PepT1 oligopeptide transporter (SLC15A1) gene polymorphism in inflammatory bowel disease. - Wikidata - wikimedia - TriplyDB

PepT1 oligopeptide transporter (SLC15A1) gene polymorphism in inflammatory bowel disease.

PepT1 oligopeptide transporter (SLC15A1) gene polymorphism in inflammatory bowel disease.

http://www.wikidata.org/entity/Q47744754

about

Multiple polymorphisms affect expression and function of the neuropeptide S receptor (NPSR1).PepT1 mediates transport of the proinflammatory bacterial tripeptide L-Ala-{gamma}-D-Glu-meso-DAP in intestinal epithelial cells.Nod1 and nod2 are expressed in human and murine renal tubular epithelial cells and participate in renal ischemia reperfusion injury.The peptide transporter PEPT1 is expressed in distal colon in rodents and humans and contributes to water absorption.CD98 expression modulates intestinal homeostasis, inflammation, and colitis-associated cancer in mice Colonic expression of the peptide transporter PEPT1 is downregulated during intestinal inflammation and is not required for NOD2-dependent immune activation.Colonic miRNA expression/secretion, regulated by intestinal epithelial PepT1, plays an important role in cell-to-cell communication during colitis.L-Ala-γ-D-Glu-meso-diaminopimelic acid (DAP) interacts directly with leucine-rich region domain of nucleotide-binding oligomerization domain 1, increasing phosphorylation activity of receptor-interacting serine/threonine-protein kinase 2 and its int The PepT1-NOD2 signaling pathway aggravates induced colitis in mice The role and pathophysiological relevance of membrane transporter PepT1 in intestinal inflammation and inflammatory bowel disease.Apple juice greatly reduces systemic exposure to atenolol Proton-coupled oligopeptide transporter family SLC15: physiological, pharmacological and pathological implications.Identification of Susceptibility Genes of Adult Asthma in French Canadian Women Critical role of PepT1 in promoting colitis-associated cancer and therapeutic benefits of the anti-inflammatory PepT1-mediated tripeptide KPV in a murine model.Genome-wide association analysis reveals variants on chromosome 19 that contribute to childhood risk of chronic otitis media with effusion.Impact of intestinal PepT1 on the kinetics and dynamics of N-formyl-methionyl-leucyl-phenylalanine, a bacterially-produced chemotactic peptide.pH-dependent internalization of muramyl peptides from early endosomes enables Nod1 and Nod2 signaling Drug transporter pharmacogenetics in nucleoside-based therapies.Epithelial transport in inflammatory bowel diseases.Intestinal barrier dysfunction: implications for chronic inflammatory conditions of the bowel.Di- and tripeptide transport in vertebrates: the contribution of teleost fish models.Clinical relevance of intestinal peptide uptake.PepT1 expressed in immune cells has an important role in promoting the immune response during experimentally induced colitis.Lactobacillus plantarum consumption increases PepT1-mediated amino acid absorption by enhancing protein kinase C activity in spontaneously colitic mice.Association between polymorphisms in and genes and development of obesity in Chinese subjects

P2860

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P2860

PepT1 oligopeptide transporter (SLC15A1) gene polymorphism in inflammatory bowel disease.

http://www.wikidata.org/entity/Q47744754

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

@zh-hans

2009年学术文章

@zh-my

2009年学术文章

@zh-sg

2009年學術文章

@yue

2009年學術文章

@zh

2009年學術文章

@zh-hant

name

PepT1 oligopeptide transporter (SLC15A1) gene polymorphism in inflammatory bowel disease.

@en

PepT1 oligopeptide transporter

@nl

type

label

PepT1 oligopeptide transporter (SLC15A1) gene polymorphism in inflammatory bowel disease.

@en

PepT1 oligopeptide transporter

@nl

prefLabel

PepT1 oligopeptide transporter (SLC15A1) gene polymorphism in inflammatory bowel disease.

@en

PepT1 oligopeptide transporter

@nl

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Inflammatory Bowel Diseases

P1476

PepT1 oligopeptide transporter (SLC15A1) gene polymorphism in inflammatory bowel disease.

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P2093

Anna Hellquist

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Colin L Noble

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Francesca Anedda

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Francesca Bresso

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Gunnar B Lindgren

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Jack Satsangi

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Kimmo Kontula

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Leena Halme

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Leif Torkvist

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Maarit Lappalainen

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P2860

Systematic association mapping identifies NELL1 as a novel IBD disease gene

Ulcerative colitis and Crohn's disease in an unselected population of monozygotic and dizygotic twins. A study of heritability and the influence of smoking

The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease

Mechanisms of Disease: pathogenesis of Crohn's disease and ulcerative colitis

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

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

Genes mirror geography within Europe

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

Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci

Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe

P304

1562-1569

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10.1002/IBD.20963

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10

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15

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Ghazaleh Assadi

Martti Färkkilä

Jonas Halfvarson

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2009-10-01T00:00:00Z

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24446512

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19462432

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inflammatory bowel diseases