Association between genetic variants in myosin IXB and Crohn's disease. - Wikidata - wikimedia - TriplyDB

Association between genetic variants in myosin IXB and Crohn's disease.

Association between genetic variants in myosin IXB and Crohn's disease.

http://www.wikidata.org/entity/Q43981539

about

Myosins in cell junctions The myosin superfamily at a glance.Association of MYO9B gene polymorphisms with inflammatory bowel disease in Chinese Han population.Genotype/phenotype analyses for 53 Crohn's disease associated genetic polymorphisms.Association analysis of genetic variants in the myosin IXB gene in acute pancreatitis A role for myosin IXb, a motor-RhoGAP chimera, in epithelial wound healing and tight junction regulation.Mice lacking myosin IXb, an inflammatory bowel disease susceptibility gene, have impaired intestinal barrier function and superficial ulceration in the ileum.The intestinal epithelial barrier: a therapeutic target?MYO9B gene polymorphisms are associated with the risk of inflammatory bowel diseases.T300A polymorphism of ATG16L1 and susceptibility to inflammatory bowel diseases: a meta-analysis.The RhoGAP activity of myosin IXB is critical for osteoclast podosome patterning, motility, and resorptive capacity.IBD candidate genes and intestinal barrier regulation.Myosin IXb variants and their pivotal role in maintaining the intestinal barrier: a study in Crohn's disease.Cell-Cell Junctions Organize Structural and Signaling Networks.The RhoGAP Myo9b Promotes Bone Growth by Mediating Osteoblastic Responsiveness to IGF-1.Myo9B is associated with an increased risk of Barrett's esophagus and esophageal adenocarcinoma

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P2860

Association between genetic variants in myosin IXB and Crohn's disease.

http://www.wikidata.org/entity/Q43981539

description

2009 nî lūn-bûn

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2009年の論文

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年學術文章

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2009年學術文章

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2009年學術文章

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name

Association between genetic variants in myosin IXB and Crohn's disease.

@en

Association between genetic variants in myosin IXB and Crohn's disease.

@nl

type

label

Association between genetic variants in myosin IXB and Crohn's disease.

@en

Association between genetic variants in myosin IXB and Crohn's disease.

@nl

prefLabel

Association between genetic variants in myosin IXB and Crohn's disease.

@en

Association between genetic variants in myosin IXB and Crohn's disease.

@nl

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Inflammatory Bowel Diseases

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Association between genetic variants in myosin IXB and Crohn's disease

@en

P2093

Alessandra Geremia

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

Andrew Morris

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

Changcun Guo

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

Derek P Jewell

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J R Fraser Cummings

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John Beckly

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Laura Hancock

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P2860

Systematic association mapping identifies NELL1 as a novel IBD disease gene

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

Myosin IXb is a single-headed minus-end-directed processive motor

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

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

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

Haploview: analysis and visualization of LD and haplotype maps

Myosin-IXb is a single-headed and processive motor

Association analysis of MYO9B gene polymorphisms with celiac disease in a Swedish/Norwegian cohort

Physical mapping of human myosin-IXB (MYO9B), the human orthologue of the rat myosin myr 5, to chromosome 19p13.1

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1014-1021

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10.1002/IBD.20885

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15

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