Хайлтын үр дүнгүүд - David E. Timm

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  1. 1
    Conformational stability of dimeric proteins: Quantitative studies by equilibrium denaturation

    Conformational stability of dimeric proteins: Quantitative studies by equilibrium denaturation -н Kenneth Neet, David E. Timm

    Хэвлэсэн 1994
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    Revisão
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  2. 2
    Structural basis of pheromone binding to mouse major urinary protein (MUP‐I)

    Structural basis of pheromone binding to mouse major urinary protein (MUP‐I) -н David E. Timm, L. Baker, Heather Mueller, Lukáš Žı́dek, Miloš V. Novotný

    Хэвлэсэн 2001
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    Artigo
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  3. 3
    Crystal structure of human homogentisate dioxygenase.

    Crystal structure of human homogentisate dioxygenase. -н David E. Timm, Greg P. Titus, H.A. Mueller, John Burgner, Santiago Rodrı́guez de Córdoba, Miguel Á. Peñalva

    Хэвлэсэн 2000
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    Artigo
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  4. 4
    Structural and functional analysis of mutations in alkaptonuria

    Structural and functional analysis of mutations in alkaptonuria -н Javier M. Rodrı́guez, David E. Timm, Gail Titus, Daniel Beltrán-Valero de Bernabé, Olga Criado‐García, H. Mueller, Santiago Rodrı́guez de Córdoba, Miguel Á. Peñalva

    Хэвлэсэн 2000
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    Artigo
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  5. 5
    Merestinib (LY2801653) inhibits neurotrophic receptor kinase (NTRK) and suppresses growth of NTRK fusion bearing tumors

    Merestinib (LY2801653) inhibits neurotrophic receptor kinase (NTRK) and suppresses growth of NTRK fusion bearing tumors -н Bruce W. Konicek, Andrew Capen, Kelly M. Credille, Philip J. Ebert, Beverly L. Falcón, Gary L. Heady, Bharvin K.R. Patel, Victoria L. Peek, Jennifer R. Stephens, Julie Stewart, Stephanie L. Stout, David E. Timm, Suzane L. Um, Melinda D. Willard, Isabella H. Wulur, Yi Arial Zeng, Yong Wang, Richard A. Walgren, S. Betty Yan

    Хэвлэсэн 2018
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    Artigo
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  6. 6
    Robust Central Reduction of Amyloid-β in Humans with an Orally Available, Non-Peptidic β-Secretase Inhibitor

    Robust Central Reduction of Amyloid-β in Humans with an Orally Available, Non-Peptidic β-Secretase Inhibitor -н Patrick C. May, Robert A. Dean, Stephen L. Lowe, Ferenc Martényi, Scott M. Sheehan, Leonard N. Boggs, Scott A. Monk, Brian M. Mathes, Dustin J. Mergott, Brian M. Watson, Stephanie L. Stout, David E. Timm, Elizabeth LaBell, Celedon Gonzales, Masako Nakano, Stanford S. Jhee, Mark Yen, Larry Ereshefsky, Terry D. Lindstrom, David O. Calligaro, Patrick J. Cocke, Dennis G. Hall, Stuart Friedrich, Martin Citron, James E. Audia

    Хэвлэсэн 2011
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    Artigo
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  7. 7
    Discovery of a First-in-Class Inhibitor of the PRMT5–Substrate Adaptor Interaction

    Discovery of a First-in-Class Inhibitor of the PRMT5–Substrate Adaptor Interaction -н David C. McKinney, Brian J. McMillan, Matthew J. Ranaghan, Jamie A. Moroco, Merissa Brousseau, Zachary Mullin-Bernstein, Meghan O’Keefe, Patrick McCarren, Michael F. Mesleh, Kathleen M. Mulvaney, Foxy P. Robinson, Ritu Singh, Besnik Bajrami, Florence F. Wagner, Robert Hilgraf, Martin J. Drysdale, Arthur J. Campbell, Adam Skepner, David E. Timm, Dale Porter, Virendar K. Kaushik, William R. Sellers, Alessandra Ianari

    Хэвлэсэн 2021
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    Artigo
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  8. 8
    The Potent BACE1 Inhibitor LY2886721 Elicits Robust Central Aβ Pharmacodynamic Responses in Mice, Dogs, and Humans

    The Potent BACE1 Inhibitor LY2886721 Elicits Robust Central Aβ Pharmacodynamic Responses in Mice, Dogs, and Humans -н Patrick C. May, Brian A. Willis, Stephen L. Lowe, Robert A. Dean, Scott A. Monk, Patrick J. Cocke, James E. Audia, Leonard N. Boggs, Anthony R. Borders, Richard A. Brier, David O. Calligaro, Theresa A. Day, Larry Ereshefsky, Jon A. Erickson, Hykop Gevorkyan, Celedon Gonzales, Douglas E. James, Stanford S. Jhee, Steven F. Komjathy, Lin Li, Terry D. Lindstrom, Brian M. Mathes, Ferenc Martényi, Scott M. Sheehan, Stephanie L. Stout, David E. Timm, Grant M. Vaught, Brian M. Watson, Leonard L. Winneroski, Zhixiang Yang, Dustin J. Mergott

    Хэвлэсэн 2015
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    Artigo
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