γ-Secretase Partitioning into Lipid Bilayers Remodels Membrane Microdomains after Direct Insertion von Barros, Marilia, Houlihan, William J, Paresi, Chelsea J, Brendel, Matthew, Rynearson, Kevin D, Lee, Chang-Wook, Prikhodko, Olga, Cregger, Cristina, Chang, Geoffrey, Wagner, Steven L, Gilchrist, M Lane, Li, Yue-Ming

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Molecular mechanisms underlying the heterogeneous barrier responses of two primary endothelial cell types to sphingosine-1-phosphate von Salminen, Alec T., McCloskey, Molly C., Ahmad, S. Danial, Romanick, Samantha S., Chen, Kaihua, Houlihan, William, Klaczko, Michael E., Flax, Jonathan, Waugh, Richard E., McGrath, James L.

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Partitioning of γ-Secretase and its Substrates in Lipid Microdomains von Barros, Marilia, Houlihan, William, Gilchrist, Lane, Li, Yueming

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Three-Dimensional Quantitative Structure−Activity Relationships of Mazindol Analogues at the Dopamine Transporter von Kulkarni, Santosh S, Newman, Amy Hauck, Houlihan, William J

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Mazindol Analogues as Potential Inhibitors of the Cocaine Binding Site at the Dopamine Transporter von Houlihan, William J, Kelly, Lawrence, Pankuch, Jessica, Koletar, Judith, Brand, Leonard, Janowsky, Aaron, Kopajtic, Theresa A

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Assessment of mazindane, a pro-drug form of mazindol, in assays used to define cocaine treatment agents von Houlihan, William J., Kelly, Lawrence

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Benzo- and Cyclohexanomazindol Analogues as Potential Inhibitors of the Cocaine Binding Site at the Dopamine Transporter von Houlihan, William J, Ahmad, Umer F, Koletar, Judith, Kelly, Lawrence, Brand, Leonard, Kopajtic, Theresa A

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Antitumor Activity of 5-Aryl-2,3-dihydroimidazo[2,1-a]isoquinolines von Houlihan, William J, Munder, Paul G, Handley, Dean A, Cheon, Seung H, Parrino, Vincent A

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Halogenated Mazindol Analogs as Potential Inhibitors of the Cocaine Binding Site at the Dopamine Transporter von Houlihan, William J, Boja, John W, Parrino, Vincent A, Kopajtic, Theresa A, Kuhar, Michael J

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Anti‐Obesity Drugs von Houlihan, William J.

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Structural modification of 5-aryl-2,3-dihydroimidazo[2,1-a]isoquinoline platelet activating factor receptor antagonists von Houlihan, William J, Cheon, Seung H, Parrino, Vincent A, Handley, Dean A, Larson, Douglas A

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Dimeric Products from the Base-Catalyzed Condensation of Benzaldehyde with 2,3-Dihydro-1H-inden-1-one or 2-(Phenylmethylene)-2,3-dihydro-1H- inden-1-one von Houlihan, William J, Shapiro, Michael J, Chin, Jefferson A

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High affinity recognition of serotonin transporter antagonists defined by species-scanning mutagenesis. An aromatic residue in transmembrane domain I dictates species-selective rec... von Barker, E L, Perlman, M A, Adkins, E M, Houlihan, W J, Pristupa, Z B, Niznik, H B, Blakely, R D

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Antitumor Activity of the R- and S-Enantiomers of RS-2-[[Hydroxy[[2-[(octadecyloxy)methyl]tetrahydrofuran-2-yl]methoxy]phosphinyl]oxy]-N,N,N-trimethylethylaminium Hydroxide Inner S... von Houlihan, William J, Prasad, Kapa, Underwood, Russell, Repič, Oljan, Munder, Paul G

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Phospholipid antitumor agents von Houlihan, William J., Lohmeyer, Matthias, Workman, Paul, Cheon, Seung H.

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Lithiation of N-(2-alkylphenyl)alkanamides and related compounds. A modified Madelung indole synthesis von Houlihan, William J, Parrino, Vincent A, Uike, Yasuyuki

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High Affinity Recognition of Serotonin Transporter Antagonists Defined by Species-scanning Mutagenesis von Barker, Eric L., Perlman, Melody A., Adkins, Erika M., Houlihan, William J., Pristupa, Zdenek B., Niznik, Hyman B., Blakely, Randy D.

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Directed lithiation of 2-phenyl- and 2-(o-methylphenyl)imidazoline von Houlihan, William J, Parrino, Vincent A

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Novel cycloaddition products formed by the modified Madelung indole synthesis von Houlihan, William J, Uike, Yasuyuki, Parrino, Vincent A

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Sleep-inducing N-alkyl-5-[m-(trifluoromethyl)phenyl]-5-hydroxy-2-pyrrolidinones and N-alkyl-3-(trifluoromethyl)cinnamamides von Houlihan, William J, Gogerty, John H, Ryan, Eileen A, Schmitt, Gemma

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