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Titlebook: Drug Resistance; William N. Hait Book 1996 Kluwer Academic Publishers 1996 DNA.Drogen.apoptosis.breast cancer.cancer.chemotherapy.drug.dru

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https://doi.org/10.1007/978-1-4613-1267-3DNA; Drogen; apoptosis; breast cancer; cancer; chemotherapy; drug; drug resistance; hormones; immunodeficienc
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978-1-4612-8540-3Kluwer Academic Publishers 1996
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https://doi.org/10.1057/9781137477972istance (MDR) is an important mechanism of cellular resistance to the cytotoxic activity of certain chemotherapeutic agents. Tumor cells selected for the MDR phenotype overexpress the .1 gene product, P-glycoprotein (P-gp), a membrane-bound drug efflux pump that confers resistance to a broad range o
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M. Ramesh,Xun Wu,Michael Howlett of tumors, such as non-small cell lung carcinomas, this resistance is inherent, while in others (e.g., acute myelogenous leukemia) it is acquired during treatment. The problem of drug resistance has been studied in the laboratory primarily by using drug-selected, cultured tumor cell lines as model
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“Cosmonaut 13”: Vladimir Shatalovnts includes the methylating agents, temozolomide, procarbazine, dacarbazine (DTIC), and steptozotocin, and the chloroethylating agents, carmustine (1,3 bis-chloroethyl 2-nitrosourea, BCNU), lomustine (3-cyclohexyl-1-chloroethyl-nitrosourea, CCNU), (2-chloroethyl)-3-sarcosinamide-1-nitrosourea (SarC
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https://doi.org/10.1057/9781137485335oncept of antimetabolite was conceived in 1940 when Woods and Fildes described the activity of sulfonamides on bacteria and suggested that the antimicrobial effect was related to some sort of competition with the normal utilization of p-aminobenzoic acid, a fundamental metabolite for bacteria [1,2].
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