Similar articles for PMID: 16790556

Year	Number of Results
1987	1
1988	1
1992	4
1993	1
1994	3
1995	5
1996	14
1997	9
1998	9
1999	6
2000	9
2001	16
2002	6
2003	12
2004	15
2005	12
2006	15
2007	15
2008	5
2009	12
2010	11
2011	10
2012	7
2013	13
2014	7
2015	4
2016	9
2017	10
2018	16
2019	18
2020	18
2021	10
2022	11
2023	6
2024	0

1

Inhibition of the human liver microsomal and human cytochrome P450 1A2 and 3A4 metabolism of estradiol by deployment-related and other chemicals.

Usmani KA, Cho TM, Rose RL, Hodgson E. Usmani KA, et al. Drug Metab Dispos. 2006 Sep;34(9):1606-14. doi: 10.1124/dmd.106.010439. Epub 2006 Jun 21. Drug Metab Dispos. 2006. PMID: 16790556

2

Inhibition and activation of the human liver microsomal and human cytochrome P450 3A4 metabolism of testosterone by deployment-related chemicals.

Usmani KA, Rose RL, Hodgson E. Usmani KA, et al. Drug Metab Dispos. 2003 Apr;31(4):384-91. doi: 10.1124/dmd.31.4.384. Drug Metab Dispos. 2003. PMID: 12642463

3

In vitro metabolism of carbofuran by human, mouse, and rat cytochrome P450 and interactions with chlorpyrifos, testosterone, and estradiol.

Usmani KA, Hodgson E, Rose RL. Usmani KA, et al. Chem Biol Interact. 2004 Dec 7;150(3):221-32. doi: 10.1016/j.cbi.2004.09.015. Chem Biol Interact. 2004. PMID: 15560889

4

In vitro metabolism of carbaryl by human cytochrome P450 and its inhibition by chlorpyrifos.

Tang J, Cao Y, Rose RL, Hodgson E. Tang J, et al. Chem Biol Interact. 2002 Oct 20;141(3):229-41. doi: 10.1016/s0009-2797(02)00074-1. Chem Biol Interact. 2002. PMID: 12385721

5

The kinetics of aflatoxin B1 oxidation by human cDNA-expressed and human liver microsomal cytochromes P450 1A2 and 3A4.

Gallagher EP, Kunze KL, Stapleton PL, Eaton DL. Gallagher EP, et al. Toxicol Appl Pharmacol. 1996 Dec;141(2):595-606. doi: 10.1006/taap.1996.0326. Toxicol Appl Pharmacol. 1996. PMID: 8975785

6

In vitro metabolism and drug interaction potential of a new highly potent anti-cytomegalovirus molecule, CMV423 (2-chloro 3-pyridine 3-yl 5,6,7,8-tetrahydroindolizine I-carboxamide).

Bournique B, Lambert N, Boukaiba R, Martinet M. Bournique B, et al. Br J Clin Pharmacol. 2001 Jul;52(1):53-63. doi: 10.1046/j.0306-5251.2001.01413.x. Br J Clin Pharmacol. 2001. PMID: 11453890 Free PMC article.

7

Interindividual variation in relative CYP1A2/3A4 phenotype influences susceptibility of clozapine oxidation to cytochrome P450-specific inhibition in human hepatic microsomes.

Zhang WV, D'Esposito F, Edwards RJ, Ramzan I, Murray M. Zhang WV, et al. Drug Metab Dispos. 2008 Dec;36(12):2547-55. doi: 10.1124/dmd.108.023671. Epub 2008 Sep 22. Drug Metab Dispos. 2008. PMID: 18809730

8

In vitro metabolism of the calmodulin antagonist DY-9760e (3-[2-[4-(3-chloro-2-methylphenyl)-1-piperazinyl]ethyl]-5,6-dimethoxy-1-(4-imidazolylmethyl)-1H-indazole dihydrochloride 3.5 hydrate) by human liver microsomes: involvement of cytochromes p450 in atypical kinetics and potential drug interactions.

Tachibana S, Fujimaki Y, Yokoyama H, Okazaki O, Sudo K. Tachibana S, et al. Drug Metab Dispos. 2005 Nov;33(11):1628-36. doi: 10.1124/dmd.105.004903. Epub 2005 Jul 27. Drug Metab Dispos. 2005. PMID: 16049129

9

Human metabolic interactions of environmental chemicals.

Hodgson E, Rose RL. Hodgson E, et al. J Biochem Mol Toxicol. 2007;21(4):182-6. doi: 10.1002/jbt.20175. J Biochem Mol Toxicol. 2007. PMID: 17936932 Review.

10

Further assessment of 17alpha-ethinyl estradiol as an inhibitor of different human cytochrome P450 forms in vitro.

Chang SY, Chen C, Yang Z, Rodrigues AD. Chang SY, et al. Drug Metab Dispos. 2009 Aug;37(8):1667-75. doi: 10.1124/dmd.109.026997. Epub 2009 May 19. Drug Metab Dispos. 2009. PMID: 19454483

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