檢索結果 - Christopher E. Dempsey

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  1. 1
    Structure, Location, and Lipid Perturbations of Melittin at the Membrane Interface

    Structure, Location, and Lipid Perturbations of Melittin at the Membrane Interface 由 Kalina Hristova, Christopher E. Dempsey, Stephen H. White

    出版 2001
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  2. 2
    Origin of Low Mammalian Cell Toxicity in a Class of Highly Active Antimicrobial Amphipathic Helical Peptides

    Origin of Low Mammalian Cell Toxicity in a Class of Highly Active Antimicrobial Amphipathic Helical Peptides 由 Ayman Hawrani, Robin Howe, Timothy R. Walsh, Christopher E. Dempsey

    出版 2008
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  3. 3
    The Interaction of Guanidinium Ions with a Model Peptide

    The Interaction of Guanidinium Ions with a Model Peptide 由 Philip E. Mason, John W. Brady, George W. Neilson, Christopher E. Dempsey

    出版 2007
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  4. 4
    Arginine side chain interactions and the role of arginine as a gating charge carrier in voltage sensitive ion channels

    Arginine side chain interactions and the role of arginine as a gating charge carrier in voltage sensitive ion channels 由 Craig T. Armstrong, Philip E. Mason, J. L. Ross Anderson, Christopher E. Dempsey

    出版 2016
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  5. 5
    Ranolazine inhibition of hERG potassium channels: Drug–pore interactions and reduced potency against inactivation mutants

    Ranolazine inhibition of hERG potassium channels: Drug–pore interactions and reduced potency against inactivation mutants 由 Chunyun Du, Yihong Zhang, Aziza El Harchi, Christopher E. Dempsey, Jules C. Hancox

    出版 2014
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  6. 6
    Molecular basis of hERG potassium channel blockade by the class Ic antiarrhythmic flecainide

    Molecular basis of hERG potassium channel blockade by the class Ic antiarrhythmic flecainide 由 Dario Melgari, Yihong Zhang, Aziza El Harchi, Christopher E. Dempsey, Jules C. Hancox

    出版 2015
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  7. 7
    An Update on the Structure of hERG

    An Update on the Structure of hERG 由 Andrew S. Butler, Matthew V. Helliwell, Yihong Zhang, Jules C. Hancox, Christopher E. Dempsey

    出版 2020
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  8. 8
    Assessing hERG Pore Models As Templates for Drug Docking Using Published Experimental Constraints: The Inactivated State in the Context of Drug Block

    Assessing hERG Pore Models As Templates for Drug Docking Using Published Experimental Constraints: The Inactivated State in the Context of Drug Block 由 Christopher E. Dempsey, Dominic Wright, Charlotte K. Colenso, Richard B. Sessions, Jules C. Hancox

    出版 2014
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  9. 9
    Contribution of proline‐14 to the structure and actions of melittin

    Contribution of proline‐14 to the structure and actions of melittin 由 Christopher E. Dempsey, Renzo Bazzo, Timothy S. Harvey, Inge Syperek, G. Boheim, Iain D. Campbell

    出版 1991
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  10. 10
    Structural implications of hERG K+ channel block by a high-affinity minimally structured blocker

    Structural implications of hERG K+ channel block by a high-affinity minimally structured blocker 由 Matthew V. Helliwell, Yihong Zhang, Aziza El Harchi, Chunyun Du, Jules C. Hancox, Christopher E. Dempsey

    出版 2018
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  11. 11
    Pro-arrhythmic effects of gain-of-function potassium channel mutations in the short QT syndrome

    Pro-arrhythmic effects of gain-of-function potassium channel mutations in the short QT syndrome 由 Jules C. Hancox, Chongyang Du, Andrew S. Butler, Yihong Zhang, Christopher E. Dempsey, Stephen C. Harmer, Henggui Zhang

    出版 2023
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  12. 12
    Interactions between amiodarone and the hERG potassium channel pore determined with mutagenesis and in silico docking

    Interactions between amiodarone and the hERG potassium channel pore determined with mutagenesis and in silico docking 由 Yihong Zhang, Charlotte K. Colenso, Aziza El Harchi, Hongwei Cheng, Harry J. Witchel, Christopher E. Dempsey, Jules C. Hancox

    出版 2016
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  13. 13
    Glycophorin A dimerization is driven by specific interactions between transmembrane alpha-helices.

    Glycophorin A dimerization is driven by specific interactions between transmembrane alpha-helices. 由 Mark A. Lemmon, John M. Flanagan, J.F. Hunt, Brian D. Adair, Barbara J. Bormann, Christopher E. Dempsey, Donald M. Engelman

    出版 1992
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  14. 14
    Distinct subcellular localisations of the putative inositol 1,3,4,5-tetrakisphosphate receptors GAP1 IP4BP and GAP1 m result from the GAP1 IP4BP PH domain directing plasma membrane targeting

    Distinct subcellular localisations of the putative inositol 1,3,4,5-tetrakisphosphate receptors GAP1 IP4BP and GAP1 m result from the GAP1 IP4BP PH domain directing plasma membrane... 由 Peter J. Lockyer, Joanna Bottomley, Jon S. Reynolds, Tracy J. McNulty, Venkateswarlu Kanamarlapudi, B. V. L. POTTER, Christopher E. Dempsey, Peter J. Cullen

    出版 1997
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  15. 15
    hERG Potassium Channel Blockade by the HCN Channel Inhibitor Bradycardic Agent Ivabradine

    hERG Potassium Channel Blockade by the HCN Channel Inhibitor Bradycardic Agent Ivabradine 由 Dario Melgari, Kieran E. Brack, Chuan Zhang, Yihong Zhang, Aziza El Harchi, John S. Mitcheson, Christopher E. Dempsey, G. André Ng, Jules C. Hancox

    出版 2015
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  16. 16
    Tunable Protease-Activatable Virus Nanonodes

    Tunable Protease-Activatable Virus Nanonodes 由 Justin Judd, Michelle Ho, Abhinav Tiwari, Eric Gomez, Christopher E. Dempsey, Kim Van Vliet, Oleg A. Igoshin, Jonathan J. Silberg, Mavis Agbandje‐McKenna, Junghae Suh

    出版 2014
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