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Journal Abstract Search

255 related items for PubMed ID: 8717154

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  • 4. How efficacious are 5-HT1B/D receptor ligands: an answer from GTP gamma S binding studies with stably transfected C6-glial cell lines.
    Pauwels PJ, Tardif S, Palmier C, Wurch T, Colpaert FC.
    Neuropharmacology; 1997; 36(4-5):499-512. PubMed ID: 9225275
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  • 7. Pharmacological characterizations of recombinant human 5-HT1D alpha and 5-HT1D beta receptor subtypes coupled to adenylate cyclase inhibition in clonal cell lines: apparent differences in drug intrinsic efficacies between human 5-HT1D subtypes.
    Zgombick JM, Schechter LE, Adham N, Kucharewicz SA, Weinshank RL, Branchek TA.
    Naunyn Schmiedebergs Arch Pharmacol; 1996; 354(3):226-36. PubMed ID: 8878051
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  • 10. Selective antagonism of human 5-HT1D and 5-HT1B receptor-mediated responses in stably transfected C6-glial cells by ketanserin and GR 127,935.
    Pauwels PJ, Colpaert FC.
    Eur J Pharmacol; 1996 Apr 04; 300(1-2):141-5. PubMed ID: 8741180
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  • 11. Ketanserin-sensitive depressant actions of 5-HT receptor agonists in the neonatal rat spinal cord.
    Manuel NA, Wallis DI, Crick H.
    Br J Pharmacol; 1995 Nov 04; 116(6):2647-54. PubMed ID: 8590984
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  • 13. Functional effects of the 5-HT1D receptor antagonist GR 127,935 at human 5-HT1D alpha, 5-HT1D beta, 5-HT1A and opossum 5-HT1B receptors.
    Pauwels PJ, Palmier C.
    Eur J Pharmacol; 1995 Jul 18; 290(2):95-103. PubMed ID: 8575538
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  • 16. 5-Hydroxytryptamine (5-HT)-induced endothelium-dependent relaxation of pig coronary arteries is mediated by 5-HT receptors similar to the 5-HT1D receptor subtype.
    Schoeffter P, Hoyer D.
    J Pharmacol Exp Ther; 1990 Jan 18; 252(1):387-95. PubMed ID: 2137176
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  • 19. Activation of recombinant h 5-HT1B and h 5-HT1D receptors stably expressed in C6 glioma cells produces increases in Ca2+-dependent K+ current.
    Le Grand B, Panissié A, Pauwels PJ, John GW.
    Naunyn Schmiedebergs Arch Pharmacol; 1998 Dec 18; 358(6):608-15. PubMed ID: 9879718
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