The Plasmodium falciparum cytoplasmic translation apparatus: a promising therapeutic target not yet exploited by clinically approved anti-malarials
Author:
Funder
UCSF Discovery Fellows
National Institutes of Health
Chan Zuckerberg Biohub
Publisher
Springer Science and Business Media LLC
Subject
Infectious Diseases,Parasitology
Link
http://link.springer.com/content/pdf/10.1186/s12936-018-2616-7.pdf
Reference46 articles.
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3. Jiménez-Díaz MB, Ebert D, Salinas Y, Pradhan A, Lehane AM, Myrand-Lapierre M-E, et al. (+)-SJ733, a clinical candidate for malaria that acts through ATP4 to induce rapid host-mediated clearance of Plasmodium. Proc Natl Acad Sci USA. 2014;111:E5455–62.
4. Rosenthal PJ. Azithromycin for malaria? Am J Trop Med Hyg. 2016;95:2–4.
5. Budimulja AS, Syafruddin, Tapchaisri P, Wilairat P, Marzuki S. The sensitivity of Plasmodium protein synthesis to prokaryotic ribosomal inhibitors. Mol Biochem Parasitol. 1997;84:137–41.
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