FUT2: filling the gap between genes and environment in Behçet's disease? - Wikidata - wikimedia - TriplyDB

FUT2: filling the gap between genes and environment in Behçet's disease?

FUT2: filling the gap between genes and environment in Behçet's disease?

http://www.wikidata.org/entity/Q39606833

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Advances in the genetically complex autoinflammatory diseases The immunogenetics of Behçet's disease: A comprehensive review Genetic polymorphisms of C-type lectin receptors in Behcet's disease in a Chinese Han population.Intestinal fucose as a mediator of host-microbe symbiosis.Genetic Variants Underlying Risk of Intracranial Aneurysms: Insights from a GWAS in Portugal.Multicentric Genome-Wide Association Study for Primary Spontaneous Pneumothorax.High-Salt Enhances the Inflammatory Response by Retina Pigment Epithelium Cells following Lipopolysaccharide Stimulation.The potential of genetically guided treatment in Behçet's disease.Dense genotyping of immune-related loci implicates host responses to microbial exposure in Behçet's disease susceptibility.Epithelial glycosylation in gut homeostasis and inflammation.Brief report: association of CCR1, KLRC4, IL12A-AS1, STAT4, and ERAP1 With Behçet's disease in Iranians.Genetics and immunodysfunction underlying Behçet's disease and immunomodulant treatment approaches.A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways.Is Behçet's disease a 'class 1-opathy'? The role of HLA-B*51 in the pathogenesis of Behçet's disease.Behçet syndrome: a contemporary view.GWAS-identified CCR1 and IL10 loci contribute to M1 macrophage-predominant inflammation in Behçet's disease.Vasculitis Pathogenesis: Can We Talk About Precision Medicine?

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P2860

FUT2: filling the gap between genes and environment in Behçet's disease?

http://www.wikidata.org/entity/Q39606833

description

2013 nî lūn-bûn

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FUT2: filling the gap between genes and environment in Behçet's disease?

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FUT2: filling the gap between genes and environment in Behçet's disease?

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FUT2: filling the gap between genes and environment in Behçet's disease?

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FUT2: filling the gap between genes and environment in Behçet's disease?

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FUT2: filling the gap between genes and environment in Behçet's disease?

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FUT2: filling the gap between genes and environment in Behçet's disease?

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ANNRHEUMDIS-2013-204475

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Annals of the Rheumatic Diseases

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FUT2: filling the gap between genes and environment in Behçet's disease?

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Abdolhadi Nadji

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Bahar Sadeghi Abdollahi

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Fahmida Ghaderibarim

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Farhad Shahram

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Inês Sousa

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Mafalda Matos

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Niloofar Mojarad Shafiee

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Sofia A Oliveira

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P2860

Sequence and expression of a candidate for the human Secretor blood group alpha(1,2)fucosyltransferase gene (FUT2). Homozygosity for an enzyme-inactivating nonsense mutation commonly correlates with the non-secretor phenotype

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

Identification of disease causing loci using an array-based genotyping approach on pooled DNA.

Haploview: analysis and visualization of LD and haplotype maps

Human susceptibility and resistance to Norwalk virus infection

Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study

Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet's disease susceptibility loci

Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1

Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

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3

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Fereydoun Davatchi

Manuela M. Oliveira

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2013-12-10T00:00:00Z

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259270361

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Behcet's disease