Identification of a potent synthetic FXR agonist with an unexpected mode of binding and activation von Soisson, Stephen M, Parthasarathy, Gopalakrishnan, Adams, Alan D, Sahoo, Soumya, Sitlani, Ayesha, Sparrow, Carl, Cui, Jisong, Becker, Joseph W

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A Potent Synthetic LXR Agonist Is More Effective than Cholesterol Loading at Inducing ABCA1 mRNA and Stimulating Cholesterol Efflux von Sparrow, Carl P., Baffic, Joanne, Lam, My-Hanh, Lund, Erik G., Adams, Alan D., Fu, Xuan, Hayes, Nancy, Jones, A. Brian, Macnaul, Karen L., Ondeyka, John, Singh, Sheo, Wang, Jianhua, Zhou, Gaochao, Moller, David E., Wright, Samuel D., Menke, John G.

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Distinct Properties and Advantages of a Novel Peroxisome Proliferator-Activated Protein γ Selective Modulator von Berger, Joel P, Petro, Ann E, Macnaul, Karen L, Kelly, Linda J, Zhang, Bei B, Richards, Karen, Elbrecht, Alex, Johnson, Bruce A, Zhou, Gaochao, Doebber, Thomas W, Biswas, Chhabi, Parikh, Mona, Sharma, Neelam, Tanen, Michael R, Thompson, G. Marie, Ventre, John, Adams, Alan D, Mosley, Ralph, Surwit, Richard S, Moller, David E

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Different roles of liver X receptor α and β in lipid metabolism: Effects of an α-selective and a dual agonist in mice deficient in each subtype von Lund, Erik G., Peterson, Laurence B., Adams, Alan D., Lam, My-Hanh N., Burton, Charlotte A., Chin, Jayne, Guo, Qiu, Huang, Shaei, Latham, Melanie, Lopez, Jacqueline C., Menke, John G., Milot, Denise P., Mitnaul, Lyndon J., Rex-Rabe, Sandra E., Rosa, Raymond L., Tian, Jenny Y., Wright, Samuel D., Sparrow, Carl P.

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Design of potent and selective GPR119 agonists for type II diabetes von Szewczyk, Jason W., Acton, John, Adams, Alan D., Chicchi, Gary, Freeman, Stanley, Howard, Andrew D., Huang, Yong, Li, Cai, Meinke, Peter T., Mosely, Ralph, Murphy, Elizabeth, Samuel, Rachel, Santini, Conrad, Yang, Meng, Zhang, Yong, Zhao, Kake, Wood, Harold B.

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Amphipathic 3-Phenyl-7-propylbenzisoxazoles; human pPaR γ, δ and α agonists von Adams, Alan D, Yuen, Winston, Hu, Zao, Santini, Conrad, Jones, A.Brian, MacNaul, Karen L, Berger, Joel P, Doebber, Thomas W, Moller, David E

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SAR studies: Designing potent and selective LXR agonists von Szewczyk, Jason W., Huang, Shaei, Chin, Jayne, Tian, Jenny, Mitnaul, Lyndon, Rosa, Raymond L., Peterson, Larry, Sparrow, Carl P., Adams, Alan D.

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O-Arylmandelic acids as highly selective human PPAR α/γ agonists von Adams, Alan D, Hu, Zao, von Langen, Derek, Dadiz, Adonis, Elbrecht, Alex, MacNaul, Karen L, Berger, Joel P, Zhou, Gaochao, Doebber, Thomas W, Meurer, Roger, Forrest, Michael J, Moller, David E, Brian Jones, A

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Miniaturization of cell-based beta-lactamase-dependent FRET assays to ultra-high throughput formats to identify agonists of human liver X receptors von Chin, Jayne, Adams, Alan D, Bouffard, Aileen, Green, Ahren, Lacson, Raul G, Smith, Todd, Fischer, Paul A, Menke, John G, Sparrow, Carl P, Mitnaul, Lyndon J

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Retrofit propulsion apparatus for an avian decoy von Adams, Alan D

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An approach to erythronolide A seco acid via a simple tetronic acid von Schlessinger, Richard H, Mjalli, Adnan M. M, Adams, Alan D, Springer, James P, Hoogsteen, Karst

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Selective steroid chlorinations directed by attached pyridine ester templates von Breslow, Ronald, Brandl, Michael, Hunger, Juergen, Adams, Alan D

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The structure and kinetic reactivity of a pyrrolidine-derived vinylogous urethane lithium enolate von Adams, Alan D, Schlessinger, R. H, Tata, J. R, Venit, J. J

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Amphipathic 3-phenyl-7-propylbenzisoxazoles; human PPaA γ, δ and α agonists von ADAMS, Alan D, YUEN, Winston, ZAO HU, SANTINI, Conrad, JONES, A. Brian, MACNAUL, Karen L, BERGER, Joel P, DOEBBER, Thomas W, MOLLER, David E

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Distinct properties and advantages of a novel peroxisome proliferator-activated protein [gamma] selective modulator von Berger, Joel P, Petro, Ann E, Macnaul, Karen L, Kelly, Linda J, Zhang, Bei B, Richards, Karen, Elbrecht, Alex, Johnson, Bruce A, Zhou, Gaochao, Doebber, Thomas W, Biswas, Chhabi, Parikh, Mona, Sharma, Neelam, Tanen, Michael R, Thompson, G Marie, Ventre, John, Adams, Alan D, Mosley, Ralph, Surwit, Richard S, Moller, David E

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Reactive intermediates in the photochemistry of 4-diazo-2-pyrazolin-5-ones von Umrigar, Pesi, Griffin, Gary W, Ege, Seyhan N, Adams, Alan D, Das, Paritosh K

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Tetrapeptide derived inhibitors of complexation of a class II MHC: fully unnatural ligands von Brian Jones, A., Acton, John J., Adams, Alan D., Yuen, Winston, Nichols, Elizabeth A., Schwartz, Cheryl D., Wicker, Linda S., Hermes, Jeffrey D.

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SUBSTITUTED CYCLOPROPYL COMPOUNDS, COMPOSITIONS CONTAINING SUCH COMPOUNDS AND METHODS OF TREATMENT von YANG, Meng, WOOD, Harold, B, SZEWCZYK, Jason, W, ZHANG, Yong, ADAMS, Alan, D

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Oxopyrazoline-spiro-oxirans. A new class of reactive heterocycles von Eḡe, Seyhan N., Adams, Alan D., Gess, E. Joseph, Ragone, Katherine S., Kober, Brian J., Lampert, Mark B., Umrigar, Pesi, Lankin, David C., Griffin, Gary W.

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Pyridine, Pyrimidine and Pyrazine Derivatives as Cxcr3 Receptor Modulators von ADAMS ALAN D, SANTINI CONRAD

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