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1
NK-1 receptor mediation of neurogenic plasma extravasation in rat skin.
Br J Pharmacol. 1989 Aug;97(4):1232-8. doi: 10.1111/j.1476-5381.1989.tb12583.x.
5
Novel selective agonists and antagonists confirm neurokinin NK1 receptors in guinea-pig vas deferens.
Br J Pharmacol. 1991 Feb;102(2):511-7. doi: 10.1111/j.1476-5381.1991.tb12202.x.
6
Tachykinin receptors in smooth muscles: a study with agonists (substance P, neurokinin A) and antagonists.
Eur J Pharmacol. 1985 Nov 26;118(1-2):25-36. doi: 10.1016/0014-2999(85)90659-4.
9
Comparison of cardiovascular and bronchoconstrictor effects of substance P, substance K and other tachykinins.
Naunyn Schmiedebergs Arch Pharmacol. 1984 Dec;328(2):196-201. doi: 10.1007/BF00512072.
10
The mechanism of tachykinin-induced bronchoconstriction in the rat.
Am Rev Respir Dis. 1988 May;137(5):1038-44. doi: 10.1164/ajrccm/137.5.1038.

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Neurobiological mechanisms of pelvic pain.
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A non-peptide NK1-receptor antagonist, RP 67580, inhibits neurogenic inflammation postsynaptically.
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Pharmacology of the neurogenic oedema response to electrical stimulation of the saphenous nerve in the rat.
Naunyn Schmiedebergs Arch Pharmacol. 1980 Nov;314(3):271-6. doi: 10.1007/BF00498549.
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Receptors for substance P. III. Classification by competitive antagonists.
Eur J Pharmacol. 1984 Jan 27;97(3-4):179-89. doi: 10.1016/0014-2999(84)90449-7.
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The possible existence of multiple receptors for substance P.
Naunyn Schmiedebergs Arch Pharmacol. 1982 Mar;318(4):281-7. doi: 10.1007/BF00501166.
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Intrathecal morphine inhibits substance P release from mammalian spinal cord in vivo.
Nature. 1980 Jul 10;286(5769):155-7. doi: 10.1038/286155a0.
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Novel pharmacology of substance K-binding sites: a third type of tachykinin receptor.
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