Resultados de procura - Louis DiDone

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  1. 1
    Identification, <i>in Vitro</i> Activity and Mode of Action of Phosphoinositide-Dependent-1 Kinase Inhibitors as Antifungal Molecules

    Identification, <i>in Vitro</i> Activity and Mode of Action of Phosphoinositide-Dependent-1 Kinase Inhibitors as Antifungal Molecules por Bonnie K. Baxter, Louis DiDone, Duana Ogu, Stanford Schor, Damian J. Krysan

    Publicado 2011
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  2. 2
    The Unfolded Protein Response Is Induced by the Cell Wall Integrity Mitogen-activated Protein Kinase Signaling Cascade and Is Required for Cell Wall Integrity in<i>Saccharomyces cerevisiae</i>

    The Unfolded Protein Response Is Induced by the Cell Wall Integrity Mitogen-activated Protein Kinase Signaling Cascade and Is Required for Cell Wall Integrity in<i>Saccharomyces ce... por Thomas Scrimale, Louis DiDone, Karen L. de Mesy Bentley, Damian J. Krysan

    Publicado 2008
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  3. 3
    Antifungal Activity of Tamoxifen: In Vitro and In Vivo Activities and Mechanistic Characterization

    Antifungal Activity of Tamoxifen: In Vitro and In Vivo Activities and Mechanistic Characterization por Kristy Dolan, Sara Montgomery, Bradley M. Buchheit, Louis DiDone, Melanie Wellington, Damian J. Krysan

    Publicado 2009
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  4. 4
    Adenylate Kinase Release as a High-Throughput-Screening-Compatible Reporter of Bacterial Lysis for Identification of Antibacterial Agents

    Adenylate Kinase Release as a High-Throughput-Screening-Compatible Reporter of Bacterial Lysis for Identification of Antibacterial Agents por Anna C. Jacobs, Louis DiDone, Jennielle Jobson, Madeline K. Sofia, Damian J. Krysan, Paul M. Dunman

    Publicado 2012
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  5. 5
    A Repurposing Approach Identifies Off-Patent Drugs with Fungicidal Cryptococcal Activity, a Common Structural Chemotype, and Pharmacological Properties Relevant to the Treatment of Cryptococcosis

    A Repurposing Approach Identifies Off-Patent Drugs with Fungicidal Cryptococcal Activity, a Common Structural Chemotype, and Pharmacological Properties Relevant to the Treatment of... por Arielle Butts, Louis DiDone, Kristy Koselny, Bonnie K. Baxter, Yeissa Chabrier‐Roselló, Melanie Wellington, Damian J. Krysan

    Publicado 2012
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  6. 6
    Antitumor/Antifungal Celecoxib Derivative AR-12 is a Non-Nucleoside Inhibitor of the ANL-Family Adenylating Enzyme Acetyl CoA Synthetase

    Antitumor/Antifungal Celecoxib Derivative AR-12 is a Non-Nucleoside Inhibitor of the ANL-Family Adenylating Enzyme Acetyl CoA Synthetase por Kristy Koselny, Julianne Green, Lacey J. Favazzo, Virginia E. Glazier, Louis DiDone, Shea Ransford, Damian J. Krysan

    Publicado 2016
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  7. 7
    The Celecoxib Derivative AR-12 Has Broad-Spectrum Antifungal Activity <i>In Vitro</i> and Improves the Activity of Fluconazole in a Murine Model of Cryptococcosis

    The Celecoxib Derivative AR-12 Has Broad-Spectrum Antifungal Activity <i>In Vitro</i> and Improves the Activity of Fluconazole in a Murine Model of Cryptococcosis por Kristy Koselny, Julianne Green, Louis DiDone, Justin P. Halterman, Annette W. Fothergill, Nathan P. Wiederhold, Thomas F. Patterson, Melanie T. Cushion, Chad Rappelye, Melanie Wellington, Damian J. Krysan

    Publicado 2016
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  8. 8
    Estrogen Receptor Antagonists Are Anti-Cryptococcal Agents That Directly Bind EF Hand Proteins and Synergize with Fluconazole <i>In Vivo</i>

    Estrogen Receptor Antagonists Are Anti-Cryptococcal Agents That Directly Bind EF Hand Proteins and Synergize with Fluconazole <i>In Vivo</i> por Arielle Butts, Kristy Koselny, Yeissa Chabrier‐Roselló, Camile P. Semighini, Jessica C. S. Brown, Xuying Wang, Sivakumar Annadurai, Louis DiDone, Julie M. Tabroff, Wayne E. Childers, Magid Abou‐Gharbia, Melanie Wellington, María E. Cárdenas, Hiten D. Madhani, Joseph Heitman, Damian J. Krysan

    Publicado 2014
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