-
1
-
-
0026633686
-
Discriminative stimulus properties of 8-OH-DPAT in pigeons: Antagonism studies with putative 5-HT1A receptor antagonists BMY 7378 and NAN-190
-
Barrett JE, Gleeson S (1992). Discriminative stimulus properties of 8-OH-DPAT in pigeons: antagonism studies with putative 5-HT1A receptor antagonists BMY 7378 and NAN-190. Eur J Pharmacol 217:163-171.
-
(1992)
Eur J Pharmacol
, vol.217
, pp. 163-171
-
-
Barrett, J.E.1
Gleeson, S.2
-
2
-
-
33748578640
-
WAY 100635 is a potent dopamine D4 receptor agonist
-
Chemel BR, Roth BL, Armbruster B, Watts VJ, Nichols DE (2006). WAY 100635 is a potent dopamine D4 receptor agonist. Psychopharmacology (Berl) 188:244-251.
-
(2006)
Psychopharmacology (Berl)
, vol.188
, pp. 244-251
-
-
Chemel, B.R.1
Roth, B.L.2
Armbruster, B.3
Watts, V.J.4
Nichols, D.E.5
-
3
-
-
0035986335
-
Effect of chronic fluoxetine and WAY 100635 treatment on serotonergic neurotransmission in the frontal cortex
-
Dawson LA, Nguyen HQ, Smith DL, Schechter LE (2002). Effect of chronic fluoxetine and WAY 100635 treatment on serotonergic neurotransmission in the frontal cortex. J Psychopharmacol 16:145-152.
-
(2002)
J Psychopharmacol
, vol.16
, pp. 145-152
-
-
Dawson, L.A.1
Nguyen, H.Q.2
Smith, D.L.3
Schechter, L.E.4
-
4
-
-
0031910091
-
Characterization of the aminomethylchroman derivative BAY x 3702 as a highly potent 5-hydroxytryptamine1 A receptor agonist
-
De Vry J, Schohe-Loop R, Heine HG, Greuel JM, Mauler F, Schmidt B, et al. (1998). Characterization of the aminomethylchroman derivative BAY x 3702 as a highly potent 5-hydroxytryptamine1 A receptor agonist. J Pharmacol Exp Ther 284: 1082-1094.
-
(1998)
J Pharmacol Exp Ther
, vol.284
, pp. 1082-1094
-
-
De Vry, J.1
Schohe-Loop, R.2
Heine, H.G.3
Greuel, J.M.4
Mauler, F.5
Schmidt, B.6
-
5
-
-
0030070276
-
Electrophysiological, biochemical, neurohormonal and behavioural studies with WAY 100635, a potent, selective and silent 5-HT1A receptor antagonist
-
Fletcher A, Forster EA, Bill DJ, Brown G, Cliffe IA, Hartley JE, et al. (1996). Electrophysiological, biochemical, neurohormonal and behavioural studies with WAY 100635, a potent, selective and silent 5-HT1A receptor antagonist. Behav Brain Res 73: 337-353.
-
(1996)
Behav Brain Res
, vol.73
, pp. 337-353
-
-
Fletcher, A.1
Forster, E.A.2
Bill, D.J.3
Brown, G.4
Cliffe, I.A.5
Hartley, J.E.6
-
7
-
-
0029132789
-
A pharmacological profile of the selective silent 5-HT1A receptor antagonist, WAY 100635
-
Forster EA, Cliffe IA, Bill DJ, Dover GM, Jones D, Reilly Y, Fletcher A (1995). A pharmacological profile of the selective silent 5-HT1A receptor antagonist, WAY 100635. Eur J Pharmacol 281:81 -88.
-
(1995)
Eur J Pharmacol
, vol.281
, pp. 81-88
-
-
Forster, E.A.1
Cliffe, I.A.2
Bill, D.J.3
Dover, G.M.4
Jones, D.5
Reilly, Y.6
Fletcher, A.7
-
8
-
-
0033799217
-
Two-lever drug-drug discrimination with the 5-HT1 receptor agonists flesinoxan and eltoprazine
-
Gommans J, Hijzen TH, Maes RA, Olivier B (2000). Two-lever drug-drug discrimination with the 5-HT1 receptor agonists flesinoxan and eltoprazine. Int J Neuropsychopharmacol 3:221 -228.
-
(2000)
Int J Neuropsychopharmacol
, vol.3
, pp. 221-228
-
-
Gommans, J.1
Hijzen, T.H.2
Maes, R.A.3
Olivier, B.4
-
9
-
-
33745076212
-
WAY 100635 antagonist-induced plasticity of 5-HT receptors: Regulatory differences between a stable cell line and an in vivo native system
-
Khawaja XZ, Smith DL, Nawoschik SP, Zhang J, Dunlop J, Dilks DW, et al. (2006). WAY 100635 antagonist-induced plasticity of 5-HT receptors: regulatory differences between a stable cell line and an in vivo native system. J Neurochem 98:134-145.
-
(2006)
J Neurochem
, vol.98
, pp. 134-145
-
-
Khawaja, X.Z.1
Smith, D.L.2
Nawoschik, S.P.3
Zhang, J.4
Dunlop, J.5
Dilks, D.W.6
-
12
-
-
84951384024
-
A simplified method of evaluating dose-effect experiments
-
Litchfield JT Jr, Wilcoxon F (1949). A simplified method of evaluating dose-effect experiments. J Pharmacol Exp Ther 96:99-112.
-
(1949)
J Pharmacol Exp Ther
, vol.96
, pp. 99-112
-
-
Litchfield Jr, J.T.1
Wilcoxon, F.2
-
13
-
-
0028232981
-
Behavioral effects of the highly selective serotonin releasing agent 5-methoxy-6-methyl-2-aminoindan
-
Marona-Lewicka D, Nichols DE (1994). Behavioral effects of the highly selective serotonin releasing agent 5-methoxy-6-methyl-2-aminoindan. Eur J Pharmacol 258:1-13.
-
(1994)
Eur J Pharmacol
, vol.258
, pp. 1-13
-
-
Marona-Lewicka, D.1
Nichols, D.E.2
-
14
-
-
2442547256
-
1A receptor agonist LY 293284 in the drug discrimination assay in rats
-
1A receptor agonist LY 293284 in the drug discrimination assay in rats. Psychopharmacology 172:415-421.
-
(2004)
Psychopharmacology
, vol.172
, pp. 415-421
-
-
Marona-Lewicka, D.1
Nichols, D.E.2
-
15
-
-
61849169763
-
-
4 receptor involvement in the discriminative stimulus effects in rats of LSD, but not the phenethylamine hallucinogen DOI. Psychopharmacology Jul 6. [Epub ahead of print, PM: 18604600].
-
4 receptor involvement in the discriminative stimulus effects in rats of LSD, but not the phenethylamine hallucinogen DOI. Psychopharmacology Jul 6. [Epub ahead of print, PM: 18604600].
-
-
-
-
16
-
-
34848820567
-
WAY 100635 has high selectivity for serotonin 5-HT(1A) versus dopamine D(4) receptors
-
Martel JC, Leduc N, Ormiere AM, Faucillon V, Danty N, Culie C, et al. (2007). WAY 100635 has high selectivity for serotonin 5-HT(1A) versus dopamine D(4) receptors. Eur J Pharmacol 574:15-19.
-
(2007)
Eur J Pharmacol
, vol.574
, pp. 15-19
-
-
Martel, J.C.1
Leduc, N.2
Ormiere, A.M.3
Faucillon, V.4
Danty, N.5
Culie, C.6
-
17
-
-
21344456516
-
2-[4-(3,4-Dimethylphenyl)piperazin-1-ylmethyl]-1H benzoimidazole (A-381393), a selective dopamine D4 receptor antagonist
-
Nakane M, Cowart MD, Hsieh GC, Miller L, Uchic ME, Chang R, et al. (2005). 2-[4-(3,4-Dimethylphenyl)piperazin-1-ylmethyl]-1H benzoimidazole (A-381393), a selective dopamine D4 receptor antagonist. Neuropharmacology 49: 112-121.
-
(2005)
Neuropharmacology
, vol.49
, pp. 112-121
-
-
Nakane, M.1
Cowart, M.D.2
Hsieh, G.C.3
Miller, L.4
Uchic, M.E.5
Chang, R.6
-
20
-
-
0029941536
-
(S)-(-)-4-[4-[2-(isochroman-1 -yl)ethyl]-piperazin-1 -yl] benzenesulfonamide, a selective dopamine D4 antagonist
-
Tenbrink RE, Bergh CL, Duncan JN, Harris DW, Huff RM, Lahti RA, et al. (1996). (S)-(-)-4-[4-[2-(isochroman-1 -yl)ethyl]-piperazin-1 -yl] benzenesulfonamide, a selective dopamine D4 antagonist. J Med Chem 39:2435-2437.
-
(1996)
J Med Chem
, vol.39
, pp. 2435-2437
-
-
Tenbrink, R.E.1
Bergh, C.L.2
Duncan, J.N.3
Harris, D.W.4
Huff, R.M.5
Lahti, R.A.6
-
23
-
-
0004252445
-
-
4th ed. Upper Saddle River, New Jersey: Prentice-Hall. pp, Section 24.6
-
Zar J (1999). Biostatistical analysis. 4th ed. Upper Saddle River, New Jersey: Prentice-Hall. pp. 533-538. (Section 24.6).
-
(1999)
Biostatistical analysis
, pp. 533-538
-
-
Zar, J.1
|