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PUBMED FOR HANDHELDS

Journal Abstract Search


322 related items for PubMed ID: 10940356

  • 1.
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  • 2. In vitro inhibitory effects of J-113397 on nociceptin/orphanin FQ-stimulated.
    Ichikawa D, Ozaki S, Azuma T, Nambu H, Kawamoto H, Iwasawa Y, Takeshima H, Ohta H.
    Neuroreport; 2001 Jun 13; 12(8):1757-61. PubMed ID: 11409754
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  • 4. Pharmacological characterization of the nociceptin/orphanin FQ receptor antagonist SB-612111 [(-)-cis-1-methyl-7-[[4-(2,6-dichlorophenyl)piperidin-1-yl]methyl]-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-ol]: in vitro studies.
    Spagnolo B, Carrà G, Fantin M, Fischetti C, Hebbes C, McDonald J, Barnes TA, Rizzi A, Trapella C, Fanton G, Morari M, Lambert DG, Regoli D, Calò G.
    J Pharmacol Exp Ther; 2007 Jun 13; 321(3):961-7. PubMed ID: 17329552
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  • 5. Identification of the G-protein-coupled ORL1 receptor in the mouse spinal cord by [35S]-GTPgammaS binding and immunohistochemistry.
    Narita M, Mizoguchi H, Oji DE, Dun NJ, Hwang BH, Nagase H, Tseng LF.
    Br J Pharmacol; 1999 Nov 13; 128(6):1300-6. PubMed ID: 10578145
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  • 7. Cloning and characterization of the rhesus monkey nociceptin/orphanin FQ receptor.
    Koga K, Ichikawa D, Nambu H, Azuma-Kanoh T, Sakai N, Takaki-Kawagoe H, Ozaki S, Ohta H.
    Genes Genet Syst; 2009 Oct 13; 84(5):319-25. PubMed ID: 20154418
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  • 10. Comparison of pharmacological activities of buprenorphine and norbuprenorphine: norbuprenorphine is a potent opioid agonist.
    Huang P, Kehner GB, Cowan A, Liu-Chen LY.
    J Pharmacol Exp Ther; 2001 May 13; 297(2):688-95. PubMed ID: 11303059
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  • 12. Effects of [(pF)Phe(4)]nociceptin/orphanin FQ-(1-13)NH(2) on GTPgamma(35)S binding and cAMP formation in Chinese hamster ovary cells expressing the human nociceptin/orphanin FQ receptor.
    McDonald J, Barnes TA, Calo G, Guerrini R, Rowbotham DJ, Lambert DG.
    Eur J Pharmacol; 2002 May 17; 443(1-3):7-12. PubMed ID: 12044785
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  • 14. In vitro and ex vivo effects of a selective nociceptin/orphanin FQ (N/OFQ) peptide receptor antagonist, CompB, on specific binding of [3H]N/OFQ and [35S]GTPgammaS in rat brain and spinal cord.
    Yamada S, Kusaka T, Urayama A, Kimura R, Watanabe Y.
    Br J Pharmacol; 2003 Aug 17; 139(8):1462-8. PubMed ID: 12922933
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  • 15. Binding and GTPgammaS autoradiographic analysis of preproorphanin precursor peptide products at the ORL1 and opioid receptors.
    Neal CR, Owens CE, Taylor LP, Hoversten MT, Akil H, Watson SJ.
    J Chem Neuroanat; 2003 Jul 17; 25(4):233-47. PubMed ID: 12842269
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  • 16. N-terminal modifications leading to peptide ORL1 partial agonists and antagonists.
    Judd AK, Kaushanskaya A, Tuttle DJ, Sanchez A, Khroyan T, Polgar W, Toll L.
    J Pept Res; 2003 Nov 17; 62(5):191-8. PubMed ID: 14531842
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  • 17. Nociceptin (orphanin FQ): high-affinity and high-capacity binding site coupled to low-potency stimulation of guanylyl-5'-O-(gamma-thio)-triphosphate binding in rat brain membranes.
    Albrecht E, Samovilova NN, Oswald S, Baeger I, Berger H.
    J Pharmacol Exp Ther; 1998 Aug 17; 286(2):896-902. PubMed ID: 9694948
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  • 18. (2S,3R) beta-methyl-2',6'-dimethyltyrosine-L-tetrahydroisoquinoline-3-carboxylic acid [(2S,3R)TMT-L-Tic-OH] is a potent, selective delta-opioid receptor antagonist in mouse brain.
    Hosohata K, Varga EV, Alfaro-Lopez J, Tang X, Vanderah TW, Porreca F, Hruby VJ, Roeske WR, Yamamura HI.
    J Pharmacol Exp Ther; 2003 Feb 17; 304(2):683-8. PubMed ID: 12538822
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  • 20. G protein activation and cyclic AMP modulation by naloxone benzoylhydrazone in distinct layers of rat olfactory bulb.
    Onali P, Olianas MC.
    Br J Pharmacol; 2004 Nov 17; 143(5):638-48. PubMed ID: 15451772
    [Abstract] [Full Text] [Related]


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