These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
281 related articles for article (PubMed ID: 16891617)
1. Calpain mediates the dioxin-induced activation and down-regulation of the aryl hydrocarbon receptor. Dale YR; Eltom SE Mol Pharmacol; 2006 Nov; 70(5):1481-7. PubMed ID: 16891617 [TBL] [Abstract][Full Text] [Related]
2. Aryl hydrocarbon receptor expression and activity in cerebellar granule neuroblasts: implications for development and dioxin neurotoxicity. Williamson MA; Gasiewicz TA; Opanashuk LA Toxicol Sci; 2005 Feb; 83(2):340-8. PubMed ID: 15537747 [TBL] [Abstract][Full Text] [Related]
3. Dietary flavonols quercetin and kaempferol are ligands of the aryl hydrocarbon receptor that affect CYP1A1 transcription differentially. Ciolino HP; Daschner PJ; Yeh GC Biochem J; 1999 Jun; 340 ( Pt 3)(Pt 3):715-22. PubMed ID: 10359656 [TBL] [Abstract][Full Text] [Related]
4. Dioxin-mediated up-regulation of aryl hydrocarbon receptor target genes is dependent on the calcium/calmodulin/CaMKIalpha pathway. Monteiro P; Gilot D; Le Ferrec E; Rauch C; Lagadic-Gossmann D; Fardel O Mol Pharmacol; 2008 Mar; 73(3):769-77. PubMed ID: 18089838 [TBL] [Abstract][Full Text] [Related]
5. The induction of CYP1A1 by oltipraz is mediated through calcium-dependent-calpain. Dale Y; Eltom SE Toxicol Lett; 2006 Oct; 166(2):150-9. PubMed ID: 16891067 [TBL] [Abstract][Full Text] [Related]
6. Activation of mitogen-activated protein kinases (MAPKs) by aromatic hydrocarbons: role in the regulation of aryl hydrocarbon receptor (AHR) function. Tan Z; Chang X; Puga A; Xia Y Biochem Pharmacol; 2002 Sep; 64(5-6):771-80. PubMed ID: 12213569 [TBL] [Abstract][Full Text] [Related]
7. Metabolism-based polycyclic aromatic acetylene inhibition of CYP1B1 in 10T1/2 cells potentiates aryl hydrocarbon receptor activity. Alexander DL; Zhang L; Foroozesh M; Alworth WL; Jefcoate CR Toxicol Appl Pharmacol; 1999 Dec; 161(2):123-39. PubMed ID: 10581206 [TBL] [Abstract][Full Text] [Related]
8. Activation of the aryl hydrocarbon receptor by the calcium/calmodulin-dependent protein kinase kinase inhibitor 7-oxo-7H-benzimidazo[2,1-a]benz[de]isoquinoline-3-carboxylic acid (STO-609). Monteiro P; Gilot D; Langouet S; Fardel O Drug Metab Dispos; 2008 Dec; 36(12):2556-63. PubMed ID: 18755850 [TBL] [Abstract][Full Text] [Related]
9. Flavone antagonists bind competitively with 2,3,7, 8-tetrachlorodibenzo-p-dioxin (TCDD) to the aryl hydrocarbon receptor but inhibit nuclear uptake and transformation. Henry EC; Kende AS; Rucci G; Totleben MJ; Willey JJ; Dertinger SD; Pollenz RS; Jones JP; Gasiewicz TA Mol Pharmacol; 1999 Apr; 55(4):716-25. PubMed ID: 10101030 [TBL] [Abstract][Full Text] [Related]
10. A potential endogenous ligand for the aryl hydrocarbon receptor has potent agonist activity in vitro and in vivo. Henry EC; Bemis JC; Henry O; Kende AS; Gasiewicz TA Arch Biochem Biophys; 2006 Jun; 450(1):67-77. PubMed ID: 16545771 [TBL] [Abstract][Full Text] [Related]
11. Curcumin suppresses the transformation of an aryl hydrocarbon receptor through its phosphorylation. Nishiumi S; Yoshida K; Ashida H Arch Biochem Biophys; 2007 Oct; 466(2):267-73. PubMed ID: 17880909 [TBL] [Abstract][Full Text] [Related]
12. Dephosphorylation of Sp1 at Ser-59 by protein phosphatase 2A (PP2A) is required for induction of CYP1A1 transcription after treatment with 2,3,7,8-tetrachlorodibenzo-p-dioxin or omeprazole. Shimoyama S; Kasai S; Kahn-Perlès B; Kikuchi H Biochim Biophys Acta; 2014 Feb; 1839(2):107-15. PubMed ID: 24382322 [TBL] [Abstract][Full Text] [Related]
13. Role of the carboxy-terminal transactivation domain and active transcription in the ligand-induced and ligand-independent degradation of the mouse Ahb-1 receptor. Pollenz RS; Popat J; Dougherty EJ Biochem Pharmacol; 2005 Nov; 70(11):1623-33. PubMed ID: 16226227 [TBL] [Abstract][Full Text] [Related]
14. 2,3,7,8-tetrachlorodibenzo-p-dioxin-induced degradation of aryl hydrocarbon receptor (AhR) by the ubiquitin-proteasome pathway. Role of the transcription activaton and DNA binding of AhR. Ma Q; Baldwin KT J Biol Chem; 2000 Mar; 275(12):8432-8. PubMed ID: 10722677 [TBL] [Abstract][Full Text] [Related]
15. The aryl hydrocarbon receptor mediates degradation of estrogen receptor alpha through activation of proteasomes. Wormke M; Stoner M; Saville B; Walker K; Abdelrahim M; Burghardt R; Safe S Mol Cell Biol; 2003 Mar; 23(6):1843-55. PubMed ID: 12612060 [TBL] [Abstract][Full Text] [Related]
16. Aryl hydrocarbon receptor-dependent suppression by 2,3,7, 8-tetrachlorodibenzo-p-dioxin of IgM secretion in activated B cells. Sulentic CE; Holsapple MP; Kaminski NE Mol Pharmacol; 1998 Apr; 53(4):623-9. PubMed ID: 9547351 [TBL] [Abstract][Full Text] [Related]
17. Suppression of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-mediated aryl hydrocarbon receptor transformation and CYP1A1 induction by the phosphatidylinositol 3-kinase inhibitor 2-(4-morpholinyl)-8-phenyl-4H-1- benzopyran-4-one (LY294002). Guo M; Joiakim A; Reiners JJ Biochem Pharmacol; 2000 Sep; 60(5):635-42. PubMed ID: 10927021 [TBL] [Abstract][Full Text] [Related]
18. Signal transduction-mediated activation of the aryl hydrocarbon receptor in rat hepatoma H4IIE cells. Backlund M; Johansson I; Mkrtchian S; Ingelman-Sundberg M J Biol Chem; 1997 Dec; 272(50):31755-63. PubMed ID: 9395520 [TBL] [Abstract][Full Text] [Related]
19. Superinduction of CYP1A1 in MCF10A cultures by cycloheximide, anisomycin, and puromycin: a process independent of effects on protein translation and unrelated to suppression of aryl hydrocarbon receptor proteolysis by the proteasome. Joiakim A; Mathieu PA; Elliott AA; Reiners JJ Mol Pharmacol; 2004 Oct; 66(4):936-47. PubMed ID: 15385644 [TBL] [Abstract][Full Text] [Related]
20. 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) induces plasminogen activator inhibitor-1 through an aryl hydrocarbon receptor-mediated pathway in mouse hepatoma cell lines. Son DS; Rozman KK Arch Toxicol; 2002 Jul; 76(7):404-13. PubMed ID: 12111005 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]