Search Results - "McClue, S J"
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Alpha 2-C10 adrenergic receptors expressed in rat 1 fibroblasts can regulate both adenylylcyclase and phospholipase D-mediated hydrolysis of phosphatidylcholine by interacting with pertussis toxin-sensitive guanine nucleotide-binding proteins
Published in The Journal of biological chemistry (05-02-1992)“…The alpha 2-C10 adrenergic receptor from human platelets was expressed permanently in Rat-1 fibroblasts. A series of clones that varied in expression of the…”
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Molecular interaction of the human alpha 2-C10-adrenergic receptor, when expressed in Rat-1 fibroblasts, with multiple pertussis toxin-sensitive guanine nucleotide-binding proteins: studies with site-directed antisera
Published in Molecular pharmacology (01-11-1991)“…DNA encoding the human alpha 2-C-10-adrenergic receptor was transfected into Rat-1 fibroblasts by CaPO4 precipitation, and clones expressing the receptor were…”
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5-Hydroxytryptamine-stimulated inositol phospholipid hydrolysis in the mouse cortex has pharmacological characteristics compatible with mediation via 5-HT2 receptors but this response does not reflect altered 5-HT2 function after 5,7-dihydroxytryptamine lesioning or repeated antidepressant treatments
Published in Journal of neurochemistry (01-03-1988)“…5-Hydroxytryptamine (5-HT; 3 x 10(-8)-1 x 10(-5)M) produced a dose-dependent increase in phosphatidylinositol/polyphosphoinositide (PI) turnover in mouse…”
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Serotonergic agonists stimulate inositol lipid metabolism in rabbit platelets
Published in Life sciences (1973) (28-10-1985)“…The metabolism of inositol phospholipids in response to serotonergic agonists was investigated in rabbit platelets. In platelets prelabelled with…”
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Hallucinogenic drugs are partial agonists of the human platelet shape change response: a physiological model of the 5-HT2 receptor
Published in Biological psychiatry (1969) (01-07-1989)“…We have assayed several phenylalkylamine and indolealkylamine hallucinogens, as well as structurally similar nonhallucinogens, for their effect on human…”
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5-Hydroxytryptamine (5-HT)-induced shape change in human platelets determined by computerized data acquisition: correlation with [125I]-iodoLSD binding at 5-HT2 receptors
Published in Blood coagulation & fibrinolysis (01-02-1991)“…The 5-HT-induced shape change and subsequent aggregation of platelets provides a functional assay for 5-HT2 receptors. In the present study we describe a…”
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Subacute and chronic in vivo lithium treatment inhibits agonist- and sodium fluoride-stimulated inositol phosphate production in rat cortex
Published in Journal of neurochemistry (01-02-1989)“…We have investigated the effects of in vivo lithium treatment on cerebral inositol phospholipid metabolism. Twice-daily treatment of rats with LiCl (3 mEq/kg)…”
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Gi3 does not contribute to the inhibition of adenylate cyclase when stimulation of an α2-adrenergic receptor causes activation of both Gi2 and Gi3
Published in Biochemical journal (01-06-1992)“…Agonist occupancy of the alpha 2-C10 adrenergic receptor in a stable clone (1C) of Rat 1 fibroblasts produced by transfection of cells with genomic DNA…”
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Gi3 does not contribute to the inhibition of adenylate cyclase when stimulation of an alpha 2-adrenergic receptor causes activation of both Gi2 and Gi3
Published in Biochemical journal (01-06-1992)“…Agonist occupancy of the alpha 2-C10 adrenergic receptor in a stable clone (1C) of Rat 1 fibroblasts produced by transfection of cells with genomic DNA…”
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The role and specificity of guanine nucleotide binding proteins in receptor-effector coupling
Published in Symposia of the Society for Experimental Biology (1990)“…Nine distinct alpha subunits of guanine nucleotide binding proteins (G-proteins) have now been identified by cDNA cloning. Each of these functions to allow…”
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Expression of human M2 muscarinic receptors in Sf9 cells: characterisation and reconstitution with G-proteins
Published in Journal of receptors and signal transduction (01-01-1995)“…The gene for the human m2 muscarinic receptor was expressed in Sf9 cells using the baculovirus expression system. As assessed by [3H]NMS binding, Sf9 cells…”
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In vitro and in vivo antitumor properties of the cyclin dependent kinase inhibitor CYC202 (R‐roscovitine)
Published in International journal of cancer (10-12-2002)“…CDK2 inhibitors have been proposed as effective anti‐cancer therapeutics. We show here that CYC202 (R‐roscovitine) is a potent inhibitor of recombinant…”
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Discovery of a Novel Family of CDK Inhibitors with the Program LIDAEUS: Structural Basis for Ligand-Induced Disordering of the Activation Loop
Published in Structure (London) (01-04-2003)“…A family of 4-heteroaryl-2-amino-pyrimidine CDK2 inhibitor lead compounds was discovered with the new database-mining program LIDAEUS through in silico…”
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Metabolism and pharmacokinetics of the cyclin-dependent kinase inhibitor R-roscovitine in the mouse
Published in Molecular cancer therapeutics (01-01-2005)“…R -roscovitine (seliciclib, CYC202) is a cyclin-dependent kinase inhibitor currently in phase II clinical trials in patients with cancer. Here, we describe its…”
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The alpha 2B adrenergic receptor of undifferentiated neuroblastoma x glioma hybrid NG108-15 cells, interacts directly with the guanine nucleotide binding protein, Gi2
Published in FEBS letters (03-09-1990)“…In membranes of undifferentiated neuroblastoma x glioma hybrid cell line NG108-15, the apparent specific binding of [3H]yohimbine measured in the presence of 1…”
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The alpha sub(2) B adrenergic receptor of undifferentiated neuroblastoma x glioma hybrid NG108-15 cells, interacts directly with the guanine nucleotide binding protein, G sub(i)2
Published in FEBS letters (01-01-1990)“…In membranes of undifferentiated neuroblastoma x glioma hybrid cell line NG108-15, the apparent specific binding of ( super(3)H)yohimbine measured in the…”
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Activation of Gi protein by peptide structures of the muscarinic M2 receptor second intracellular loop
Published in European journal of pharmacology (15-04-1994)“…The muscarinic M2 receptor that normally couples via Gi to inhibit adenylyl cyclase was made to couple to Gs by exchange of its third intracellular loop for…”
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Synthesis and configuration of the cyclin-dependent kinase inhibitor roscovitine and its enantiomer
Published in Tetrahedron: asymmetry (13-11-2001)“…The cyclin-dependent kinase inhibitor ( R)-2-(6-benzylamino-9-isopropyl-9 H-purin-2-ylamino)butan-1-ol (roscovitine, 1a), as well as its ( S)-enantiomer 1b,…”
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G sub(i)3 does not contribute to the inhibition of adenylate cyclase when stimulation of an alpha sub(2)-adrenergic receptor causes activation of both G sub(i)2 and G sub(i)3
Published in Biochemical journal (01-01-1992)“…Agonist occupancy of the alpha sub(2)-C10 adrenergic receptor in a stable clone (1C) of rat 1 fibroblasts produced by transfection of cells with genomic DNA…”
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