Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease. - Wikidata - awgldk - TriplyDB

Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease.

Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease.

http://www.wikidata.org/entity/Q35597793

about

Systematic association mapping identifies NELL1 as a novel IBD disease gene Crohn's disease: an immune deficiency state Functional role of the 503F variant of the organic cation transporter OCTN1 in Crohn's disease Role of genetics in the diagnosis and prognosis of Crohn's disease Role of discs large homolog 5 OCTNs: will the real IBD5 gene please stand up?Single nucleotide polymorphisms of OCTN1, OCTN2, and DLG5 genes in Greek patients with Crohn's disease The promise and perils of interpreting genetic associations in Crohn's disease.The NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants Xenobiotic, bile acid, and cholesterol transporters: function and regulation.Contribution of genetics to a new vision in the understanding of inflammatory bowel disease.Prevalence of SLC22A4, SLC22A5 and CARD15 gene mutations in Hungarian pediatric patients with Crohn's disease.Is the disease course predictable in inflammatory bowel diseases?Role of CARD15, DLG5 and OCTN genes polymorphisms in children with inflammatory bowel diseases.Novel genetic markers in inflammatory bowel disease.The role of heredity in pterygium development PTGER4 expression-modulating polymorphisms in the 5p13.1 region predispose to Crohn's disease and affect NF-κB and XBP1 binding sites Role of genetics in the diagnosis and prognosis of Crohn's disease The NOD2 Single Nucleotide Polymorphism rs72796353 (IVS4+10 A>C) Is a Predictor for Perianal Fistulas in Patients with Crohn's Disease in the Absence of Other NOD2 Mutations Evidence for association of OCTN genes and IBD5 with ulcerative colitis Analysis of the influence of OCTN1/2 variants within the IBD5 locus on disease susceptibility and growth indices in early onset inflammatory bowel disease Current status of genetics research in inflammatory bowel disease.Spontaneous development of intestinal and colonic atrophy and inflammation in the carnitine-deficient jvs (OCTN2(-/-)) mice Role of the IBD5 susceptibility locus in the inflammatory bowel diseases.Current concept on the pathogenesis of inflammatory bowel disease-crosstalk between genetic and microbial factors: pathogenic bacteria and altered bacterial sensing or changes in mucosal integrity take "toll" ?Genetic variants and the risk of Crohn's disease: what does it mean for future disease management?Review article: genetic susceptibility and application of genetic testing in clinical management of inflammatory bowel disease.Genetics of inflammatory bowel disease: current status and future directions.Transport of butyryl-L-carnitine, a potential prodrug, via the carnitine transporter OCTN2 and the amino acid transporter ATB(0,+)Genetics of the innate immune response in inflammatory bowel disease.Molecular pathogenesis of inflammatory bowel disease: genotypes, phenotypes and personalized medicine.Genetic factors associated with the development of inflammatory bowel disease.Inflammatory bowel disease: genetic and epidemiologic considerations Meta-analysis of associations between DLG5 R30Q and P1371Q polymorphisms and susceptibility to inflammatory bowel disease OCTN and CARD15 gene polymorphism in Chinese patients with inflammatory bowel disease.Genetic dissection of inflammatory bowel disease: unravelling etiology and improving diagnostics.NOD2/CARD15 genotype influences MDP-induced cytokine release and basal IL-12p40 levels in primary isolated peripheral blood monocytes.New IBD genes?Association between genetic variants in myosin IXB and Crohn's disease.

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Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease.

http://www.wikidata.org/entity/Q35597793

description

2005 nî lūn-bûn

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2005年论文

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2005年论文

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2005年论文

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name

Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease.

@ast

Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease.

@en

type

label

Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease.

@ast

Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease.

@en

prefLabel

Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease.

@ast

Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease.

@en

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Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease

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B Müller-Myhsok

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C Folwaczny

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C Neugebauer

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C Tillack

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F Schnitzler

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G Brünnler

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H-P Török

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J Glas

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J Seiderer

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L Tonenchi

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P2860

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

A New Statistical Method for Haplotype Reconstruction from Population Data

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

Functional variants of OCTN cation transporter genes are associated with Crohn disease

Genetic variation in DLG5 is associated with inflammatory bowel disease

A risk haplotype in the Solute Carrier Family 22A4/22A5 gene cluster influences phenotypic expression of Crohn's disease

A comparison of bayesian methods for haplotype reconstruction from population genotype data.

A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetes

Genetic evidence for interaction of the 5q31 cytokine locus and the CARD15 gene in Crohn disease.

IBD5 is a general risk factor for inflammatory bowel disease: replication of association with Crohn disease and identification of a novel association with ulcerative colitis.

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