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Molecular Pharmacology

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Table of Contents

June 01, 1998; Volume 53,Issue 6

Accelerated Communications

  • You have access
    Trinitrophenyl-Substituted Nucleotides Are Potent Antagonists Selective for P2X1, P2X3, and Heteromeric P2X2/3 Receptors
    Caterina Virginio, Graeme Robertson, Annmarie Surprenant and R. Alan North
    Molecular Pharmacology June 1998, 53 (6) 969-973;
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    Privileged Access to Mitochondria of Calcium Influx throughN-Methyl-d-Aspartate Receptors
    Tsung-I Peng and J. Timothy Greenamyre
    Molecular Pharmacology June 1998, 53 (6) 974-980;

Articles

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    Receptor-Mediated Activation of Gsα: Evidence for Intramolecular Signal Transduction
    Stephen R. Marsh, Galina Grishina, Paul T. Wilson and Catherine H. Berlot
    Molecular Pharmacology June 1998, 53 (6) 981-990;
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    A Comparison of the Oxidation of Clozapine and Olanzapine to Reactive Metabolites and the Toxicity of these Metabolites to Human Leukocytes
    Iain Gardner, Nasir Zahid, Duncan MacCrimmon and Jack P. Uetrecht
    Molecular Pharmacology June 1998, 53 (6) 991-998;
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    A Comparison of the Covalent Binding of Clozapine and Olanzapine to Human Neutrophils In Vitro and In Vivo
    Iain Gardner, J. Steven Leeder, Terrence Chin, Nasir Zahid and Jack P. Uetrecht
    Molecular Pharmacology June 1998, 53 (6) 999-1008;
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    Interleukin-1β Induces Bradykinin B2 Receptor Gene Expression through a Prostanoid Cyclic AMP-Dependent Pathway in Human Bronchial Smooth Muscle Cells
    Fabien Schmidlin, Didier Scherrer, Laurent Daeffler, Claude Bertrand, Yves Landry and Jean-Pierre Gies
    Molecular Pharmacology June 1998, 53 (6) 1009-1015;
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    Negative Regulation of the Rat GlutathioneS-Transferase A2 Gene by Glucocorticoids Involves a Canonical Glucocorticoid Consensus Sequence
    K. Cameron Falkner, Thomas H. Rushmore, Mark W. Linder and Russell A. Prough
    Molecular Pharmacology June 1998, 53 (6) 1016-1026;
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    C/EBPα Is a Regulator of the UDP GlucuronosyltransferaseUGT2B1 Gene
    Antony J. Hansen, Ying-Hue Lee, Esta Sterneck, Frank J. Gonzalez and Peter I. Mackenzie
    Molecular Pharmacology June 1998, 53 (6) 1027-1033;
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    Selective Inhibition of α1B-Adrenergic Receptor Expression and Function Using a Phosphorothioate Antisense Oligodeoxynucleotide
    Pedro J. Gonzalez-Cabrera, Patrick L. Iversen, Marvin F. Liu, Margaret A. Scofield and William B. Jeffries
    Molecular Pharmacology June 1998, 53 (6) 1034-1039;
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    Characterization of Human Cellular γ-Glutamyl Hydrolase
    M. S. Rhee, B. Lindau-Shepard, K. J. Chave, J. Galivan and T. J. Ryan
    Molecular Pharmacology June 1998, 53 (6) 1040-1046;
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    Contribution of Phospholipase C-β3 Phosphorylation to the Rapid Attenuation of Opioid-Activated Phosphoinositide Response
    Derek Strassheim, Ping-Yee Law and Horace H. Loh
    Molecular Pharmacology June 1998, 53 (6) 1047-1053;
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    Evidence for the Involvement of Protein Kinase C in the Inhibition of Prolactin Gene Expression by Transforming Growth Factor-β2
    Chuan-Chang Chuang, Sai-Koong Tan, Lung-Kuo Tai, Jin-Ping Hsin and Fung-Fang Wang
    Molecular Pharmacology June 1998, 53 (6) 1054-1061;
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    Adenosine Triphosphate-Dependent Transport of Anionic Conjugates by the Rabbit Multidrug Resistance-Associated Protein Mrp2 Expressed in Insect Cells
    Rémon A. M. H. van Aubel, Marcel A. van Kuijck, Jan B. Koenderink, Peter M. T. Deen, Carel H. van Os and Frans G. M. Russel
    Molecular Pharmacology June 1998, 53 (6) 1062-1067;
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    Hepatic Expression of Multidrug Resistance-Associated Protein-Like Proteins Maintained in Eisai Hyperbilirubinemic Rats
    Tomoko Hirohashi, Hiroshi Suzuki, Kousei Ito, Kotaro Ogawa, Kazuhiko Kume, Takao Shimizu and Yuichi Sugiyama
    Molecular Pharmacology June 1998, 53 (6) 1068-1075;
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    Reactive Oxygen Species Regulate Macrophage Scavenger Receptor Type I, but Not Type II, in the Human Monocytic Cell Line THP-1
    Sjef J. De Kimpe, Erik E. Änggård and Martin J. Carrier
    Molecular Pharmacology June 1998, 53 (6) 1076-1082;
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    Allosteric Activation of the Ca2+ Receptor Expressed in Xenopus laevis Oocytes by NPS 467 or NPS 568
    Lance G. Hammerland, James E. Garrett, Benjamin C. P. Hung, Cynthia Levinthal and Edward F. Nemeth
    Molecular Pharmacology June 1998, 53 (6) 1083-1088;
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    Kinetics of Inhibition of Rabbit Reticulocyte Peptidyltransferase by Anisomycin and Sparsomycin
    Margarita Ioannou, Charalambos Coutsogeorgopoulos and Dennis Synetos
    Molecular Pharmacology June 1998, 53 (6) 1089-1096;
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    Inhibition of Human Immunodeficiency Virus Type 1 Replication and Cytokine Production by Fluoroquinoline Derivatives
    Masanori Baba, Mika Okamoto, Masaki Kawamura, Masahiko Makino, Tomoe Higashida, Tohru Takashi, Youichi Kimura, Tohru Ikeuchi, Toshifumi Tetsuka and Takashi Okamoto
    Molecular Pharmacology June 1998, 53 (6) 1097-1103;
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    Pharmacological Properties of the T-Type Ca2+ Current of Mouse Spermatogenic Cells
    Christophe Arnoult, Michel Villaz and Harvey M. Florman
    Molecular Pharmacology June 1998, 53 (6) 1104-1111;
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    Glycosylation within the Cysteine Loop and Six Residues Near Conserved Cys192/Cys193 Are Determinants of Neuronal Bungarotoxin Sensitivity on the Neuronal Nicotinic Receptor α3 Subunit
    Charles W. Luetje, Floyd N. Maddox and Scott C. Harvey
    Molecular Pharmacology June 1998, 53 (6) 1112-1119;
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    On the Unique Binding and Activating Properties of Xanomeline at the M1 Muscarinic Acetylcholine Receptor
    Arthur Christopoulos, Tracie L. Pierce, Jennifer L. Sorman and Esam E. El-Fakahany
    Molecular Pharmacology June 1998, 53 (6) 1120-1130;
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    Specific Activation of the Nuclear Receptors PPARγ and RORA by the Antidiabetic Thiazolidinedione BRL 49653 and the Antiarthritic Thiazolidinedione Derivative CGP 52608
    Irmgard Wiesenberg, Michele Chiesi, Martin Missbach, Carsten Spanka, Werner Pignat and Carsten Carlberg
    Molecular Pharmacology June 1998, 53 (6) 1131-1138;
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    Gi- and Protein Kinase C-Mediated Heterologous Potentiation of Phospholipase C Signaling by G Protein-Coupled Receptors
    Martina Schmidt, Barbara Lohmann, Kerstin Hammer, Stephan Haupenthal, Matthias Voß, Christoph Nehls and Karl H. Jakobs
    Molecular Pharmacology June 1998, 53 (6) 1139-1148;
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In this issue

Molecular Pharmacology: 53 (6)
Molecular Pharmacology
Vol. 53, Issue 6
1 Jun 1998
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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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