Search Results - "Montana, V G"

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    Structural basis for autorepression of retinoid X receptor by tetramer formation and the AF-2 helix by Gampe, Jr, R T, Montana, V G, Lambert, M H, Wisely, G B, Milburn, M V, Xu, H E

    Published in Genes & development (01-09-2000)
    “…The 9-cis-retinoic acid receptors (RXRalpha, RXRbeta, and RXRgamma) are nuclear receptors that play key roles in multiple hormone-signaling pathways…”
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    Journal Article
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    Structural basis for antagonist-mediated recruitment of nuclear co-repressors by PPAR α by Xu, H. Eric, Stanley, Thomas B, Montana, Valerie G, Lambert, Millard H, Shearer, Barry G, Cobb, Jeffery E, McKee, David D, Galardi, Cristin M, Plunket, Kelli D, Nolte, Robert T, Parks, Derek J, Moore, John T, Kliewer, Steven A, Willson, Timothy M, Stimmel, Julie B

    Published in Nature (London) (07-02-2002)
    “…Repression of gene transcription by nuclear receptors is mediated by interactions with co-repressor proteins such as SMRT and N-CoR, which in turn recruit…”
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    Asymmetry in the PPARγ/RXRα Crystal Structure Reveals the Molecular Basis of Heterodimerization among Nuclear Receptors by Gampe, Robert T., Montana, Valerie G., Lambert, Millard H., Miller, Aaron B., Bledsoe, Randy K., Milburn, Michael V., Kliewer, Steven A., Willson, Timothy M., Xu, H.Eric

    Published in Molecular cell (01-03-2000)
    “…The nuclear receptor PPAR gamma /RXR alpha heterodimer regulates glucose and lipid homeostasis and is the target for the antidiabetic drugs GI262570 and the…”
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    Journal Article
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    Molecular Recognition of Fatty Acids by Peroxisome Proliferator–Activated Receptors by Xu, H.Eric, Lambert, Millard H, Montana, Valerie G, Parks, Derek J, Blanchard, Steven G, Brown, Peter J, Sternbach, Daniel D, Lehmann, Jürgen M, Wisely, G.Bruce, Willson, Timothy M, Kliewer, Steven A, Milburn, Michael V

    Published in Molecular cell (01-03-1999)
    “…The peroxisome proliferator–activated receptors (PPARs) are nuclear receptors for fatty acids (FAs) that regulate glucose and lipid homeostasis. We report the…”
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    Crystal Structure of the Catalytic Domain of the Human Cell Cycle Control Phosphatase, Cdc25A by Fauman, Eric B., Cogswell, John P., Lovejoy, Brett, Rocque, Warren J., Holmes, William, Montana, Valerie G., Piwnica-Worms, Helen, Rink, Martin J., Saper, Mark A.

    Published in Cell (15-05-1998)
    “…Cdc25 phosphatases activate the cell division kinases throughout the cell cycle. The 2.3 Å structure of the human Cdc25A catalytic domain reveals a small α/β…”
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    Structure-Based Design of Potent Retinoid X Receptor α Agonists by Haffner, Curt D., Lenhard, James M., Miller, Aaron B., McDougald, Darryl L., Dwornik, Kate, Ittoop, Olivia R., Gampe, Robert T., Xu, H. Eric, Blanchard, Steve, Montana, Valerie G., Consler, Tom G., Bledsoe, Randy K., Ayscue, Andrea, Croom, Dallas

    Published in Journal of medicinal chemistry (08-04-2004)
    “…A series of tetrahydrobenzofuranyl and tetrahydrobenzothienyl propenoic acids that showed potent agonist activity against RXRα were synthesized via a…”
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    Journal Article
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    Asymmetry in the PPARgamma/RXRalpha crystal structure reveals the molecular basis of heterodimerization among nuclear receptors by Gampe, Jr, R T, Montana, V G, Lambert, M H, Miller, A B, Bledsoe, R K, Milburn, M V, Kliewer, S A, Willson, T M, Xu, H E

    Published in Molecular cell (01-03-2000)
    “…The nuclear receptor PPARgamma/RXRalpha heterodimer regulates glucose and lipid homeostasis and is the target for the antidiabetic drugs GI262570 and the…”
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    Journal Article
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    Subtype Specific Effects of Peroxisome Proliferator-Activated Receptor Ligands on Corepressor Affinity by Stanley, Thomas B, Leesnitzer, Lisa M, Montana, Valerie G, Galardi, Cristin M, Lambert, Millard H, Holt, Jason A, Xu, H. Eric, Moore, Linda B, Blanchard, Steven G, Stimmel, Julie B

    Published in Biochemistry (Easton) (12-08-2003)
    “…Natural ligands for nuclear receptors are believed to activate gene transcription by causing dissociation of corepressors and promoting the association of…”
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    Alteration of a Single Amino Acid in Peroxisome Proliferator-Activated Receptor-α (PPARα) Generates a PPARδ Phenotype by Takada, Ichiro, Yu, Ruth T, Xu, H. Eric, Lambert, Millard H, Montana, Valerie G, Kliewer, Steven A, Evans, Ronald M, Umesono, Kazuhiko

    Published in Molecular endocrinology (Baltimore, Md.) (01-05-2000)
    “…Three pharmacologically important nuclear receptors, the peroxisome proliferator-activated receptors (PPARs α,γ , and δ), mediate key transcriptional responses…”
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    Journal Article