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425 related items for PubMed ID: 20935161
1. Aryl hydrocarbon receptor nuclear translocator in hepatocytes is required for aryl hydrocarbon receptor-mediated adaptive and toxic responses in liver. Nukaya M, Walisser JA, Moran SM, Kennedy GD, Bradfield CA. Toxicol Sci; 2010 Dec; 118(2):554-63. PubMed ID: 20935161 [Abstract] [Full Text] [Related]
2. Hypoxia perturbs aryl hydrocarbon receptor signaling and CYP1A1 expression induced by PCB 126 in human skin and liver-derived cell lines. Vorrink SU, Severson PL, Kulak MV, Futscher BW, Domann FE. Toxicol Appl Pharmacol; 2014 Feb 01; 274(3):408-16. PubMed ID: 24355420 [Abstract] [Full Text] [Related]
7. Dioxin toxicity in vivo results from an increase in the dioxin-independent transcriptional activity of the aryl hydrocarbon receptor. Céspedes MA, Galindo MI, Couso JP. PLoS One; 2010 Nov 08; 5(11):e15382. PubMed ID: 21079739 [Abstract] [Full Text] [Related]
8. The transcription factor aryl hydrocarbon receptor nuclear translocator functions as an estrogen receptor beta-selective coactivator, and its recruitment to alternative pathways mediates antiestrogenic effects of dioxin. Rüegg J, Swedenborg E, Wahlström D, Escande A, Balaguer P, Pettersson K, Pongratz I. Mol Endocrinol; 2008 Feb 08; 22(2):304-16. PubMed ID: 17991765 [Abstract] [Full Text] [Related]
9. The aryl hydrocarbon receptor-interacting protein (AIP) is required for dioxin-induced hepatotoxicity but not for the induction of the Cyp1a1 and Cyp1a2 genes. Nukaya M, Lin BC, Glover E, Moran SM, Kennedy GD, Bradfield CA. J Biol Chem; 2010 Nov 12; 285(46):35599-605. PubMed ID: 20829355 [Abstract] [Full Text] [Related]
10. Distinct roles for aryl hydrocarbon receptor nuclear translocator and ah receptor in estrogen-mediated signaling in human cancer cell lines. Labrecque MP, Takhar MK, Hollingshead BD, Prefontaine GG, Perdew GH, Beischlag TV. PLoS One; 2012 Nov 12; 7(1):e29545. PubMed ID: 22235307 [Abstract] [Full Text] [Related]
11. 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 12; 76(7):404-13. PubMed ID: 12111005 [Abstract] [Full Text] [Related]
13. Expression of the mediators of dioxin toxicity, aryl hydrocarbon receptor (AHR) and the AHR nuclear translocator (ARNT), is developmentally regulated in mouse teeth. Sahlberg C, Pohjanvirta R, Gao Y, Alaluusua S, Tuomisto J, Lukinmaa PL. Int J Dev Biol; 2002 May 12; 46(3):295-300. PubMed ID: 12068950 [Abstract] [Full Text] [Related]
14. Novel roles for AhR and ARNT in the regulation of alcohol dehydrogenases in human hepatic cells. Attignon EA, Leblanc AF, Le-Grand B, Duval C, Aggerbeck M, Rouach H, Blanc EB. Arch Toxicol; 2017 Jan 12; 91(1):313-324. PubMed ID: 27055685 [Abstract] [Full Text] [Related]
19. High-resolution genome-wide mapping of AHR and ARNT binding sites by ChIP-Seq. Lo R, Matthews J. Toxicol Sci; 2012 Dec 12; 130(2):349-61. PubMed ID: 22903824 [Abstract] [Full Text] [Related]
20. 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 12; 83(2):340-8. PubMed ID: 15537747 [Abstract] [Full Text] [Related] Page: [Next] [New Search]