Spratt TE - Search Results

1

A transcriptional inhibitor induced in human melanoma cells upon ultraviolet irradiation.

Yang YM, Rutberg SE, Luo FC, Spratt TE, Halaban R, Ferrone S, Ronai Z. Yang YM, et al. Among authors: spratt te. Cell Growth Differ. 1993 Jul;4(7):595-602. Cell Growth Differ. 1993. PMID: 8398900

2

Evaluation of cysteine adduct formation in rat hemoglobin by 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone and related compounds.

Carmella SG, Kagan SS, Spratt TE, Hecht SS. Carmella SG, et al. Among authors: spratt te. Cancer Res. 1990 Sep 1;50(17):5453-9. Cancer Res. 1990. PMID: 2201436

3

A fluoroquinolone antibiotic with a methoxy group at the 8 position yields reduced generation of 8-oxo-7,8-dihydro-2'-deoxyguanosine after ultraviolet-A irradiation.

Rosen JE, Chen D, Prahalad AK, Spratt TE, Schluter G, Williams GM. Rosen JE, et al. Among authors: spratt te. Toxicol Appl Pharmacol. 1997 Aug;145(2):381-7. doi: 10.1006/taap.1997.8183. Toxicol Appl Pharmacol. 1997. PMID: 9266812

4

Identification of sulfate and glucuronic acid conjugates of the 5-hydroxy derivative as major metabolites of 2-amino-3-methylimidazo[4,5-f]quinoline in rats.

Luks HJ, Spratt TE, Vavrek MT, Roland SF, Weisburger JH. Luks HJ, et al. Among authors: spratt te. Cancer Res. 1989 Aug 15;49(16):4407-11. Cancer Res. 1989. PMID: 2743329

5

Tobacco-specific nitrosamines.

Hecht SS, Peterson LA, Spratt TE. Hecht SS, et al. Among authors: spratt te. IARC Sci Publ. 1994;(125):91-106. IARC Sci Publ. 1994. PMID: 7806343 Review. No abstract available.

6

Inhibition of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) metabolism in human hepatic microsomes by ipomeanol analogs--an exploratory study.

Nunes MG, Desai D, Koehl W, Spratt TE, Guengerich FP, Amin S. Nunes MG, et al. Among authors: spratt te. Cancer Lett. 1998 Jul 17;129(2):131-8. doi: 10.1016/s0304-3835(98)00049-4. Cancer Lett. 1998. PMID: 9719453

7

Different mechanisms for the photoinduced production of oxidative DNA damage by fluoroquinolones differing in photostability.

Spratt TE, Schultz SS, Levy DE, Chen D, Schlüter G, Williams GM. Spratt TE, et al. Chem Res Toxicol. 1999 Sep;12(9):809-15. doi: 10.1021/tx980224j. Chem Res Toxicol. 1999. PMID: 10490502

8

Reaction and binding of oligodeoxynucleotides containing analogues of O6-methylguanine with wild-type and mutant human O6-alkylguanine-DNA alkyltransferase.

Spratt TE, Wu JD, Levy DE, Kanugula S, Pegg AE. Spratt TE, et al. Biochemistry. 1999 May 25;38(21):6801-6. doi: 10.1021/bi982908w. Biochemistry. 1999. PMID: 10346901

9

Synthesis of oligodeoxynucleotides containing analogs of O6-methylguanine and reaction with O6-alkylguanine-DNA alkyltransferase.

Spratt TE, Campbell CR. Spratt TE, et al. Biochemistry. 1994 Sep 20;33(37):11364-71. doi: 10.1021/bi00203a035. Biochemistry. 1994. PMID: 7727387

10

Pyridyloxobutyl adduct O6-[4-oxo-4-(3-pyridyl)butyl]guanine is present in 4-(acetoxymethylnitrosamino)-1-(3-pyridyl)-1-butanone-treated DNA and is a substrate for O6-alkylguanine-DNA alkyltransferase.

Wang L, Spratt TE, Liu XK, Hecht SS, Pegg AE, Peterson LA. Wang L, et al. Among authors: spratt te. Chem Res Toxicol. 1997 May;10(5):562-7. doi: 10.1021/tx9602067. Chem Res Toxicol. 1997. PMID: 9168254

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