Select Publications
Conference Papers
, 2018, 'Abstract B143: The formation of redox active complexes is important for the induction of the UPR by Dp44mT', in Molecular Cancer Therapeutics, American Association for Cancer Research (AACR), pp. b143 - b143, http://dx.doi.org/10.1158/1535-7163.targ-17-b143
, 2016, '287 The Redox Active Anti-Cancer Drug, Dp44mT, Induces Endoplasmic Reticulum Stress Activating Pro-Apoptotic Pathways of the Unfolded Protein Response in Cancer Cells', in Free Radical Biology and Medicine, Elsevier, pp. s126, http://dx.doi.org/10.1016/j.freeradbiomed.2016.10.328
, 2016, '288 Dissecting the Role of the Iron-Regulated Metastasis Suppressor NDRG1 in Regulating Endoplasmic Reticulum Stress and Cancer Cell Survival', in Free Radical Biology and Medicine, Elsevier, pp. s126, http://dx.doi.org/10.1016/j.freeradbiomed.2016.10.329
, 2014, 'EXPLOITING HSA TO STIMULATE THE DELIVERY AND ANTI-TUMOUR ACTIVITY OF THE ANTI-CANCER THIOSEMICARBAZONE, DP44MT, TO CANCER CELLS', in ASIA-PACIFIC JOURNAL OF CLINICAL ONCOLOGY, WILEY-BLACKWELL, pp. 19 - 19, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000344745100040&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
, 2013, 'THE INTERACTION OF NOVEL ANTI-CANCER IRON CHELATORS WITH ALBUMIN: MECHANISMS OF CELLULAR UPTAKE', in AMERICAN JOURNAL OF HEMATOLOGY, WILEY-BLACKWELL, pp. E169 - E169, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000318043500284&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
, 2012, '116 Transport of the Anticancer Agent, Dp44mT, via a Receptor-mediated Process', in European Journal of Cancer, Elsevier, pp. 36, http://dx.doi.org/10.1016/s0959-8049(12)71914-7
, 2011, 'Abstract A112: Enhanced accumulation of anticancer drug in tumor cells through albumin interactions: A novel drug delivery mechanism.', in Molecular Cancer Therapeutics, American Association for Cancer Research (AACR), pp. a112 - a112, http://dx.doi.org/10.1158/1535-7163.targ-11-a112