Variants in ZNF365 isoform D are associated with Crohn's disease. - Wikidata - awgldk - TriplyDB

Variants in ZNF365 isoform D are associated with Crohn's disease.

Variants in ZNF365 isoform D are associated with Crohn's disease.

http://www.wikidata.org/entity/Q35648463

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Genome-wide association analysis and genomic prediction of Mycobacterium avium subspecies paratuberculosis infection in US Jersey cattle Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained.Nutrigenetics, nutrigenomics and inflammatory bowel diseases.Genome-wide association study and admixture mapping reveal new loci associated with total IgE levels in Latinos.11q13 is a susceptibility locus for hormone receptor positive breast cancer.Nutrigenomics: A controversy.A genome-wide association study of central corneal thickness in Latinos.Trans-ethnic fine mapping identifies a novel independent locus at the 3' end of CDKAL1 and novel variants of several susceptibility loci for type 2 diabetes in a Han Chinese population Genetic associations with adverse events from anti-tumor necrosis factor therapy in inflammatory bowel disease patients.

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P2860

Variants in ZNF365 isoform D are associated with Crohn's disease.

http://www.wikidata.org/entity/Q35648463

description

2011 nî lūn-bûn

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2011年の論文

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2011年論文

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2011年论文

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name

Variants in ZNF365 isoform D are associated with Crohn's disease.

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Variants in ZNF365 isoform D are associated with Crohn's disease.

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type

label

Variants in ZNF365 isoform D are associated with Crohn's disease.

@ast

Variants in ZNF365 isoform D are associated with Crohn's disease.

@en

prefLabel

Variants in ZNF365 isoform D are associated with Crohn's disease.

@ast

Variants in ZNF365 isoform D are associated with Crohn's disease.

@en

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Variants in ZNF365 isoform D are associated with Crohn's disease.

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Andrew Ippoliti

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Arie Levine

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Carrie Derkowski

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David Q Shih

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Debra Dutridge

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Dermot P B McGovern

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Emebet Mengesha

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

Eric A Vasilauskas

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Gil Y Melmed

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Kent D Taylor

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

P2860

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

Centrosomal proteins Nde1 and Su48 form a complex regulated by phosphorylation

Identification of a novel gene and a common variant associated with uric acid nephrolithiasis in a Sardinian genetic isolate.

Identification of a new candidate locus for uric acid nephrolithiasis.

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

A second generation human haplotype map of over 3.1 million SNPs

Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

PLINK: a tool set for whole-genome association and population-based linkage analyses

An isoform of ZBP-89 predisposes the colon to colitis

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Talin Haritunians

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Jerome I Rotter

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Crohn's disease

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