PTPN22 c.1858CC ...... children with type 1 diabetes.

@nl

prefLabel

Coincidence of PTPN22 c.1858CC ...... children with type 1 diabetes.

@en

Coincidence of PTPN22 c.1858CC ...... children with type 1 diabetes.

@nl

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Coincidence of PTPN22 c.1858CC ...... children with type 1 diabetes

@en

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Anna Balcerska

http://www.w3.org/2001/XMLSchema#string

Grzegorz Krzykowski

http://www.w3.org/2001/XMLSchema#string

Janusz Limon

http://www.w3.org/2001/XMLSchema#string

Julia Kulczycka

http://www.w3.org/2001/XMLSchema#string

Lucyna Morzuch

http://www.w3.org/2001/XMLSchema#string

Małgorzata Pawłowicz

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P2860

Role of PTPN22 in type 1 diabetes and other autoimmune diseases

Protein tyrosine phosphatase PTPN22 in human autoimmunity

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

Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.

Fall in C-peptide during first 2 years from diagnosis: evidence of at least two distinct phases from composite Type 1 Diabetes TrialNet data

The PTPN22 C1858T gene variant is associated with proinsulin in new-onset type 1 diabetes.

Expression of the autoimmune susceptibility gene FcRL3 on human regulatory T cells is associated with dysfunction and high levels of programmed cell death-1.

Why is PTPN22 a good candidate susceptibility gene for autoimmune disease?

Defective suppressor function in CD4(+)CD25(+) T-cells from patients with type 1 diabetes.

Rheumatoid arthritis association with the FCRL3 -169C polymorphism is restricted to PTPN22 1858T-homozygous individuals in a Canadian population.

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696-705

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scholarly article

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10.1111/PEDI.12429

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http://www.w3.org/2001/XMLSchema#string

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http://www.w3.org/2001/XMLSchema#string

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A Stanisławska-Sachadyn

Rafał Filipów

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2016-09-12T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

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27615679

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type-1 diabetes

Coincidence of PTPN22 c.1858CC and FCRL3 -169CC genotypes as a biomarker of preserved residual β-cell function in children with type 1 diabetes.

about

P2860

P2860

Coincidence of PTPN22 c.1858CC and FCRL3 -169CC genotypes as a biomarker of preserved residual β-cell function in children with type 1 diabetes.

description

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type

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P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921