-
2
-
-
0014511179
-
The mechanism of irreversible adrenergic blockade by N-carbethoxydihydroquinolines. Model studies with typical serine hydrolases
-
Belleau B., DiTullio V., Godin D. The mechanism of irreversible adrenergic blockade by N-carbethoxydihydroquinolines. Model studies with typical serine hydrolases. Biochem. Pharmacol. 18:1969;1039-1044.
-
(1969)
Biochem. Pharmacol.
, vol.18
, pp. 1039-1044
-
-
Belleau, B.1
Ditullio, V.2
Godin, D.3
-
3
-
-
0023026089
-
Adaptive changes in the 5-HT2 binding site after chronic administration of agonists and antagonists
-
Blackshear M.A., Martin L.L., Sanders-Bush E. Adaptive changes in the 5-HT2 binding site after chronic administration of agonists and antagonists. Neuropharmacology. 25:1986;1267-1271.
-
(1986)
Neuropharmacology
, vol.25
, pp. 1267-1271
-
-
Blackshear, M.A.1
Martin, L.L.2
Sanders-Bush, E.3
-
4
-
-
0028245619
-
Molecular biology of 5-HT receptors
-
Boess F.G., Martin I.L. Molecular biology of 5-HT receptors. Neuropharmacology. 33:1994;275-317.
-
(1994)
Neuropharmacology
, vol.33
, pp. 275-317
-
-
Boess, F.G.1
Martin, I.L.2
-
5
-
-
0025783810
-
Recovery of 5-HT receptors after irreversible blockade by N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ)
-
Bolanos F.J., Schechter L.E., Laporte A.-M., Hamon M., Gozlan H. Recovery of 5-HT receptors after irreversible blockade by N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ). Proc. West. Pharmacol. Soc. 34:1991;387-393.
-
(1991)
Proc. West. Pharmacol. Soc.
, vol.34
, pp. 387-393
-
-
Bolanos, F.J.1
Schechter, L.E.2
Laporte, A.-M.3
Hamon, M.4
Gozlan, H.5
-
6
-
-
0021346626
-
Inositol phospholipid hydrolysis in rat cerebral cortical slices. I. Receptor characterisation
-
Brown E., Kendall D.A., Nahorski S.R. Inositol phospholipid hydrolysis in rat cerebral cortical slices. I. Receptor characterisation. J. Neurochem. 42:1984;1379-1387.
-
(1984)
J. Neurochem.
, vol.42
, pp. 1379-1387
-
-
Brown, E.1
Kendall, D.A.2
Nahorski, S.R.3
-
8
-
-
0039166383
-
Mechanism of cholinergic antagonism by N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ)
-
Chang K.J., Moran J.F., Triggle D.J. Mechanism of cholinergic antagonism by N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ). Pharmacol. Res. Commun. 2:1970;63-66.
-
(1970)
Pharmacol. Res. Commun.
, vol.2
, pp. 63-66
-
-
Chang, K.J.1
Moran, J.F.2
Triggle, D.J.3
-
10
-
-
0024513997
-
Neurotransmitter receptors and phosphoinositide turnover
-
Chuang D.-M. Neurotransmitter receptors and phosphoinositide turnover. Annu. Rev. Pharmacol. Toxicol. 29:1990;71-110.
-
(1990)
Annu. Rev. Pharmacol. Toxicol.
, vol.29
, pp. 71-110
-
-
Chuang, D.-M.1
-
11
-
-
0021248714
-
Selective 5-HT2 antagonists inhibit serotonin-stimulated phosphatidylinositol metabolism in cerebral cortex
-
Conn P.J., Sanders-Bush E. Selective 5-HT2 antagonists inhibit serotonin-stimulated phosphatidylinositol metabolism in cerebral cortex. Neuropharmacology. 23:1984;993-996.
-
(1984)
Neuropharmacology
, vol.23
, pp. 993-996
-
-
Conn, P.J.1
Sanders-Bush, E.2
-
12
-
-
0021875393
-
2 binding site in rat cerebral cortex but not in subcortical regions
-
2 binding site in rat cerebral cortex but not in subcortical regions. J. Pharmacol. Exp. Ther. 234:1985;195-203.
-
(1985)
J. Pharmacol. Exp. Ther.
, vol.234
, pp. 195-203
-
-
Conn, P.J.1
Sanders-Bush, E.2
-
13
-
-
0022630728
-
Biochemical characterisation of serotonin-stimulated phosphoinositide turnover
-
Conn P.J., Sanders-Bush E. Biochemical characterisation of serotonin-stimulated phosphoinositide turnover. Life Sci. 38:1986;663-669.
-
(1986)
Life Sci.
, vol.38
, pp. 663-669
-
-
Conn, P.J.1
Sanders-Bush, E.2
-
15
-
-
0026611099
-
2 receptor agonistic action on phosphatidylinositol metabolism in the rat fronto-cingulate and entorhinal cortex
-
2 receptor agonistic action on phosphatidylinositol metabolism in the rat fronto-cingulate and entorhinal cortex. Neuropharmacology. 31:1992;615-621.
-
(1992)
Neuropharmacology
, vol.31
, pp. 615-621
-
-
Edwards, E.1
Ashby, C.R.2
Wang, R.Y.3
-
16
-
-
0025921998
-
3 receptor agonists on phosphoinositides hydrolysis in the rat fronto-cingulate and entortinal cortices
-
3 receptor agonists on phosphoinositides hydrolysis in the rat fronto-cingulate and entortinal cortices. J. Pharmacol. Exp. Ther. 256:1991;1025-1032.
-
(1991)
J. Pharmacol. Exp. Ther.
, vol.256
, pp. 1025-1032
-
-
Edwards, E.1
Harkins, K.2
Ashby, C.R.3
Wang, R.Y.4
-
19
-
-
0030608845
-
2A receptor-mediated inositol phosphate production in the spontaneously hypertensive rat and Lewis rat strains
-
2A receptor-mediated inositol phosphate production in the spontaneously hypertensive rat and Lewis rat strains. Neurosci. Lett. 236:1997;112-116.
-
(1997)
Neurosci. Lett.
, vol.236
, pp. 112-116
-
-
Gauffre, J.-C.1
Aguerre, S.2
Mormède, P.3
Chaouloff, F.4
-
20
-
-
0028290841
-
Differential effects of N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ) on various 5-HT receptor binding sites in the rat brain
-
Gozlan H., Laporte A.-M., Thibault S., Schechter L.E., Bolanos F., Hamon M. Differential effects of N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ) on various 5-HT receptor binding sites in the rat brain. Neuropharmacology. 33:1994;423-431.
-
(1994)
Neuropharmacology
, vol.33
, pp. 423-431
-
-
Gozlan, H.1
Laporte, A.-M.2
Thibault, S.3
Schechter, L.E.4
Bolanos, F.5
Hamon, M.6
-
21
-
-
0020582473
-
Behavioural and radioligand binding evidence for irreversible dopamine receptor blockade by N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline
-
Hamblin M.W., Creese I. Behavioural and radioligand binding evidence for irreversible dopamine receptor blockade by N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline. Life Sci. 32:1983;2247-2255.
-
(1983)
Life Sci.
, vol.32
, pp. 2247-2255
-
-
Hamblin, M.W.1
Creese, I.2
-
23
-
-
0001503815
-
2 receptor blockade to study serotonin-induced pathology
-
2 receptor blockade to study serotonin-induced pathology. Trends Pharmacol. Sci. 4:1983;198-206.
-
(1983)
Trends Pharmacol. Sci.
, vol.4
, pp. 198-206
-
-
Janssen, P.A.J.1
-
24
-
-
0021963089
-
5-Hydroxytryptamine-stimulated inositol phospholipid hydrolysis in rat cerebral cortex slices: Pharmacological characterization and effects of antidepressants
-
Kendall D.A., Nahorski S.R. 5-Hydroxytryptamine-stimulated inositol phospholipid hydrolysis in rat cerebral cortex slices: pharmacological characterization and effects of antidepressants. J. Pharmacol. Exp. Ther. 223:1985;474-479.
-
(1985)
J. Pharmacol. Exp. Ther.
, vol.223
, pp. 474-479
-
-
Kendall, D.A.1
Nahorski, S.R.2
-
27
-
-
0020004528
-
2 receptor binding sites. Binding properties, brain distribution, and functional role
-
2 receptor binding sites. Binding properties, brain distribution, and functional role. Mol. Pharmacol. 21:1982;301-314.
-
(1982)
Mol. Pharmacol.
, vol.21
, pp. 301-314
-
-
Leysen, J.E.1
Niemegeers, C.J.E.2
Van Nueten, J.M.3
Laduron, P.M.4
-
28
-
-
0022595471
-
Down-regulation of serotonin-S2 receptor sites in rat brain by chronic treatment with the serotonin antagonists ritanserin and setoperone
-
Leysen J.E., Van-Gompel P., Gommeren W., Woestenborghs R., Janssen P.A. Down-regulation of serotonin-S2 receptor sites in rat brain by chronic treatment with the serotonin antagonists ritanserin and setoperone. Psychopharmacology. 88:1986;434-444.
-
(1986)
Psychopharmacology
, vol.88
, pp. 434-444
-
-
Leysen, J.E.1
Van-Gompel, P.2
Gommeren, W.3
Woestenborghs, R.4
Janssen, P.A.5
-
33
-
-
0019061918
-
LIGAND: A versatile computerized approach for characterisation of ligand-binding systems
-
Munson P.J., Rodbard D. LIGAND: a versatile computerized approach for characterisation of ligand-binding systems. Anal. Biochem. 107:1980;229-239.
-
(1980)
Anal. Biochem.
, vol.107
, pp. 229-239
-
-
Munson, P.J.1
Rodbard, D.2
-
34
-
-
0021748014
-
Mesulergine, a selective serotonin-2 ligand in the rat cortex, does not label these receptors in porcine and human cortex: Evidence for species differences in brain serotonin-2 receptors
-
Pazos A., Hoyer D., Palacios J.M. Mesulergine, a selective serotonin-2 ligand in the rat cortex, does not label these receptors in porcine and human cortex: evidence for species differences in brain serotonin-2 receptors. Eur. J. Pharmacol. 106:1984;531-538.
-
(1984)
Eur. J. Pharmacol.
, vol.106
, pp. 531-538
-
-
Pazos, A.1
Hoyer, D.2
Palacios, J.M.3
-
35
-
-
0023751817
-
5-Hydroxytryptamine receptor subtypes: Molecular, biochemical and physiological characterization
-
Peroutka S.J. 5-Hydroxytryptamine receptor subtypes: molecular, biochemical and physiological characterization. Trends Neurosci. 11:1988;496-500.
-
(1988)
Trends Neurosci.
, vol.11
, pp. 496-500
-
-
Peroutka, S.J.1
-
36
-
-
0025690446
-
5-Hydroxytryptamine receptor subtypes
-
Peroutka S.J. 5-Hydroxytryptamine receptor subtypes. Pharmacol. Toxicol. 67:1990;373-383.
-
(1990)
Pharmacol. Toxicol.
, vol.67
, pp. 373-383
-
-
Peroutka, S.J.1
-
38
-
-
0019432957
-
Two distinct serotonin receptors: Regional variations in receptor binding in mammalian brain
-
Peroutka S.J., Snyder S.H. Two distinct serotonin receptors: regional variations in receptor binding in mammalian brain. Brain Res. 208:1981;339-347.
-
(1981)
Brain Res.
, vol.208
, pp. 339-347
-
-
Peroutka, S.J.1
Snyder, S.H.2
-
40
-
-
0345463304
-
Physiological and pharmacological aspects of 5-HT3 receptor function
-
T.W. Stone. London: Taylor and Francis
-
Peters J.A., Lambert J.J., Malone H.M. Physiological and pharmacological aspects of 5-HT3 receptor function. Stone T.W. Aspects of Synaptic Transmission: LTP, Galanin, Opioids, Autonomic and 5-HT. 1991;283-313 Taylor and Francis, London.
-
(1991)
Aspects of Synaptic Transmission: LTP, Galanin, Opioids, Autonomic and 5-HT
, pp. 283-313
-
-
Peters, J.A.1
Lambert, J.J.2
Malone, H.M.3
-
41
-
-
0024165856
-
2 receptor-mediated phosphatidylinositol turnover by D-lysergic acid diethylamide
-
2 receptor-mediated phosphatidylinositol turnover by D-lysergic acid diethylamide. J. Pharmacol. Exp. Ther. 247:1988;918-925.
-
(1988)
J. Pharmacol. Exp. Ther.
, vol.247
, pp. 918-925
-
-
Pierce, P.A.1
Peroutka, S.J.2
-
43
-
-
0025923909
-
2 receptors in rat cortex: Studies with a putative selective agonist and an antagonist
-
2 receptors in rat cortex: studies with a putative selective agonist and an antagonist. Biochem. Pharmacol. 42:1991;1099-1105.
-
(1991)
Biochem. Pharmacol.
, vol.42
, pp. 1099-1105
-
-
Pranzatelli, M.R.1
-
44
-
-
0024462718
-
Dopamine receptor occupancy in vivo: Measurement using N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ)
-
Saller C.F., Kreamer L.D., Adamovage L.A., Saloma A.I. Dopamine receptor occupancy in vivo: measurement using N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ). Life Sci. 45:1989;917-929.
-
(1989)
Life Sci.
, vol.45
, pp. 917-929
-
-
Saller, C.F.1
Kreamer, L.D.2
Adamovage, L.A.3
Saloma, A.I.4
-
45
-
-
0023163413
-
2 binding sites after mianserin: Comparison of loss of sites and brain levels of drug
-
2 binding sites after mianserin: comparison of loss of sites and brain levels of drug. Eur. J. Pharmacol. 133:1987;199-204.
-
(1987)
Eur. J. Pharmacol.
, vol.133
, pp. 199-204
-
-
Sanders-Bush, E.1
Breeding, M.2
Roznoski, M.3
-
47
-
-
0030610894
-
2C receptor is a prominent serotonin receptor in basal ganglia: Evidence from functional studies on serotonin-mediated phosphoinositide production
-
2C receptor is a prominent serotonin receptor in basal ganglia: evidence from functional studies on serotonin-mediated phosphoinositide production. J. Neurochem. 69:1997;1449-1458.
-
(1997)
J. Neurochem.
, vol.69
, pp. 1449-1458
-
-
Wolf, W.A.1
Schutz, L.J.2
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