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dc.contributor.advisorSmith, Owen
dc.contributor.authorBalding, Joanna
dc.date.accessioned2019-04-29T14:10:07Z
dc.date.available2019-04-29T14:10:07Z
dc.date.issued2004
dc.identifier.citationJoanna Balding, 'The monocyte protein C pathway : implications in human diseases', [thesis], Trinity College (Dublin, Ireland). Department of Genetics, 2004, pp 293
dc.identifier.otherTHESIS 7544
dc.description.abstractThe protein C (PC) pathway provides an important link between the coagulation, fibrinolytic, and inflammatory pathways. PC/activated protein C (APC) is one o f very few therapies shown to effectively reduce the morbidity and mortality states seen in severe sepsis and septic shock. Originally identified as a naturally occurring anti-coagulant, PC has subsequently been shown to have potent anti-inflammatory properties. Given the significance of activated monocytes in the pathophysiology of severe sepsis and the recent discovery of expression of the endothelial protein C receptor (EPCR) on the monocyte cell surface, we investigated the effect of PC on the gene expression profile of the monocytic cell line THP-1. Microarray technology was used to determine the effect of PC on the expression levels of approximately ten thousand human genes in untreated and LPS activated THP-1 cells. Results were confirmed by investigating the expression of a number of genes included in the microarray by real-time PCR and ELISA.
dc.format1 volume
dc.language.isoen
dc.publisherTrinity College (Dublin, Ireland). Department of Genetics
dc.relation.isversionofhttp://stella.catalogue.tcd.ie/iii/encore/record/C__Rb12426526
dc.subjectGenetics, Ph.D.
dc.subjectPh.D. Trinity College Dublin
dc.titleThe monocyte protein C pathway : implications in human diseases
dc.typethesis
dc.type.supercollectionthesis_dissertations
dc.type.supercollectionrefereed_publications
dc.type.qualificationlevelDoctoral
dc.type.qualificationnameDoctor of Philosophy (Ph.D.)
dc.rights.ecaccessrightsopenAccess
dc.format.extentpaginationpp 293
dc.description.noteTARA (Trinity's Access to Research Archive) has a robust takedown policy. Please contact us if you have any concerns: rssadmin@tcd.ie
dc.identifier.urihttp://hdl.handle.net/2262/86202


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