Butyrate produced by commensal bacteria potentiates phorbol esters induced AP-1 response in human intestinal epithelial cells - Wikidata - awgldk - TriplyDB

Butyrate produced by commensal bacteria potentiates phorbol esters induced AP-1 response in human intestinal epithelial cells

Butyrate produced by commensal bacteria potentiates phorbol esters induced AP-1 response in human intestinal epithelial cells

http://www.wikidata.org/entity/Q34541325

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Gut/brain axis and the microbiota Brain-gut microbiome interactions and functional bowel disorders Probiotics, prebiotics and immunomodulation of gut mucosal defences: homeostasis and immunopathology Resistant starch: promise for improving human health A potential anti-tumor effect of leukotriene C4 through the induction of 15-hydroxyprostaglandin dehydrogenase expression in colon cancer cells Exploring the influence of the gut microbiota and probiotics on health: a symposium report.Mechanisms of intestinal adaptation.Antibiotics, birth mode, and diet shape microbiome maturation during early life.A phylogenomic view of ecological specialization in the Lachnospiraceae, a family of digestive tract-associated bacteria.Commensal gut bacteria modulate phosphorylation-dependent PPARγ transcriptional activity in human intestinal epithelial cells.Breaking down the gut microbiome composition in multiple sclerosis.Investigation of faecal volatile organic metabolites as novel diagnostic biomarkers in inflammatory bowel disease.Dietary inhibitors of histone deacetylases in intestinal immunity and homeostasis An Integrated Outlook on the Metagenome and Metabolome of Intestinal Diseases.Role of intestinal flora in colorectal cancer from the metabolite perspective: a systematic review.Killed Whole-Cell Oral Cholera Vaccine Induces CCL20 Secretion by Human Intestinal Epithelial Cells in the Presence of the Short-Chain Fatty Acid, Butyrate.Human Gut Microbiota and Gastrointestinal Cancer.Screening of genotoxicity and mutagenicity in extractable organics from oil sands process-affected water.Butyrate produced by gut commensal bacteria activates TGF-beta1 expression through the transcription factor SP1 in human intestinal epithelial cells.

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Butyrate produced by commensal bacteria potentiates phorbol esters induced AP-1 response in human intestinal epithelial cells

http://www.wikidata.org/entity/Q34541325

description

2012 nî lūn-bûn

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2012 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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name

Butyrate produced by commensal ...... an intestinal epithelial cells

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Butyrate produced by commensal ...... an intestinal epithelial cells

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Butyrate produced by commensal ...... an intestinal epithelial cells

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Butyrate produced by commensal ...... an intestinal epithelial cells

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Butyrate produced by commensal ...... an intestinal epithelial cells

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Butyrate produced by commensal ...... an intestinal epithelial cells

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Butyrate produced by commensal ...... an intestinal epithelial cells

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Butyrate produced by commensal ...... an intestinal epithelial cells

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Butyrate produced by commensal ...... an intestinal epithelial cells

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Butyrate produced by commensal ...... an intestinal epithelial cells

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Antonietta Cultrone

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Fabienne Béguet-Crespel

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

Hervé M Blottière

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Joël Doré

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Karine Le Roux

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Malgorzata Nepelska

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Vermulugesan Arulampalam

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P2860

Fusobacterium nucleatum infection is prevalent in human colorectal carcinoma

Genomic analysis identifies association of Fusobacterium with colorectal carcinoma

A human gut microbial gene catalogue established by metagenomic sequencing

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Towards the human intestinal microbiota phylogenetic core

Association between low colonic short-chain fatty acids and high bile acids in high colon cancer risk populations

Signal transduction by the c-Jun N-terminal kinase (JNK)--from inflammation to development

AP-1 subunits: quarrel and harmony among siblings

The role of Jun, Fos and the AP-1 complex in cell-proliferation and transformation

Anticancer activities of histone deacetylase inhibitors

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