dc.contributor.advisor | Smith, Owen | |
dc.contributor.author | Galligan, Leeona | |
dc.date.accessioned | 2019-07-25T10:43:06Z | |
dc.date.available | 2019-07-25T10:43:06Z | |
dc.date.issued | 2003 | |
dc.identifier.citation | Leeona Galligan, 'Isolation and characterisation of a monocyte protein C receptor : implications for novel therapeutic strategies in sepsis', [thesis], Trinity College (Dublin, Ireland). School of Medicine. Discipline of Haematology, 2003, pp 272 | |
dc.identifier.other | THESIS 7339 | |
dc.identifier.uri | http://hdl.handle.net/2262/88852 | |
dc.description.abstract | The protein C (PC) pathway provides a unique interface between the processes of coagulation, inflammation and fibrinolysis. Used as an adjunct to standard treatment,
PC/activated PC to date, has been shown to be the only effective therapeutic intervention to reduce morbidity and mortality levels associated with severe sepsis/septic shock. Although its exact mechanism of action remains to be established, PC binding to the recently described endothelial protein C receptor (EPCR) appears to be a key feature. Given the significance of monocytes in the pathophysiology of severe sepsis, the possible
expression of a protein C receptor on the monocyte membrane was investigated. | |
dc.format | 1 volume | |
dc.language.iso | en | |
dc.publisher | Trinity College (Dublin, Ireland). School of Medicine. Discipline of Haematology | |
dc.relation.isversionof | http://stella.catalogue.tcd.ie/iii/encore/record/C__Rb12406368 | |
dc.subject | Haematology, Ph.D. | |
dc.subject | Ph.D. Trinity College Dublin | |
dc.title | Isolation and characterisation of a monocyte protein C receptor : implications for novel therapeutic strategies in sepsis | |
dc.type | thesis | |
dc.type.supercollection | thesis_dissertations | |
dc.type.supercollection | refereed_publications | |
dc.type.qualificationlevel | Doctoral | |
dc.type.qualificationname | Doctor of Philosophy (Ph.D.) | |
dc.rights.ecaccessrights | openAccess | |
dc.format.extentpagination | pp 272 | |
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