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Molecular Pharmacology

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Table of Contents

January 01, 2023; Volume 103,Issue 1

Articles

  • You have access
    A Regional and Projection-Specific Role of RGSz1 in the Ventrolateral Periaqueductal Grey in the Modulation of Morphine Reward
    Farhana Sakloth, Omar B. Sanchez-Reyes, Anne Ruiz, Andrew Nicolais, Randal A. Serafini, Kerri D. Pryce, Feodora Bertherat, Angélica Torres-Berrío, Ivone Gomes, Lakshmi A. Devi, Daniel Wacker and Venetia Zachariou
    Molecular Pharmacology January 2023, 103 (1) 1-8; DOI: https://doi.org/10.1124/molpharm.122.000528
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    Functional Assessment of Cancer-Linked Mutations in Sensitive Regions of Regulators of G Protein Signaling Predicted by Three-Dimensional Missense Tolerance Ratio Analysis
    Carolina Montañez-Miranda, Riley E. Perszyk, Nicholas H. Harbin, Jennifer Okalova, Suneela Ramineni, Stephen F. Traynelis and John R. Hepler
    Molecular Pharmacology January 2023, 103 (1) 21-37; DOI: https://doi.org/10.1124/molpharm.122.000614

Emerging Concepts

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    Targeting Circuit Abnormalities in Neurodegenerative Disease
    Sharan Ram Srinivasan
    Molecular Pharmacology January 2023, 103 (1) 38-44; DOI: https://doi.org/10.1124/molpharm.122.000563

Minireview

  • Protein Kinases and Cross-talk between Post-translational Modifications in the Regulation of Drug Transporters
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    Protein Kinases and Cross-talk between Post-translational Modifications in the Regulation of Drug Transporters
    Xuyang Wang and Mei Hong
    Molecular Pharmacology January 2023, 103 (1) 9-20; DOI: https://doi.org/10.1124/molpharm.122.000604
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In this issue

Molecular Pharmacology: 103 (1)
Molecular Pharmacology
Vol. 103, Issue 1
1 Jan 2023
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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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