-
2
-
-
0035283073
-
Orphan G-protein-coupled receptors and natural ligand discovery
-
Howard AD, McAllister G, Feighner SD, Liu Q, Nargund RP, van der Ploeg LH, et al: Orphan G-protein-coupled receptors and natural ligand discovery. Trends Pharmacol Sci 2001;22:132-140.
-
(2001)
Trends Pharmacol Sci
, vol.22
, pp. 132-140
-
-
Howard, A.D.1
McAllister, G.2
Feighner, S.D.3
Liu, Q.4
Nargund, R.P.5
Van Der Ploeg, L.H.6
-
3
-
-
0035213854
-
Patent status of the therapeutically important G-protein-coupled receptors
-
Bailey WJ, Vanti WB, George SR, Blevins R, Swaminathan S, Bonini JA, et al: Patent status of the therapeutically important G-protein-coupled receptors. Expert Opin Ther Patents 2001;11:1861-1887.
-
(2001)
Expert Opin Ther Patents
, vol.11
, pp. 1861-1887
-
-
Bailey, W.J.1
Vanti, W.B.2
George, S.R.3
Blevins, R.4
Swaminathan, S.5
Bonini, J.A.6
-
4
-
-
0037024360
-
Identification of G protein-coupled receptor genes from the human genome sequence
-
Takeda S, Kadowaki S, Haga T, Takaesu H, Mitaku S: Identification of G protein-coupled receptor genes from the human genome sequence. FEBS Lett 2002;520:97-101.
-
(2002)
FEBS Lett
, vol.520
, pp. 97-101
-
-
Takeda, S.1
Kadowaki, S.2
Haga, T.3
Takaesu, H.4
Mitaku, S.5
-
5
-
-
1342281272
-
The identification of ligands at orphan G-protein coupled receptors
-
Wise A, Jupe SC, Rees S: The identification of ligands at orphan G-protein coupled receptors. Annu Rev Pharmacol Toxicol 2004;44:43-66.
-
(2004)
Annu Rev Pharmacol Toxicol
, vol.44
, pp. 43-66
-
-
Wise, A.1
Jupe, S.C.2
Rees, S.3
-
6
-
-
0001238111
-
Evaluation of a CRE-directed luciferase reporter gene assay as an alternative to measuring cAMP accumulation
-
George SE, Bungay PJ, Naylor LH: Evaluation of a CRE-directed luciferase reporter gene assay as an alternative to measuring cAMP accumulation. J Biomol Screen 1997;2:235-240.
-
(1997)
J Biomol Screen
, vol.2
, pp. 235-240
-
-
George, S.E.1
Bungay, P.J.2
Naylor, L.H.3
-
7
-
-
0030843887
-
Functional coupling of endogenous serotonin (5-HT1B) and calcitonin (Cla) receptors in CHO cells to a cyclic AMP-responsive luciferase reporter gene
-
George SE, Bungay PJ, Naylor LH: Functional coupling of endogenous serotonin (5-HT1B) and calcitonin (Cla) receptors in CHO cells to a cyclic AMP-responsive luciferase reporter gene. J Neurochem 1997;69:1278-1285.
-
(1997)
J Neurochem
, vol.69
, pp. 1278-1285
-
-
George, S.E.1
Bungay, P.J.2
Naylor, L.H.3
-
8
-
-
0032981148
-
Partial agonism at serotonin 5-HT1B and dopamine D2L receptors using a luciferase reporter gene assay
-
Kemp DM, George SE, Bungay PJ, Naylor LH: Partial agonism at serotonin 5-HT1B and dopamine D2L receptors using a luciferase reporter gene assay. Eur J Pharmacol 1999;373:215-222.
-
(1999)
Eur J Pharmacol
, vol.373
, pp. 215-222
-
-
Kemp, D.M.1
George, S.E.2
Bungay, P.J.3
Naylor, L.H.4
-
9
-
-
0345735308
-
Synthesis and pharmacological identification of neutral histamine H1-receptor antagonists
-
Govoni M, Bakker RA, van de Wetering I, Smit MJ, Menge WM, Timmerman H, et al: Synthesis and pharmacological identification of neutral histamine H1-receptor antagonists. J Med Chem 2003;46:5812-5824.
-
(2003)
J Med Chem
, vol.46
, pp. 5812-5824
-
-
Govoni, M.1
Bakker, R.A.2
Van De Wetering, I.3
Smit, M.J.4
Menge, W.M.5
Timmerman, H.6
-
10
-
-
0030910439
-
Constitutive activity of native thyrotropin-releasing hormone receptors revealed using a protein kinase C-responsive reporter gene
-
Jinsi-Parimoo A, Gershengorn MC: Constitutive activity of native thyrotropin-releasing hormone receptors revealed using a protein kinase C-responsive reporter gene. Endocrinology 1997;138:1471-1475.
-
(1997)
Endocrinology
, vol.138
, pp. 1471-1475
-
-
Jinsi-Parimoo, A.1
Gershengorn, M.C.2
-
11
-
-
0037107027
-
High-throughput cell analysis using multiplexed array technologies
-
Beske OE, Goldbard S: High-throughput cell analysis using multiplexed array technologies. Drug Discov Today 2002;7:S131-S135.
-
(2002)
Drug Discov Today
, vol.7
-
-
Beske, O.E.1
Goldbard, S.2
-
13
-
-
0034212465
-
Use of a dual firefly and Renilla luciferase reporter gene assay to simultaneously determine drug selectivity at human corticotrophin releasing hormone 1 and 2 receptors
-
Parsons SJ, Rhodes SA, Connor HE, Rees S, Brown J, Giles H: Use of a dual firefly and Renilla luciferase reporter gene assay to simultaneously determine drug selectivity at human corticotrophin releasing hormone 1 and 2 receptors. Anal Biochem 2000;281:187-192.
-
(2000)
Anal Biochem
, vol.281
, pp. 187-192
-
-
Parsons, S.J.1
Rhodes, S.A.2
Connor, H.E.3
Rees, S.4
Brown, J.5
Giles, H.6
-
14
-
-
0027532674
-
Functional testing of human dopamine D1 and D5 receptors expressed in stable cAMP-responsive luciferase reporter cell lies
-
Himmler A, Stratowa C, Czernilofsky AP: Functional testing of human dopamine D1 and D5 receptors expressed in stable cAMP-responsive luciferase reporter cell lies. J Recept Res 1993;13:79-94.
-
(1993)
J Recept Res
, vol.13
, pp. 79-94
-
-
Himmler, A.1
Stratowa, C.2
Czernilofsky, A.P.3
-
15
-
-
0033003760
-
A simple statistical parameter for use in evaluation and validation of high throughput screening assays
-
Zhang JH, Chung TD, Oldenburg KR: A simple statistical parameter for use in evaluation and validation of high throughput screening assays. J Biomol Screen 1999;4:67-73.
-
(1999)
J Biomol Screen
, vol.4
, pp. 67-73
-
-
Zhang, J.H.1
Chung, T.D.2
Oldenburg, K.R.3
-
16
-
-
0035863914
-
A chimeric reporter gene allowing for clone selection and high-throughput screening of reporter cell lines expressing G-protein-coupled receptors
-
Kotarsky K, Owman C, Olde B: A chimeric reporter gene allowing for clone selection and high-throughput screening of reporter cell lines expressing G-protein-coupled receptors. Anal Biochem 2001;288:209-215.
-
(2001)
Anal Biochem
, vol.288
, pp. 209-215
-
-
Kotarsky, K.1
Owman, C.2
Olde, B.3
-
17
-
-
0026800892
-
The cloning of a family of genes that encode the melanocortin receptors
-
Mountjoy KG, Robbins LS, Mortrud MT, Cone RD: The cloning of a family of genes that encode the melanocortin receptors. Science 1992;257:1248-1251.
-
(1992)
Science
, vol.257
, pp. 1248-1251
-
-
Mountjoy, K.G.1
Robbins, L.S.2
Mortrud, M.T.3
Cone, R.D.4
-
18
-
-
0030564894
-
Major pharmacological distinction of the ACTH receptor from other melanocortin receptors
-
Schioth HB, Chhajlani V, Muceniece R, Klusa V, Wikberg JE: Major pharmacological distinction of the ACTH receptor from other melanocortin receptors. Life Sci 1996;59:797-801.
-
(1996)
Life Sci
, vol.59
, pp. 797-801
-
-
Schioth, H.B.1
Chhajlani, V.2
Muceniece, R.3
Klusa, V.4
Wikberg, J.E.5
-
19
-
-
0031786114
-
Discovery of a novel superpotent and selective melanocortin-4 receptor antagonist (HS024): Evaluation in vitro and in vivo
-
Kask A, Mutulis F, Muceniece R, Pahkla R, Mutule I, Wikberg JE, et al: Discovery of a novel superpotent and selective melanocortin-4 receptor antagonist (HS024): evaluation in vitro and in vivo. Endocrinology 1998;139:5006-5014.
-
(1998)
Endocrinology
, vol.139
, pp. 5006-5014
-
-
Kask, A.1
Mutulis, F.2
Muceniece, R.3
Pahkla, R.4
Mutule, I.5
Wikberg, J.E.6
-
20
-
-
0032584441
-
Asp10 in Lys-gamma2-MSH determines selective activation of the melanocortin MC3 receptor
-
Oosterom J, Burbach JP, Gispen WH, Adan RA: Asp10 in Lys-gamma2-MSH determines selective activation of the melanocortin MC3 receptor. Eur J Pharmacol 1998;354:R9-R11.
-
(1998)
Eur J Pharmacol
, vol.354
-
-
Oosterom, J.1
Burbach, J.P.2
Gispen, W.H.3
Adan, R.A.4
-
21
-
-
0030609042
-
Comparison of the Ca2+ movement by activation of alpha1-adrenoceptor subtypes in HEK-293 cells
-
Tao L, Guan YY, He H, Han C, Zhang YY, Sun JJ: Comparison of the Ca2+ movement by activation of alpha1-adrenoceptor subtypes in HEK-293 cells. Life Sci 1997;61:2127-2136.
-
(1997)
Life Sci
, vol.61
, pp. 2127-2136
-
-
Tao, L.1
Guan, Y.Y.2
He, H.3
Han, C.4
Zhang, Y.Y.5
Sun, J.J.6
-
23
-
-
0029822338
-
A constitutively active mutant of the alpha 1B-adrenergic receptor can cause greater agonist-dependent down-regulation of the G-proteins G9 alpha and G11 alpha than the wild-type receptor
-
Lee TW, Wise A, Cotecchia S, Milligan G: A constitutively active mutant of the alpha 1B-adrenergic receptor can cause greater agonist-dependent down-regulation of the G-proteins G9 alpha and G11 alpha than the wild-type receptor. Biochem J 1996;320(Pt 1):79-86.
-
(1996)
Biochem J
, vol.320
, Issue.PART 1
, pp. 79-86
-
-
Lee, T.W.1
Wise, A.2
Cotecchia, S.3
Milligan, G.4
-
24
-
-
0029649771
-
Degradation of G11 alpha/Gq alpha is accelerated by agonist occupancy of alpha 1A/D, alpha 1B, and alpha 1C adrenergic receptors
-
Wise A, Lee TW, MacEwan DJ, Milligan G: Degradation of G11 alpha/Gq alpha is accelerated by agonist occupancy of alpha 1A/D, alpha 1B, and alpha 1C adrenergic receptors. J Biol Chem 1995;270:17196-17203.
-
(1995)
J Biol Chem
, vol.270
, pp. 17196-17203
-
-
Wise, A.1
Lee, T.W.2
MacEwan, D.J.3
Milligan, G.4
-
25
-
-
0029957669
-
Carboxyl-terminal mutations of Gq alpha and Gs alpha that alter the fidelity of receptor activation
-
Conklin BR, Herzmark P, Ishida S, Voyno-Yasenetskaya TA, Sun Y, Farfel Z, et al: Carboxyl-terminal mutations of Gq alpha and Gs alpha that alter the fidelity of receptor activation. Mol Pharmacol 1996;50:885-890.
-
(1996)
Mol Pharmacol
, vol.50
, pp. 885-890
-
-
Conklin, B.R.1
Herzmark, P.2
Ishida, S.3
Voyno-Yasenetskaya, T.A.4
Sun, Y.5
Farfel, Z.6
-
26
-
-
0028173259
-
D2-dopamine agonists inhibit adenosine 3′:5′-cyclic monophosphate (cAMP) production in human term trophoblastic cells
-
Vaillancourt C, Petit A, Belisle S: D2-dopamine agonists inhibit adenosine 3′:5′-cyclic monophosphate (cAMP) production in human term trophoblastic cells. Life Sci 1994;55:1545-1552.
-
(1994)
Life Sci
, vol.55
, pp. 1545-1552
-
-
Vaillancourt, C.1
Petit, A.2
Belisle, S.3
-
27
-
-
0035800852
-
Agonist regulation of D(2) dopamine receptor/G protein interaction: Evidence for agonist selection of G protein subtype
-
Cordeaux Y, Nickolls SA, Flood LA, Graber SG, Strange PG: Agonist regulation of D(2) dopamine receptor/G protein interaction: evidence for agonist selection of G protein subtype. J Biol Chem 2001;276:28667-28675.
-
(2001)
J Biol Chem
, vol.276
, pp. 28667-28675
-
-
Cordeaux, Y.1
Nickolls, S.A.2
Flood, L.A.3
Graber, S.G.4
Strange, P.G.5
-
28
-
-
0035051547
-
Mechanisms of inverse agonism of antipsychotic drugs at the D(2) dopamine receptor: Use of a mutant D(2) dopamine receptor that adopts the activated conformation
-
Wilson J, Lin H, Fu D, Javitch JA, Strange PG: Mechanisms of inverse agonism of antipsychotic drugs at the D(2) dopamine receptor: use of a mutant D(2) dopamine receptor that adopts the activated conformation. J Neurochem 2001;77:493-504.
-
(2001)
J Neurochem
, vol.77
, pp. 493-504
-
-
Wilson, J.1
Lin, H.2
Fu, D.3
Javitch, J.A.4
Strange, P.G.5
-
29
-
-
1542598049
-
Comparative analysis of functional assays for characterization of agonist ligands at G protein-coupled receptors
-
Niedernberg A, Tunaru S, Blaukat A, Harris B, Kostenis E: Comparative analysis of functional assays for characterization of agonist ligands at G protein-coupled receptors. J Biomol Screen 2003;8:500-510.
-
(2003)
J Biomol Screen
, vol.8
, pp. 500-510
-
-
Niedernberg, A.1
Tunaru, S.2
Blaukat, A.3
Harris, B.4
Kostenis, E.5
-
30
-
-
0033788831
-
Influence of receptor number on functional responses elicited by agonists acting at the human adenosine A(1) receptor: Evidence for signaling pathway-dependent changes in agonist potency and relative intrinsic activity
-
Cordeaux Y, Briddon SJ, Megson AE, McDonnell J, Dickenson JM, Hill SJ: Influence of receptor number on functional responses elicited by agonists acting at the human adenosine A(1) receptor: evidence for signaling pathway-dependent changes in agonist potency and relative intrinsic activity. Mol Pharmacol 2000;58:1075-1084.
-
(2000)
Mol Pharmacol
, vol.58
, pp. 1075-1084
-
-
Cordeaux, Y.1
Briddon, S.J.2
Megson, A.E.3
McDonnell, J.4
Dickenson, J.M.5
Hill, S.J.6
-
31
-
-
12644296023
-
Agonist potency at the cloned human beta-3 adrenoceptor depends on receptor expression level and nature of assay
-
Wilson S, Chambers JK, Park JE, Ladurner A, Cronk DW, Chapman CG, et al: Agonist potency at the cloned human beta-3 adrenoceptor depends on receptor expression level and nature of assay. J Pharmacol Exp Ther 1996;279:214-221.
-
(1996)
J Pharmacol Exp Ther
, vol.279
, pp. 214-221
-
-
Wilson, S.1
Chambers, J.K.2
Park, J.E.3
Ladurner, A.4
Cronk, D.W.5
Chapman, C.G.6
-
32
-
-
0037462728
-
Inhibitory effect of AP-1 complex on 5-aminolevulinate synthase gene expression through sequestration of cAMP-response element protein (CRE)-binding protein (CBP) coactivator
-
Guberman AS, Scassa ME, Giono LE, Varone CL, Canepa ET: Inhibitory effect of AP-1 complex on 5-aminolevulinate synthase gene expression through sequestration of cAMP-response element protein (CRE)-binding protein (CBP) coactivator. J Biol Chem 2003;278:2317-2326.
-
(2003)
J Biol Chem
, vol.278
, pp. 2317-2326
-
-
Guberman, A.S.1
Scassa, M.E.2
Giono, L.E.3
Varone, C.L.4
Canepa, E.T.5
-
33
-
-
0028947365
-
A colorimetric assay for measuring activation of Gs- and Gq-coupled signaling pathways
-
Chen W, Shields TS, Stork PJ, Cone RD: A colorimetric assay for measuring activation of Gs- and Gq-coupled signaling pathways. Anal Biochem 1995;226:349-354.
-
(1995)
Anal Biochem
, vol.226
, pp. 349-354
-
-
Chen, W.1
Shields, T.S.2
Stork, P.J.3
Cone, R.D.4
-
34
-
-
0034633263
-
A reporter gene assay for high-throughput screening of G-protein-coupled receptors stably or transiently expressed in HEK293 EBNA cells grown in suspension culture
-
Durocher Y, Perret S, Thibaudeau E, Gaumond MH, Kamen A, Stocco R, et al: A reporter gene assay for high-throughput screening of G-protein-coupled receptors stably or transiently expressed in HEK293 EBNA cells grown in suspension culture. Anal Biochem 2000;284:316-326.
-
(2000)
Anal Biochem
, vol.284
, pp. 316-326
-
-
Durocher, Y.1
Perret, S.2
Thibaudeau, E.3
Gaumond, M.H.4
Kamen, A.5
Stocco, R.6
-
35
-
-
0035083109
-
Inverse, protean, and ligand-selective agonism: Matters of receptor conformation
-
Kenakin T: Inverse, protean, and ligand-selective agonism: matters of receptor conformation. FASEB J 2001;15:598-611.
-
(2001)
FASEB J
, vol.15
, pp. 598-611
-
-
Kenakin, T.1
-
36
-
-
0037085583
-
Cellular platforms for HTS: Three case studies
-
Johnston PA, Johnston PA: Cellular platforms for HTS: three case studies. Drug Discov Today 2002;7:353-363.
-
(2002)
Drug Discov Today
, vol.7
, pp. 353-363
-
-
Johnston, P.A.1
Johnston, P.A.2
|