New medicines to improve control and contribute to the eradication of malaria
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[1] P. Olliaro,et al. Associate Editor: P. Winstanley An Overview of Chemotherapeutic Targets for Antimalarial Drug Discovery , 1999 .
[2] R. Benner,et al. A multicenter study of azithromycin, alone and in combination with chloroquine, for the treatment of acute uncomplicated Plasmodium falciparum malaria in India. , 2005, The Journal of infectious diseases.
[3] Jonathan E. Allen,et al. Genome sequence of the human malaria parasite Plasmodium falciparum , 2002, Nature.
[4] W. Milhous,et al. Assessment of Azithromycin in Combination with Other Antimalarial Drugs against Plasmodium falciparum In Vitro , 2002, Antimicrobial Agents and Chemotherapy.
[5] Organización Mundial de la Salud. Guidelines for the treatment of malaria , 2010 .
[6] Nicholas J White,et al. Vivax malaria: neglected and not benign. , 2007, The American journal of tropical medicine and hygiene.
[7] N. Waters,et al. Protein kinases of malaria parasites: an update. , 2008, Trends in parasitology.
[8] James M. Woolven,et al. Synthesis and structure-activity relationships of 4-pyridones as potential antimalarials. , 2008, Journal of medicinal chemistry.
[9] M. Green. Antimalarial drug resistance and the importance of drug quality monitoring. , 2006, Journal of Postgraduate Medicine.
[10] A. Janowsky,et al. Discovery of dual function acridones as a new antimalarial chemotype , 2009, Nature.
[11] P. Hunter,et al. A systematic review and meta-analysis of the effectiveness and safety of atovaquone proguanil (Malarone) for chemoprophylaxis against malaria. , 2007, The Journal of antimicrobial chemotherapy.
[12] K. Lasseter,et al. First-time-in-humans safety and pharmacokinetics of WR 238605, a new antimalarial. , 1998, The American journal of tropical medicine and hygiene.
[13] R. Price,et al. Vivax malaria: a major cause of morbidity in early infancy. , 2009, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.
[14] D. Conway,et al. Plasmodium knowlesi malaria in humans is widely distributed and potentially life threatening. , 2008, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.
[15] John P. Overington,et al. Genomic-scale prioritization of drug targets: the TDR Targets database , 2008, Nature Reviews Drug Discovery.
[16] Ernest Beutler,et al. Glucose-6-phosphate dehydrogenase deficiency and antimalarial drug development. , 2007, The American journal of tropical medicine and hygiene.
[17] J. Sattabongkot,et al. Cultivation of Plasmodium vivax. , 2008, Trends in parasitology.
[18] Identification and Characterization of Small Molecule Inhibitors of a Class I Histone Deacetylase from Plasmodium falciparum , 2009, Journal of medicinal chemistry.
[19] L. Rénia,et al. A pre-emptive strike against malaria's stealthy hepatic forms , 2009, Nature Reviews Drug Discovery.
[20] Linda S. Brinen,et al. Structures of Falcipain-2 and Falcipain-3 Bound to Small Molecule Inhibitors: Implications for Substrate Specificity‡ , 2009, Journal of medicinal chemistry.
[21] C. Withers-Martinez,et al. Subcellular Discharge of a Serine Protease Mediates Release of Invasive Malaria Parasites from Host Erythrocytes , 2007, Cell.
[22] G. Coatney,et al. A Naturally Acquired Quotidian-Type Malaria in Man Transferable to Monkeys , 1965, Science.
[23] H. Vial,et al. A Class of Potent Antimalarials and Their Specific Accumulation in Infected Erythrocytes , 2002, Science.
[24] Peter D Gibbons,et al. Two-step synthesis of achiral dispiro-1,2,4,5-tetraoxanes with outstanding antimalarial activity, low toxicity, and high-stability profiles. , 2008, Journal of medicinal chemistry.
[25] Arjen Dondorp,et al. Artesunate versus quinine for treatment of severe falciparum malaria: a randomised trial , 2005, The Lancet.
[26] C. Gee,et al. Structural basis for selective inhibition of Mycobacterium tuberculosis protein tyrosine phosphatase PtpB. , 2007, Structure.
[27] M. Dietrich,et al. Stronger host response per parasitized erythrocyte in Plasmodium vivax or ovale than in Plasmodium falciparum malaria , 2006, Tropical medicine & international health : TM & IH.
[28] P. Newton,et al. Mixed-species malaria infections in humans. , 2004, Trends in parasitology.
[29] V. Schramm,et al. Plasmodium falciparum Purine Nucleoside Phosphorylase Is Critical for Viability of Malaria Parasites* , 2008, Journal of Biological Chemistry.
[30] J. Sachs,et al. The economic burden of malaria. , 2001, The American journal of tropical medicine and hygiene.
[31] David M. Shackleford,et al. Identification of a metabolically stable triazolopyrimidine-based dihydroorotate dehydrogenase inhibitor with antimalarial activity in mice. , 2009, Journal of medicinal chemistry.
[32] Q. Bassat,et al. Insights into Long-Lasting Protection Induced by RTS,S/AS02A Malaria Vaccine: Further Results from a Phase IIb Trial in Mozambican Children , 2009, PloS one.
[33] X. Luo,et al. The chemistry, pharmacology, and clinical applications of qinghaosu (Artemisinin) and its derivatives , 1987, Medicinal research reviews.
[34] Peter G. Schultz,et al. In silico activity profiling reveals the mechanism of action of antimalarials discovered in a high-throughput screen , 2008, Proceedings of the National Academy of Sciences.
[35] Joel S. Freundlich,et al. X-ray Structural Analysis of Plasmodium falciparum Enoyl Acyl Carrier Protein Reductase as a Pathway toward the Optimization of Triclosan Antimalarial Efficacy* , 2007, Journal of Biological Chemistry.
[36] N. White,et al. Antimalarial drug resistance and combination chemotherapy. , 1999, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.
[37] G. Stygall. “Did They Really Say That?” , 2008 .
[38] Yingyao Zhou,et al. Evidence-Based Annotation of the Malaria Parasite's Genome Using Comparative Expression Profiling , 2008, PloS one.
[39] K. Silamut,et al. Artemisinin resistance in Plasmodium falciparum malaria. , 2009, The New England journal of medicine.
[40] V. Schramm,et al. Transition states and inhibitors of the purine nucleoside phosphorylase family. , 2005, Current topics in medicinal chemistry.
[41] P. Olliaro,et al. The Global Portfolio of New Antimalarial Medicines Under Development , 2009, Clinical pharmacology and therapeutics.
[42] S. Hoffman,et al. Rationale and plans for developing a non-replicating, metabolically active, radiation-attenuated Plasmodium falciparum sporozoite vaccine , 2003, Journal of Experimental Biology.
[43] K. Johnson. An Update. , 1984, Journal of food protection.
[44] M. Fukuda,et al. Evidence of artemisinin-resistant malaria in western Cambodia. , 2008, The New England journal of medicine.
[45] B. Mordmüller,et al. Selection of a trioxaquine as an antimalarial drug candidate , 2008, Proceedings of the National Academy of Sciences.
[46] Christian Scheurer,et al. Identification of an antimalarial synthetic trioxolane drug development candidate , 2004, Nature.
[47] Jonathan Crabtree,et al. Comparative genomics of the neglected human malaria parasite Plasmodium vivax , 2008, Nature.
[48] S. Meshnick,et al. Artemisinin: mechanisms of action, resistance and toxicity. , 2002, International journal for parasitology.
[49] P. Garnham,et al. Relapses in primate malaria: discovery of two populations of exoerythrocytic stages. Preliminary note. , 1980, British medical journal.
[50] Pedro Alonso,et al. Efficacy and safety of intermittent preventive treatment with sulfadoxine-pyrimethamine for malaria in African infants: a pooled analysis of six randomised, placebo-controlled trials , 2009, The Lancet.
[51] P. Rathod,et al. High-throughput Screening for Potent and Selective Inhibitors of Plasmodium falciparum Dihydroorotate Dehydrogenase* , 2005, Journal of Biological Chemistry.
[52] G. McFadden,et al. The apicoplast: a review of the derived plastid of apicomplexan parasites. , 2005, Current issues in molecular biology.
[53] M. Enserink,et al. Did They Really Say ... Eradication? , 2007, Science.
[54] Md. Mizanur Rahman,et al. Pre-referral rectal artesunate to prevent death and disability in severe malaria: a placebo-controlled trial , 2009, The Lancet.
[55] J. Luft,et al. Structures of substrate- and inhibitor-bound adenosine deaminase from a human malaria parasite show a dramatic conformational change and shed light on drug selectivity. , 2008, Journal of molecular biology.