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130 related items for PubMed ID: 12488544
1. Mechanism of rat UDP-glucuronosyltransferase 1A6 induction by oltipraz: evidence for a contribution of the Aryl hydrocarbon receptor pathway. Auyeung DJ, Kessler FK, Ritter JK. Mol Pharmacol; 2003 Jan; 63(1):119-27. PubMed ID: 12488544 [Abstract] [Full Text] [Related]
2. Oltipraz inhibits 3-methylcholanthrene induction of CYP1A1 by CCAAT/enhancer-binding protein activation. Cho IJ, Kim SG. J Biol Chem; 2003 Nov 07; 278(45):44103-12. PubMed ID: 12941938 [Abstract] [Full Text] [Related]
3. Aryl hydrocarbon receptor and NF-E2-related factor 2 are key regulators of human MRP4 expression. Xu S, Weerachayaphorn J, Cai SY, Soroka CJ, Boyer JL. Am J Physiol Gastrointest Liver Physiol; 2010 Jul 07; 299(1):G126-35. PubMed ID: 20395535 [Abstract] [Full Text] [Related]
5. Oltipraz is a bifunctional inducer activating both phase I and phase II drug-metabolizing enzymes via the xenobiotic responsive element. Miao W, Hu L, Kandouz M, Batist G. Mol Pharmacol; 2003 Aug 01; 64(2):346-54. PubMed ID: 12869639 [Abstract] [Full Text] [Related]
6. Transcriptional activation of the UDP-glucuronosyltransferase 1A7 gene in rat liver by aryl hydrocarbon receptor ligands and oltipraz. Metz RP, Ritter JK. J Biol Chem; 1998 Mar 06; 273(10):5607-14. PubMed ID: 9488689 [Abstract] [Full Text] [Related]
7. Aryl hydrocarbon receptor-inducible or constitutive expression of human UDP glucuronosyltransferase UGT1A6. Münzel PA, Lehmköster T, Brück M, Ritter JK, Bock KW. Arch Biochem Biophys; 1998 Feb 01; 350(1):72-8. PubMed ID: 9466822 [Abstract] [Full Text] [Related]
12. Regulation of the Cyp2a5 gene involves an aryl hydrocarbon receptor-dependent pathway. Arpiainen S, Raffalli-Mathieu F, Lang MA, Pelkonen O, Hakkola J. Mol Pharmacol; 2005 Apr 01; 67(4):1325-33. PubMed ID: 15657367 [Abstract] [Full Text] [Related]
13. Inhibition of the transcription of CYP1A1 gene by the upstream stimulatory factor 1 in rabbits. Competitive binding of USF1 with AhR.Arnt complex. Takahashi Y, Nakayama K, Itoh S, Fujii-Kuriyama Y, Kamataki T. J Biol Chem; 1997 Nov 28; 272(48):30025-31. PubMed ID: 9374477 [Abstract] [Full Text] [Related]
14. The aryl hydrocarbon receptor interacts with estrogen receptor alpha and orphan receptors COUP-TFI and ERRalpha1. Klinge CM, Kaur K, Swanson HI. Arch Biochem Biophys; 2000 Jan 01; 373(1):163-74. PubMed ID: 10620335 [Abstract] [Full Text] [Related]
15. Identification of a novel domain in the aryl hydrocarbon receptor required for DNA binding. Fukunaga BN, Hankinson O. J Biol Chem; 1996 Feb 16; 271(7):3743-9. PubMed ID: 8631989 [Abstract] [Full Text] [Related]
16. Competitive inhibition of the transcription of rabbit CYP1A1 gene by upstream stimulatory factor 1 (USF1). Takahashi Y, Kamataki T. Drug Metab Rev; 2001 Feb 16; 33(1):37-47. PubMed ID: 11270661 [Abstract] [Full Text] [Related]
17. Analysis of aryl hydrocarbon receptor-mediated signaling during physiological hypoxia reveals lack of competition for the aryl hydrocarbon nuclear translocator transcription factor. Pollenz RS, Davarinos NA, Shearer TP. Mol Pharmacol; 1999 Dec 16; 56(6):1127-37. PubMed ID: 10570039 [Abstract] [Full Text] [Related]
18. The same xenobiotic response element is required for constitutive and inducible expression of the mammalian aldehyde dehydrogenase-3 gene. Boesch JS, Miskimins R, Miskimins WK, Lindahl R. Arch Biochem Biophys; 1999 Jan 15; 361(2):223-30. PubMed ID: 9882450 [Abstract] [Full Text] [Related]
20. Induction of 26S proteasome subunit PSMB5 by the bifunctional inducer 3-methylcholanthrene through the Nrf2-ARE, but not the AhR/Arnt-XRE, pathway. Kwak MK, Kensler TW. Biochem Biophys Res Commun; 2006 Jul 14; 345(4):1350-7. PubMed ID: 16723119 [Abstract] [Full Text] [Related] Page: [Next] [New Search]