Staub RE - Search Results

1

Mechanism for benomyl action as a mitochondrial aldehyde dehydrogenase inhibitor in mice.

Staub RE, Quistad GB, Casida JE. Staub RE, et al. Chem Res Toxicol. 1998 May;11(5):535-43. doi: 10.1021/tx980002l. Chem Res Toxicol. 1998. PMID: 9585485

2

S-methylation as a bioactivation mechanism for mono- and dithiocarbamate pesticides as aldehyde dehydrogenase inhibitors.

Staub RE, Sparks SE, Quistad GB, Casida JE. Staub RE, et al. Chem Res Toxicol. 1995 Dec;8(8):1063-9. doi: 10.1021/tx00050a010. Chem Res Toxicol. 1995. PMID: 8605289

3

S-methyl N-butylthiocarbamate sulfoxide: selective carbamoylating agent for mouse mitochondrial aldehyde dehydrogenase.

Staub RE, Quistad GB, Casida JE. Staub RE, et al. Biochem Pharmacol. 1999 Nov 1;58(9):1467-73. doi: 10.1016/s0006-2952(99)00239-7. Biochem Pharmacol. 1999. PMID: 10513990

4

Fate of 3,3'-diindolylmethane in cultured MCF-7 human breast cancer cells.

Staub RE, Onisko B, Bjeldanes LF. Staub RE, et al. Chem Res Toxicol. 2006 Mar;19(3):436-42. doi: 10.1021/tx050325z. Chem Res Toxicol. 2006. PMID: 16544949

5

Fate of indole-3-carbinol in cultured human breast tumor cells.

Staub RE, Feng C, Onisko B, Bailey GS, Firestone GL, Bjeldanes LF. Staub RE, et al. Chem Res Toxicol. 2002 Feb;15(2):101-9. doi: 10.1021/tx010056m. Chem Res Toxicol. 2002. PMID: 11849035

6

1-Benzyl-indole-3-carbinol is a novel indole-3-carbinol derivative with significantly enhanced potency of anti-proliferative and anti-estrogenic properties in human breast cancer cells.

Nguyen HH, Lavrenov SN, Sundar SN, Nguyen DH, Tseng M, Marconett CN, Kung J, Staub RE, Preobrazhenskaya MN, Bjeldanes LF, Firestone GL. Nguyen HH, et al. Among authors: staub re. Chem Biol Interact. 2010 Aug 5;186(3):255-66. doi: 10.1016/j.cbi.2010.05.015. Epub 2010 Jun 2. Chem Biol Interact. 2010. PMID: 20570586 Free PMC article.

7

Convenient synthesis of 5,6,11,12,17,18- hexahydrocyclononal[1,2-b:4,5-b':7,8-b'']triindole, a novel phytoestrogen.

Staub RE, Bjeldanes LF. Staub RE, et al. J Org Chem. 2003 Jan 10;68(1):167-9. doi: 10.1021/jo020415y. J Org Chem. 2003. PMID: 12515475

8

Liquiritigenin is a plant-derived highly selective estrogen receptor beta agonist.

Mersereau JE, Levy N, Staub RE, Baggett S, Zogovic T, Chow S, Ricke WA, Tagliaferri M, Cohen I, Bjeldanes LF, Leitman DC. Mersereau JE, et al. Among authors: staub re. Mol Cell Endocrinol. 2008 Feb 13;283(1-2):49-57. doi: 10.1016/j.mce.2007.11.020. Epub 2007 Nov 26. Mol Cell Endocrinol. 2008. PMID: 18177995 Free PMC article.

9

Drug and cell type-specific regulation of genes with different classes of estrogen receptor beta-selective agonists.

Paruthiyil S, Cvoro A, Zhao X, Wu Z, Sui Y, Staub RE, Baggett S, Herber CB, Griffin C, Tagliaferri M, Harris HA, Cohen I, Bjeldanes LF, Speed TP, Schaufele F, Leitman DC. Paruthiyil S, et al. Among authors: staub re. PLoS One. 2009 Jul 17;4(7):e6271. doi: 10.1371/journal.pone.0006271. PLoS One. 2009. PMID: 19609440 Free PMC article.

10

Metabolism of cycloate in radish leaf: metabolite identification by packed capillary flow fast atom bombardment tandem mass spectrometry.

Onisko BC, Barnes JP, Staub RE, Walker FH, Kerlinger N. Onisko BC, et al. Among authors: staub re. Biol Mass Spectrom. 1994 Oct;23(10):626-36. doi: 10.1002/bms.1200231005. Biol Mass Spectrom. 1994. PMID: 7986833

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