-
1
-
-
0027229310
-
1 receptor stimulation on rotation and c-fos expression
-
1 receptor stimulation on rotation and c-fos expression. Eur. J. Pharmacol. 235 (1993) 167-168
-
(1993)
Eur. J. Pharmacol.
, vol.235
, pp. 167-168
-
-
Asin, K.E.1
Wirtshafter, D.2
-
2
-
-
0015861774
-
I) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction
-
I) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction. Biochem. Pharmacol. 22 (1973) 3099-3108
-
(1973)
Biochem. Pharmacol.
, vol.22
, pp. 3099-3108
-
-
Cheng, Y.1
Prusoff, W.H.2
-
3
-
-
0025832748
-
A68930: a potent agonist selective for the dopamine D1 receptor
-
DeNinno M.P., Schoenleber R., MacKenzie R., Britton D.R., Asin K.E., Briggs C., Trugman J.M., Ackerman M., Artman L., and Bednarz L. A68930: a potent agonist selective for the dopamine D1 receptor. Eur. J. Pharmacol. 199 (1991) 209-219
-
(1991)
Eur. J. Pharmacol.
, vol.199
, pp. 209-219
-
-
DeNinno, M.P.1
Schoenleber, R.2
MacKenzie, R.3
Britton, D.R.4
Asin, K.E.5
Briggs, C.6
Trugman, J.M.7
Ackerman, M.8
Artman, L.9
Bednarz, L.10
-
4
-
-
0026075790
-
Synthesis and dopaminergic activity of 3-substituted 1-(aminomethyl)-3,4-dihydro-5,6-dihydroxy-1H-2-benzopyrans: characterization of an auxiliary binding region in the D1 receptor
-
DeNinno M.P., Schoenleber R., Perner R.J., Lijewski L., Asin K.E., Britton D.R., MacKenzie R., and Kebabian J.W. Synthesis and dopaminergic activity of 3-substituted 1-(aminomethyl)-3,4-dihydro-5,6-dihydroxy-1H-2-benzopyrans: characterization of an auxiliary binding region in the D1 receptor. J. Med. Chem. 34 (1991) 2561-2569
-
(1991)
J. Med. Chem.
, vol.34
, pp. 2561-2569
-
-
DeNinno, M.P.1
Schoenleber, R.2
Perner, R.J.3
Lijewski, L.4
Asin, K.E.5
Britton, D.R.6
MacKenzie, R.7
Kebabian, J.W.8
-
5
-
-
0018079026
-
Dopamine receptors: pharmacological and anatomical evidences indicate that two distinct dopamine receptor populations are present in rat striatum
-
Garau L., Govoni S., Stefanini E., Trabucchi M., and Spano P.F. Dopamine receptors: pharmacological and anatomical evidences indicate that two distinct dopamine receptor populations are present in rat striatum. Life Sci. 23 (1978) 1745-1750
-
(1978)
Life Sci.
, vol.23
, pp. 1745-1750
-
-
Garau, L.1
Govoni, S.2
Stefanini, E.3
Trabucchi, M.4
Spano, P.F.5
-
6
-
-
0035137099
-
The role of phosphorylation/dephosphorylation in agonist-induced desensitization of D1 dopamine receptor function: evidence for a novel pathway for receptor dephosphorylation
-
Gardner B., Liu Z.F., Jiang D., and Sibley D.R. The role of phosphorylation/dephosphorylation in agonist-induced desensitization of D1 dopamine receptor function: evidence for a novel pathway for receptor dephosphorylation. Mol. Pharmacol. 59 (2001) 310-321
-
(2001)
Mol. Pharmacol.
, vol.59
, pp. 310-321
-
-
Gardner, B.1
Liu, Z.F.2
Jiang, D.3
Sibley, D.R.4
-
7
-
-
0029664618
-
9-Dihydroxy-2,3,7,11b-tetrahydro-1H-naph[1,2,3-de]isoquinoline: a potent full dopamine D1 agonist containing a rigid-beta-phenyldopamine pharmacophore
-
Ghosh D., Snyder S.E., Watts V.J., Mailman R.B., and Nichols D.E. 9-Dihydroxy-2,3,7,11b-tetrahydro-1H-naph[1,2,3-de]isoquinoline: a potent full dopamine D1 agonist containing a rigid-beta-phenyldopamine pharmacophore. J. Med. Chem. 39 (1996) 549-555
-
(1996)
J. Med. Chem.
, vol.39
, pp. 549-555
-
-
Ghosh, D.1
Snyder, S.E.2
Watts, V.J.3
Mailman, R.B.4
Nichols, D.E.5
-
8
-
-
1542301679
-
8,9-Dihydroxy-1,2,3,11b-tetrahydrochromeno[4, 3,2,-de]isoquinoline (dinoxyline), a high affinity and potent agonist at all dopamine receptor isoforms
-
Grubbs R.A., Lewis M.M., Owens-Vance C., Gay E.A., Jassen A.K., Mailman R.B., and Nichols D.E. 8,9-Dihydroxy-1,2,3,11b-tetrahydrochromeno[4, 3,2,-de]isoquinoline (dinoxyline), a high affinity and potent agonist at all dopamine receptor isoforms. Bioorg. Med. Chem. 12 (2004) 1403-1412
-
(2004)
Bioorg. Med. Chem.
, vol.12
, pp. 1403-1412
-
-
Grubbs, R.A.1
Lewis, M.M.2
Owens-Vance, C.3
Gay, E.A.4
Jassen, A.K.5
Mailman, R.B.6
Nichols, D.E.7
-
10
-
-
0016820947
-
Femtomole sensitive radioimmunoassay for cyclic AMP and cyclic GMP after 2′-O-acetylation by acetic anhydride in aqueous solution
-
Harper J.F., and Brooker G. Femtomole sensitive radioimmunoassay for cyclic AMP and cyclic GMP after 2′-O-acetylation by acetic anhydride in aqueous solution. J. Cyclic Nucleotide Res. 1 (1975) 207-218
-
(1975)
J. Cyclic Nucleotide Res.
, vol.1
, pp. 207-218
-
-
Harper, J.F.1
Brooker, G.2
-
12
-
-
0026610957
-
Comparison of the D1-dopamine agonists SKF-38393 and A-68930 in neonatal 6-hydroxydopamine-lesioned rats: behavioral effects and induction of c-fos-like immunoreactivity
-
Johnson K.B., Criswell H.E., Jensen K.F., Simson P.E., Mueller R.A., and Breese G.R. Comparison of the D1-dopamine agonists SKF-38393 and A-68930 in neonatal 6-hydroxydopamine-lesioned rats: behavioral effects and induction of c-fos-like immunoreactivity. J. Pharmacol. Exp. Ther. 262 (1992) 855-865
-
(1992)
J. Pharmacol. Exp. Ther.
, vol.262
, pp. 855-865
-
-
Johnson, K.B.1
Criswell, H.E.2
Jensen, K.F.3
Simson, P.E.4
Mueller, R.A.5
Breese, G.R.6
-
13
-
-
0027062847
-
A-77636: a potent and selective dopamine D1 receptor agonist with antiparkinsonian activity in marmosets
-
Kebabian J.W., Britton D.R., DeNinno M.P., Perner R., Smith L., Jenner P., Schoenleber R., and Williams M. A-77636: a potent and selective dopamine D1 receptor agonist with antiparkinsonian activity in marmosets. Eur. J. Pharmacol. 229 (1992) 203-209
-
(1992)
Eur. J. Pharmacol.
, vol.229
, pp. 203-209
-
-
Kebabian, J.W.1
Britton, D.R.2
DeNinno, M.P.3
Perner, R.4
Smith, L.5
Jenner, P.6
Schoenleber, R.7
Williams, M.8
-
14
-
-
0018378511
-
Multiple receptors for dopamine
-
Kebabian J.W., and Calne D.B. Multiple receptors for dopamine. Nature 277 (1979) 93-96
-
(1979)
Nature
, vol.277
, pp. 93-96
-
-
Kebabian, J.W.1
Calne, D.B.2
-
15
-
-
1542349921
-
The role of phosphorylation in D1 dopamine receptor desensitization: evidence for a novel mechanism of arrestin association
-
Kim O.J., Gardner B.R., Williams D.B., Marinec P.S., Cabrera D.M., Peters J.D., Mak C.C., Kim K.M., and Sibley D.R. The role of phosphorylation in D1 dopamine receptor desensitization: evidence for a novel mechanism of arrestin association. J. Biol. Chem. 279 (2004) 7999-8010
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 7999-8010
-
-
Kim, O.J.1
Gardner, B.R.2
Williams, D.B.3
Marinec, P.S.4
Cabrera, D.M.5
Peters, J.D.6
Mak, C.C.7
Kim, K.M.8
Sibley, D.R.9
-
16
-
-
0031597626
-
Homologous desensitization of the D1A dopamine receptor: efficacy in causing desensitization dissociates from both receptor occupancy and functional potency
-
Lewis M.M., Watts V.J., Lawler C.P., Nichols D.E., and Mailman R.B. Homologous desensitization of the D1A dopamine receptor: efficacy in causing desensitization dissociates from both receptor occupancy and functional potency. J. Pharmacol. Exp. Ther. 286 (1998) 345-353
-
(1998)
J. Pharmacol. Exp. Ther.
, vol.286
, pp. 345-353
-
-
Lewis, M.M.1
Watts, V.J.2
Lawler, C.P.3
Nichols, D.E.4
Mailman, R.B.5
-
17
-
-
0030111239
-
1 receptor contributes to prolonged receptor desensitization: studies with A-77636
-
1 receptor contributes to prolonged receptor desensitization: studies with A-77636. J. Pharmacol. Exp. Ther. 276 (1996) 1022-1029
-
(1996)
J. Pharmacol. Exp. Ther.
, vol.276
, pp. 1022-1029
-
-
Lin, C.W.1
Bianchi, B.R.2
Miller, T.R.3
Stashko, M.A.4
Wang, S.S.5
Curzon, P.6
Bednarz, L.7
Asin, K.E.8
Britton, D.R.9
-
18
-
-
7044272919
-
2 dopamine receptors (a lesson for drug discovery)
-
2 dopamine receptors (a lesson for drug discovery). Med. Chem. Res. 13 (2004) 115-126
-
(2004)
Med. Chem. Res.
, vol.13
, pp. 115-126
-
-
Mailman, R.B.1
Gay, E.A.2
-
19
-
-
0002287121
-
Functional effects of novel dopamine ligands: dihydrexidine and Parkinson's disease as a first step
-
Jenner P., and Demirdemar R. (Eds), IOS Stockton Press
-
Mailman R.B., Nichols D.E., Lewis M.M., Blake B.L., and Lawler C.P. Functional effects of novel dopamine ligands: dihydrexidine and Parkinson's disease as a first step. In: Jenner P., and Demirdemar R. (Eds). Dopamine Receptor Subtypes: From Basic Science to Clinical Application (1998), IOS Stockton Press 64-83
-
(1998)
Dopamine Receptor Subtypes: From Basic Science to Clinical Application
, pp. 64-83
-
-
Mailman, R.B.1
Nichols, D.E.2
Lewis, M.M.3
Blake, B.L.4
Lawler, C.P.5
-
20
-
-
0036211021
-
Regulation of dopamine D-1 receptor trafficking by protein kinase A-dependent phosphorylation
-
Mason J.N., Kozell L.B., and Neve K.A. Regulation of dopamine D-1 receptor trafficking by protein kinase A-dependent phosphorylation. Mol. Pharmacol. 61 (2002) 806-816
-
(2002)
Mol. Pharmacol.
, vol.61
, pp. 806-816
-
-
Mason, J.N.1
Kozell, L.B.2
Neve, K.A.3
-
22
-
-
0034595860
-
Differential affinities of visual arrestin, beta arrestin1, and beta arrestin2 for G protein-coupled receptors delineate two major classes of receptors
-
Oakley R.H., Laporte S.A., Holt J.A., Caron M.G., and Barak L.S. Differential affinities of visual arrestin, beta arrestin1, and beta arrestin2 for G protein-coupled receptors delineate two major classes of receptors. J. Biol. Chem. 275 (2000) 17201-17210
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 17201-17210
-
-
Oakley, R.H.1
Laporte, S.A.2
Holt, J.A.3
Caron, M.G.4
Barak, L.S.5
-
23
-
-
0037838870
-
The nature of the arrestin x receptor complex determines the ultimate fate of the internalized receptor
-
Pan L., Gurevich E.V., and Gurevich V.V. The nature of the arrestin x receptor complex determines the ultimate fate of the internalized receptor. J. Biol. Chem. 278 (2003) 11623-11632
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 11623-11632
-
-
Pan, L.1
Gurevich, E.V.2
Gurevich, V.V.3
-
24
-
-
25144499754
-
Differential activation of adenylate cyclase and receptor internalization by novel dopamine D1 receptor agonists
-
Ryman-Rasmussen J.P., Nichols D.E., and Mailman R.B. Differential activation of adenylate cyclase and receptor internalization by novel dopamine D1 receptor agonists. Mol. Pharmacol. 68 (2005) 1039-1048
-
(2005)
Mol. Pharmacol.
, vol.68
, pp. 1039-1048
-
-
Ryman-Rasmussen, J.P.1
Nichols, D.E.2
Mailman, R.B.3
-
25
-
-
22544440017
-
Functional selectivity, ligand-directed trafficking, conformation-specific agonism: What's in a name?
-
Simmons M.A. Functional selectivity, ligand-directed trafficking, conformation-specific agonism: What's in a name?. Mol. Interv. 5 (2005) 154-157
-
(2005)
Mol. Interv.
, vol.5
, pp. 154-157
-
-
Simmons, M.A.1
-
26
-
-
0030020424
-
Differential regulation of dopamine D1A receptor responsiveness by various G protein-coupled receptor kinases
-
Tiberi M., Nash S.R., Bertrand L., Lefkowitz R.J., and Caron M.G. Differential regulation of dopamine D1A receptor responsiveness by various G protein-coupled receptor kinases. J. Biol. Chem. 271 (1996) 3771-3778
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 3771-3778
-
-
Tiberi, M.1
Nash, S.R.2
Bertrand, L.3
Lefkowitz, R.J.4
Caron, M.G.5
-
27
-
-
1942487807
-
First principles predictions of the structure and function of G-protein coupled receptors: validation for bovine rhodopsin
-
Trabanino R.J., Hall S.E., Vaidehi N., Floriano W.B., Kam V., and Goddard III W.A. First principles predictions of the structure and function of G-protein coupled receptors: validation for bovine rhodopsin. Biophys. J. 86 (2004) 1904-1921
-
(2004)
Biophys. J.
, vol.86
, pp. 1904-1921
-
-
Trabanino, R.J.1
Hall, S.E.2
Vaidehi, N.3
Floriano, W.B.4
Kam, V.5
Goddard III, W.A.6
-
28
-
-
0023619677
-
A study of some variables in a tetrazolium dye (MTT) based assay for cell growth and chemosensitivity
-
Twentyman P.R., and Luscombe M. A study of some variables in a tetrazolium dye (MTT) based assay for cell growth and chemosensitivity. Br. J. Cancer 56 (1987) 279-285
-
(1987)
Br. J. Cancer
, vol.56
, pp. 279-285
-
-
Twentyman, P.R.1
Luscombe, M.2
-
29
-
-
33751172589
-
Functional selectivity and classical concepts of quantitative pharmacology
-
epub 06/27/2006. PM:16803859
-
Urban J.D., Clarke W.P., von Zastrow M., Nichols D.E., Kobilka B.K., Weinstein H., Javitch J.A., Roth B.L., Christopoulos A., Sexton P., Miller K., Spedding M., and Mailman R.B. Functional selectivity and classical concepts of quantitative pharmacology. J. Pharmacol. Exp. Ther. (2006) epub 06/27/2006. PM:16803859
-
(2006)
J. Pharmacol. Exp. Ther.
-
-
Urban, J.D.1
Clarke, W.P.2
von Zastrow, M.3
Nichols, D.E.4
Kobilka, B.K.5
Weinstein, H.6
Javitch, J.A.7
Roth, B.L.8
Christopoulos, A.9
Sexton, P.10
Miller, K.11
Spedding, M.12
Mailman, R.B.13
-
30
-
-
0036790954
-
Prediction of structure and function of G protein-coupled receptors
-
Vaidehi N., Floriano W.B., Trabanino R., Hall S.E., Freddolino P., Choi E.J., Zamanakos G., and Goddard III W.A. Prediction of structure and function of G protein-coupled receptors. Proc. Natl. Acad. Sci. USA 99 (2002) 12622-12627
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 12622-12627
-
-
Vaidehi, N.1
Floriano, W.B.2
Trabanino, R.3
Hall, S.E.4
Freddolino, P.5
Choi, E.J.6
Zamanakos, G.7
Goddard III, W.A.8
-
32
-
-
0033545208
-
Distinct dynamin-dependent and -independent mechanisms target structurally homologous dopamine receptors to different endocytic membranes
-
Vickery R.G., and von Zastrow M. Distinct dynamin-dependent and -independent mechanisms target structurally homologous dopamine receptors to different endocytic membranes. J. Cell Biol. 144 (1999) 31-43
-
(1999)
J. Cell Biol.
, vol.144
, pp. 31-43
-
-
Vickery, R.G.1
von Zastrow, M.2
-
33
-
-
0022506797
-
Multiple tritium labeling of (+)-7-chloro-8-hydroxy-3-methyl-1- phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine (SCH23390)
-
Wyrick S., McDougald D.L., and Mailman R.B. Multiple tritium labeling of (+)-7-chloro-8-hydroxy-3-methyl-1- phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine (SCH23390). J. Label. Compd. Radiopharm. 23 (1986) 685-692
-
(1986)
J. Label. Compd. Radiopharm.
, vol.23
, pp. 685-692
-
-
Wyrick, S.1
McDougald, D.L.2
Mailman, R.B.3
-
34
-
-
0033574430
-
Cellular trafficking of G protein-coupled receptor/beta-arrestin endocytic complexes
-
Zhang J., Barak L.S., Anborgh P.H., Laporte S.A., Caron M.G., and Ferguson S.S. Cellular trafficking of G protein-coupled receptor/beta-arrestin endocytic complexes. J. Biol. Chem. 274 (1999) 10999-11006
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 10999-11006
-
-
Zhang, J.1
Barak, L.S.2
Anborgh, P.H.3
Laporte, S.A.4
Caron, M.G.5
Ferguson, S.S.6
|