-
1
-
-
0003089394
-
Neurotransmitter, hormone, or drug receptor binding methods
-
Raven Press, New York, H.I. Yamamura, S.J. Enna, M.J. Kuhar (Eds.)
-
Bennett J.P., Yamamura H.I. Neurotransmitter, hormone, or drug receptor binding methods. Neurotransmitter receptor binding 1985, 61-89. Raven Press, New York. 2nd ed. H.I. Yamamura, S.J. Enna, M.J. Kuhar (Eds.).
-
(1985)
Neurotransmitter receptor binding
, pp. 61-89
-
-
Bennett, J.P.1
Yamamura, H.I.2
-
2
-
-
0016828210
-
Quantitative aspects of hormone-receptor interactions of high affinity. Effect of receptor concentration and measurement of dissociation constants of labeled and unlabeled hormones
-
Chang K.J., Jacobs S., Cuatrecasas P. Quantitative aspects of hormone-receptor interactions of high affinity. Effect of receptor concentration and measurement of dissociation constants of labeled and unlabeled hormones. Biochim. Biophys. Acta 1975, 406:294-303.
-
(1975)
Biochim. Biophys. Acta
, vol.406
, pp. 294-303
-
-
Chang, K.J.1
Jacobs, S.2
Cuatrecasas, P.3
-
3
-
-
0015861774
-
Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction
-
Cheng Y., Prusoff W.H. Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction. Biochem. Pharmacol. 1973, 22:3099-3108.
-
(1973)
Biochem. Pharmacol.
, vol.22
, pp. 3099-3108
-
-
Cheng, Y.1
Prusoff, W.H.2
-
4
-
-
0028012102
-
Activation of heterologously expressed D3 dopamine receptors: comparison with D2 dopamine receptors
-
Chio C.L., Lajiness M.E., Huff R.M. Activation of heterologously expressed D3 dopamine receptors: comparison with D2 dopamine receptors. Mol. Pharmacol. 1994, 45:51-60.
-
(1994)
Mol. Pharmacol.
, vol.45
, pp. 51-60
-
-
Chio, C.L.1
Lajiness, M.E.2
Huff, R.M.3
-
5
-
-
0037169991
-
A novel series of hybrid compounds derived by combining 2-aminotetralin and piperazine fragments: binding activity at D2 and D3 receptors
-
Dutta A.K., Fei X.S., Reith M.E. A novel series of hybrid compounds derived by combining 2-aminotetralin and piperazine fragments: binding activity at D2 and D3 receptors. Bioorg. Med. Chem. Lett. 2002, 12:619-622.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 619-622
-
-
Dutta, A.K.1
Fei, X.S.2
Reith, M.E.3
-
6
-
-
0029976759
-
Pharmacological analysis of dopamine stimulation of [35S]-GTP gamma S binding via human D2short and D2long dopamine receptors expressed in recombinant cells
-
Gardner B., Hall D.A., Strange P.G. Pharmacological analysis of dopamine stimulation of [35S]-GTP gamma S binding via human D2short and D2long dopamine receptors expressed in recombinant cells. Br. J. Pharmacol. 1996, 118:1544-1550.
-
(1996)
Br. J. Pharmacol.
, vol.118
, pp. 1544-1550
-
-
Gardner, B.1
Hall, D.A.2
Strange, P.G.3
-
7
-
-
2442467014
-
The neurobiology of dopamine signaling
-
Girault J.A., Greengard P. The neurobiology of dopamine signaling. Arch. Neurol. 2004, 61:641-644.
-
(2004)
Arch. Neurol.
, vol.61
, pp. 641-644
-
-
Girault, J.A.1
Greengard, P.2
-
8
-
-
0016762525
-
Estimation of hormone receptor affinity by competitive displacement of labeled ligand: effect of concentration of receptor and of labeled ligand
-
Jacobs S., Chang K.-J., Cuatrecasas P. Estimation of hormone receptor affinity by competitive displacement of labeled ligand: effect of concentration of receptor and of labeled ligand. Biochem. Biophys. Res. Commun. 1975, 66:687-692.
-
(1975)
Biochem. Biophys. Res. Commun.
, vol.66
, pp. 687-692
-
-
Jacobs, S.1
Chang, K.-J.2
Cuatrecasas, P.3
-
9
-
-
0030610305
-
The D3 dopamine receptor: neurobiology and potential clinical relevance
-
Levant B. The D3 dopamine receptor: neurobiology and potential clinical relevance. Pharmacol. Rev. 1997, 49:231-252.
-
(1997)
Pharmacol. Rev.
, vol.49
, pp. 231-252
-
-
Levant, B.1
-
10
-
-
0020446693
-
Calculating the dissociation constant of an unlabeled compound from the concentration required to displace radiolabel binding by 50%
-
Linden J. Calculating the dissociation constant of an unlabeled compound from the concentration required to displace radiolabel binding by 50%. J. Cyclic. Nucleotide. Res. 1982, 8:163-172.
-
(1982)
J. Cyclic. Nucleotide. Res.
, vol.8
, pp. 163-172
-
-
Linden, J.1
-
11
-
-
0031595788
-
Mapping of dopamine D3 receptor binding site by pharmacological characterization of mutants expressed in CHO cells with the Semliki Forest virus system
-
Lundstrom K., Turpin M.P., Large C., Robertson G., Thomas P., Lewell X.Q. Mapping of dopamine D3 receptor binding site by pharmacological characterization of mutants expressed in CHO cells with the Semliki Forest virus system. J. Recept. Signal. Transduct. Res. 1998, 18:133-150.
-
(1998)
J. Recept. Signal. Transduct. Res.
, vol.18
, pp. 133-150
-
-
Lundstrom, K.1
Turpin, M.P.2
Large, C.3
Robertson, G.4
Thomas, P.5
Lewell, X.Q.6
-
12
-
-
0037449354
-
Synthesis of 2-(5-bromo-2,3-dimethoxyphenyl)-5-(aminomethyl)-1H-pyrrole analogues and their binding affinities for dopamine D2, D3, and D4 receptors
-
Mach R.H., Huang Y., Freeman R.A., Wu L., Blair S., Luedtke R.R. Synthesis of 2-(5-bromo-2,3-dimethoxyphenyl)-5-(aminomethyl)-1H-pyrrole analogues and their binding affinities for dopamine D2, D3, and D4 receptors. Bioorg. Med. Chem. 2003, 11:225-233.
-
(2003)
Bioorg. Med. Chem.
, vol.11
, pp. 225-233
-
-
Mach, R.H.1
Huang, Y.2
Freeman, R.A.3
Wu, L.4
Blair, S.5
Luedtke, R.R.6
-
13
-
-
0026940770
-
Site-directed mutagenesis of the human dopamine D2 receptor
-
Mansour A., Meng F., Meador-Woodruff J.H., Taylor L.P., Civelli O., Akil H. Site-directed mutagenesis of the human dopamine D2 receptor. Eur. J. Pharmacol. 1992, 227:205-214.
-
(1992)
Eur. J. Pharmacol.
, vol.227
, pp. 205-214
-
-
Mansour, A.1
Meng, F.2
Meador-Woodruff, J.H.3
Taylor, L.P.4
Civelli, O.5
Akil, H.6
-
14
-
-
23944521608
-
Sumanirole, a highly dopamine D2-selective receptor agonist: in vitro and in vivo pharmacological characterization and efficacy in animal models of Parkinson's disease
-
McCall R.B., Lookingland K.J., Bedard P.J., Huff R.M. Sumanirole, a highly dopamine D2-selective receptor agonist: in vitro and in vivo pharmacological characterization and efficacy in animal models of Parkinson's disease. J. Pharmacol. Exp. Ther. 2005, 314:1248-1256.
-
(2005)
J. Pharmacol. Exp. Ther.
, vol.314
, pp. 1248-1256
-
-
McCall, R.B.1
Lookingland, K.J.2
Bedard, P.J.3
Huff, R.M.4
-
15
-
-
0023918636
-
An exact correction to the " Cheng-Prusoff" correction
-
Munson P.J., Rodbard D. An exact correction to the " Cheng-Prusoff" correction. J. Recept. Res. 1988, 8:533-546.
-
(1988)
J. Recept. Res.
, vol.8
, pp. 533-546
-
-
Munson, P.J.1
Rodbard, D.2
-
16
-
-
0033045716
-
Role of conserved serine residues in the interaction of agonists with D3 dopamine receptors
-
Sartania N., Strange P.G. Role of conserved serine residues in the interaction of agonists with D3 dopamine receptors. J. Neurochem. 1999, 72:2621-2624.
-
(1999)
J. Neurochem.
, vol.72
, pp. 2621-2624
-
-
Sartania, N.1
Strange, P.G.2
-
17
-
-
34250847652
-
N-(4-(4-(2-Halogenophenyl)piperazin-1-yl)butyl) substituted cinnamoyl amide derivatives as dopamine D2 and D3 receptor ligands
-
Saur O., Hackling A.E., Perachon S., Schwartz J.C., Sokoloff P., Stark H. N-(4-(4-(2-Halogenophenyl)piperazin-1-yl)butyl) substituted cinnamoyl amide derivatives as dopamine D2 and D3 receptor ligands. Arch. Pharm. (Weinheim) 2007, 340:178-184.
-
(2007)
Arch. Pharm. (Weinheim)
, vol.340
, pp. 178-184
-
-
Saur, O.1
Hackling, A.E.2
Perachon, S.3
Schwartz, J.C.4
Sokoloff, P.5
Stark, H.6
-
18
-
-
0025179967
-
Molecular cloning and characterization of a novel dopamine receptor (D3) as a target for neuroleptics
-
Sokoloff P., Giros B., Martres M.P., Bouthenet M.L., Schwartz J.C. Molecular cloning and characterization of a novel dopamine receptor (D3) as a target for neuroleptics. Nature 1990, 347:146-151.
-
(1990)
Nature
, vol.347
, pp. 146-151
-
-
Sokoloff, P.1
Giros, B.2
Martres, M.P.3
Bouthenet, M.L.4
Schwartz, J.C.5
-
19
-
-
0026510136
-
The third dopamine receptor (D3) as a novel target for antipsychotics
-
Sokoloff P., Martres M.P., Giros B., Bouthenet M.L., Schwartz J.C. The third dopamine receptor (D3) as a novel target for antipsychotics. Biochem. Pharmacol. 1992, 43:659-666.
-
(1992)
Biochem. Pharmacol.
, vol.43
, pp. 659-666
-
-
Sokoloff, P.1
Martres, M.P.2
Giros, B.3
Bouthenet, M.L.4
Schwartz, J.C.5
-
20
-
-
0035101404
-
Antipsychotic drugs: importance of dopamine receptors for mechanisms of therapeutic actions and side effects
-
Strange P.G. Antipsychotic drugs: importance of dopamine receptors for mechanisms of therapeutic actions and side effects. Pharmacol. Rev. 2001, 53:119-133.
-
(2001)
Pharmacol. Rev.
, vol.53
, pp. 119-133
-
-
Strange, P.G.1
-
21
-
-
44549087928
-
Antipsychotic drug action: antagonism, inverse agonism or partial agonism
-
Strange P.G. Antipsychotic drug action: antagonism, inverse agonism or partial agonism. Trends Pharmacol. Sci. 2008, 29:314-321.
-
(2008)
Trends Pharmacol. Sci.
, vol.29
, pp. 314-321
-
-
Strange, P.G.1
-
22
-
-
0023921625
-
Potential misconceptions arising from the application of enzyme kinetic equations to ligand-receptor systems at equilibrium
-
Tomlinson G. Potential misconceptions arising from the application of enzyme kinetic equations to ligand-receptor systems at equilibrium. Can. J. Physiol. Pharmacol. 1988, 66:342-349.
-
(1988)
Can. J. Physiol. Pharmacol.
, vol.66
, pp. 342-349
-
-
Tomlinson, G.1
-
23
-
-
0032194951
-
Selective activation of Galphao by D2L dopamine receptors in NS20Y neuroblastoma cells
-
Watts V.J., Wiens B.L., Cumbay M.G., Vu M.N., Neve R.L., Neve K.A. Selective activation of Galphao by D2L dopamine receptors in NS20Y neuroblastoma cells. J. Neurosci. 1998, 18:8692-8699.
-
(1998)
J. Neurosci.
, vol.18
, pp. 8692-8699
-
-
Watts, V.J.1
Wiens, B.L.2
Cumbay, M.G.3
Vu, M.N.4
Neve, R.L.5
Neve, K.A.6
-
24
-
-
0029664508
-
D2, D3, and D4 dopamine receptors couple to G protein-regulated potassium channels in Xenopus oocytes
-
Werner P., Hussy N., Buell G., Jones K.A., North R.A. D2, D3, and D4 dopamine receptors couple to G protein-regulated potassium channels in Xenopus oocytes. Mol. Pharmacol. 1996, 49:656-661.
-
(1996)
Mol. Pharmacol.
, vol.49
, pp. 656-661
-
-
Werner, P.1
Hussy, N.2
Buell, G.3
Jones, K.A.4
North, R.A.5
-
25
-
-
0032714409
-
Efficient functional coupling of the human D3 dopamine receptor to G(o) subtype of G proteins in SH-SY5Y cells
-
Zaworski P.G., Alberts G.L., Pregenzer J.F., Im W.B., Slightom J.L., Gill G.S. Efficient functional coupling of the human D3 dopamine receptor to G(o) subtype of G proteins in SH-SY5Y cells. Br. J. Pharmacol. 1999, 128:1181-1188.
-
(1999)
Br. J. Pharmacol.
, vol.128
, pp. 1181-1188
-
-
Zaworski, P.G.1
Alberts, G.L.2
Pregenzer, J.F.3
Im, W.B.4
Slightom, J.L.5
Gill, G.S.6
-
26
-
-
9644280929
-
Interaction between a hydroxypiperidine analogue of 4-(2-benzhydryloxy-ethyl)-1-(4-fluorobenzyl)piperidine and Aspartate 68 in the human dopamine transporter
-
Zhen J., Maiti S., Chen N., Dutta A.K., Reith M.E. Interaction between a hydroxypiperidine analogue of 4-(2-benzhydryloxy-ethyl)-1-(4-fluorobenzyl)piperidine and Aspartate 68 in the human dopamine transporter. Eur. J. Pharmacol. 2004, 506:17-26.
-
(2004)
Eur. J. Pharmacol.
, vol.506
, pp. 17-26
-
-
Zhen, J.1
Maiti, S.2
Chen, N.3
Dutta, A.K.4
Reith, M.E.5
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