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Molecular Pharmacology

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Table of Contents

May 01, 1991; Volume 39,Issue 5
  • You have access
    Reduction of desensitization of a glutamate ionotropic receptor by antagonists.
    M Geoffroy, B Lambolez, E Audinat, B Hamon, F Crepel, J Rossier and R T Kado
    Molecular Pharmacology May 1991, 39 (5) 587-591;
  • You have access
    Tetrahydroaminoacridine block of N-methyl-D-aspartate-activated cation channels in cultured hippocampal neurons.
    N Hershkowitz and M A Rogawski
    Molecular Pharmacology May 1991, 39 (5) 592-598;
  • You have access
    Regulation of gamma-aminobutyric acidA receptor subunit expression by activation of N-methyl-D-aspartate-selective glutamate receptors.
    M Memo, P Bovolin, E Costa and D R Grayson
    Molecular Pharmacology May 1991, 39 (5) 599-603;
  • You have access
    SkM2, a Na+ channel cDNA clone from denervated skeletal muscle, encodes a tetrodotoxin-insensitive Na+ channel.
    M M White, L Q Chen, R Kleinfield, R G Kallen and R L Barchi
    Molecular Pharmacology May 1991, 39 (5) 604-608;
  • You have access
    Aminoalkyl structural requirements for interaction of lidocaine with the class I antiarrhythmic drug receptor on rat cardiac myocytes.
    R S Sheldon, R J Hill, M Taouis and L M Wilson
    Molecular Pharmacology May 1991, 39 (5) 609-614;
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    Pharmacological characterization of type B cholecystokinin binding sites on the human JURKAT T lymphocyte cell line.
    M F Lignon, N Bernad and J Martinez
    Molecular Pharmacology May 1991, 39 (5) 615-620;
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    A synthetic pseudosubstrate peptide of protein kinase C inhibits the phorbol-12,13-dibutyrate effect on permeabilized coronary artery smooth muscle.
    T S Guthrie, J Tsuji and J N Wells
    Molecular Pharmacology May 1991, 39 (5) 621-624;
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    Effect of anti-human immunodeficiency virus nucleoside analogs on mitochondrial DNA and its implication for delayed toxicity.
    C H Chen, M Vazquez-Padua and Y C Cheng
    Molecular Pharmacology May 1991, 39 (5) 625-628;
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    Application of pattern recognition methods to the analysis and classification of toxicological data derived from proton nuclear magnetic resonance spectroscopy of urine.
    K P Gartland, C R Beddell, J C Lindon and J K Nicholson
    Molecular Pharmacology May 1991, 39 (5) 629-642;
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    Production of antisera selective for m1 muscarinic receptors using fusion proteins: distribution of m1 receptors in rat brain.
    S J Wall, R P Yasuda, F Hory, S Flagg, B M Martin, E I Ginns and B B Wolfe
    Molecular Pharmacology May 1991, 39 (5) 643-649;
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    Agonist-induced desensitization of D2 dopamine receptors in human Y-79 retinoblastoma cells.
    A C Barton, L E Black and D R Sibley
    Molecular Pharmacology May 1991, 39 (5) 650-658;
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    Dopamine receptor reappearance after irreversible receptor blockade: effect of chronic estradiol treatment of ovariectomized rats.
    D Lévesque and T Di Paolo
    Molecular Pharmacology May 1991, 39 (5) 659-665;
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    Effects of (+)-HA-966 and 7-chlorokynurenic acid on the kinetics of N-methyl-D-aspartate receptor agonist responses in rat cultured cortical neurons.
    J A Kemp and T Priestley
    Molecular Pharmacology May 1991, 39 (5) 666-670;
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    12-hydroperoxyeicosatetraenoic acid inhibits main platelet functions by activation of soluble guanylate cyclase.
    B Brüne and V Ullrich
    Molecular Pharmacology May 1991, 39 (5) 671-678;
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    Characterization of multiple [3H]ryanodine binding sites on the Ca2+ release channel of sarcoplasmic reticulum from skeletal and cardiac muscle: evidence for a sequential mechanism in ryanodine action.
    I N Pessah and I Zimanyi
    Molecular Pharmacology May 1991, 39 (5) 679-689;
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In this issue

Molecular Pharmacology
Vol. 39, Issue 5
1 May 1991
  • Table of Contents
  • Table of Contents (PDF)
  • Index by author
  • Back Matter (PDF)
  • Editorial Board (PDF)
  • Front Matter (PDF)
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  • Proteomic Analysis of GPCR Cell Biology
  • Phosphoproteomic Analysis of cAMP-Dependent Pathways
  • Phosphoproteomic Identification of Signaling Pathways
  • How Many G Protein-Coupled Receptors are Drug Targets?
  • Characterization of GRD and LCCH3 from Human Louse
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