检索结果 - D Kuntz

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  1. 1
    Structure-based identification of an inducer of the low-pH conformational change in the influenza virus hemagglutinin: irreversible inhibition of infectivity

    Structure-based identification of an inducer of the low-pH conformational change in the influenza virus hemagglutinin: irreversible inhibition of infectivity 由 Laura Hoffman, Irwin D. Kuntz, J White

    出版 1997
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  2. 2
    Spectroscopic recognition of guanine dimeric hairpin quadruplexes by a carbocyanine dye.

    Spectroscopic recognition of guanine dimeric hairpin quadruplexes by a carbocyanine dye. 由 Q Chen, Irwin D. Kuntz, Richard H. Shafer

    出版 1996
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  3. 3
    Blood monocyte activation in rheumatoid arthritis: increased monocyte adhesiveness, integrin expression, and cytokine release

    Blood monocyte activation in rheumatoid arthritis: increased monocyte adhesiveness, integrin expression, and cytokine release 由 Frédéric Lioté, B. BOVAL-BOIZARD, D Weill, D Kuntz, JL Wautier

    出版 1996
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  4. 4
    Molecular cloning and nucleotide sequence of the streptavidin gene

    Molecular cloning and nucleotide sequence of the streptavidin gene 由 Carlos E. Argaraña, Irwin D. Kuntz, Steven Birken, Richard Axel, Charles R. Cantor

    出版 1986
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  5. 5
    Mutational and secondary structural analysis of the basolateral sorting signal of the polymeric immunoglobulin receptor.

    Mutational and secondary structural analysis of the basolateral sorting signal of the polymeric immunoglobulin receptor. 由 Benjamin Aroeti, Phyllis Anne Kosen, Irwin D. Kuntz, Fred E. Cohen, Keith E. Mostov

    出版 1993
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  6. 6
    Urinary Pharmacokinetic Profile of Cannabinoids Following Administration of Vaporized and Oral Cannabidiol and Vaporized CBD-Dominant Cannabis

    Urinary Pharmacokinetic Profile of Cannabinoids Following Administration of Vaporized and Oral Cannabidiol and Vaporized CBD-Dominant Cannabis 由 Tory R. Spindle, Edward J. Cone, D Kuntz, John M. Mitchell, George E. Bigelow, Ronald Flegel, Ryan G. Vandrey

    出版 2019
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  7. 7
    Computer-assisted Mutagenesis of Ecotin to Engineer Its Secondary Binding Site for Urokinase Inhibition

    Computer-assisted Mutagenesis of Ecotin to Engineer Its Secondary Binding Site for Urokinase Inhibition 由 Martha C.A. Laboissière, Malin M. Young, Rilva G. Pinho, Stephen Todd, Robert J. Fletterick, Irwin D. Kuntz, Charles S. Craik

    出版 2002
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  8. 8
    High throughput protein fold identification by using experimental constraints derived from intramolecular cross-links and mass spectrometry

    High throughput protein fold identification by using experimental constraints derived from intramolecular cross-links and mass spectrometry 由 Malin M. Young, Ning Tang, Judith C. Hempel, Connie Oshiro, Eric W. Taylor, Irwin D. Kuntz, Bradford W. Gibson, Gavin Dollinger

    出版 2000
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  9. 9
    Structure-based design and combinatorial chemistry yield low nanomolar inhibitors of cathepsin D

    Structure-based design and combinatorial chemistry yield low nanomolar inhibitors of cathepsin D 由 Ellen K. Kick, Diana C. Roe, A. Geoffrey Skillman, Guangcheng Liu, Todd Ewing, Yaxiong Sun, Irwin D. Kuntz, Jonathan A. Ellman

    出版 1997
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  10. 10
    Apolipoprotein (apo) E4 enhances amyloid β peptide production in cultured neuronal cells: ApoE structure as a potential therapeutic target

    Apolipoprotein (apo) E4 enhances amyloid β peptide production in cultured neuronal cells: ApoE structure as a potential therapeutic target 由 Shiming Ye, Yadong Huang, Karin Müllendorff, Liming Dong, Gretchen Giedt, Elaine C. Meng, Fred E. Cohen, Irwin D. Kuntz, Karl H. Weisgraber, Robert W. Mahley

    出版 2005
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  11. 11
    Structure-based design of nonpeptide inhibitors specific for the human immunodeficiency virus 1 protease.

    Structure-based design of nonpeptide inhibitors specific for the human immunodeficiency virus 1 protease. 由 Renée L. DesJarlais, George Seibel, Irwin D. Kuntz, Paul S. Furth, Juan C. Alvarez, P.R. Ortiz de Montellano, Dianne L. DeCamp, Lilia M. Babé, Charles S. Craik

    出版 1990
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  12. 12
    DOCK 6: Combining techniques to model RNA–small molecule complexes

    DOCK 6: Combining techniques to model RNA–small molecule complexes 由 P. Therese Lang, Scott R. Brozell, Sudipto Mukherjee, Eric F. Pettersen, Elaine C. Meng, Veena Thomas, Robert C. Rizzo, David A. Case, Thomas Leroy James, Irwin D. Kuntz

    出版 2009
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  13. 13
    Structure of a non-peptide inhibitor complexed with HIV-1 protease. Developing a cycle of structure-based drug design

    Structure of a non-peptide inhibitor complexed with HIV-1 protease. Developing a cycle of structure-based drug design 由 Earl Rutenber, Eric B. Fauman, Robert J. Keenan, Sherman Fong, Paul S. Furth, P.R. Ortiz de Montellano, E Meng, Irwin D. Kuntz, Dianne L. DeCamp, Rafael Salto

    出版 1993
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  14. 14
    Adenosine Analogues as Selective Inhibitors of Glyceraldehyde-3-phosphate Dehydrogenase of <i>Trypanosomatidae</i> via Structure-Based Drug Design

    Adenosine Analogues as Selective Inhibitors of Glyceraldehyde-3-phosphate Dehydrogenase of <i>Trypanosomatidae</i> via Structure-Based Drug Design 由 Jerome C. Bressi, Christophe L. M. J. Verlinde, Alex M. Aronov, My Le Shaw, Sam Sik Shin, Lisa N. Nguyen, Stephen Suresh, Frederick S. Buckner, Wesley C. Van Voorhis, Irwin D. Kuntz, Wim G. J. Hol, Michael H. Gelb

    出版 2001
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