-
1
-
-
0017184389
-
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
-
Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248-254.
-
(1976)
Anal Biochem
, vol.72
, pp. 248-254
-
-
Bradford, M.M.1
-
2
-
-
0034748486
-
Sensitization of adenylate cyclase induced by a dopamine D2 receptor mutant: Inverse agonism by D2 receptor antagonists
-
Bullock CM, Li C, Li M, Bermak JC, and Zhou QY (2001) Sensitization of adenylate cyclase induced by a dopamine D2 receptor mutant: Inverse agonism by D2 receptor antagonists. Prog Neuropsychopharmacol Biol Psychiatry 25:1387-1402.
-
(2001)
Prog Neuropsychopharmacol Biol Psychiatry
, vol.25
, pp. 1387-1402
-
-
Bullock, C.M.1
Li, C.2
Li, M.3
Bermak, J.C.4
Zhou, Q.Y.5
-
3
-
-
0031037633
-
Pharmacology of muscarinic receptor subtypes constitutively activated by G proteins
-
Burstein ES, Spalding TA, and Brann MR (1997) Pharmacology of muscarinic receptor subtypes constitutively activated by G proteins. Mol Pharmacol 51:312-319.
-
(1997)
Mol Pharmacol
, vol.51
, pp. 312-319
-
-
Burstein, E.S.1
Spalding, T.A.2
Brann, M.R.3
-
5
-
-
0029993115
-
Chimeric mutagenesis of putative G-protein coupling domains of the α2A-adrenergic receptor. Localization of two redundant and fully competent Gi coupling domains
-
Eason MG and Liggett SB (1996) Chimeric mutagenesis of putative G-protein coupling domains of the α2A-adrenergic receptor. Localization of two redundant and fully competent Gi coupling domains. J Biol Chem 271:12826-12832.
-
(1996)
J Biol Chem
, vol.271
, pp. 12826-12832
-
-
Eason, M.G.1
Liggett, S.B.2
-
6
-
-
0030912961
-
Evidence that antipsychotic drugs are inverse agonists at D2 dopamine receptors
-
Hall DA and Strange PG (1997) Evidence that antipsychotic drugs are inverse agonists at D2 dopamine receptors. Br J Pharmacol 121:731-736.
-
(1997)
Br J Pharmacol
, vol.121
, pp. 731-736
-
-
Hall, D.A.1
Strange, P.G.2
-
7
-
-
0029098028
-
Catalepsy as a rodent model for detecting antipsychotic drugs with extrapyramidal side effect liability
-
Hoffman DC and Donovan H (1995) Catalepsy as a rodent model for detecting antipsychotic drugs with extrapyramidal side effect liability. Psychopharmacology 120:128-133.
-
(1995)
Psychopharmacology
, vol.120
, pp. 128-133
-
-
Hoffman, D.C.1
Donovan, H.2
-
8
-
-
0032506047
-
Agonist-mediated down-regulation of Gαi via the α2-adrenergic receptor is targeted by receptor-Gi interaction and is independent of receptor signaling and regulation
-
Jewell-Motz EA, Donnelly ET, Eason MG, and Liggett SB (1998) Agonist-mediated down-regulation of Gαi via the α2-adrenergic receptor is targeted by receptor-Gi interaction and is independent of receptor signaling and regulation. Biochemistry 37:15720-15725.
-
(1998)
Biochemistry
, vol.37
, pp. 15720-15725
-
-
Jewell-Motz, E.A.1
Donnelly, E.T.2
Eason, M.G.3
Liggett, S.B.4
-
9
-
-
0034666151
-
α2A/α2C-adrenergic receptor third loop chimera show that agonist interaction with receptor subtype backbone establishes G protein-coupled receptor kinase phosphorylation
-
Jewell-Motz EA, Small KM, Theiss CT, and Liggett SB (2000) α2A/α2C-adrenergic receptor third loop chimera show that agonist interaction with receptor subtype backbone establishes G protein-coupled receptor kinase phosphorylation. J Biol Chem 275:28989-28993.
-
(2000)
J Biol Chem
, vol.275
, pp. 28989-28993
-
-
Jewell-Motz, E.A.1
Small, K.M.2
Theiss, C.T.3
Liggett, S.B.4
-
10
-
-
0031434924
-
Differences between natural and recombinant G protein-coupled receptor systems with varying receptor/G protein stoichiometry
-
Kenakin T (1997) Differences between natural and recombinant G protein-coupled receptor systems with varying receptor/G protein stoichiometry. Trends Pharmacol Sci 18:456-464.
-
(1997)
Trends Pharmacol Sci
, vol.18
, pp. 456-464
-
-
Kenakin, T.1
-
11
-
-
0035083109
-
Inverse, protean and ligand-selective agonism: Matters of receptor conformation
-
Kenakin T (2001) Inverse, protean and ligand-selective agonism: Matters of receptor conformation. FASEB J 15:598-611.
-
(2001)
FASEB J
, vol.15
, pp. 598-611
-
-
Kenakin, T.1
-
12
-
-
0026592357
-
Constitutive activation of the α1B-adrenergic receptor by all amino acid substitutions at a single site. Evidence for a region which constrains receptor activation
-
Kjelsberg MA, Cotecchia S, Ostrowski J, Caron MG, and Lefkowitz RJ (1992) Constitutive activation of the α1B-adrenergic receptor by all amino acid substitutions at a single site. Evidence for a region which constrains receptor activation. J Biol Chem 267:1430-1433.
-
(1992)
J Biol Chem
, vol.267
, pp. 1430-1433
-
-
Kjelsberg, M.A.1
Cotecchia, S.2
Ostrowski, J.3
Caron, M.G.4
Lefkowitz, R.J.5
-
13
-
-
0023889603
-
Chimeric α2-, β2-adrenergic receptors: Delineation of domains involved in effector coupling and ligand binding specificity
-
Kobilka BK, Kobilka TS, Daniel K, Regan JW, Caron MG, and Lefkowitz RJ (1988) Chimeric α2-, β2-adrenergic receptors: Delineation of domains involved in effector coupling and ligand binding specificity. Science (Wash DC) 240:1310-1316.
-
(1988)
Science (Wash DC)
, vol.240
, pp. 1310-1316
-
-
Kobilka, B.K.1
Kobilka, T.S.2
Daniel, K.3
Regan, J.W.4
Caron, M.G.5
Lefkowitz, R.J.6
-
14
-
-
0031439585
-
Constitutive activity of a chimeric D2/D1 dopamine receptor
-
Kozell LB and Neve KA (1997) Constitutive activity of a chimeric D2/D1 dopamine receptor. Mol Pharmacol 52:1137-1149.
-
(1997)
Mol Pharmacol
, vol.52
, pp. 1137-1149
-
-
Kozell, L.B.1
Neve, K.A.2
-
15
-
-
0031593972
-
Effects of the D3 and autoreceptor-preferring dopamine antagonist (+)-UH232 in schizophrenia
-
Lahti AC, Weiler M, Carlsson A, and Tamminga CA (1998) Effects of the D3 and autoreceptor-preferring dopamine antagonist (+)-UH232 in schizophrenia. J Neural Transm 105:719-734.
-
(1998)
J Neural Transm
, vol.105
, pp. 719-734
-
-
Lahti, A.C.1
Weiler, M.2
Carlsson, A.3
Tamminga, C.A.4
-
16
-
-
0025834814
-
Desensitization of the beta-adrenergic receptor: Distinct molecular determinants of phosphorylation by specific kinases
-
Liggett SB (1991) Desensitization of the beta-adrenergic receptor: Distinct molecular determinants of phosphorylation by specific kinases. Pharmacol Res 24 (Suppl 1):29-41.
-
(1991)
Pharmacol Res
, vol.24
, Issue.SUPPL. 1
, pp. 29-41
-
-
Liggett, S.B.1
-
18
-
-
0030200664
-
Inverse agonism at dopamine D2 receptors. Haloperidol-induced prolactin release from GH4C1 cells transfected with the human D2 receptor is antagonized by R(-)-n-propylnorapomorphine, raclopride and phenoxybenzamine
-
Nilsson CL, Ekman A, Hellstrand M, and Eriksson E (1996) Inverse agonism at dopamine D2 receptors. Haloperidol-induced prolactin release from GH4C1 cells transfected with the human D2 receptor is antagonized by R(-)-n-propylnorapomorphine, raclopride and phenoxybenzamine. Neuropsychopharmacology 15:53-61.
-
(1996)
Neuropsychopharmacology
, vol.15
, pp. 53-61
-
-
Nilsson, C.L.1
Ekman, A.2
Hellstrand, M.3
Eriksson, E.4
-
24
-
-
0032239841
-
Amino acid domains involved in constitutive activation of G protein-coupled receptors: A target for inverse agonists
-
Pauwels PJ and Wurch T (1998) Amino acid domains involved in constitutive activation of G protein-coupled receptors: A target for inverse agonists. Mol Neurobiol 17:109-136.
-
(1998)
Mol Neurobiol
, vol.17
, pp. 109-136
-
-
Pauwels, P.J.1
Wurch, T.2
-
27
-
-
0026767427
-
Reverse intrinsic activity of antagonists on G protein-coupled receptors
-
Schutz W and Freissmuth M (1992) Reverse intrinsic activity of antagonists on G protein-coupled receptors. Trends Pharmacol Sci 13:376-380.
-
(1992)
Trends Pharmacol Sci
, vol.13
, pp. 376-380
-
-
Schutz, W.1
Freissmuth, M.2
-
28
-
-
0028815402
-
Cloning and pharmacological characterization of human α-1 adrenergic receptors: Sequence corrections and direct comparison with other species homologues
-
Schwinn DA, Johnston GI, Page SO, Mosley MJ, Wilson KH, Worman NP, Campbell S, Fidock MD, Furness M, Parry-Smith DJ, et al. (1995) Cloning and pharmacological characterization of human α-1 adrenergic receptors: Sequence corrections and direct comparison with other species homologues. J Pharmacol Exp Ther 272:134-142.
-
(1995)
J Pharmacol Exp Ther
, vol.272
, pp. 134-142
-
-
Schwinn, D.A.1
Johnston, G.I.2
Page, S.O.3
Mosley, M.J.4
Wilson, K.H.5
Worman, N.P.6
Campbell, S.7
Fidock, M.D.8
Furness, M.9
Parry-Smith, D.J.10
-
29
-
-
0035101404
-
Antipsychotic drugs: Importance of dopamine receptors for mechanisms of therapeutic actions and side effects
-
Strange PG (2001) Antipsychotic drugs: Importance of dopamine receptors for mechanisms of therapeutic actions and side effects. Pharmacol Rev 53:119-133.
-
(2001)
Pharmacol Rev
, vol.53
, pp. 119-133
-
-
Strange, P.G.1
-
30
-
-
0036468505
-
Mechanisms of inverse agonism at G protein-coupled receptors
-
Strange PG (2002) Mechanisms of inverse agonism at G protein-coupled receptors. Trends Pharmacol Sci 23:89-95.
-
(2002)
Trends Pharmacol Sci
, vol.23
, pp. 89-95
-
-
Strange, P.G.1
-
31
-
-
0028925608
-
Analysis of receptor-G protein interaction in permeabilized cells
-
Wieland T, Liedel K, Kaldenberg-Stasch S, Meyer zu Heringdorf D, Schmidt M, and Jakobs KH (1995) Analysis of receptor-G protein interaction in permeabilized cells. Naunyn-Schmiedeberg's Arch Pharmacol 351:329-336.
-
(1995)
Naunyn-Schmiedeberg's Arch Pharmacol
, vol.351
, pp. 329-336
-
-
Wieland, T.1
Liedel, K.2
Kaldenberg-Stasch, S.3
Meyer zu Heringdorf, D.4
Schmidt, M.5
Jakobs, K.H.6
-
34
-
-
0031718841
-
A modified overlap extension PCR method to create chimaeric genes in the absence of restriction sites
-
Wurch T, Lestienne F, and Pauwels PJ (1998) A modified overlap extension PCR method to create chimaeric genes in the absence of restriction sites. Biotechnol Tech 12:653-657.
-
(1998)
Biotechnol Tech
, vol.12
, pp. 653-657
-
-
Wurch, T.1
Lestienne, F.2
Pauwels, P.J.3
|