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PGP |
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Abstract P-glycoprotein (P-gp)-mediated multiple drug resistance (MDR) is perhaps the most thoroughly studied cellular mechanism of cytotoxic drug resistance. Werbeloff (2001) explains that phase 1 involves the action of cytochrome P450 and P-glycoprotein which remove toxic substances that if not cleared will often manifest as an external skin condition. now say they have successfully spliced the human p-glycoprotein gene into mouse embryos to make strains of mice whose marrow cells can resist a wide variety of anticancer drugs. |
P-glycoprotein |
P-CTSIB P-cymene P-cymene P-D P-D ratio P-day P-day P-DD-PLL P-DF P-DFD p-diaminodiphenyl P-dihydroxybenzene P-dihydroxybenzene P-dihydroxybenzene p-dimethylaminoazobenzene p-dimethylaminobenzaldehyde P-dioxane P-E ratio P-EPON P-ERK P-F P-FCCS P-FFT P-FLAG P-form P-form P-FSA P-FSG P-Funk P-glycoprotein P-GMCP-GTC P-GVSG P-HDD P-HOUR P-HTTP P-Hydroxy-Benzoate Hydroxylase P-hydroxybenzoic acid P-hydroxyphenylacetate Decarboxylase P-Hydroxyphenylpyruvate P-I BD P-I-N P-I-N P-i-n diode P-IMDF P-Induced Blocking Factor P-integrable function p-intrinsic-n Field Effect Transistor P-ISCAS P-K antibodies P-K antibodies P-K antibodies P-K reaction P-KSFI P-LAD P-LCBR P-LCR | |||||
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