抗疟药物开发和新靶点

I Macreadie , H Ginsburg , W Sirawaraporn , L Tilley
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引用次数: 61

摘要

疟疾分子方法(MAM2000)会议于2000年2月2日至5日在澳大利亚洛恩举行,汇集了世界一流的疟疾研究科学家。新工具和技术的发展——转染、DNA微阵列和蛋白质组学分析——以及疟疾基因组计划产生的DNA序列的可用性,以及更经典的方法,促进了新的药物靶点的鉴定、新的抗疟疾药物的开发以及对疟疾耐药性分子机制的更深入理解。正如在MAM2000上讨论并由Ian Macreadie及其同事在这里概述的那样,希望这些技术的组合能够导致能够开发有效、高效和负担得起的新药来克服耐药疟疾的战略。
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Antimalarial Drug Development and New Targets

The Molecular Approaches to Malaria (MAM2000) conference, Lorne, Australia, 2–5 February 2000, brought together world-class malaria research scientists. The development of new tools and technologies – transfection, DNA microarrays and proteomic analysis – and the availability of DNA sequences generated by the Malaria Genome Project, along with more classic approaches, have facilitated the identification of novel drug targets, the development of new antimalarials and the generation of a deeper understanding of the molecular mechanism(s) of drug resistance in malaria. It is hoped that combinations of these technologies could lead to strategies that enable the development of effective, efficient and affordable new drugs to overcome drug-resistant malaria, as discussed at MAM2000 and outlined here by Ian Macreadie and colleagues.

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Websites of interest Neosporosis. Seeking new targets for antiparasitic agents Response from A. Serero et al. Parasitology nomenclature – a recommendation Implications for neonatal HIV/AIDS and TB of sensitization in utero to helminths
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