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Molecular Pharmacology

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Table of Contents

October 01, 2016; Volume 90,Issue 4

Announcement

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    Announcement
    Mary Vore
    Molecular Pharmacology October 2016, 90 (4) 414; DOI: https://doi.org/10.1124/mol.115.106443

Accelerated Communication

  • AMP Kinase Activation Alters Oxidant-Induced Stress Granule Assembly by Modulating Cell Signaling and Microtubule Organization
    You have access
    AMP Kinase Activation Alters Oxidant-Induced Stress Granule Assembly by Modulating Cell Signaling and Microtubule Organization
    Hicham Mahboubi, Antonis E. Koromilas and Ursula Stochaj
    Molecular Pharmacology October 2016, 90 (4) 460-468; DOI: https://doi.org/10.1124/mol.116.105494

Articles

  • Open Access
    S-Nitrosoglutathione Attenuates Airway Hyperresponsiveness in Murine Bronchopulmonary Dysplasia
    Thomas M. Raffay, Andrew M. Dylag, Juliann M. Di Fiore, Laura A. Smith, Helly J. Einisman, Yuejin Li, Mitchell M. Lakner, Ahmad M. Khalil, Peter M. MacFarlane, Richard J. Martin and Benjamin Gaston
    Molecular Pharmacology October 2016, 90 (4) 418-426; DOI: https://doi.org/10.1124/mol.116.104125
  • You have access
    Molecular Mechanisms of Action of M5 Muscarinic Acetylcholine Receptor Allosteric Modulators
    Alice E. Berizzi, Patrick R. Gentry, Patricia Rueda, Sandra Den Hoedt, Patrick M. Sexton, Christopher J. Langmead and Arthur Christopoulos
    Molecular Pharmacology October 2016, 90 (4) 427-436; DOI: https://doi.org/10.1124/mol.116.104182
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    A Fibroblast Growth Factor 21–Pregnane X Receptor Pathway Downregulates Hepatic CYP3A4 in Nonalcoholic Fatty Liver Disease
    Sarah J. Woolsey, Melanie D. Beaton, Sara E. Mansell, Matilde Leon-Ponte, Janice Yu, Christopher L. Pin, Paul C. Adams, Richard B. Kim and Rommel G. Tirona
    Molecular Pharmacology October 2016, 90 (4) 437-446; DOI: https://doi.org/10.1124/mol.116.104687
  • WNT Stimulation Dissociates a Frizzled 4 Inactive-State Complex with G<em>α</em><sub>12/13</sub>
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    WNT Stimulation Dissociates a Frizzled 4 Inactive-State Complex with Gα12/13
    Elisa Arthofer, Belma Hot, Julian Petersen, Katerina Strakova, Stefan Jäger, Manuel Grundmann, Evi Kostenis, J. Silvio Gutkind and Gunnar Schulte
    Molecular Pharmacology October 2016, 90 (4) 447-459; DOI: https://doi.org/10.1124/mol.116.104919
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    Ginsenoside Rg3, a Gating Modifier of EAG Family K+ Channels
    Wei Wu, Alison Gardner, Frank B. Sachse and Michael C. Sanguinetti
    Molecular Pharmacology October 2016, 90 (4) 469-482; DOI: https://doi.org/10.1124/mol.116.104091
  • CXC Chemokine Receptor 3 Alternative Splice Variants Selectively Activate Different Signaling Pathways
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    CXC Chemokine Receptor 3 Alternative Splice Variants Selectively Activate Different Signaling Pathways
    Yamina A. Berchiche and Thomas P. Sakmar
    Molecular Pharmacology October 2016, 90 (4) 483-495; DOI: https://doi.org/10.1124/mol.116.105502
  • Differential Inhibition of Water and Ion Channel Activities of Mammalian Aquaporin-1 by Two Structurally Related Bacopaside Compounds Derived from the Medicinal Plant <em>Bacopa monnieri</em>
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    Differential Inhibition of Water and Ion Channel Activities of Mammalian Aquaporin-1 by Two Structurally Related Bacopaside Compounds Derived from the Medicinal Plant Bacopa monnieri
    Jinxin V. Pei, Mohamad Kourghi, Michael L. De Ieso, Ewan M. Campbell, Hilary S. Dorward, Jennifer E. Hardingham and Andrea J. Yool
    Molecular Pharmacology October 2016, 90 (4) 496-507; DOI: https://doi.org/10.1124/mol.116.105882

Erratum

  • You have access
    Corrections to “Molecular interaction of α-conotoxin RgIA with the rat α9α10 nicotinic acetylcholine receptor”
    Molecular Pharmacology October 2016, 90 (4) 415-417; DOI: https://doi.org/10.1124/mol.114.096511err
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In this issue

Molecular Pharmacology: 90 (4)
Molecular Pharmacology
Vol. 90, Issue 4
1 Oct 2016
  • Table of Contents
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  • SB-431542 Is a Potent and Specific Inhibitor of Transforming Growth Factor-β Superfamily Type I Activin Receptor-Like Kinase (ALK) Receptors ALK4, ALK5, and ALK7
  • The G-Protein-Coupled Receptors in the Human Genome Form Five Main Families. Phylogenetic Analysis, Paralogon Groups, and Fingerprints
  • Pharmacological Properties of Y-27632, a Specific Inhibitor of Rho-Associated Kinases
  • Pharmacological characterization of five cloned voltage-gated K+ channels, types Kv1.1, 1.2, 1.3, 1.5, and 3.1, stably expressed in mammalian cell lines.
  • The Orphan Human Pregnane X Receptor Mediates the Transcriptional Activation of CYP3A4 by Rifampicin through a Distal Enhancer Module
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