Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2008-5-23
pubmed:abstractText
HIF plays a central role in the transcriptional response to changes in oxygen availability. The PHD family of oxygen-dependent prolyl hydroxylases plays a pivotal role in regulating HIF stability. The biochemical properties of these enzymes make them well suited to act as oxygen sensors. They also respond to other intracellular signals, including reactive oxygen species, nitric oxide, and certain metabolites, that can modulate the hypoxic response. HIF transcriptional activity is further tuned by FIH1-mediated asparagine hydroxylation. HIF affects signaling pathways that influence development, metabolism, inflammation, and integrative physiology. Accordingly, HIF-modulatory drugs are now being developed for diverse diseases.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Ascorbic Acid, http://linkedlifedata.com/resource/pubmed/chemical/Asparagine, http://linkedlifedata.com/resource/pubmed/chemical/HIF1AN protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Hypoxia-Inducible Factor 1, http://linkedlifedata.com/resource/pubmed/chemical/Iron, http://linkedlifedata.com/resource/pubmed/chemical/Isoenzymes, http://linkedlifedata.com/resource/pubmed/chemical/Mixed Function Oxygenases, http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide, http://linkedlifedata.com/resource/pubmed/chemical/Oxygen, http://linkedlifedata.com/resource/pubmed/chemical/Procollagen-Proline Dioxygenase, http://linkedlifedata.com/resource/pubmed/chemical/Reactive Oxygen Species, http://linkedlifedata.com/resource/pubmed/chemical/Repressor Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1097-4164
pubmed:author
pubmed:issnType
Electronic
pubmed:day
23
pubmed:volume
30
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
393-402
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:18498744-Animals, pubmed-meshheading:18498744-Ascorbic Acid, pubmed-meshheading:18498744-Asparagine, pubmed-meshheading:18498744-Citric Acid Cycle, pubmed-meshheading:18498744-Enzyme Stability, pubmed-meshheading:18498744-Gene Expression Regulation, pubmed-meshheading:18498744-Humans, pubmed-meshheading:18498744-Hypoxia-Inducible Factor 1, pubmed-meshheading:18498744-Iron, pubmed-meshheading:18498744-Isoenzymes, pubmed-meshheading:18498744-Mixed Function Oxygenases, pubmed-meshheading:18498744-Nitric Oxide, pubmed-meshheading:18498744-Oxygen, pubmed-meshheading:18498744-Procollagen-Proline Dioxygenase, pubmed-meshheading:18498744-Reactive Oxygen Species, pubmed-meshheading:18498744-Repressor Proteins, pubmed-meshheading:18498744-Signal Transduction, pubmed-meshheading:18498744-Transcription, Genetic, pubmed-meshheading:18498744-Transcription Factors
pubmed:year
2008
pubmed:articleTitle
Oxygen sensing by metazoans: the central role of the HIF hydroxylase pathway.
pubmed:affiliation
Howard Hughes Medical Institute, Boston, MA 02115, USA. william_kaelin@dfci.harvard.edu
pubmed:publicationType
Journal Article, Review, Research Support, Non-U.S. Gov't