Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2011-1-4
pubmed:abstractText
Several studies have shown that regions of hypoxia develop in the liver during chronic injury. Furthermore, it has been demonstrated that hypoxia stimulates the release of mediators from hepatic stellate cells (HSCs) that may affect the progression of fibrosis. The mechanism by which hypoxia modulates gene expression in HSCs is not known. Recent studies demonstrated that the hypoxia-activated transcription factor, hypoxia-inducible factor (HIF)-1?, is critical for the development of fibrosis. Accordingly, the hypothesis was tested that HIF-1? is activated in HSCs and regulates the expression of genes important for HSC activation and liver fibrosis.
pubmed:grant
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Basic Helix-Loop-Helix..., http://linkedlifedata.com/resource/pubmed/chemical/Ccr1 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers, http://linkedlifedata.com/resource/pubmed/chemical/Hypoxia-Inducible Factor 1, alpha..., http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-13 Receptor alpha1..., http://linkedlifedata.com/resource/pubmed/chemical/Intramolecular Oxidoreductases, http://linkedlifedata.com/resource/pubmed/chemical/Macrophage Migration-Inhibitory..., http://linkedlifedata.com/resource/pubmed/chemical/Mif protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, CCR1, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, CCR5, http://linkedlifedata.com/resource/pubmed/chemical/endothelial PAS domain-containing...
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1478-3231
pubmed:author
pubmed:copyrightInfo
© 2010 John Wiley & Sons A/S.
pubmed:issnType
Electronic
pubmed:volume
31
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
230-44
pubmed:dateRevised
2011-5-24
pubmed:meshHeading
pubmed-meshheading:20880076-Animals, pubmed-meshheading:20880076-Basic Helix-Loop-Helix Transcription Factors, pubmed-meshheading:20880076-Blotting, Western, pubmed-meshheading:20880076-Cell Hypoxia, pubmed-meshheading:20880076-DNA Primers, pubmed-meshheading:20880076-Gene Expression Regulation, pubmed-meshheading:20880076-Hepatic Stellate Cells, pubmed-meshheading:20880076-Hypoxia-Inducible Factor 1, alpha Subunit, pubmed-meshheading:20880076-Interleukin-13 Receptor alpha1 Subunit, pubmed-meshheading:20880076-Intramolecular Oxidoreductases, pubmed-meshheading:20880076-Liver Cirrhosis, pubmed-meshheading:20880076-Macrophage Migration-Inhibitory Factors, pubmed-meshheading:20880076-Male, pubmed-meshheading:20880076-Mice, pubmed-meshheading:20880076-Mice, Inbred C57BL, pubmed-meshheading:20880076-Microarray Analysis, pubmed-meshheading:20880076-Receptors, CCR1, pubmed-meshheading:20880076-Receptors, CCR5, pubmed-meshheading:20880076-Reverse Transcriptase Polymerase Chain Reaction
pubmed:year
2011
pubmed:articleTitle
Hypoxia-inducible factor-1? regulates the expression of genes in hypoxic hepatic stellate cells important for collagen deposition and angiogenesis.
pubmed:affiliation
Department of Pharmacology, Toxicology, and Experimental Therapeutics, University of Kansas Medical Center, Kansas City, KS 66160, USA. bcopple@kumc.edu
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural