Titlebook: Drug Targets in Kinetoplastid Parasites; Hemanta K. Majumder Book 2008 The Editor(s) (if applicable) and The Author(s), under exclusive li

malcontented

書目名稱Drug Targets in Kinetoplastid Parasites影響因子(影響力)




書目名稱Drug Targets in Kinetoplastid Parasites影響因子(影響力)學(xué)科排名




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書目名稱Drug Targets in Kinetoplastid Parasites網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Drug Targets in Kinetoplastid Parasites被引頻次




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書目名稱Drug Targets in Kinetoplastid Parasites年度引用學(xué)科排名




書目名稱Drug Targets in Kinetoplastid Parasites讀者反饋




書目名稱Drug Targets in Kinetoplastid Parasites讀者反饋學(xué)科排名

暴露他抗議

Selective Lead Compounds against Kinetoplastid Tubulin,ments against cancer and helminths, suggesting that kinetoplastid tubulin is also a suitable target for antiprotozoal compounds. Selective lead compounds against kinetoplastid tubulin have been identified that could represent a starting point for the development of new drug candidates against these parasites.

epicardium

Wave Propagation in Infinite Domainsiplinary approach that includes protein structure and function and high throughput screening of random and directed chemical libraries, followed by in vivo testing in animals and humans. We outline the opportunities that are made possible by recent technologies, and potential problems that need to be overcome.

Grating

不斷的變動(dòng)

curriculum

curriculum

使入迷

0065-2598 ozoan parasites like Leishmania and Trypanosoma continue as a cause of suffering for many millions of people in both tropical and subtropical regions of the world. Leishmania species are found throughout Latin America, Africa and Asia. Trypanosoma cruzi that cause Chagas’ disease is endemic in Latin

嘴唇可修剪

Offshore wind energy conversion systemsments against cancer and helminths, suggesting that kinetoplastid tubulin is also a suitable target for antiprotozoal compounds. Selective lead compounds against kinetoplastid tubulin have been identified that could represent a starting point for the development of new drug candidates against these parasites.

談判

Begriff und Ziele des Wettbewerbsrechtscation of free detached minicircles and catenated maxicircles, and the generation of two progeny kDNA networks. It is catalyzed by an enzymatic machinery, consisting of kDNA replication proteins that are located at defined sites flanking the kDNA disk in the mitochondrial matrix (for recent reviews on kDNA see refs. 1-8).