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dc.contributor.authorPasic, Sara
dc.contributor.supervisorNina Tirnitz-Parkeren_US
dc.contributor.supervisorPieter Eichhornen_US
dc.contributor.supervisorBorut Klopcicen_US
dc.date.accessioned2023-09-20T00:54:38Z
dc.date.available2023-09-20T00:54:38Z
dc.date.issued2023en_US
dc.identifier.urihttp://hdl.handle.net/20.500.11937/93361
dc.description.abstract

The HGF/c-MET signalling pathway is known to be antifibrotic in the liver. However, its influence on liver progenitor cell (LPC) and hepatic stellate cell (HSC) communication during chronic liver disease (CLD) is unknown. Here, CRISPR/Cas9 technology was utilised to create a c-MET knockout LPC line, which altered LPC biology and diminished the HSC-regulatory potential of LPCs. These findings suggest that HGF/c-MET signalling is important for maintaining LPC biology and regulating HSC behaviour in CLD.

en_US
dc.publisherCurtin Universityen_US
dc.titleThe role of the HGF/c-MET signalling pathway in cellular crosstalk during chronic liver injuryen_US
dc.typeThesisen_US
dcterms.educationLevelPhDen_US
curtin.departmentCurtin Medical Schoolen_US
curtin.accessStatusOpen accessen_US
curtin.facultyHealth Sciencesen_US
curtin.contributor.orcidPasic, Sara [0000-0002-6168-7518]en_US


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