scholarly article | Q13442814 |
P2093 | author name string | A Bell | |
J P Dalton | |||
S G Machado | |||
C S Gavigan | |||
P2860 | cites work | Hemoglobin metabolism in the malaria parasite Plasmodium falciparum | Q27973732 |
Synergistic drug combinations in AIDS therapy. Dipyridamole/3'-azido-3'-deoxythymidine in particular and principles of analysis in general | Q28328662 | ||
Hemoglobin degradation in the malaria parasite Plasmodium falciparum: an ordered process in a unique organelle | Q28972254 | ||
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A malarial cysteine proteinase is necessary for hemoglobin degradation by Plasmodium falciparum | Q35592776 | ||
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Structure-based inhibitor design by using protein models for the development of antiparasitic agents | Q36252297 | ||
Statistical analysis of drug-drug and site-site interactions with isobolograms | Q38699327 | ||
Disease problems in the Third World | Q38776269 | ||
Malaria, the submerged disease | Q39322893 | ||
Synergy, additivism and antagonism in immunosuppression. A critical review | Q39622779 | ||
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The role of aminopeptidases in haemoglobin degradation in Plasmodium falciparum-infected erythrocytes | Q43733737 | ||
A Method for Testing for Synergy with Any Number of Agents | Q44778227 | ||
Generation of hemoglobin peptides in the acidic digestive vacuole of Plasmodium falciparum implicates peptide transport in amino acid production | Q48037131 | ||
Lecture on the Antagonism between the Actions of Active Substances. | Q48582933 | ||
Application of a new approach for the quantitation of drug synergism to the combination of cis-diamminedichloroplatinum and 1-beta-D-arabinofuranosylcytosine. | Q52473169 | ||
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Localization and characterization of hemoglobin-degrading aspartic proteinases from the malarial parasite Plasmodium falciparum | Q68017340 | ||
Plasmodium falciparum: differential sensitivity in vitro to E-64 (cysteine protease inhibitor) and Pepstatin A (aspartyl protease inhibitor) | Q68041234 | ||
Toxicological studies on bestatin. I. Acute toxicity test in mice, rats and dogs | Q71207493 | ||
A direct, general approach based on isobolograms for assessing the joint action of drugs in pre-clinical experiments | Q72544025 | ||
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Plasmodium chabaudi chabaudi and P. falciparum: inhibition of aminopeptidase and parasite growth by bestatin and nitrobestatin | Q77051404 | ||
P433 | issue | 11 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | statistics | Q12483 |
antimalarial | Q521616 | ||
P304 | page(s) | 3175-3181 | |
P577 | publication date | 2001-11-01 | |
P1433 | published in | Antimicrobial Agents and Chemotherapy | Q578004 |
P1476 | title | Analysis of antimalarial synergy between bestatin and endoprotease inhibitors using statistical response-surface modelling | |
P478 | volume | 45 |
Q27671783 | Bestatin-based chemical biology strategy reveals distinct roles for malaria M1- and M17-family aminopeptidases |
Q36870833 | Chemical target validation studies of aminopeptidase in malaria parasites using alpha-aminoalkylphosphonate and phosphonopeptide inhibitors |
Q39017667 | Overexpression of leucyl aminopeptidase in Plasmodium falciparum parasites. Target for the antimalarial activity of bestatin |
Q27653672 | Structural basis for the inhibition of the essential Plasmodium falciparum M1 neutral aminopeptidase |
Q36018855 | The aminopeptidase inhibitor CHR-2863 is an orally bioavailable inhibitor of murine malaria |
Q47988678 | The antimalarial action of FK506 and rapamycin: evidence for a direct effect on FK506-binding protein PfFKBP35. |
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