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Publications by Amanda Hott
Correction for Breglio Et Al., “Kelch Mutations in Plasmodium Falciparum Protein K13 Do Not Modulate Dormancy After Artemisinin Exposure and Sorbitol Selection in Vitro”
Antimicrobial Agents and Chemotherapy
Infectious Diseases
Pharmacology
Related publications
Natural Selection of K13 Mutants of Plasmodium Falciparum in Response to Artemisinin Combination Therapies in Thailand
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Evolution and Genetic Diversity of the K13 Gene Associated With Artemisinin Delayed Parasite Clearance in Plasmodium Falciparum
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Plasmodium Falciparum Founder Populations in Western Cambodia Have Reduced Artemisinin Sensitivity in Vitro
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Molecular Evidence for Plasmodium Falciparum Resistance to Sulfadoxine–Pyrimethamine but Absence of K13 Mutations in Mangaluru, Southwestern India
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Alternative Pathway to Reduced Artemisinin Susceptibility in Plasmodium Falciparum
Proceedings of the National Academy of Sciences of the United States of America
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In Vitro Cultivation of Plasmodium Falciparum *
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Parasitology
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Experimentally Engineered Mutations in a Ubiquitin Hydrolase, UBP-1, Modulate in Vivo Resistance to Artemisinin and Chloroquine in Plasmodium Berghei.
Sequence Analysis of the K13-Propeller Gene in Artemisinin Challenging Plasmodium Falciparum Isolates From Malaria Endemic Areas of Odisha, India: A Molecular Surveillance Study
BioMed Research International
Immunology
Molecular Biology
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