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Science, ISSN 0036-8075, 9/2010, Volume 329, Issue 5996, pp. 1175 - 1180
Recent reports of increased tolerance to artemisinin derivatives—the most recently adopted class of antimalarials— have prompted a need for new treatments. The... 
Malaria | Artemisinins | RESEARCH ARTICLES | Genomics | Adenosine triphosphatases | Antimalarials | Parasites | Inhibitory concentration 50 | Drug resistance | Dosage | Genetic mutation | VIVAX | MULTIDISCIPLINARY SCIENCES | PARASITE PLASMODIUM-FALCIPARUM | ERADICATION | CALCIUM-PUMP | DRUG-RESISTANCE | SARCOPLASMIC-RETICULUM | ANTIMALARIALS | IDENTIFICATION | CHLOROQUINE | ARTEMISININ | Parasitic Sensitivity Tests | Humans | Male | Plasmodium falciparum - drug effects | Indoles - administration & dosage | Plasmodium falciparum - genetics | Protein Synthesis Inhibitors - pharmacology | Mutant Proteins - antagonists & inhibitors | Antimalarials - pharmacokinetics | Adenosine Triphosphatases - metabolism | Models, Molecular | Rats | Spiro Compounds - pharmacokinetics | Adenosine Triphosphatases - antagonists & inhibitors | Antimalarials - administration & dosage | Malaria - parasitology | Adenosine Triphosphatases - genetics | Mice | Mutation | Erythrocytes - parasitology | Plasmodium berghei - drug effects | Plasmodium vivax - growth & development | Protein Synthesis Inhibitors - chemistry | Rats, Wistar | Spiro Compounds - administration & dosage | Genes, Protozoan | Protozoan Proteins - genetics | Protein Synthesis Inhibitors - administration & dosage | Protozoan Proteins - metabolism | Female | Indoles - pharmacology | Protozoan Proteins - chemistry | Drug Resistance | Spiro Compounds - chemistry | Cell Line | Plasmodium vivax - drug effects | Mutant Proteins - metabolism | Drug Discovery | Protozoan Proteins - biosynthesis | Antimalarials - pharmacology | Protein Synthesis Inhibitors - pharmacokinetics | Animals | Mutant Proteins - chemistry | Antimalarials - chemistry | Adenosine Triphosphatases - chemistry | Indoles - pharmacokinetics | Malaria - drug therapy | Plasmodium falciparum - growth & development | Indoles - chemistry | Spiro Compounds - pharmacology | Research | Pharmacology | Inhibitor drugs | Drug therapy | Protein synthesis
Journal Article
Journal Article
Nature, ISSN 0028-0836, 04/2015, Volume 520, Issue 7549, pp. 683 - 687
Journal Article
Immunity, ISSN 1074-7613, 03/2015, Volume 42, Issue 3, pp. 580 - 590
Journal Article
Journal Article
Science, ISSN 0036-8075, 1/2013, Volume 339, Issue 6116, pp. 227 - 230
Journal Article
Immunity, ISSN 1074-7613, 02/2016, Volume 44, Issue 2, pp. 246 - 258
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 12/2010, Volume 285, Issue 49, pp. 37964 - 37975
Using a pharmacological inhibitor of Hsp90 in cultured malarial parasite, we have previously implicated Plasmodium falciparum Hsp90 (PfHsp90) as a drug target... 
CELLS | HSP90 MOLECULAR CHAPERONE | ATPASE ACTIVITY | INHIBITION | HEAT-SHOCK-PROTEIN-90 | PLASMODIUM-FALCIPARUM | HUMAN ERYTHROCYTES | GELDANAMYCIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | GROWTH | EXPRESSION | Malaria, Falciparum - enzymology | Plasmodium falciparum - enzymology | Malaria, Falciparum - genetics | Protozoan Proteins - antagonists & inhibitors | Trypanosoma - genetics | Humans | Plasmodium berghei - genetics | Trypanosomiasis - enzymology | Protozoan Proteins - genetics | Protozoan Proteins - metabolism | Plasmodium berghei - enzymology | Plasmodium falciparum - genetics | HSP90 Heat-Shock Proteins - genetics | Trypanosoma - enzymology | Disease Models, Animal | Protein Structure, Tertiary | Malaria, Falciparum - drug therapy | Trypanosomiasis - genetics | Enzyme Inhibitors - pharmacology | Adenosine Triphosphatases - metabolism | Lactams, Macrocyclic - pharmacology | Antiprotozoal Agents - pharmacology | Benzoquinones - pharmacology | Trypanosomiasis - drug therapy | Adenosine Triphosphatases - antagonists & inhibitors | Acetylation - drug effects | Animals | HSP90 Heat-Shock Proteins - antagonists & inhibitors | HSP90 Heat-Shock Proteins - metabolism | Adenosine Triphosphatases - genetics | Mice | Hsp90 | Trypanosoma evansi | Molecular Bases of Disease | Plasmodium falciparum | Parasitology | Post-translational Modification | Protozoan | Geldanamycin | Preclinical Study | Protein-Drug Interactions | Heat Shock Protein
Journal Article
PLoS Biology, ISSN 1544-9173, 2014, Volume 12, Issue 7, pp. 1 - 16
The malaria parasite Plasmodium falciparum exports several hundred proteins into the infected erythrocyte that are involved in cellular remodeling and severe... 
CHONDROITIN SULFATE | FALCIPARUM-INFECTED ERYTHROCYTES | IN-VITRO | PLASMODIUM-FALCIPARUM | HOST-CELL |