https://nova.newcastle.edu.au/vital/access/ /manager/Index ${session.getAttribute("locale")} 5 miR-323a-3p regulates lung fibrosis by targeting multiple profibrotic pathways https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:29820 Sat 24 Mar 2018 07:40:51 AEDT ]]> Role of iron in the pathogenesis of lung disease https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:33233 Mon 23 Sep 2019 10:39:37 AEST ]]> Role of Lung Microbiome in Innate Immune Response Associated With Chronic Lung Diseases https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:42345 Mon 22 Aug 2022 13:54:38 AEST ]]> Identification and optimization of mechanism-based fluoroallylamine inhibitors of lysyl oxidase-like 2/3 https://nova.newcastle.edu.au/vital/access/ /manager/Repository/uon:41886 PXS-5120A (12k), a potent, irreversible inhibitor that is >300-fold selective for LOXL2 over LOX. PXS-5120A also shows potent inhibition of LOXL3, an emerging therapeutic target for lung fibrosis. Key to the development of this compound was the utilization of a compound oxidation assay. PXS-5120A was optimized to show negligible substrate activity in vitro for related amine oxidase family members, leading to metabolic stability. PXS-5120A, in a pro-drug form (PXS-5129A, 12o), displayed anti-fibrotic activity in models of liver and lung fibrosis, thus confirming LOXL2 as an important target in diseases where collagen cross-linking is implicated.]]> Mon 15 Aug 2022 15:37:55 AEST ]]>