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Journal Abstract Search

112 related items for PubMed ID: 1977191

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  • 2. Serotonin-2 receptor-mediated regulation of release of acetylcholine by minaprine in cholinergic nerve terminal of hippocampus of rat.
    Muramatsu M, Tamaki-Ohashi J, Usuki C, Araki H, Aihara H.
    Neuropharmacology; 1988 Jun; 27(6):603-9. PubMed ID: 3419543
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  • 4. Attenuation of serotonin-suppressed [3H]acetylcholine release by tetrahydroaminoacridine and dendrotoxin: interaction with minaprine binding site.
    Muramatsu M, Chaki S, Usuki-ito C, Otomo S.
    Res Commun Chem Pathol Pharmacol; 1990 May; 68(2):131-42. PubMed ID: 2353129
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  • 5. Characterization of the inhibition of excitatory amino acid-induced neurotransmitter release in the rat striatum by phencyclidine-like drugs.
    Snell LD, Johnson KM.
    J Pharmacol Exp Ther; 1986 Sep; 238(3):938-46. PubMed ID: 2875174
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  • 8. Interaction of L-glutamate and magnesium with phencyclidine recognition sites in rat brain: evidence for multiple affinity states of the phencyclidine/N-methyl-D-aspartate receptor complex.
    Loo PS, Braunwalder AF, Lehmann J, Williams M, Sills MA.
    Mol Pharmacol; 1987 Dec; 32(6):820-30. PubMed ID: 2892125
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  • 13. Inhibition of N-methyl-D-aspartate-induced hippocampal [3H]norepinephrine release by phencyclidine is dependent on potassium concentration.
    Snell LD, Jones SM, Johnson KM.
    Neurosci Lett; 1987 Aug 05; 78(3):333-7. PubMed ID: 2888064
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  • 14. Decreased density, but not number, of N-methyl-D-aspartate, glycine and phencyclidine binding sites in hippocampus of senescent rats.
    Bonhaus DW, Perry WB, McNamara JO.
    Brain Res; 1990 Nov 05; 532(1-2):82-6. PubMed ID: 2178039
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  • 15. Modulation of [3H]MK-801 binding to NMDA receptors in vivo and in vitro.
    Murray F, Kennedy J, Hutson PH, Elliot J, Huscroft I, Mohnen K, Russell MG, Grimwood S.
    Eur J Pharmacol; 2000 Jun 02; 397(2-3):263-70. PubMed ID: 10844123
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  • 16. 5-HT2 antagonists and minaprine block the 5-HT-induced inhibition of dopamine release from rat brain striatal slices.
    Muramatsu M, Tamaki-Ohashi J, Usuki C, Araki H, Chaki S, Aihara H.
    Eur J Pharmacol; 1988 Aug 09; 153(1):89-95. PubMed ID: 2975224
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  • 20. 3-((+/-)2-carboxypiperazin-4-yl)propyl-1-phosphonic acid (CPP) more potently antagonizes the high-affinity Mg2+ binding site on the N-methyl-D-aspartate/phencyclidine receptor ion channel complex than the L-glutamate recognition site.
    Hatta K, Yamamato T, Hori T, Okuwa M, Moroji T.
    Neurosci Lett; 1991 Apr 01; 124(2):229-31. PubMed ID: 1712440
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