UK‐78,282, a novel piperidine compound that potently blocks the Kv1.3 voltage‐gated potassium channel and inhibits human T cell activation von Hanson, Douglas C, Nguyen, Angela, Mather, Robert J, Rauer, Heiko, Koch, Kevin, Burgess, Laurence E, Rizzi, James P, Donovan, Carol B, Bruns, Matthew J, Canniff, Paul C, Cunningham, Ann C, Verdries, Kimberly A, Mena, Edward, Kath, John C, Gutman, George A, Cahalan, Michael D, Grissmer, Stephan, Chandy, K George

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Potent Selective Nonpeptidic Inhibitors of Human Lung Tryptase von Burgess, Laurence E., Newhouse, Bradley J., Ibrahim, Prabha, Rizzi, James, Kashem, Mohammed A., Hartman, Ann, Brandhuber, Barbara J., Wright, Clifford D., Thomson, David S., Guy P. A. Vigers, Koch, Kevin

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Inhibition of allergen-induced pulmonary responses by the selective tryptase inhibitor 1,5-bis-{4-[(3-carbamimidoyl-benzenesulfonylamino)-methyl]-phenoxy}-pentane (AMG-126737) von Wright, Clifford D, Havill, Andrew M, Middleton, Scot C, Kashem, Mohammed A, Dripps, David J, Abraham, William M, Thomson, David S, Burgess, Laurence E

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A simple asymmetric synthesis of 2-substituted pyrrolidines and 5-substituted pyrrolidinones von Burgess, Laurence E, Meyers, A. I

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High-efficiency p +- n - n + back-surface-field silicon solar cells von Fossum, J. G., Burgess, E. L.

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A simple asymmetric synthesis of 2-substituted pyrrolidines from 3-acylpropionic acids von Meyers, A. I, Burgess, Laurence E

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DNA-dependent protein kinase inhibitors as drug candidates for the treatment of cancer von Kashishian, Adam, Douangpanya, Heather, Clark, Darcey, Schlachter, Stephen T, Eary, C Todd, Schiro, Justin G, Huang, Hongmei, Burgess, Larry E, Kesicki, Edward A, Halbrook, James

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A formal total synthesis of (+)-macbecin I von Martin, Stephen F, Dodge, Jeffrey A, Burgess, Laurence E, Hartmann, Michael

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The SAR of UK-78,282: A novel blocker of human T cell Kv1.3 potassium channels von Burgess, Laurence E., Koch, Kevin, Cooper, Kelvin, Biggers, Michael S., Ramchandani, Mukesh, Smitrovich, Jacqueline H., Gilbert, Eric J., Bruns, Matthew J., Mather, Robert J., Donovan, Carol B., Hanson, Douglas C.

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Discovery and SAR of trisubstituted thiazolidinones as CCR4 antagonists von Allen, Shelley, Newhouse, Bradley, Anderson, Aaron S., Fauber, Benjamin, Allen, Andrew, Chantry, David, Eberhardt, Christine, Odingo, Joshua, Burgess, Laurence E.

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Progress in light ion beam fusion research on PBFA II von Cook, D L, Allshouse, G O, Bailey, J, Barr, G W, Boyes, J D, Burgess, E L, Boyer, W B, Cap, J S, Coats, R S, Dreike, P L, Fifer, H G, Furaus, J P, Gerber, R A, Goldsmith, S, Goldstein, S A, Hamil, R A, Humphreys, D R, Leeper, R J, McDaniel, D H, Martin, T H, Jr, C W Mendel, Miller, P A, Mix, L P, Neau, E L, Olsen, J N, Peterson, G D, Prestwich, K R, Quintenz, J P, Rochau, G E, Rosenthal, S E, Rovang, D C, Ruiz, C L, Schneider, L, Seamons, L O, Seidel, D B, Simmons, T N, Slutz, S A, Stinnett, R W, Stygar, W A, Sweeney, M A, Tolk, K M, Turman, B N, Wilson, J M, VanDevender, J P

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Tryptase activates peripheral blood mononuclear cells causing the synthesis and release of TNF-α, IL-6 and IL-1β: possible relevance to multiple sclerosis von Malamud, Vivian, Vaaknin, Ady, Abramsky, Oded, Mor, Michal, Burgess, Laurence E., Ben-Yehudah, Ahmi, Lorberboum-Galski, Haya

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Silicon solar cell designs based on physical behavior in concentrated sunlight von Fossum, J.G., Burgess, E.L., Lindholm, F.A.

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Potent Nonpeptide Antagonists of the Bradykinin B1 Receptor:  Structure−Activity Relationship Studies with Novel Diaminochroman Carboxamides von Biswas, Kaustav, Li, Aiwen, Chen, Jian Jeffrey, D'Amico, Derin C, Fotsch, Christopher, Han, Nianhe, Human, Jason, Liu, Qingyian, Norman, Mark H, Riahi, Bobby, Yuan, Chester, Suzuki, Hideo, Mareska, David A, Zhan, James, Clarke, David E, Toro, Andras, Groneberg, Robert D, Burgess, Laurence E, Lester-Zeiner, Dianna, Biddlecome, Gloria, Manning, Barton H, Arik, Leyla, Dong, Hong, Huang, Ming, Kamassah, Augustus, Loeloff, Richard, Sun, Hong, Hsieh, Feng-Yin, Kumar, Gondi, Ng, Gordon Y, Hungate, Randall W, Askew, Benny C, Johnson, Eileen

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Racemic and chiral lactams as potent, selective and functionally active CCR4 antagonists von Newhouse, Bradley, Allen, Shelley, Fauber, Benjamin, Anderson, Aaron S., Eary, C. Todd, Hansen, Joshua D., Schiro, Justin, Gaudino, John J., Laird, Ellen, Chantry, David, Eberhardt, Christine, Burgess, Laurence E.

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Precipitation of Dopants in Silicon-Germanium Thermoelectric Alloys von Nasby, R. D., Burgess, E. L.

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A perspective on future photovoltaic systems von Burgess, E.L.

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Application of the superposition principle to solar-cell analysis von Lindholm, F.A., Fossum, J.G., Burgess, E.L.

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4-KETOUNDECANOIC ACID

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The preparation of α-substituted, β-hydroxy piperidines and pyrrolidines: The total synthesis of febrifugine von Burgess, Laurence E., Gross, Elizabeth K.M., Jurka, Joe

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