Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients. - Wikidata - wikimedia - TriplyDB

Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.

Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.

http://www.wikidata.org/entity/Q37213674

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Association of a TNIP1 polymorphism with Vogt-Koyanagi-Harada syndrome but not with ocular Behcet's disease in Han Chinese.A functional variant of PTPN22 confers risk for Vogt-Koyanagi-Harada syndrome but not for ankylosing spondylitis.Influence of molecular genetics in Vogt-Koyanagi-Harada disease.

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Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.

http://www.wikidata.org/entity/Q37213674

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 03 June 2009

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.

@en

Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.

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type

label

Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.

@en

Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.

@nl

prefLabel

Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.

@en

Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients.

@nl

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Molecular Vision

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Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients

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Hidetoshi Inoko

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

Kazuhiko Yoshida

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

Masao Ota

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

Nobuhisa Mizuki

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

Nobuyoshi Kitaichi

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

Shigeaki Ohno

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

Susumu Ishida

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

Toshie Miura

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

Yoshihiko Katsuyama

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

Yukihiro Horie

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P2860

Allele frequencies and haplotypic associations defined by allelic DNA typing at HLA class I and class II loci in the Japanese population

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

A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis.

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

Score tests for association between traits and haplotypes when linkage phase is ambiguous

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

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

Small ubiquitin-like modifier 4 (SUMO4) polymorphisms and Vogt-Koyanagi-Harada (VKH) syndrome in the Chinese Han population.

PDCD1 genes may protect against extraocular manifestations in Chinese Han patients with Vogt-Koyanagi-Harada syndrome

Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism.

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1115-1119

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scholarly article

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15

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2009-06-03T00:00:00Z

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2690962

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