CEACAM6 gene variants in inflammatory bowel disease - Test2 - elhamkhani - TriplyDB

CEACAM6 gene variants in inflammatory bowel disease

CEACAM6 gene variants in inflammatory bowel disease

http://www.wikidata.org/entity/Q28740558

about

The role of osteopontin (OPN/SPP1) haplotypes in the susceptibility to Crohn's disease PTPN2 gene variants are associated with susceptibility to both Crohn's disease and ulcerative colitis supporting a common genetic disease background Analysis of IL12B gene variants in inflammatory bowel disease.Recent advances in adherence and invasion of pathogenic Escherichia coli IRGM variants and susceptibility to inflammatory bowel disease in the German population.Characterization of adherent-invasive Escherichia coli isolated from pediatric patients with inflammatory bowel disease.Tsr Chemoreceptor Interacts With IL-8 Provoking E. coli Transmigration Across Human Lung Epithelial Cells.Diet-induced hypoxia responsive element demethylation increases CEACAM6 expression, favouring Crohn's disease-associated Escherichia coli colonisation.

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P2860

CEACAM6 gene variants in inflammatory bowel disease

http://www.wikidata.org/entity/Q28740558

description

2011 nî lūn-bûn

@nan

2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2011年の論文

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2011年論文

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2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

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name

CEACAM6 gene variants in inflammatory bowel disease

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CEACAM6 gene variants in inflammatory bowel disease

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CEACAM6 gene variants in inflammatory bowel disease

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type

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CEACAM6 gene variants in inflammatory bowel disease

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CEACAM6 gene variants in inflammatory bowel disease

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CEACAM6 gene variants in inflammatory bowel disease

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prefLabel

CEACAM6 gene variants in inflammatory bowel disease

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CEACAM6 gene variants in inflammatory bowel disease

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CEACAM6 gene variants in inflammatory bowel disease

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JOURNAL.PONE.0019319

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CEACAM6 gene variants in inflammatory bowel disease

@en

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Burkhard Göke

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

Christiane Wolf

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Christoph Fries

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Cornelia Tillack

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Florian Beigel

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Julia Diegelmann

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Julia Seiderer

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Jürgen Glas

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

Maria Weidinger

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

Peter Lohse

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

P2860

Inflammatory Bowel Disease

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

XBP1 links ER stress to intestinal inflammation and confers genetic risk for human inflammatory bowel disease

Reduced Paneth cell alpha-defensins in ileal Crohn's disease

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

Induction of intestinal Th17 cells by segmented filamentous bacteria

rs224136 on chromosome 10q21.1 and variants in PHOX2B, NCF4, and FAM92B are not major genetic risk factors for susceptibility to Crohn's disease in the German population

CEACAM1: contact-dependent control of immunity

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e19319

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scholarly article

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4172301

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10.1371/JOURNAL.PONE.0019319

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4

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6

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Bertram Müller-Myhsok

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2011-04-29T00:00:00Z

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51114467

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21559399

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inflammatory bowel diseases

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3084820

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