Calibration of Microscopic Traffic Simulation in an Urban Environment Using GPS-Data von Stang, Christopher, Bogenberger, Klaus

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Dopamine D4 Receptor-Selective Compounds Reveal Structure–Activity Relationships that Engender Agonist Efficacy von Keck, Thomas M, Free, R. Benjamin, Day, Marilyn M, Brown, Sonvia L, Maddaluna, Michele S, Fountain, Griffin, Cooper, Charles, Fallon, Brooke, Holmes, Matthew, Stang, Christopher T, Burkhardt, Russell, Bonifazi, Alessandro, Ellenberger, Michael P, Newman, Amy H, Sibley, David R, Wu, Chun, Boateng, Comfort A

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Dopamine D 4 Receptor-Selective Compounds Reveal Structure-Activity Relationships that Engender Agonist Efficacy von Keck, Thomas M, Free, R Benjamin, Day, Marilyn M, Brown, Sonvia L, Maddaluna, Michele S, Fountain, Griffin, Cooper, Charles, Fallon, Brooke, Holmes, Matthew, Stang, Christopher T, Burkhardt, Russell, Bonifazi, Alessandro, Ellenberger, Michael P, Newman, Amy H, Sibley, David R, Wu, Chun, Boateng, Comfort A

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Design, synthesis, and biological evaluation of lipophilically modified bisphenol Z derivatives von Stitzlein, Lea M., Stang, Christopher R. T., Inbody, Laura R., Rao, P. S. S., Schneider, Ryan A., Dudley, Richard W.

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Implementation of a Pharmacist-Led Antimicrobial Time-Out for Medical-Surgery Services in an Academic Pediatric Hospital von Stang, Christopher R T, Jaggi, Preeti, Tansmore, Jessica, Parson, Katelyn, Nuss, Kathryn E, Sapko, Matthew, Thompson, R Zachary, Gallup, Nathaniel, Buckingham, Don, Abdel-Rasoul, Mahmoud, Watson, Joshua R

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22 Implementation of a pharmacist-driven antimicrobial time-out for medical-surgery services in an academic pediatric hospital von Stang, Christopher, Tansmore, Jessica, Parson, Katelyn, Nuss, Kathryn, Sapko, Matthew, Thompson, Zachary, Buckingham, Don, Abdel-Rasoul, Mahmoud, Watson, Joshua, Jaggi, Preeti

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Screening of a Small Flavonoid Library for Anti‐Cancer Activity Against Glioblastoma von Faler, Ashton D., Stang, Christopher R.T., Khupse, Rahul S., Schneider, Ryan A.

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Characterization of a Novel Series of D4 Dopamine Receptor Ligands Reveals Structure‐Activity Relationships for Selective Partial Agonists von Day, Marilyn M., Free, R. Benjamin, Stang, Christopher R.T., Boateng, Comfort A., Keck, Thomas M., Sibley, David R.

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Structure‐Activity Analysis of Bisphenol‐Z Derivatives for Anticancer Activity von Stang, Christopher R.T., Inbody, Laura R., Stitzlein, Lea M., Dick, Matt J., Eichel, Amanda M., Orahood, Cassandra B., Mohamed, Ahmed H., Dudley, Richard W., Schneider, Ryan A.

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Investigating the Selectivity of Novel Chalcones for Human Cancer Cells Compared to Non‐Cancerous Human Cell Lines von Stang, Christopher R.T., Inbody, Laura R., Hickey, Mikaela C., Mohamed, Ahmed H., Hollenbacher, Courtney A., Orahood, Cassandra B., Dick, Matt J., Eichel, Amanda M., Khupse, Rahul S., Schneider, Ryan A.

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Investigating the Selectivity of Putative Sigma‐2 Receptor Compounds in Human Cancer Cells Compared to Non‐Cancerous Cell Lines von Inbody, Laura R., Stang, Christopher R.T., Mohamed, Ahmed H., Hickey, Mikaela C., Orahood, Cassandra B., Dick, Matt J., Eichel, Amanda M., Zaibek, Ann E., Kinder, David H., Schneider, Ryan A.

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Investigation of Non‐Caspase Mediated Mechanisms of Death in Response to Treatment with Novel Chalcone in Glioblastoma Cell Lines von Inbody, Laura R., Stang, Christopher R.T., Eichel, Amanda M., Orahood, Cassandra B., Dick, Matt J., Mohamed, Ahmed H., Hickey, Mikaela C., Khupse, Rahul S., Schneider, Ryan A.

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Modulation of COX‐1 and COX‐2 Protein Levels by Selective and Non‐Selective NSAIDs von Schneider, Ryan, Whited, Tawna, Adams, Bryce, Miller, Ian, Stang, Christopher, Kim, Lindsay, Dudley, Richard, Kinder, David

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Novel Chalcone Derivatives Show Anti‐Cancer Effects in Several Human Cancer Cell Lines von Whited, Tawna, Adams, Bryce, Stang, Christopher, Pierson, Thomas, Khupse, Rahul, Dudley, Richard, Schneider, Ryan

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Optimization of a Series of Novel Chalcone Derivatives for Anti‐Cancer Activity von Whited, Tawna L., Stang, Christopher R.T., Adams, Bryce R., Khupse, Rahul S., Dudley, Richard W., Schneider, Ryan A.

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Modulation of Autophagy Proteins in Response to a Compound Designed as a Sigma‐2 Receptor Agonist Derived from Tamoxifen von Stang, Christopher R.T., Adams, Bryce R., Faler, Ashton D., Schuler, Brian R., Kinder, David H., Sabol, Patrick, Carlston, Leah, Schneider, Ryan A.

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Structure‐Activity Relationship of Novel Compounds Based on Tamoxifen with Proposed Sigma‐2 Receptor Activity von Stang, Christopher R.T., Inbody, Laura R., Orahood, Cassandra B., Dick, Matt J., Eichel, Amanda M., Mohamed, Ahmed H., Faler, Ashton D., Zaibek, Ann E., Kinder, David H., Schneider, Ryan A.

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Optimization of a Novel D 2 Dopamine Receptor Antagonist Scaffold Reveals Exceptionally Selective and Potent Lead Molecules von Day, Marilyn M., Dulcey, Andres E., Bayron, Diane, Stang, Christopher R.T., Moritz, Amy E., Doyle, Trevor, Javitch, Jonathan A., Southall, Noel T., Ferrer, Marc, Marugan, Juan J., Sibley, David R., Free, R. Benjamin

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Induction of Apoptosis and Generation of Reactive Oxygen Species by Novel Chalcone Derivatives von Stang, Christopher R.T., Adams, Bryce R., Faler, Ashton D., Schuler, Brian R., Eichel, Amanda M., Dick, Matt J., Orahood, Cassandra B., Whited, Tawna L., Rao, P.S.S., Dudley, Richard W., Khupse, Rahul S., Schneider, Ryan A.

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Anti‐Cancer Effects of a Proposed Sigma‐2 Receptor Agonist Structurally Similar to Tamoxifen von Adams, Bryce R., Stang, Christopher R.T., Carlston, Leah, Faler, Ashton D., Thomas, Colin D., Schuler, Brian R., Eichel, Amanda M., Whited, Tawna L., Kinder, David H., Schneider, Ryan A.

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