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dc.contributor.authorMain, Nathan Michael
dc.contributor.supervisorNina Tirnitz-Parkeren_US
dc.contributor.supervisorBen Dwyeren_US
dc.contributor.supervisorPieter Eichhornen_US
dc.date.accessioned2024-10-15T05:30:49Z
dc.date.available2024-10-15T05:30:49Z
dc.date.issued2024en_US
dc.identifier.urihttp://hdl.handle.net/20.500.11937/96122
dc.description.abstract

This study investigated the molecular mechanisms regulating TWEAKindependent Fn14 signalling to identify barriers preventing successful targeting of the TWEAK/Fn14 signalling pathway. The principal discovery was that alternative splicing produces a novel Fn14 Isoform, called Fn14 Isoform 2, which has the capacity to activate in the absence of TWEAK.

en_US
dc.publisherCurtin Universityen_US
dc.titleNovel mechanisms of Fn14 signalling and its regulationen_US
dc.typeThesisen_US
dcterms.educationLevelPhDen_US
curtin.departmentCurtin Medical Schoolen_US
curtin.accessStatusFulltext not availableen_US
curtin.facultyHealth Sciencesen_US
curtin.contributor.orcidMain, Nathan Michael [0000-0003-0966-0745]en_US
dc.date.embargoEnd2026-10-02


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