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Molecular Pharmacology

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Table of Contents

November 01, 1988; Volume 34,Issue 5
  • You have access
    Determination and characterization of a cannabinoid receptor in rat brain.
    W A Devane, F A Dysarz, M R Johnson, L S Melvin and A C Howlett
    Molecular Pharmacology November 1988, 34 (5) 605-613;
  • You have access
    Identification of endogenous opioid receptor components in rat brain using a monoclonal antibody.
    L A Bero, S Roy and N M Lee
    Molecular Pharmacology November 1988, 34 (5) 614-620;
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    Immunohistochemical localization of glutamine transaminase K, a rat kidney cysteine conjugate beta-lyase, and the relationship to the segment specificity of cysteine conjugate nephrotoxicity.
    T W Jones, C Qin, V H Schaeffer and J L Stevens
    Molecular Pharmacology November 1988, 34 (5) 621-627;
  • You have access
    On the substrate specificity of cytochrome P450IIIA1.
    M J Namkung, H L Yang, J E Hulla and M R Juchau
    Molecular Pharmacology November 1988, 34 (5) 628-637;
  • You have access
    Examination of the substrate specificity of cloned rat kidney phenol UDP-glucuronyltransferase expressed in COS-7 cells.
    M R Jackson, S Fournel-Gigleux, D Harding and B Burchell
    Molecular Pharmacology November 1988, 34 (5) 638-642;
  • You have access
    Distribution of alpha-bungarotoxin binding sites over residues 173-204 of the alpha subunit of the acetylcholine receptor.
    P T Wilson, E Hawrot and T L Lentz
    Molecular Pharmacology November 1988, 34 (5) 643-650;
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    Iodination of [Tyr11]somatostatin yields a super high affinity ligand for somatostatin receptors in GH4C1 pituitary cells.
    D H Presky and A Schonbrunn
    Molecular Pharmacology November 1988, 34 (5) 651-658;
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    Determinants of stereospecific binding of type I antiarrhythmic drugs to cardiac sodium channels.
    R J Hill, H J Duff and R S Sheldon
    Molecular Pharmacology November 1988, 34 (5) 659-663;
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    The role of caffeine-sensitive calcium stores in the regulation of the intracellular free calcium concentration in rat sympathetic neurons in vitro.
    S A Thayer, L D Hirning and R J Miller
    Molecular Pharmacology November 1988, 34 (5) 664-673;
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    The metabolism of N-acetyl-3,5-dimethyl-p-benzoquinone imine in isolated hepatocytes involves N-deacetylation.
    L Rossi, L G McGirr, J Silva and P J O'Brien
    Molecular Pharmacology November 1988, 34 (5) 674-681;
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    A competitive binding assay for 2,3,7,8-tetrachlorodibenzo-p-dioxin and related ligands of the Ah receptor.
    C A Bradfield and A Poland
    Molecular Pharmacology November 1988, 34 (5) 682-688;
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    Characterization of opioid, sigma, and phencyclidine receptors in the neuroblastoma-brain hybrid cell line NCB-20.
    L Kushner, S R Zukin and R S Zukin
    Molecular Pharmacology November 1988, 34 (5) 689-694;
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    Oxygen-dependent hepatotoxicity due to doxorubicin: role of reducing equivalent supply in perfused rat liver.
    P E Ganey, F C Kauffman and R G Thurman
    Molecular Pharmacology November 1988, 34 (5) 695-701;
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    Methyl mercury stimulates chain elongation by purified HeLa RNA polymerase II.
    G D Frenkel and J Ducote
    Molecular Pharmacology November 1988, 34 (5) 702-706;
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    Local anesthetics: comparison of effects on batrachotoxin-elicited sodium flux and phosphoinositide breakdown in guinea pig cerebral cortical synaptoneurosomes.
    Y Nishizawa, F Gusovsky and J W Daly
    Molecular Pharmacology November 1988, 34 (5) 707-713;
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In this issue

Molecular Pharmacology
Vol. 34, Issue 5
1 Nov 1988
  • 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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