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Molecular Pharmacology

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Table of Contents

December 01, 1987; Volume 32,Issue 6
  • You have access
    Purification of the bifunctional thymidylate synthase-dihydrofolate reductase complex from the human malaria parasite Plasmodium falciparum.
    G X Chen and J W Zolg
    Molecular Pharmacology December 1987, 32 (6) 723-730;
  • You have access
    Interaction of some estrogenic drugs with tubulin. Formation of twisted ribbon structures.
    M M Chaudoreille, V Peyrot, D Braguer and A Crevat
    Molecular Pharmacology December 1987, 32 (6) 731-736;
  • You have access
    Agonists and phorbol esters desensitize beta-adrenergic receptors by different mechanisms.
    M L Toews, M Liang and J P Perkins
    Molecular Pharmacology December 1987, 32 (6) 737-742;
  • You have access
    Calmodulin activates adenylate cyclase from rat anterior pituitary.
    D V Greenlee and S Okada
    Molecular Pharmacology December 1987, 32 (6) 743-748;
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    Effect of avermectin B1a on chick neuronal gamma-aminobutyrate receptor channels expressed in Xenopus oocytes.
    E Sigel and R Baur
    Molecular Pharmacology December 1987, 32 (6) 749-752;
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    Role of high affinity cAMP phosphodiesterase activities in the response of S49 cells to agonists.
    R Barber, T J Goka and R W Butcher
    Molecular Pharmacology December 1987, 32 (6) 753-759;
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    Dopamine D1 and D2 receptors are sensitive to the cationic form of apomorphine.
    P Seeman and H C Guan
    Molecular Pharmacology December 1987, 32 (6) 760-763;
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    3H-neurokinin A labels a specific tachykinin-binding site in the rat duodenal smooth muscle.
    L Bergström, J C Beaujouan, Y Torrens, M Saffroy, J Glowinski, S Lavielle, G Chassaing, A Marquet, P D'Orleans-Juste and S Dion
    Molecular Pharmacology December 1987, 32 (6) 764-771;
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    Structural determinants of sigma receptor affinity.
    B L Largent, H Wikström, A L Gundlach and S H Snyder
    Molecular Pharmacology December 1987, 32 (6) 772-784;
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    Depolarization of chick myotubes triggers the appearance of (+)-[3H]PN 200-110-binding sites.
    P J Pauwels, H P Van Assouw and J E Leysen
    Molecular Pharmacology December 1987, 32 (6) 785-791;
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    Characterization of the alpha +-like Na+,K+-ATPase which mediates ouabain inhibition of adrenergic induction of N-acetyltransferase (EC 2.3.1.87) activity: studies with isolated pinealocytes.
    C González-García, V Ceña and D C Klein
    Molecular Pharmacology December 1987, 32 (6) 792-797;
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    2',3'-Dideoxycytidine: regulation of its metabolism and anti-retroviral potency by natural pyrimidine nucleosides and by inhibitors of pyrimidine nucleotide synthesis.
    J Balzarini, D A Cooney, M Dalal, G J Kang, J E Cupp, E DeClercq, S Broder and D G Johns
    Molecular Pharmacology December 1987, 32 (6) 798-806;
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    Hydroquinone inhibits bone marrow pre-B cell maturation in vitro.
    A G King, K S Landreth and D Wierda
    Molecular Pharmacology December 1987, 32 (6) 807-812;
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    Human and rat liver phenol sulfotransferase: structure-activity relationships for phenolic substrates.
    N R Campbell, J A Van Loon, R S Sundaram, M M Ames, C Hansch and R Weinshilboum
    Molecular Pharmacology December 1987, 32 (6) 813-819;
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    Interaction of L-glutamate and magnesium with phencyclidine recognition sites in rat brain: evidence for multiple affinity states of the phencyclidine/N-methyl-D-aspartate receptor complex.
    P S Loo, A F Braunwalder, J Lehmann, M Williams and M A Sills
    Molecular Pharmacology December 1987, 32 (6) 820-830;
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    Effect of ethanol on intracellular ionized calcium concentrations in synaptosomes and hepatocytes.
    L C Daniell, E P Brass and R A Harris
    Molecular Pharmacology December 1987, 32 (6) 831-837;
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In this issue

Molecular Pharmacology
Vol. 32, Issue 6
1 Dec 1987
  • Table of Contents
  • Table of Contents (PDF)
  • Index by author
  • Back Matter (PDF)
  • Editorial Board (PDF)
  • Front Matter (PDF)
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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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