[Phe1 ψ (CH2 -NH)Gly2 ]nociceptin-(1-13)-NH2 activation of an inward rectifier as a partial agonist of ORL1 receptors in rat periaqueductal gray
Author:
Publisher
Wiley
Subject
Pharmacology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1038/sj.bjp.0702746/fullpdf
Reference33 articles.
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4. [Phe1ψ(CH2-NH)Gly2]nociceptin-(1-13)-NH2 is an agonist of the nociceptin (ORL1) receptor;BUTOUR;Eur. J. Pharmacol.,1998
5. Pharmacological characterization of the nociceptin receptor mediating hyperalgesia in the mouse tail withdrawal assay;CALO;Br. J. Pharmacol.,1998
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