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Titlebook: Deoxynucleoside Analogs in Cancer Therapy; Godefridus J. Peters (Professor of Medical Oncolog Book 2006 Humana Press 2006 HIV.cancer.cance

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Gemcitabine,h as non-small cell lung carcinoma and pancreatic and bladder cancer. In this chapter, we summarize the role of the key enzymes in its metabolic activation and deactivation pathways, the role of the various targets, the associated mechanisms of acquired and inherent resistance, and the changes in DN
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Hydrostatik (Statik der Flüssigkeiten)n of the substrates by their transporters. This will be a key point in the development of rationally designed new drugs. Other aspects of nucleoside transporters are also relevant to their function as drug transporters. On the one hand, several polymorphisms have been described in CNT and ENT protei
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J. Lackmann,H. Mertens,R. Liebichl drug zidovudine (AZT) and, to a lesser degree, d4T (stavudine). Until recently, the two mitochondrial deoxynucleoside kinases, thymidine kinase 2 (TK2) and dGK (deoxyguanosine kinase), have not been in focus as drug-targeting enzymes, but the accumulating knowledge of the role these kinases play f
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Hydrostatik (Statik der Flüssigkeiten)vation and thereby contribute to drug resistance. Because cloned 5′_nucleotidases have been described in human tissues, it is not always possible to assess which particular 5′-nucleotidase is important in nucleoside drug catabolism. In this chapter, we review the properties of all cloned 5′-nucleoti
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