The subdomains of the transactivation domain of the aryl hydrocarbon receptor (AhR) inhibit AhR and estrogen receptor transcriptional activity (original ) (raw )ERα-AHR-ARNT Protein-Protein Interactions Mediate Estradiol-dependent Transrepression of Dioxin-inducible Gene Transcription
Gary Perdew
Journal of Biological Chemistry, 2005
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The aryl hydrocarbon receptor (AHR)/AHR nuclear translocator (ARNT) heterodimer interacts with naturally occurring estrogen response elements
Hollie Swanson
Molecular and Cellular Endocrinology, 1999
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ER -AHR-ARNT Protein-Protein Interactions Mediate Estradiol-dependent Transrepression of Dioxin-inducible Gene Transcription
Timothy Beischlag
Journal of Biological Chemistry, 2005
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The Q-Rich Subdomain of the Human AhReceptor Transactivation Domain Is Required for Dioxin-Mediated Transcriptional Activity
Gary Perdew
Journal of Biological …, 2001
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Evidence that ligand binding is a key determinant of Ah receptor-mediated transcriptional activity
Laura Bonati
Archives of Biochemistry and Biophysics, 2005
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DETECTION OF NEW POTENTIALLY ACTIVE DRE SITES IN REGULATORY REGION OF HUMAN GENES ENCODING COMPONENTS OF Ah RECEPTOR CYTOSOLIC COMPLEX
Viatcheslav Mordvinov , Dmitry Oshchepkov
Journal of Alloys and Compounds
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The aryl hydrocarbon receptor interacts with estrogen receptor alpha and orphan receptors COUP-TFI and ERRα1
Hollie Swanson
2000
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Detection of New Potentially Active DRE Sites in Regulatory Region of Human Genes Encoding Components of Ah Receptor Cytosolyc Complex
Dmitry Oshchepkov
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AhR and ARNT modulate ER signaling
Ingemar Pongratz
Toxicology, 2010
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The Ah receptor inhibits estrogen-induced estrogen receptor � in breast cancer cells
Katarina Pettersson
Biochem Biophys Res Commun, 2004
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Repression of Aryl Hydrocarbon Receptor (AHR) signaling by AHR repressor: Role of DNA binding and competition for AHR nuclear translocator
R. Pollenz
Molecular Pharmacology, 2008
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Advance Access publication October 16, 2008 TOXICOLOGICAL HIGHLIGHT Ah Receptor Binding to its Cognate Response Element is Required for
Gary Perdew
2008
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Differential Recruitment of Coactivator RIP140 by Ah and Estrogen Receptors. ABSENCE OF A ROLE FOR LXXLL MOTIFS
Gary Perdew
Journal of Biological Chemistry, 1999
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Ah receptor binding to its cognate response element is required for dioxin-mediated toxicity
Gary Perdew
2008
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Binding of transformed Ah receptor complex to a dioxin responsive transcriptional enhancer: Evidence for two distinct heteromeric DNA-binding forms
Hollie Swanson
Biochemistry, 1993
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Ligand-dependent interactions of the Ah receptor with coactivators in a mammalian two-hybrid assay
Craig Rowlands
Toxicology and Applied Pharmacology, 2008
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AhR signaling pathways and regulatory functions
Xavier Coumoul
Biochimie Open
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Transgenic humanized AHR mouse reveals differences between human and mouse AHR ligand selectivity
Gary Perdew
2009
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Differential Regulation of Mouse Ah Receptor Gene Expression in Cell Lines of Different Tissue Origins
Pedro Fernandez-salguero
Archives of Biochemistry and Biophysics, 1996
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Species-specific binding of transformed Ah receptor to a dioxin responsive transcriptional enhancer
Cynthia Phelps
European Journal of Pharmacology: Environmental Toxicology and Pharmacology, 1992
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The Ah receptor inhibits estrogen-induced estrogen receptor β in breast cancer cells
Katarina Pettersson
Biochemical and Biophysical Research Communications, 2004
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Distinct Roles for Aryl Hydrocarbon Receptor Nuclear Translocator and Ah Receptor in Estrogen-Mediated Signaling in Human Cancer Cell Lines
Timothy Beischlag
PLoS ONE, 2012
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Dioxin Increases the Interaction Between Aryl Hydrocarbon Receptor and Estrogen Receptor Alpha at Human Promoters
Md. Sohel Ahmed
Toxicological Sciences, 2009
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Estrogen Receptor Subtype and Promoter-Specific Modulation of Aryl Hydrocarbon Receptor-Dependent Transcription
Sohel Ahmed
Molecular Cancer Research, 2009
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The Transcription Factor Aryl Hydrocarbon Receptor Nuclear Translocator Functions as an Estrogen Receptor Selective Coactivator, and Its Recruitment to Alternative Pathways Mediates Antiestrogenic Effects of Dioxin
Ingemar Pongratz , Joëlle Rüegg
Molecular Endocrinology, 2007
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The Transcription Factor Aryl Hydrocarbon Receptor Nuclear Translocator Functions as an Estrogen Receptor β-Selective Coactivator, and Its Recruitment to Alternative Pathways Mediates Antiestrogenic Effects of Dioxin
Elin Swedenborg , Ingemar Pongratz , Joëlle Rüegg
Molecular Endocrinology, 2008
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The Active Form of Human Aryl Hydrocarbon Receptor (AHR) Repressor Lacks Exon 8, and Its Pro185 and Ala185 Variants Repress both AHR and Hypoxia-Inducible Factor
Ann Tarrant
Molecular and Cellular Biology, 2009
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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
Katarina Pettersson , Joëlle Rüegg , Ingemar Pongratz
Molecular endocrinology (Baltimore, Md.), 2008
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