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библиографическое описание краткийполный
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Общее количество найденных документов : 12
Показаны документы с 1 по 12
1.
Chen The fallacy of using adrenochrome reaction for measurement of reactive oxygen species formed during cytochrome P450-mediated metabolism of xenobiotics // J. Pharmacol. and Exp. Ther., 2002. Vol. 300, N 2.-С.417-420

2.
Chen The fallacy of using adrenochrome reaction for measurement of reactive oxygen species formed during cytochrome P450-mediated metabolism of xenobiotics // J. Pharmacol. and Exp. Ther., 2002. Vol. 300, N 2.-С.417-420

3.
Cytochrome P450 reductase dependent inhibition of cytochrome P450 2B1 activity: Implications for gene directed enzyme prodrug therapy // Biochem. Pharmacol., 2006. Vol. 72, N 7.-С.893-901

4.
Cytochrome P450 reductase dependent inhibition of cytochrome P450 2B1 activity: Implications for gene directed enzyme prodrug therapy // Biochem. Pharmacol., 2006. Vol. 72, N 7.-С.893-901

5.
Delahoussaye Yvette M. Metabolism of tirapazamine by multiple reductases in the nucleus // Biochem. Pharmacol., 2001. Vol. 62, N 9.-С.1201-1209

6.
Delahoussaye Yvette M. Metabolism of tirapazamine by multiple reductases in the nucleus // Biochem. Pharmacol., 2001. Vol. 62, N 9.-С.1201-1209

7.
Henderson Colin J. The hepatic cytochrome P450 reductase null mouse as a tool to identify a successful candidate entity // Toxicol. Lett., 2006. Vol. 162, N 1.-С.111-117

8.
Hepatic, extrahepatic, microsomal, and mitochondrial activation of the N-hydroxylated prodrugs benzamidoxime, guanoxabenz, and RO48-3656 ([[1-[(2S)-2-[[4-[(hydroxyamino)iminomethyl]benzoyl]amino]-1-oxopropyl]-4-piperidinyl]oxy]-acetic acid) // Drug Metab. and Dispos., 2005. Vol. 33, N 11.-С.1740-1747

9.
Hidestrand M. Human cytochromes P450 expressed in Saccharomyces cerevisiae for prediction of in vivo human drug metabolism // MDO 2000. -Torino, 2000.-С.169

10.
Korytko P.J. Expression and activity of a housefly cytochrome P450, CYP6D1, in Drosophila melanogaster // Insect. Mol. Biol., 2000. Vol. 9, N 5.-С.441-449

11.
The relative importance of NADPH: Cytochrome c (P450) reductase for determining the sensitivity of human tumour cells to the indolequinone EO9 and related analogues lacking functionality at the C-2 and C-3 positions // Biochem. Pharmacol., 2000. Vol. 59, N 8.-С.993-996

12.
The relative importance of NADPH: Cytochrome c (P450) reductase for determining the sensitivity of human tumour cells to the indolequinone EO9 and related analogues lacking functionality at the C-2 and C-3 positions // Biochem. Pharmacol., 2000. Vol. 59, N 8.-С.993-996

 




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