Differences in TCDD-elicited gene expression profiles in human HepG2, mouse Hepa1c1c7 and rat H4IIE hepatoma cells
暂无分享,去创建一个
[1] V. K. Rowe,et al. Toxicology of chlorinated dibenzo-p-dioxins. , 1973, Environmental health perspectives.
[2] J. Zinkl,et al. Toxicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in C57B1/6 mice. , 1974, Toxicology and applied pharmacology.
[3] E. Glover,et al. Stereospecific, high affinity binding of 2,3,7,8-tetrachlorodibenzo-p-dioxin by hepatic cytosol. Evidence that the binding species is receptor for induction of aryl hydrocarbon hydroxylase. , 1976, The Journal of biological chemistry.
[4] R. A. Neal,et al. Toxicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin in the golden Syrian hamster. , 1980, Toxicology and applied pharmacology.
[5] B. Schwetz,et al. Toxicity of 2, 3, 7, 8-tetrachlorodibenzo-p-dioxin (TCDD). , 1982, Drug metabolism reviews.
[6] A Poland,et al. 2,3,7,8-tetrachlorodibenzo-p-dioxin and related halogenated aromatic hydrocarbons: examination of the mechanism of toxicity. , 1982, Annual review of pharmacology and toxicology.
[7] M. Denison,et al. Structure and function of the Ah receptor for 2,3,7,8-tetrachlorodibenzo-p-dioxin. Species difference in molecular properties of the receptors from mouse and rat hepatic cytosols. , 1986, The Journal of biological chemistry.
[8] L. Wu,et al. Superinduction of CYP1A1 transcription by cycloheximide. Role of the DNA binding site for the liganded Ah receptor. , 1992, The Journal of biological chemistry.
[9] O. Hankinson. The aryl hydrocarbon receptor complex. , 1995, Annual review of pharmacology and toxicology.
[10] C. Bradfield,et al. Ah receptor signaling pathways. , 1996, Annual review of cell and developmental biology.
[11] M. Denison,et al. The Ah Receptor: A Regulator of the Biochemical and Toxicological Actions of Structurally Diverse Chemicals , 1998, Bulletin of environmental contamination and toxicology.
[12] M. Medvedovic,et al. The transcriptional signature of dioxin in human hepatoma HepG2 cells. , 2000, Biochemical pharmacology.
[13] P Smith,et al. Concordance of the toxicity of pharmaceuticals in humans and in animals. , 2000, Regulatory toxicology and pharmacology : RTP.
[14] D. Nebert,et al. Role of the aromatic hydrocarbon receptor and [Ah] gene battery in the oxidative stress response, cell cycle control, and apoptosis. , 2000, Biochemical pharmacology.
[15] Kiyoshi Nagata,et al. Selective suppressions of human CYP3A forms, CYP3A5 and CYP3A7, by troglitazone in HepG2 cells. , 2002, Drug metabolism and pharmacokinetics.
[16] T. Speed,et al. Design issues for cDNA microarray experiments , 2002, Nature Reviews Genetics.
[17] Q. Ma. Induction and superinduction of 2,3,7,8-tetrachlorodibenzo-rho-dioxin-inducible poly(ADP-ribose) polymerase: role of the aryl hydrocarbon receptor/aryl hydrocarbon receptor nuclear translocator transcription activation domains and a labile transcription repressor. , 2002, Archives of biochemistry and biophysics.
[18] Brad T. Sherman,et al. DAVID: Database for Annotation, Visualization, and Integrated Discovery , 2003, Genome Biology.
[19] L D Burgoon,et al. Comparative analysis of dioxin response elements in human, mouse and rat genomic sequences. , 2004, Nucleic acids research.
[20] D. Ryu,et al. Microarray analysis of gene regulation in the Hepa1c1c7 cell line following exposure to the DNA methylation inhibitor 5-aza-2'-deoxycytidine and 2,3,7,8-tetrachlorodibenzo-p-dioxin. , 2004, Toxicology in vitro : an international journal published in association with BIBRA.
[21] S Miyano,et al. Open source clustering software. , 2004, Bioinformatics.
[22] C Gennings,et al. Empirical Bayes Gene Screening Tool for Time-Course or Dose–Response Microarray Data , 2004, Journal of biopharmaceutical statistics.
[23] Alok J. Saldanha,et al. Java Treeview - extensible visualization of microarray data , 2004, Bioinform..
[24] J. Reiners,et al. 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. , 2004, Molecular pharmacology.
[25] H. Hellmold,et al. 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) alters the mRNA expression of critical genes associated with cholesterol metabolism, bile acid biosynthesis, and bile transport in rat liver: a microarray study. , 2005, Toxicology and applied pharmacology.
[26] M. Bickel. Polychlorinated persistent compounds , 1982, Experientia.
[27] Terry M. Therneau,et al. Normalization of two-channel microarray experiments: a semiparametric approach , 2005, Bioinform..
[28] C. Gennings,et al. Protocols for the assurance of microarray data quality and process control , 2005, Nucleic acids research.
[29] T. Zacharewski,et al. In vivo – in vitro toxicogenomic comparison of TCDD-elicited gene expression in Hepa1c1c7 mouse hepatoma cells and C57BL/6 hepatic tissue , 2006, BMC Genomics.
[30] Brock Chittim,et al. Comparative toxicogenomic analysis of the hepatotoxic effects of TCDD in Sprague Dawley rats and C57BL/6 mice. , 2006, Toxicological sciences : an official journal of the Society of Toxicology.
[31] Darrell R Boverhof,et al. Toxicogenomics in risk assessment: applications and needs. , 2006, Toxicological sciences : an official journal of the Society of Toxicology.
[32] A. Baccarelli,et al. Microarray analysis of gene expression in peripheral blood mononuclear cells from dioxin-exposed human subjects. , 2007, Toxicology.
[33] T. Zacharewski,et al. Tamoxifen-elicited uterotrophy: cross-species and cross-ligand analysis of the gene expression program , 2009, BMC Medical Genomics.
[34] W. Heideman,et al. Aryl Hydrocarbon Receptor-Mediated Down-Regulation of Sox9b Causes Jaw Malformation in Zebrafish Embryos , 2008, Molecular Pharmacology.
[35] C. McCulloch,et al. Toxicogenomic analysis of gender, chemical, and dose effects in livers of TCDD- or aroclor 1254-exposed rats using a multifactor linear model. , 2008, Toxicological sciences : an official journal of the Society of Toxicology.
[36] P. Boutros,et al. Transcriptomic responses to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in liver: Comparison of rat and mouse , 2008, BMC Genomics.
[37] Chia‐cheng Chang,et al. Comparative analysis of AhR-mediated TCDD-elicited gene expression in human liver adult stem cells. , 2009, Toxicological sciences : an official journal of the Society of Toxicology.
[38] Steven N. Hart,et al. A Comparison of Whole Genome Gene Expression Profiles of HepaRG Cells and HepG2 Cells to Primary Human Hepatocytes and Human Liver Tissues , 2010, Drug Metabolism and Disposition.
[39] Christina Magkoufopoulou,et al. Comparison of HepG2 and HepaRG by whole-genome gene expression analysis for the purpose of chemical hazard identification. , 2010, Toxicological sciences : an official journal of the Society of Toxicology.
[40] Lyle D Burgoon,et al. Genome-wide computational analysis of dioxin response element location and distribution in the human, mouse, and rat genomes. , 2011, Chemical research in toxicology.