Discovery and Pharmacology of a Novel Somatostatin Subtype 5 (SSTR5) Antagonist: Synergy with DPP‑4 Inhibition by Liu, Weiguo, Shao, Pengcheng P, Liang, Gui-Bai, Bawiec, John, He, Jiafang, Aster, Susan D, Wu, Margaret, Chicchi, Garry, Wang, John, Tsao, Kwei-Lan, Shang, Jin, Salituro, Gino, Zhou, Yun-Ping, Li, Cai, Akiyama, Taro E, Metzger, Daniel E, Murphy, Beth Ann, Howard, Andrew D, Weber, Ann E, Duffy, Joseph L

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Adamantyl triazoles as selective inhibitors of 11β-hydroxysteroid dehydrogenase type 1 by Olson, Steven, Aster, Susan D., Brown, Kai, Carbin, Linda, Graham, Donald W., Hermanowski-Vosatka, Anne, LeGrand, Cheryl B., Mundt, Steven S., Robbins, Michael A., Schaeffer, James M., Slossberg, Llnon H., Szymonifka, Michael J., Thieringer, Rolf, Wright, Samuel D., Balkovec, James M.

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Bis-aryl triazoles as selective inhibitors of 11β-hydroxysteroid dehydrogenase type 1 by Aster, Susan D., Graham, Donald W., Kharbanda, Divya, Patel, Gool, Ponpipom, Mitree, Santorelli, Gina M., Szymonifka, Michael J., Mundt, Steven S., Shah, Kashmira, Springer, Marty S., Thieringer, Rolf, Hermanowski-Vosatka, Anne, Wright, Samuel D., Xiao, Jianying, Zokian, Hratch, Balkovec, James M.

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Design and synthesis of novel antibacterial agents with inhibitory activity against DNA polymerase III by Ali, Amjad, Aster, Susan D, Graham, Donald W, Patel, Gool F, Taylor, Gayle E, Tolman, Richard L, Painter, Ronald E, Silver, Lynn L, Young, Katherine, Ellsworth, Kenneth, Geissler, Wayne, Harris, Georgianna S

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Conformationally restricted inhibitors of angiotensin-converting enzyme. Synthesis and computations by Thorsett, Eugene D, Harris, Elbert E, Aster, Susan D, Peterson, Elwood R, Snyder, James P, Springer, James P, Hirshfield, Jordan, Tristram, Edward W, Patchett, Arthur A

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Adamantyl triazoles as selective inhibitors of 11beta-hydroxysteroid dehydrogenase type 1 by Olson, Steven, Aster, Susan D, Brown, Kai, Carbin, Linda, Graham, Donald W, Hermanowski-Vosatka, Anne, LeGrand, Cheryl B, Mundt, Steven S, Robbins, Michael A, Schaeffer, James M, Slossberg, Llnon H, Szymonifka, Michael J, Thieringer, Rolf, Wright, Samuel D, Balkovec, James M

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Bis-aryl triazoles as selective inhibitors of 11beta-hydroxysteroid dehydrogenase type 1 by Aster, Susan D, Graham, Donald W, Kharbanda, Divya, Patel, Gool, Ponpipom, Mitree, Santorelli, Gina M, Szymonifka, Michael J, Mundt, Steven S, Shah, Kashmira, Springer, Marty S, Thieringer, Rolf, Hermanowski-Vosatka, Anne, Wright, Samuel D, Xiao, Jianying, Zokian, Hratch, Balkovec, James M

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Emerging Concepts and Technologies for the Discovery of Microorganisms Involved in Human Disease by Bullman, Susan, Meyerson, Matthew, Kostic, Aleksandar D

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Deletion-based mechanisms of Notch1 activation in T-ALL: key roles for RAG recombinase and a conserved internal translational start site in Notch1 by Ashworth, Todd D., Pear, Warren S., Chiang, Mark Y., Blacklow, Stephen C., Mastio, Jérôme, Xu, Lanwei, Kelliher, Michelle, Kastner, Philippe, Chan, Susan, Aster, Jon C.

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Notch1 Expression in Early Lymphopoiesis Influences B versus T Lineage Determination by Pui, John C, Allman, David, Xu, Lanwei, DeRocco, Susan, Karnell, Fredrick G, Bakkour, Sonia, Lee, Julia Y, Kadesch, Tom, Hardy, Richard R, Aster, Jon C, Pear, Warren S

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Meta-analysis of epigenome-wide association studies in newborns and children show widespread sex differences in blood DNA methylation by Solomon, Olivia, Huen, Karen, Yousefi, Paul, Küpers, Leanne K., González, Juan R., Suderman, Matthew, Reese, Sarah E., Page, Christian M., Gruzieva, Olena, Rzehak, Peter, Gao, Lu, Bakulski, Kelly M., Novoloaca, Alexei, Allard, Catherine, Pappa, Irene, Llambrich, Maria, Vives, Marta, Jima, Dereje D., Kvist, Tuomas, Baccarelli, Andrea, White, Cory, Rezwan, Faisal I., Sharp, Gemma C., Tindula, Gwen, Bergström, Anna, Grote, Veit, Dou, John F., Isaevska, Elena, Magnus, Maria C., Corpeleijn, Eva, Perron, Patrice, Jaddoe, Vincent W.V., Nohr, Ellen A., Maitre, Lea, Foraster, Maria, Hoyo, Cathrine, Håberg, Siri E., Lahti, Jari, DeMeo, Dawn L., Zhang, Hongmei, Karmaus, Wilfried, Kull, Inger, Koletzko, Berthold, Feinberg, Jason I., Gagliardi, Luigi, Bouchard, Luigi, Ramlau-Hansen, Cecilia Høst, Tiemeier, Henning, Santorelli, Gillian, Maguire, Rachel L., Czamara, Darina, Litonjua, Augusto A., Langhendries, Jean-Paul, Plusquin, Michelle, Lepeule, Johanna, Binder, Elisabeth B., Verduci, Elvira, Dwyer, Terence, Carracedo, Ángel, Ferre, Natalia, Eskenazi, Brenda, Kogevinas, Manolis, Nawrot, Tim S., Munthe-Kaas, Monica C., Herceg, Zdenko, Relton, Caroline, Melén, Erik, Gruszfeld, Dariusz, Breton, Carrie, Fallin, M.D., Ghantous, Akram, Nystad, Wenche, Heude, Barbara, Snieder, Harold, Hivert, Marie-France, Felix, Janine F., Sørensen, Thorkild I.A., Bustamante, Mariona, Murphy, Susan K., Raikkönen, Katri, Oken, Emily, Holloway, John W., Arshad, Syed Hasan, London, Stephanie J., Holland, Nina

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Deletion-Based Mechanisms of Notch1 Activation In T-ALL: Key Roles for RAG Recombinase and A Conserved Internal Translational Start Site In Notch1 by Aster, Jon C, Ashworth, Todd D, Chiang, Mark, Pear, Warren S., Blacklow, Stephen, Kelliher, Michelle, Kastner, Philippe, Chan, Susan

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Linkage of a Familial Platelet Disorder With a Propensity to Develop Myeloid Malignancies to Human Chromosome 21q22.1-22.2 by Ho, Carolyn Y., Otterud, Brith, Legare, Robert D., Varvil, Tena, Saxena, Richa, DeHart, David B., Kohler, Susan E., Aster, Jon C., Dowton, S. Bruce, Li, Frederick P., Leppert, Mark, Gilliland, D. Gary

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Deletion-based mechanisms of Notch 1 activation in T-ALL: key roles for RAG recombinase and a conserved internal translational start site in Notch1 by ASHWORTH, Todd D, PEAR, Warren S, CHIANG, Mark Y, BLACKLOW, Stephen C, MASTIO, Jérôme, LANWEI XU, KELLIHER, Michelle, KASTNER, Philippe, SUSAN CHAN, ASTER, Jon C

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Both Coactivator LXXLL Motif-dependent and -independent Interactions Are Required for Peroxisome Proliferator-activated Receptor γ (PPARγ) Function by Chen, Shiying, Johnson, Bruce A., Li, Ying, Aster, Susan, McKeever, Brian, Mosley, Ralph, Moller, David E., Zhou, Gaochao

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4-AZASTEROIDS AS 5α-REDUCTASE INHIBITORS: IDENTIFICATION OF 4,7β-DIMETHYL-4-AZA-5α-CHOLESTAN-3-ONE (MK-386) AS A SCALP ISOZYME SELECTIVE INHIBITOR by Tolman, Richard L., Aster, Susan, Bakshi, Raman K., Bergman, Jeffrey P., Bull, Herb G., Chang, Benedict, Cimis, George, Dolenga, Michael P., Durette, Phillippe, Ellsworth, Kenneth, Esser, Craig, Graham, Donald W., Hagmann, William K., Harris, Georgianna, Kopka, Ihor, Lanza, Thomas, Patel, Gool, Polo, Scott, Rasmusson, Gary H., Sahoo, Soumya, Toney, Jeffrey H., Von Langen, Derek, Witzel, Bruce

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