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Journal of Fungi (Basel, Switzerland)|April 16, 2020
The Dynamic Influence of Olorofim (F901318) on the Cell Morphology and Organization of Living Cells of Aspergillus fumigatusSaskia du Pré, Mike Birch, Derek Law, et al.Plos One|October 3, 2012
The Aspergillus fumigatus dihydroxyacid dehydratase Ilv3A/IlvC is required for full virulenceJason D Oliver, Sarah J Kaye, Danny Tuckwell, et al.Toxicological Sciences : an Official Journal of the Society of Toxicology|May 20, 2005
Gene ontology mapping as an unbiased method for identifying molecular pathways and processes affected by toxicant exposure: application to acute effects caused by the rodent non-genotoxic carcinogen diethylhexylphthalateRichard A Currie, Vincent Bombail, Jason D Oliver, et al.Antimicrobial Agents and Chemotherapy|June 13, 2018
Effect of the Novel Antifungal Drug F901318 (Olorofim) on Growth and Viability of Aspergillus fumigatusSaskia du Pré, Nicola Beckmann, Mariana Cruz Almeida, et al.Emerging Microbes & Infections|February 3, 2022
Resistance profiling of Aspergillus fumigatus to olorofim indicates absence of intrinsic resistance and unveils the molecular mechanisms of acquired olorofim resistanceJochem B Buil, Jason D Oliver, Derek Law, et al.The Journal of Biological Chemistry|February 12, 2004
The primary substrate binding site in the b' domain of ERp57 is adapted for endoplasmic reticulum lectin associationSarah J Russell, Lloyd W Ruddock, Kirsi E H Salo, et al.Mbio|July 20, 2017
A Nonredundant Phosphopantetheinyl Transferase, PptA, Is a Novel Antifungal Target That Directs Secondary Metabolite, Siderophore, and Lysine Biosynthesis in Aspergillus fumigatus and Is Critical for PathogenicityAnna Johns, Daniel H Scharf, Fabio Gsaller, et al.Mbio|December 5, 2019
Fluconazole Monotherapy Is a Suboptimal Option for Initial Treatment of Cryptococcal Meningitis Because of Emergence of ResistanceWilliam Hope, Neil R H Stone, Adam Johnson, et al.Proceedings of the National Academy of Sciences of the United States of America|October 30, 2016
F901318 represents a novel class of antifungal drug that inhibits dihydroorotate dehydrogenaseJason D Oliver, Graham E M Sibley, Nicola Beckmann, et al.Pageof 2