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Molecular Pharmacology|June 24, 2004
Use of 2-azido-3-[125I]iodo-7,8-dibromodibenzo-p-dioxin as a probe to determine the relative ligand affinity of human versus mouse aryl hydrocarbon receptor in cultured cellsPreeti Ramadoss, Gary H PerdewBiochemistry|August 17, 2005
The transactivation domain of the Ah receptor is a key determinant of cellular localization and ligand-independent nucleocytoplasmic shuttling propertiesPreeti Ramadoss, Gary H PerdewGut Microbes|December 31, 2020
The aryl hydrocarbon receptor as a mediator of host-microbiota interplayFangcong Dong, Gary H PerdewThe Journal of Biological Chemistry|April 20, 2005
ER alpha-AHR-ARNT protein-protein interactions mediate estradiol-dependent transrepression of dioxin-inducible gene transcriptionTimothy V Beischlag, Gary H PerdewThe Journal of Pharmacology and Experimental Therapeutics|December 7, 2007
Omeprazole stimulates the induction of human insulin-like growth factor binding protein-1 through aryl hydrocarbon receptor activationIain A Murray, Gary H PerdewMolecular and Cellular Pharmacology|September 28, 2011
Transgenic Humanized AHR Mouse Reveals Differences between Human and Mouse AHR Ligand SelectivityColin A Flaveny, Gary H PerdewBiochemistry|January 11, 2007
Carboxyl terminus of hsc70-interacting protein (CHIP) can remodel mature aryl hydrocarbon receptor (AhR) complexes and mediate ubiquitination of both the AhR and the 90 kDa heat-shock protein (hsp90) in vitroJ Luis Morales, Gary H PerdewBiochemistry|December 17, 2009
The uremic toxin 3-indoxyl sulfate is a potent endogenous agonist for the human aryl hydrocarbon receptorJennifer C Schroeder, Brett C Dinatale, Iain A Murray, et al.International Journal of Molecular Sciences|December 22, 2020
How Ah Receptor Ligand Specificity Became Important in Understanding Its Physiological FunctionIain A Murray, Gary H PerdewChemico-Biological Interactions|September 6, 2002
The role of chaperone proteins in the aryl hydrocarbon receptor core complexJohn R Petrulis, Gary H PerdewPageof 14