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Frontiers in Cellular and Infection Microbiology|October 4, 2021
Targeting Host Glycolysis as a Strategy for Antimalarial DevelopmentAndrew J Jezewski, Yu-Hsi Lin, Julie A Reisz, et al.
The Journal of Biological Chemistry|January 1, 2022
Enzymatic and structural characterization of HAD5, an essential phosphomannomutase of malaria-causing parasitesPhilip M Frasse, Justin J Miller, Alexander J Polino, et al.
The Journal of Infectious Diseases|July 23, 2016
Whole-Genome Sequencing to Evaluate the Resistance Landscape Following Antimalarial Treatment Failure With Fosmidomycin-ClindamycinAnn M Guggisberg, Sesh A Sundararaman, Miguel Lanaspa, et al.
Journal of the Pediatric Infectious Diseases Society|June 20, 2020
The Epidemiology of Severe Acute Respiratory Syndrome Coronavirus 2 in a Pediatric Healthcare Network in the United StatesWilliam R Otto, Sarah Geoghegan, Leila C Posch, et al.
RSC Medicinal Chemistry|July 19, 2024
Inhibition of DXR in the MEP pathway with lipophilic <i>N</i>-alkoxyaryl FR900098 analogsDarean Bague, Ruiqin Wang, Dana Hodge, et al.
Antimicrobial Agents and Chemotherapy|October 14, 2016
A Novel Fluorescence Resonance Energy Transfer-Based Screen in High-Throughput Format To Identify Inhibitors of Malarial and Human Glucose TransportersThomas E Kraft, Monique R Heitmeier, Marina Putanko, et al.
Scientific Reports|August 23, 2017
MEPicides: potent antimalarial prodrugs targeting isoprenoid biosynthesisRachel L Edwards, Robert C Brothers, Xu Wang, et al.
ACS Infectious Diseases|September 28, 2016
Structure-Activity Relationships of the MEPicides: N-Acyl and O-Linked Analogs of FR900098 as Inhibitors of Dxr from Mycobacterium tuberculosis and Yersinia pestisGéraldine San Jose, Emily R Jackson, Amanda Haymond, et al.
Pediatric Emergency Care|September 24, 2020
Distinguishing Multisystem Inflammatory Syndrome in Children From Kawasaki Disease and Benign Inflammatory Illnesses in the SARS-CoV-2 PandemicDaniel J Corwin, Laura F Sartori, Kathleen Chiotos, et al.
ACS Infectious Diseases|January 20, 2016
<i>Plasmodium</i> IspD (2-C-Methyl-D-erythritol 4-Phosphate Cytidyltransferase), an Essential and Druggable Antimalarial TargetLeah S Imlay, Christopher M Armstrong, Mary Clare Masters, et al.
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