Victoria Corey
Affiliations: | 2012-2016 | Pediatrics | University of California, San Diego, La Jolla, CA |
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| Bopp S, Pasaje CFA, Summers RL, et al. (2023) Potent acyl-CoA synthetase 10 inhibitors kill Plasmodium falciparum by disrupting triglyceride formation. Nature Communications. 14: 1455 |
| Morahan BJ, Abrie C, Al-Hasani K, et al. (2020) Human Aurora kinase inhibitor Hesperadin reveals epistatic interaction between Plasmodium falciparum PfArk1 and PfNek1 kinases. Communications Biology. 3: 701 |
| Cowell AN, Istvan ES, Lukens AK, et al. (2018) Mapping the malaria parasite druggable genome by using in vitro evolution and chemogenomics. Science (New York, N.Y.). 359: 191-199 |
| Vanaerschot M, Lucantoni L, Li T, et al. (2017) Hexahydroquinolines are antimalarial candidates with potent blood-stage and transmission-blocking activity. Nature Microbiology |
| Istvan ES, Mallari JP, Corey VC, et al. (2017) Esterase mutation is a mechanism of resistance to antimalarial compounds. Nature Communications. 8: 14240 |
| Magistrado PA, Corey VC, Lukens AK, et al. (2016) Plasmodium falciparum Cyclic Amine Resistance Locus (PfCARL), a Resistance Mechanism for Two Distinct Compound Classes. Acs Infectious Diseases. 2: 816-826 |
| Lim MY, LaMonte G, Lee MC, et al. (2016) UDP-galactose and acetyl-CoA transporters as Plasmodium multidrug resistance genes. Nature Microbiology. 1: 16166 |
| Kato N, Comer E, Sakata-Kato T, et al. (2016) Diversity-oriented synthesis yields novel multistage antimalarial inhibitors. Nature |
| LaMonte G, Lim MY, Wree M, et al. (2016) Mutations in the Plasmodium falciparum Cyclic Amine Resistance Locus (PfCARL) Confer Multidrug Resistance. Mbio. 7 |
| Corey VC, Lukens AK, Istvan ES, et al. (2016) A broad analysis of resistance development in the malaria parasite. Nature Communications. 7: 11901 |