Target-Oriented and Diversity-Oriented Organic Synthesis in Drug Discovery von Schreiber, Stuart L.

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Printing Proteins as Microarrays for High-Throughput Function Determination von MacBeath, Gavin, Schreiber, Stuart L.

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Small Molecule Inhibitor of Mitotic Spindle Bipolarity Identified in a Phenotype-Based Screen von Mayer, Thomas U., Kapoor, Tarun M., Haggarty, Stephen J., King, Randall W., Schreiber, Stuart L., Mitchison, Timothy J.

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A mammalian histone deacetylase related to the yeast transcriptional regulator Rpd3p von TAUNTON, J, HASSIG, C. A, SCHREIBER, S. L

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Structure of the FKBP12-Rapamycin Complex Interacting with the Binding Domain of Human FRAP von Choi, Jungwon, Chen, Jie, Schreiber, Stuart L., Clardy, Jon

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Chromatin deacetylation by an ATP-dependent nucleosome remodelling complex von Schreiber, Stuart L, Tong, Jeffrey K, Hassig, Christian A, Schnitzler, Gavin R, Kingston, Robert E

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Chemistry and Biology of the Immunophilins and Their Immunosuppressive Ligands von Schreiber, Stuart L.

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PIK-Related Kinases: DNA Repair, Recombination, and Cell Cycle Checkpoints von Keith, Curtis T., Schreiber, Stuart L.

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Regulatory intramolecular association in a tyrosine kinase of the Tec family von Andreotti, Amy Hamilton, Bunnell, Stephen C, Feng, Sibo, Berg, Leslie J, Schreiber, Stuart L

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Inhibition of Proteasome Activities and Subunit-Specific Amino-Terminal Threonine Modification by Lactacystin von Fenteany, Gabriel, Standaert, Robert F., Lane, William S., Choi, Soongyu, Corey, E. J., Schreiber, Stuart L.

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A mammalian protein targeted by G1-arresting rapamycin-receptor complex von Brown, Eric J, Albers, Mark W, Bum Shin, Tae, ichikawa, Kazuo, Keith, Curtis T, Lane, William S, Schreiber, Stuart L

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Two Binding Orientations for Peptides to the Src SH3 Domain: Development of a General Model for SH3-Ligand Interactions von Feng, Sibo, Chen, James K., Yu, Hongtao, Simon, Julian A., Schreiber, Stuart L.

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Control of p70 S6 kinase by kinase activity of FRAP in vivo von Brown, Eric J, Beal, Peter A, Keith, Curtis T, Chen, Jie, Bum Shin, Tae, Schreiber, Stuart L

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Identification of an 11-kDa FKBP12-Rapamycin-Binding Domain Within the 289- kDa FKBP12-Rapamycin-Associated Protein and Characterization of a Critical Serine Residue von Chen, Jie, Zheng, Xiao-Feng, Brown, Eric J., Schreiber, Stuart L.

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ChemBank: a small-molecule screening and cheminformatics resource database von Seiler, Kathleen Petri, George, Gregory A, Happ, Mary Pat, Bodycombe, Nicole E, Carrinski, Hyman A, Norton, Stephanie, Brudz, Steve, Sullivan, John P, Muhlich, Jeremy, Serrano, Martin, Ferraiolo, Paul, Tolliday, Nicola J, Schreiber, Stuart L., Clemons, Paul A

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Controlling Signal Transduction with Synthetic Ligands von Spencer, David M., Wandless, Thomas J., Schreiber, Stuart L., Crabtree, Gerald R.

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Atomic Structures of the Human Immunophilin FKBP-12 Complexes with FK506 and Rapamycin von Van Duyne, Gregory D., Standaert, Robert F., Karplus, P.Andrew, Schreiber, Stuart L., Clardy, Jon

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Calcineurin is a common target of cyclophilin-cyclosporin A and FKBP-FK506 complexes von Liu, Jun, Farmer, Jesse D., Lane, Willam S., Friedman, Jeff, Weissman, Irving, Schreiber, Stuart L.

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Inhibition of T cell signaling by immunophilin-ligand complexes correlates with loss of calcineurin phosphatase activity von Liu, J, Albers, M. W, Wandless, T. J, Luan, S, Alberg, D. G, Belshaw, P. J, Cohen, P, MacKintosh, C, Klee, C. B, Schreiber, S. L

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Structural basis for the binding of proline-rich peptides to SH3 domains von Yu, Hongtao, Chen, James K., Feng, Sibo, Dalgarno, David C., Brauer, Andrew W., Schrelber, Stuart L.

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