Schrag ML[au] - Search Results

Year	Number of Results
1988	1
2000	2
2001	3
2002	1
2003	2
2004	3
2005	1
2008	2
2009	1
2010	1
2023	0

1

Bacterial N-succinyl-L-diaminopimelic acid desuccinylase. Purification, partial characterization, and substrate specificity.

Lin YK, Myhrman R, Schrag ML, Gelb MH. Lin YK, et al. Among authors: schrag ml. J Biol Chem. 1988 Feb 5;263(4):1622-7. J Biol Chem. 1988. PMID: 3276674 Free article.

2

Covalent alteration of the CYP3A4 active site: evidence for multiple substrate binding domains.

Schrag ML, Wienkers LC. Schrag ML, et al. Arch Biochem Biophys. 2001 Jul 1;391(1):49-55. doi: 10.1006/abbi.2001.2401. Arch Biochem Biophys. 2001. PMID: 11414684

3

Catalytic turnover of pyrene by CYP3A4: evidence that cytochrome b5 directly induces positive cooperativity.

Jushchyshyn MI, Hutzler JM, Schrag ML, Wienkers LC. Jushchyshyn MI, et al. Among authors: schrag ml. Arch Biochem Biophys. 2005 Jun 1;438(1):21-8. doi: 10.1016/j.abb.2005.02.027. Epub 2005 Mar 5. Arch Biochem Biophys. 2005. PMID: 15910734

4

Benzodiazepine binding site occupancy by the novel GABAA receptor subtype-selective drug 7-(1,1-dimethylethyl)-6-(2-ethyl-2H-1,2,4-triazol-3-ylmethoxy)-3-(2-fluorophenyl)-1,2,4-triazolo[4,3-b]pyridazine (TPA023) in rats, primates, and humans.

Atack JR, Wong DF, Fryer TD, Ryan C, Sanabria S, Zhou Y, Dannals RF, Eng WS, Gibson RE, Burns HD, Vega JM, Vessy L, Scott-Stevens P, Beech JS, Baron JC, Sohal B, Schrag ML, Aigbirhio FI, McKernan RM, Hargreaves RJ. Atack JR, et al. Among authors: schrag ml. J Pharmacol Exp Ther. 2010 Jan;332(1):17-25. doi: 10.1124/jpet.109.157909. Epub 2009 Sep 24. J Pharmacol Exp Ther. 2010. PMID: 19779131

5

Pyrene.pyrene complexes at the active site of cytochrome P450 3A4: evidence for a multiple substrate binding site.

Dabrowski MJ, Schrag ML, Wienkers LC, Atkins WM. Dabrowski MJ, et al. Among authors: schrag ml. J Am Chem Soc. 2002 Oct 9;124(40):11866-7. doi: 10.1021/ja027552x. J Am Chem Soc. 2002. PMID: 12358527

6

Evaluation of a series of naphthamides as potent, orally active vascular endothelial growth factor receptor-2 tyrosine kinase inhibitors.

Weiss MM, Harmange JC, Polverino AJ, Bauer D, Berry L, Berry V, Borg G, Bready J, Chen D, Choquette D, Coxon A, DeMelfi T, Doerr N, Estrada J, Flynn J, Graceffa RF, Harriman SP, Kaufman S, La DS, Long A, Neervannan S, Patel VF, Potashman M, Regal K, Roveto PM, Schrag ML, Starnes C, Tasker A, Teffera Y, Whittington DA, Zanon R. Weiss MM, et al. Among authors: schrag ml. J Med Chem. 2008 Mar 27;51(6):1668-80. doi: 10.1021/jm701098w. Epub 2008 Mar 7. J Med Chem. 2008. PMID: 18324759

7

Sulfotransferase 1E1 is a low km isoform mediating the 3-O-sulfation of ethinyl estradiol.

Schrag ML, Cui D, Rushmore TH, Shou M, Ma B, Rodrigues AD. Schrag ML, et al. Drug Metab Dispos. 2004 Nov;32(11):1299-303. doi: 10.1124/dmd.32.11.. Drug Metab Dispos. 2004. PMID: 15483196

8

Topological alteration of the CYP3A4 active site by the divalent cation Mg(2+).

Schrag ML, Wienkers LC. Schrag ML, et al. Drug Metab Dispos. 2000 Oct;28(10):1198-201. Drug Metab Dispos. 2000. PMID: 10997940

9

Mechanism-based inhibition of human liver microsomal cytochrome P450 1A2 by zileuton, a 5-lipoxygenase inhibitor.

Lu P, Schrag ML, Slaughter DE, Raab CE, Shou M, Rodrigues AD. Lu P, et al. Among authors: schrag ml. Drug Metab Dispos. 2003 Nov;31(11):1352-60. doi: 10.1124/dmd.31.11.1352. Drug Metab Dispos. 2003. PMID: 14570767

10

Solvent effect on cDNA-expressed human sulfotransferase (SULT) activities in vitro.

Ma B, Shou M, Schrag ML. Ma B, et al. Among authors: schrag ml. Drug Metab Dispos. 2003 Nov;31(11):1300-5. doi: 10.1124/dmd.31.11.1300. Drug Metab Dispos. 2003. PMID: 14570759

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