Search Results - "MOY, Franklin J"

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  1. 1

    The Nuclear Hormone Receptor Farnesoid X Receptor (FXR) Is Activated by Androsterone by Wang, Shuguang, Lai, KehDih, Moy, Franklin J, Bhat, Anitha, Hartman, Helen B, Evans, Mark J

    Published in Endocrinology (Philadelphia) (01-09-2006)
    “…Farnesoid X receptor (FXR) uses bile acids as endogenous ligands. Here, we demonstrate that androsterone, a metabolic product of testosterone, is also an FXR…”
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  2. 2

    Structure-Based Design of a Novel, Potent, and Selective Inhibitor for MMP-13 Utilizing NMR Spectroscopy and Computer-Aided Molecular Design by Chen, James M, Nelson, Frances C, Levin, Jeremy I, Mobilio, Dominick, Moy, Franklin J, Nilakantan, Ramaswamy, Zask, Arie, Powers, Robert

    Published in Journal of the American Chemical Society (11-10-2000)
    “…The high-resolution NMR solution structure of the catalytic fragment of human collagenase-3 (MMP-13) was used as a starting point for structure-based design of…”
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  3. 3

    Impact of Mobility on Structure-Based Drug Design for the MMPs by Moy, Franklin J, Chanda, Pranab K, Chen, James, Cosmi, Scott, Edris, Wade, Levin, Jeremy I, Rush, Thomas S, Wilhelm, James, Powers, Robert

    Published in Journal of the American Chemical Society (30-10-2002)
    “…Structure-based approaches for drug design generally do not incorporate solvent effects and dynamic information to predict inhibitor-binding affinity because…”
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  4. 4

    Properly Oriented Heparin−Decasaccharide-Induced Dimers Are the Biologically Active Form of Basic Fibroblast Growth Factor by Moy, Franklin J, Safran, Michal, Seddon, Andrew P, Kitchen, Doug, Böhlen, Peter, Aviezer, David, Yayon, Avner, Powers, Robert

    Published in Biochemistry (Easton) (22-04-1997)
    “…Interaction of basic fibroblast growth factor (FGF-2) with heparin or heparan sulfate proteoglycans (HSPGs) is required for receptor activation and initiation…”
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  5. 5

    Chemical Diversity of Metabolites from Fungi, Cyanobacteria, and Plants Relative to FDA-Approved Anticancer Agents by El-Elimat, Tamam, Zhang, Xiaoli, Jarjoura, David, Moy, Franklin J, Orjala, Jimmy, Kinghorn, A. Douglas, Pearce, Cedric J, Oberlies, Nicholas H

    Published in ACS medicinal chemistry letters (09-08-2012)
    “…A collaborative project has been undertaken to explore filamentous fungi, cyanobacteria, and tropical plants for anticancer drug leads. Through principal…”
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  6. 6

    qNMR for profiling the production of fungal secondary metabolites by Brooks, Wilson C., Paguigan, Noemi D., Raja, Huzefa A., Moy, Franklin J., Cech, Nadja B., Pearce, Cedric J., Oberlies, Nicholas H.

    Published in Magnetic resonance in chemistry (01-07-2017)
    “…Analysis of complex mixtures is a common challenge in natural products research. Quantitative nuclear magnetic resonance spectroscopy offers analysis of…”
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  7. 7

    Assignments, Secondary Structure, Global Fold, and Dynamics of Chemotaxis Y Protein Using Three- and Four-Dimensional Heteronuclear (13C,15N) NMR Spectroscopy by Moy, Franklin J, Lowry, David F, Matsumura, Philip, Dahlquist, Frederick W, Krywko, James E, Domaille, Peter J

    Published in Biochemistry (Easton) (01-09-1994)
    “…NMR spectroscopy has been used to study recombinant Escherichia coli CheY, a 128-residue protein involved in regulating bacterial chemotaxis. Heteronuclear…”
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    Solution structure of human IL-13 and implication for receptor binding by Moy, Franklin J, Diblasio, Elizabeth, Wilhelm, James, Powers, Robert

    Published in Journal of molecular biology (29-06-2001)
    “…Interleukin-13 has been implicated as a key factor in asthma, allergy, atopy and inflammatory response, establishing the protein as a valuable therapeutic…”
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    Solution Structure of ZipA, a Crucial Component of Escherichia coli Cell Division by Moy, Franklin J, Glasfeld, Elizabeth, Mosyak, Lidia, Powers, Robert

    Published in Biochemistry (Easton) (08-08-2000)
    “…ZipA, an essential component of cell division in Escherichia coli, interacts with the FtsZ protein at the midcell in one of the initial steps of septum…”
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  13. 13

    High-resolution solution structure of the catalytic fragment of human collagenase-3 (MMP-13) complexed with a hydroxamic acid inhibitor by Moy, Franklin J, Chanda, Pranab K, Chen, James M, Cosmi, Scott, Edris, Wade, Levin, Jeremy I, Powers, Robert

    Published in Journal of molecular biology (22-09-2000)
    “…The high-resolution solution structure of the catalytic fragment of human collagenase-3 (MMP-13) complexed with a sulfonamide derivative of a hydroxamic acid…”
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  14. 14

    Design and Syntheses of 1,6-Naphthalene Derivatives as Selective HCMV Protease Inhibitors by Gopalsamy, Ariamala, Lim, Kitae, Ellingboe, John W., Mitsner, Boris, Nikitenko, Antonia, Upeslacis, Janis, Mansour, Tarek S., Olson, Matthew W., Bebernitz, Geraldine A., Grinberg, Diane, Feld, Boris, Moy, Franklin J., O'Connell, John

    Published in Journal of medicinal chemistry (08-04-2004)
    “…Through high throughput screening of various libraries, substituted styryl naphthalene 6 was identified as an HCMV protease inhibitor. Optimization of various…”
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  15. 15

    NMR Structure of Free RGS4 Reveals an Induced Conformational Change upon Binding Gα by Moy, Franklin J, Chanda, Pranab K, Cockett, Mark I, Edris, Wade, Jones, Philip G, Mason, Kim, Semus, Simon, Powers, Robert

    Published in Biochemistry (Easton) (20-06-2000)
    “…Heterotrimeric guanine nucleotide-binding proteins (G-proteins) are transducers in many cellular transmembrane signaling systems where regulators of G-protein…”
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  16. 16

    NMR Solution Structure of the Catalytic Fragment of Human Fibroblast Collagenase Complexed with a Sulfonamide Derivative of a Hydroxamic Acid Compound by Moy, Franklin J, Chanda, Pranab K, Chen, James M, Cosmi, Scott, Edris, Wade, Skotnicki, Jerauld S, Wilhelm, Jim, Powers, Robert

    Published in Biochemistry (Easton) (01-06-1999)
    “…The solution structure of the catalytic fragment of human fibroblast collagenase (MMP-1) complexed with a sulfonamide derivative of a hydroxamic acid compound…”
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  17. 17

    High-Resolution Solution Structure of Basic Fibroblast Growth Factor Determined by Multidimensional Heteronuclear Magnetic Resonance Spectroscopy by Moy, Franklin J, Seddon, Andrew P, Böhlen, Peter, Powers, Robert

    Published in Biochemistry (Easton) (22-10-1996)
    “…The high-resolution solution structure of recombinant human basic fibroblast growth factor (FGF-2), a protein of 17.2 kDa that exhibits a variety of functions…”
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  18. 18

    High-Resolution Solution Structure of the Inhibitor-Free Catalytic Fragment of Human Fibroblast Collagenase Determined by Multidimensional NMR by Moy, Franklin J, Chanda, Pranab K, Cosmi, Scott, Pisano, Michael R, Urbano, Charlotte, Wilhelm, Jim, Powers, Robert

    Published in Biochemistry (Easton) (10-02-1998)
    “…The high-resolution solution structure of the inhibitor-free catalytic fragment of human fibroblast collagenase (MMP-1), a protein of 18.7 kDa, which is a…”
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  19. 19

    Assignments, secondary structure and dynamics of the inhibitor-free catalytic fragment of human fibroblast collagenase by Moy, F J, Pisano, M R, Chanda, P K, Urbano, C, Killar, L M, Sung, M L, Powers, R

    Published in Journal of biomolecular NMR (01-07-1997)
    “…Fibroblast collagenase (MMP-1), a 169-residue protein with a molecular mass of 18.7 kDa, is a matrix metalloproteinase which has been associated with…”
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  20. 20

    Homology Model for Oncostatin M Based on NMR Structural Data by Kitchen, Douglas, Hoffman, Ross C, Moy, Franklin J, Powers, Robert

    Published in Biochemistry (Easton) (28-07-1998)
    “…Oncostatin M (OM) is a member of the cytokine family which regulates the proliferation and differentiation of a variety of cell types and includes…”
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