Low-Frequency IL23R Coding Variant Associated with Crohn's Disease Susceptibility in Japanese Subjects Identified by Personal Genomics Analysis.

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Rare variants in BRCA2 and CHEK2 are associated with the risk of urinary tract cancers.Structural Activation of Pro-inflammatory Human Cytokine IL-23 by Cognate IL-23 Receptor Enables Recruitment of the Shared Receptor IL-12Rβ1.

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Low-Frequency IL23R Coding Variant Associated with Crohn's Disease Susceptibility in Japanese Subjects Identified by Personal Genomics Analysis.

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

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Low-Frequency IL23R Coding Var ...... by Personal Genomics Analysis.

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Low-Frequency IL23R Coding Var ...... by Personal Genomics Analysis.

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Low-Frequency IL23R Coding Var ...... by Personal Genomics Analysis.

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Low-Frequency IL23R Coding Var ...... by Personal Genomics Analysis.

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Low-Frequency IL23R Coding Var ...... by Personal Genomics Analysis.

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Low-Frequency IL23R Coding Var ...... by Personal Genomics Analysis.

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P1476

Low-Frequency IL23R Coding Var ...... by Personal Genomics Analysis.

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Eiichiro Yamamoto

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Hiromu Suzuki

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

Hiroyuki Isshiki

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

Kanna Nagaishi

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Kei Onodera

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Kentaro Kawakami

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

Kentaro Yamashita

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

Kohzoh Imai

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

Takeshi Niinuma

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

Yasuhisa Shinomura

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P2860

A receptor for the heterodimeric cytokine IL-23 is composed of IL-12Rbeta1 and a novel cytokine receptor subunit, IL-23R

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

Disease gene identification strategies for exome sequencing

Exome sequencing and complex disease: practical aspects of rare variant association studies

A method and server for predicting damaging missense mutations

Haploview: analysis and visualization of LD and haplotype maps

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease

Association analysis of genetic variants in IL23R, ATG16L1 and 5p13.1 loci with Crohn's disease in Japanese patients

Functional studies on the IBD susceptibility gene IL23R implicate reduced receptor function in the protective genetic variant R381Q

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e0137801

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scholarly article

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10.1371/JOURNAL.PONE.0137801

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English

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2015-09-16T00:00:00Z

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281852514

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26375822

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Crohn's disease

P932

4574159

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Low-Frequency IL23R Coding Variant Associated with Crohn's Disease Susceptibility in Japanese Subjects Identified by Personal Genomics Analysis.

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P2860

P2860

Low-Frequency IL23R Coding Variant Associated with Crohn's Disease Susceptibility in Japanese Subjects Identified by Personal Genomics Analysis.

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