Biblio | College of Agricultural Sciences

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C. V. Gerlach, Das, S. R., Volz, D. C., Bisson, W. H., Kolluri, S. K., and Tanguay, R. L., “Mono-substituted isopropylated triaryl phosphate, a major component of Firemaster 550, is an AHR agonist that exhibits AHR-independent cardiotoxicity in zebrafish.”, Aquat Toxicol, vol. 154, pp. 71-9, 2014.

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S. Kolluri, Balduf, C., Hofmann, M., and Göttlicher, M., “Novel Target Genes of the Ah (Dioxin) Receptor Transcriptional Induction of N-Myristoyltransferase 2”, Cancer research, vol. 61, pp. 8534–8539, 2001.

S. Kolluri, Kaul, R., Banerjee, K., and Gupta, S. K., “Nucleotide sequence of cDNA encoding bonnet monkey (Macaca radiata) zona pellucida glycoprotein-ZP3”, Reproduction, Fertility and Development, vol. 7, pp. 1209–1212, 1995.

F. Luciano, Krajewska, M., Ortiz-Rubio, P., Krajewski, S., Zhai, D., Faustin, B., Bruey, J. - M., Bailly-Maitre, B., Lichtenstein, A., Kolluri, S., Satterthwait, A. C., Zhang, X. - K., and Reed, J. C., “Nur77 converts phenotype of Bcl-B, an antiapoptotic protein expressed in plasma cells and myeloma”, Blood, vol. 109, no. 9, pp. 3849 - 3855, 2007.

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B. Lin, Chen, G. -quan, Xiao, D., Kolluri, S., Cao, X., Su, H., and Zhang, X. -kun, “Orphan receptor COUP-TF is required for induction of retinoic acid receptor $\beta$, growth inhibition, and apoptosis by retinoic acid in cancer cells”, Molecular and cellular biology, vol. 20, pp. 957–970, 2000.

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S. Kolluri, Weiss, C., Koff, A., and Gottlicher, M., “p27Kip1 induction and inhibition of proliferation by the intracellular Ah receptor in developing thymus and hepatoma cells”, Genes & Development, vol. 13, no. 13, pp. 1742 - 1753, 1999.

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Y. H. Han, Cao, X., Lin, B., Lin, F., Kolluri, S., Stebbins, J., Reed, J. C., Dawson, M. I., and Zhang, X. K., “Regulation of Nur77 nuclear export by c-Jun N-terminal kinase and Akt”, Oncogene, vol. 25, pp. 2974–2986, 2006.

S. Y. James, Lin, F., Kolluri, S., Dawson, M. I., and Zhang, X. -kun, “Regulation of retinoic acid receptor $\beta$ expression by peroxisome proliferator-activated receptor $\gamma$ ligands in cancer cells”, Cancer Research, vol. 63, pp. 3531–3538, 2003.

F. Lin, Kolluri, S., Chen, G. -quan, and Zhang, X. -kun, “Regulation of retinoic acid-induced inhibition of AP-1 activity by orphan receptor chicken ovalbumin upstream promoter-transcription factor”, Journal of Biological Chemistry, vol. 277, pp. 21414–21422, 2002.

S. Kolluri, Jin, U. - H., and Safe, S., “Role of the aryl hydrocarbon receptor in carcinogenesis and potential as an anti-cancer drug target.”, Arch Toxicol, vol. 91, no. 7, pp. 2497-2513, 2017.

S

S. Kolluri, Zhu, X., Zhou, X., Lin, B., Chen, Y., Sun, K., Tian, X., Town, J., Cao, X., Lin, F., Zhai, D., Kitada, S., Luciano, F., O'Donnell, E. F., Cao, Y., He, F., Lin, J., Reed, J. C., Satterthwait, A. C., and Zhang, X. -kun, “A Short Nur77-Derived Peptide Converts Bcl-2 from a Protector to a Killer”, Cancer Cell, vol. 14, no. 4, pp. 285 - 298, 2008.

A. Perkins, Phillips, J. Lynne, Kerkvliet, N. I., Tanguay, R., Perdew, G. H., Kolluri, S., and Bisson, W. H., “A structural switch between agonist and antagonist bound conformations for a ligand-optimized model of the human aryl hydrocarbon receptor ligand binding domain”, Biology, vol. 3, pp. 645–669, 2014.

A. Perkins, Phillips, J. Lynne, Kerkvliet, N., Tanguay, R., Perdew, G., Kolluri, S., and Bisson, W. H., “A Structural Switch between Agonist and Antagonist Bound Conformations for a Ligand-Optimized Model of the Human Aryl Hydrocarbon Receptor Ligand Binding Domain”, Biology, vol. 399, no. 4, pp. 645 - 669, 2014.

A. Perkins, Phillips, J. Lynne, Kerkvliet, N. I., Tanguay, R. L., Perdew, G. H., Kolluri, S. K., and Bisson, W. H., “A Structural Switch between Agonist and Antagonist Bound Conformations for a Ligand-Optimized Model of the Human Aryl Hydrocarbon Receptor Ligand Binding Domain.”, Biology (Basel), vol. 3, no. 4, pp. 645-69, 2014.

I. A. Murray, Flaveny, C. A., Chiaro, C. R., Sharma, A. K., Tanos, R. S., Schroeder, J. C., Amin, S. G., Bisson, W. H., Kolluri, S., and Perdew, G. H., “Suppression of cytokine-mediated complement factor gene expression through selective activation of the Ah receptor with 3′, 4′-dimethoxy-$\alpha$-naphthoflavone”, Molecular pharmacology, vol. 79, pp. 508–519, 2011.

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A. K. Ehrlich, Pennington, J. M., Bisson, W. H., Kolluri, S., and Kerkvliet, N. I., “TCDD, FICZ, and other high affinity AhR ligands dose-dependently determine the fate of CD4+ T cell differentiation.”, Toxicol Sci, 2018.

C. Weiss, Faust, D., Dürk, H., Kolluri, S., Pelzer, A., Schneider, S., Dietrich, C., Oesch, F., and Göttlicher, M., “TCDD induces c-jun expression via a novel Ah (dioxin) receptor-mediated p38-MAPK-dependent pathway.”, Oncogene, vol. 24, no. 31, pp. 4975-83, 2005.

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F. Lin, Xiao, D., Kolluri, S., and Zhang, X. -kun, “Unique anti-activator protein-1 activity of retinoic acid receptor $\beta$”, Cancer research, vol. 60, pp. 3271–3280, 2000.