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dc.contributor.advisorFletcher, Jean
dc.contributor.authorCluxton, Deborah
dc.date.accessioned2019-11-05T14:52:55Z
dc.date.available2019-11-05T14:52:55Z
dc.date.issued2015
dc.identifier.citationDeborah Cluxton, 'The role of metabolism, hypoxia and immunomodulatory therapy in regulating the human Treg:Th17 cell axis', [thesis], Trinity College (Dublin, Ireland). School of Biochemistry and Immunology, 2015, pp 288
dc.identifier.otherTHESIS 11061
dc.description.abstractTh17 cells are important pathogenic effector cells in autoimmune diseases such as rheumatoid arthritis (RA), psoriasis and multiple sclerosis (MS). On the other hand, regulatory T (Treg) cells play a crucial role in maintaining tolerance and preventing autoimmunity. Under healthy conditions there is a balance between Treg and effector T cell responses, which may be perturbed in autoimmunity, cancer and other diseases; therefore, it is crucial to understand the factors that regulate this balance. Recently, a role for metabolism and hypoxia in murine T cell differentiation has been identified.
dc.format1 volume
dc.language.isoen
dc.publisherTrinity College (Dublin, Ireland). School of Biochemistry and Immunology
dc.relation.isversionofhttp://stella.catalogue.tcd.ie/iii/encore/record/C__Rb16720896
dc.subjectBiochemistry and Immunology, Ph.D.
dc.subjectPh.D. Trinity College Dublin.
dc.titleThe role of metabolism, hypoxia and immunomodulatory therapy in regulating the human Treg:Th17 cell axis
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 288
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/2262/90040


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