-
1
-
-
4944256731
-
GPCR-GIP networks: A first step in the discovery of new therapeutic drugs?
-
Bockaert J, Dumuis A, Fagni L, et al. GPCR-GIP networks: a first step in the discovery of new therapeutic drugs? Curr Opin Drug Discov Dev 2004;7:649-57
-
(2004)
Curr Opin Drug Discov Dev
, vol.7
, pp. 649-657
-
-
Bockaert, J.1
Dumuis, A.2
Fagni, L.3
-
2
-
-
34447513030
-
Emerging concepts of guanine nucleotide-binding protein-coupled receptor (GPCR) function and implications for high-throughput screening
-
Eglen R, Bosse R, Reisine T. Emerging concepts of guanine nucleotide-binding protein-coupled receptor (GPCR) function and implications for high-throughput screening. Assay Drug Dev Technol 2007;5:425-51
-
(2007)
Assay Drug Dev Technol
, vol.5
, pp. 425-451
-
-
Eglen, R.1
Bosse, R.2
Reisine, T.3
-
3
-
-
0034604451
-
Crystal structure of rhodopsin: A G protein-coupled receptor
-
Palczewski K, Kumasaka T, Hori T, et al. Crystal structure of rhodopsin: a G protein-coupled receptor. Science 2000;289:739-45
-
(2000)
Science
, vol.289
, pp. 739-745
-
-
Palczewski, K.1
Kumasaka, T.2
Hori, T.3
-
4
-
-
36448978229
-
GPCR engineering yields high-resolution structural insights into beta2-adrenergic receptor function
-
Rosenbaum D, Cherezov V, Hanson M, et al. GPCR engineering yields high-resolution structural insights into beta2-adrenergic receptor function. Science 2007;318:1266-73
-
(2007)
Science
, vol.318
, pp. 1266-1273
-
-
Rosenbaum, D.1
Cherezov, V.2
Hanson, M.3
-
5
-
-
36448995359
-
High-resolution crystal structure of all engineered human beta2-adrenergic G protein-coupled receptor
-
Cherezov V, Rosenbaum D, Hanson M, et al. High-resolution crystal structure of all engineered human beta2-adrenergic G protein-coupled receptor. Science 2007;318:1258-65
-
(2007)
Science
, vol.318
, pp. 1258-1265
-
-
Cherezov, V.1
Rosenbaum, D.2
Hanson, M.3
-
6
-
-
36248970132
-
Crystal structure of the human beta2 adrenergic G protein-coupled receptor
-
Rasmussen S, Choi H, Rosenbaum D, et al. Crystal structure of the human beta2 adrenergic G protein-coupled receptor. Nature 2007;450:383-7
-
(2007)
Nature
, vol.450
, pp. 383-387
-
-
Rasmussen, S.1
Choi, H.2
Rosenbaum, D.3
-
7
-
-
33947355865
-
G protein coupled receptor structure
-
Yeagle P, Albert A. G protein coupled receptor structure. Biochim Biophys Acta 2007;1768:808-24
-
(2007)
Biochim Biophys Acta
, vol.1768
, pp. 808-824
-
-
Yeagle, P.1
Albert, A.2
-
8
-
-
37849009111
-
Isotope labeling of mammalian GPCRs in HEK293 cells and characterization of the C-terminus of bovine rhodopsin by high resolution liquid NMR spectroscopy
-
Werner K, Richter C, Klein-Seetharaman J, et al. Isotope labeling of mammalian GPCRs in HEK293 cells and characterization of the C-terminus of bovine rhodopsin by high resolution liquid NMR spectroscopy. J Biomol NMR 2008;40:49-53
-
(2008)
J Biomol NMR
, vol.40
, pp. 49-53
-
-
Werner, K.1
Richter, C.2
Klein-Seetharaman, J.3
-
9
-
-
39549089521
-
Molecular modeling of adenosine receptors: New results and trends
-
Martinelli A, Tuccinardi T. Molecular modeling of adenosine receptors: new results and trends. Med Res Rev 2008;28:247-77
-
(2008)
Med Res Rev
, vol.28
, pp. 247-277
-
-
Martinelli, A.1
Tuccinardi, T.2
-
10
-
-
34548724959
-
Prediction of the 3D structure of FMRF-amide neuropeptides bound to the mouse MrgC11 GPCR and experimental validation
-
Heo J, Han S, Vaidehi N, et al. Prediction of the 3D structure of FMRF-amide neuropeptides bound to the mouse MrgC11 GPCR and experimental validation. Chembiochem 2007;8:1527-39
-
(2007)
Chembiochem
, vol.8
, pp. 1527-1539
-
-
Heo, J.1
Han, S.2
Vaidehi, N.3
-
11
-
-
39149107126
-
Discovery of novel chemotypes to a G protein-coupled receptor through ligand-steered homology modeling and structure-based virtual screening
-
Cavasotto C, Orry A, Murgolo N, et al. Discovery of novel chemotypes to a G protein-coupled receptor through ligand-steered homology modeling and structure-based virtual screening. J Med Chem 2008;51:581-8
-
(2008)
J Med Chem
, vol.51
, pp. 581-588
-
-
Cavasotto, C.1
Orry, A.2
Murgolo, N.3
-
12
-
-
33846245114
-
Dosage-dependent switch from G protein-coupled to G protein-independent signaling by a GPCR
-
Sun Y, Huang J, Xiang Y, et al. Dosage-dependent switch from G protein-coupled to G protein-independent signaling by a GPCR. EMBO J 2007;26:53-64
-
(2007)
EMBO J
, vol.26
, pp. 53-64
-
-
Sun, Y.1
Huang, J.2
Xiang, Y.3
-
13
-
-
33845316454
-
The V2 vasopressin receptor stimulates ERK1/2 activity independently of heterotrimeric G protein signaling
-
Charest P, Oligny-Longpre G, Bonin H, et al. The V2 vasopressin receptor stimulates ERK1/2 activity independently of heterotrimeric G protein signaling. Cell Signal 2007;19:32-41
-
(2007)
Cell Signal
, vol.19
, pp. 32-41
-
-
Charest, P.1
Oligny-Longpre, G.2
Bonin, H.3
-
14
-
-
33847781275
-
Mechanistic pathways and biological roles for receptor-independent activators of G protein signaling
-
Blumer J, Smrcka A, Lanier S. Mechanistic pathways and biological roles for receptor-independent activators of G protein signaling. Pharmacol Ther 2007;113:488-506
-
(2007)
Pharmacol Ther
, vol.113
, pp. 488-506
-
-
Blumer, J.1
Smrcka, A.2
Lanier, S.3
-
15
-
-
5644220072
-
Experimental systems for studying the role of G protein-coupled receptors in receptor tyrosine kinase signal transduction
-
Pyne N, Waters C, Moughal N, et al. Experimental systems for studying the role of G protein-coupled receptors in receptor tyrosine kinase signal transduction. Methods Enzymol 2004;390:451-75
-
(2004)
Methods Enzymol
, vol.390
, pp. 451-475
-
-
Pyne, N.1
Waters, C.2
Moughal, N.3
-
16
-
-
36448956774
-
GPCR-jacking: From a new route in RTK signaling to a new concept in GPCR activation
-
Delcourt N, Bockaert J, Marin P. GPCR-jacking: from a new route in RTK signaling to a new concept in GPCR activation. Trends Pharmacol Sci 2007;28:602-7
-
(2007)
Trends Pharmacol Sci
, vol.28
, pp. 602-607
-
-
Delcourt, N.1
Bockaert, J.2
Marin, P.3
-
17
-
-
33846260178
-
Cross-talk between G protein-coupled receptor and epidermal growth factor receptor signaling pathways contributes to growth and invasion of head and neck squamous cell carcinoma
-
Thomas S, Bhola N, Zhang Q, et al. Cross-talk between G protein-coupled receptor and epidermal growth factor receptor signaling pathways contributes to growth and invasion of head and neck squamous cell carcinoma. Cancer Res 2006;66:11831-9
-
(2006)
Cancer Res
, vol.66
, pp. 11831-11839
-
-
Thomas, S.1
Bhola, N.2
Zhang, Q.3
-
18
-
-
38449087529
-
Crosstalk between G protein-coupled receptors and epidermal growth factor receptor in cancer
-
Bhola N, Grandis J. Crosstalk between G protein-coupled receptors and epidermal growth factor receptor in cancer. Front Biosci 2008;13:1857-65
-
(2008)
Front Biosci
, vol.13
, pp. 1857-1865
-
-
Bhola, N.1
Grandis, J.2
-
20
-
-
33646531437
-
G proteins in drug screening: From analysis of receptor-G protein specificity to manipulation of GPCR-mediated signaling pathways
-
Kostenis E. G proteins in drug screening: from analysis of receptor-G protein specificity to manipulation of GPCR-mediated signaling pathways. Curr Pharm Des 2006;12:1703-15
-
(2006)
Curr Pharm Des
, vol.12
, pp. 1703-1715
-
-
Kostenis, E.1
-
21
-
-
0027435265
-
Specific interaction with rhodopsin is dependent on the gamma subunit type in a G protein
-
Kisselev O, Gautam N. Specific interaction with rhodopsin is dependent on the gamma subunit type in a G protein. J Biol Chem 1993;268:24519-22
-
(1993)
J Biol Chem
, vol.268
, pp. 24519-24522
-
-
Kisselev, O.1
Gautam, N.2
-
22
-
-
0029026880
-
Receptor-G protein coupling is established by a potential conformational switch in the beta gamma complex
-
Kisselev O, Pronin A, Ermolaeva M, et al. Receptor-G protein coupling is established by a potential conformational switch in the beta gamma complex. Proc Natl Acad Sci USA 1995;92:9102-6
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 9102-9106
-
-
Kisselev, O.1
Pronin, A.2
Ermolaeva, M.3
-
23
-
-
0027530916
-
Selectivity in signal transduction determined by gamma subunits of heterotrimeric G proteins
-
Kleuss C, Scherubl H, Hescheler J, et al. Selectivity in signal transduction determined by gamma subunits of heterotrimeric G proteins. Science 1993;259:832-4
-
(1993)
Science
, vol.259
, pp. 832-834
-
-
Kleuss, C.1
Scherubl, H.2
Hescheler, J.3
-
24
-
-
0028978141
-
Developmental expression of G alpha o and G alpha s isoforms in PC12 cells: Relationship to neurite outgrowth
-
Andreopoulos S, Li P, Warsh J. Developmental expression of G alpha o and G alpha s isoforms in PC12 cells: relationship to neurite outgrowth. Brain Res Dev Brain Res 1995;88:30-6
-
(1995)
Brain Res Dev Brain Res
, vol.88
, pp. 30-36
-
-
Andreopoulos, S.1
Li, P.2
Warsh, J.3
-
25
-
-
0028079674
-
Cellular variations in heterotrimeric G protein localization and expression in rat pituitary
-
Wilson B, Komuro M, Farquhar M. Cellular variations in heterotrimeric G protein localization and expression in rat pituitary. Endocrinology 1994;134:233-44
-
(1994)
Endocrinology
, vol.134
, pp. 233-244
-
-
Wilson, B.1
Komuro, M.2
Farquhar, M.3
-
26
-
-
1542756054
-
Cellular localization of GFP-tagged alpha subunits
-
Hynes T, Hughes T, Berlot C. Cellular localization of GFP-tagged alpha subunits. Methods Mol Biol 2004;237:233-46
-
(2004)
Methods Mol Biol
, vol.237
, pp. 233-246
-
-
Hynes, T.1
Hughes, T.2
Berlot, C.3
-
27
-
-
27444440633
-
Cell signaling diversity of the Gqalpha family of heterotrimeric G proteins
-
Hubbard K, Hepler J. Cell signaling diversity of the Gqalpha family of heterotrimeric G proteins. Cell Signal 2006;18:135-50
-
(2006)
Cell Signal
, vol.18
, pp. 135-150
-
-
Hubbard, K.1
Hepler, J.2
-
28
-
-
0033572358
-
The G protein subunit gene families
-
Downes G, Gautam N. The G protein subunit gene families. Genomics 1999;62:544-52
-
(1999)
Genomics
, vol.62
, pp. 544-552
-
-
Downes, G.1
Gautam, N.2
-
30
-
-
33947431049
-
Lipid-protein interactions in GPCR-associated signaling
-
Escriba P, Wedegaertner P, Goni F, et al. Lipid-protein interactions in GPCR-associated signaling. Biochim Biophys Acta 2007;1768:836-52
-
(2007)
Biochim Biophys Acta
, vol.1768
, pp. 836-852
-
-
Escriba, P.1
Wedegaertner, P.2
Goni, F.3
-
31
-
-
0029039937
-
The dynamic role of palmitoylation in signal transduction
-
Milligan G, Parenti M, Magee A. The dynamic role of palmitoylation in signal transduction. Trends Biochem Sci 1995;20:181-7
-
(1995)
Trends Biochem Sci
, vol.20
, pp. 181-187
-
-
Milligan, G.1
Parenti, M.2
Magee, A.3
-
32
-
-
12744274770
-
Activation of an alpha2A-adrenoceptor-Galphao1 fusion protein dynamically regulates the palmitoylation status of the G protein but not of the receptor
-
Barclay E, O'Reilly M, Milligan G. Activation of an alpha2A-adrenoceptor-Galphao1 fusion protein dynamically regulates the palmitoylation status of the G protein but not of the receptor. Biochem J 2005;385:197-206
-
(2005)
Biochem J
, vol.385
, pp. 197-206
-
-
Barclay, E.1
O'Reilly, M.2
Milligan, G.3
-
33
-
-
33745989271
-
Role of the chaperonin CCT/TRiC complex in G protein betagamma-dimer assembly
-
Wells C, Dingus J, Hildebrandt J. Role of the chaperonin CCT/TRiC complex in G protein betagamma-dimer assembly. J Biol Chem 2006;281:20221-32
-
(2006)
J Biol Chem
, vol.281
, pp. 20221-20232
-
-
Wells, C.1
Dingus, J.2
Hildebrandt, J.3
-
35
-
-
33646200560
-
Gbetagamma inhibits Galpha GTPase-activating proteins by inhibition of Galpha-GTP binding during stimulation by receptor
-
Tang W, Tu Y, Nayak S, et al. Gbetagamma inhibits Galpha GTPase-activating proteins by inhibition of Galpha-GTP binding during stimulation by receptor. J Biol Chem 2006;281:4746-53
-
(2006)
J Biol Chem
, vol.281
, pp. 4746-4753
-
-
Tang, W.1
Tu, Y.2
Nayak, S.3
-
36
-
-
0028093624
-
A farnesilated domain in the G protein gamma subunit is a specific determinant of receptor coupling
-
Kisselev O, Ermolaeva M, Gautam N. A farnesilated domain in the G protein gamma subunit is a specific determinant of receptor coupling. J Biol Chem 1994;269:21399-402
-
(1994)
J Biol Chem
, vol.269
, pp. 21399-21402
-
-
Kisselev, O.1
Ermolaeva, M.2
Gautam, N.3
-
37
-
-
0030920782
-
G protein mechanisms: Insights from structural analysis
-
Sprang S. G protein mechanisms: insights from structural analysis. Ann Rev Biochem 1997;66:639-78
-
(1997)
Ann Rev Biochem
, vol.66
, pp. 639-678
-
-
Sprang, S.1
-
38
-
-
0347364629
-
Gi protein activation in intact cells involves subunit rearrangement rather than dissociation
-
Bunemann M, Frank M, Lohse M. Gi protein activation in intact cells involves subunit rearrangement rather than dissociation. Proc Natl Acad Sci USA 2003;100:16077-82
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 16077-16082
-
-
Bunemann, M.1
Frank, M.2
Lohse, M.3
-
39
-
-
21644479599
-
G Protein activation without subunit dissociation depends on a G{alpha} (i)-specific region
-
Frank M, Thumer L, Lohse M, et al. G Protein activation without subunit dissociation depends on a G{alpha} (i)-specific region. J Biol Chem 2005;280:24584-90
-
(2005)
J Biol Chem
, vol.280
, pp. 24584-24590
-
-
Frank, M.1
Thumer, L.2
Lohse, M.3
-
40
-
-
33947407279
-
Expansion of signal transduction by G proteins. The second 15 years or so: From 3 to 16 alpha subunits plus betagamma dimers
-
Birnbaumer L. Expansion of signal transduction by G proteins. The second 15 years or so: from 3 to 16 alpha subunits plus betagamma dimers. Biochim Biophys Acta 2007;1768:772-93
-
(2007)
Biochim Biophys Acta
, vol.1768
, pp. 772-793
-
-
Birnbaumer, L.1
-
41
-
-
0347949548
-
Insights into G protein structure, function, and regulation
-
Cabrera-Vera T, Vanhauwe J, Thomas T, et al. Insights into G protein structure, function, and regulation. Endocr Rev 2003;24:765-81
-
(2003)
Endocr Rev
, vol.24
, pp. 765-781
-
-
Cabrera-Vera, T.1
Vanhauwe, J.2
Thomas, T.3
-
42
-
-
0027973625
-
Rapid kinetics of G protein subunit association: A rate-limiting conformational change?
-
Neubig R, Connolly M, Remmers A. Rapid kinetics of G protein subunit association: a rate-limiting conformational change? FEBS Lett 1994;355:251-3
-
(1994)
FEBS Lett
, vol.355
, pp. 251-253
-
-
Neubig, R.1
Connolly, M.2
Remmers, A.3
-
43
-
-
0034636206
-
Coupling between the N- and C-terminal domains influences transducin-alpha intrinsic GDP/GTP exchange
-
Muradov K, Artemyev N. Coupling between the N- and C-terminal domains influences transducin-alpha intrinsic GDP/GTP exchange. Biochemistry 2000;39:3937-42
-
(2000)
Biochemistry
, vol.39
, pp. 3937-3942
-
-
Muradov, K.1
Artemyev, N.2
-
44
-
-
0034741603
-
An intramolecular contact in Galpha transducin that participates in maintaining its intrinsic GDP release rate
-
Thomas T, Bae H, Medkova M, et al. An intramolecular contact in Galpha transducin that participates in maintaining its intrinsic GDP release rate. Mol Cell Biol Res Commun 2001;4:282-91
-
(2001)
Mol Cell Biol Res Commun
, vol.4
, pp. 282-291
-
-
Thomas, T.1
Bae, H.2
Medkova, M.3
-
45
-
-
0028083205
-
Regulation of transducin GTPase activity in bovine rod outer segments
-
Arshavsky V, Dumke C, Zhu Y, et al. Regulation of transducin GTPase activity in bovine rod outer segments. J Biol Chem 1994;269:19882-7
-
(1994)
J Biol Chem
, vol.269
, pp. 19882-19887
-
-
Arshavsky, V.1
Dumke, C.2
Zhu, Y.3
-
46
-
-
0030982264
-
Structure of RGS4 bound to AlF4-activated G(i alpha1): Stabilization of the transition state for GTP hydrolysis
-
Tesmer J, Berman D, Gilman A, et al. Structure of RGS4 bound to AlF4-activated G(i alpha1): stabilization of the transition state for GTP hydrolysis. Cell Signal 1997;89:251-61
-
(1997)
Cell Signal
, vol.89
, pp. 251-261
-
-
Tesmer, J.1
Berman, D.2
Gilman, A.3
-
47
-
-
33746012348
-
Mammalian RGS proteins: Multifunctional regulators of cellular signaling
-
Willars G. Mammalian RGS proteins: multifunctional regulators of cellular signaling. Semin Cell Dev Biol 2006;17:363-76
-
(2006)
Semin Cell Dev Biol
, vol.17
, pp. 363-376
-
-
Willars, G.1
-
48
-
-
33746030652
-
The selective interactions and functions of regulators of G protein signaling
-
Tinker A. The selective interactions and functions of regulators of G protein signaling. Semin Cell Dev Biol 2006;17:377-82
-
(2006)
Semin Cell Dev Biol
, vol.17
, pp. 377-382
-
-
Tinker, A.1
-
49
-
-
33748508863
-
Regulatory mechanisms involved in modulating RGS function
-
Jean-Baptiste G, Yang Z, Greenwood M. Regulatory mechanisms involved in modulating RGS function. Cell Mol Life Sci 2006;63:1969-85
-
(2006)
Cell Mol Life Sci
, vol.63
, pp. 1969-1985
-
-
Jean-Baptiste, G.1
Yang, Z.2
Greenwood, M.3
-
50
-
-
40349088827
-
G protein-coupled receptor phosphorylation: Where, when and by whom
-
Epub ahead of date
-
Tobin A. G protein-coupled receptor phosphorylation: where, when and by whom. Br J Pharmacol 2008 [Epub ahead of date]
-
(2008)
Br J Pharmacol
-
-
Tobin, A.1
-
51
-
-
33751533776
-
New roles for beta-arrestins in cell signaling: Not just for seven-transmembrane receptors
-
Lefkowitz R, Rajagopal K, Whalen E. New roles for beta-arrestins in cell signaling: not just for seven-transmembrane receptors. Mol Cell 2006;24:643-52
-
(2006)
Mol Cell
, vol.24
, pp. 643-652
-
-
Lefkowitz, R.1
Rajagopal, K.2
Whalen, E.3
-
52
-
-
33644778825
-
Differential efficacies of somatostatin receptor agonists for G protein activation and desensitization of somatostatin receptor subtype 4-mediated responses
-
Engstrom M, Savola J, Wurster S. Differential efficacies of somatostatin receptor agonists for G protein activation and desensitization of somatostatin receptor subtype 4-mediated responses. J Pharmacol Exp Ther 2006;316:1262-8
-
(2006)
J Pharmacol Exp Ther
, vol.316
, pp. 1262-1268
-
-
Engstrom, M.1
Savola, J.2
Wurster, S.3
-
53
-
-
0029778172
-
Morphine activates opioid receptors without causing their rapid internalization
-
Keith D, Murray S, Zaki P, et al. Morphine activates opioid receptors without causing their rapid internalization. J Biol Chem 1996;271:19021-4
-
(1996)
J Biol Chem
, vol.271
, pp. 19021-19024
-
-
Keith, D.1
Murray, S.2
Zaki, P.3
-
54
-
-
0031013532
-
Differential opioid agonist regulation of the mouse mu opioid receptor
-
Blake A, Bot G, Freeman J, et al. Differential opioid agonist regulation of the mouse mu opioid receptor. J Biol Chem 1997;272:782-90
-
(1997)
J Biol Chem
, vol.272
, pp. 782-790
-
-
Blake, A.1
Bot, G.2
Freeman, J.3
-
55
-
-
0030993594
-
Antagonist-stimulated internalization of the G protein-coupled cholecystokinin receptor
-
Roettger B, Ghanekar D, Rao R, et al. Antagonist-stimulated internalization of the G protein-coupled cholecystokinin receptor. Mol Pharmacol 1997;51:357-62
-
(1997)
Mol Pharmacol
, vol.51
, pp. 357-362
-
-
Roettger, B.1
Ghanekar, D.2
Rao, R.3
-
56
-
-
0030691760
-
Mu opioid receptor phosphorylation, desensitization, and ligand efficacy
-
Yu Y, Zhang L, Yin X, et al. Mu opioid receptor phosphorylation, desensitization, and ligand efficacy. J Biol Chem 1997;272:28869-74
-
(1997)
J Biol Chem
, vol.272
, pp. 28869-28874
-
-
Yu, Y.1
Zhang, L.2
Yin, X.3
-
57
-
-
0033049565
-
Constitutively active alpha-1b adrenergic receptor mutants display different phosphorylation and internalization features
-
Mhaouty-Kodja S, Barak L, Scheer A, et al. Constitutively active alpha-1b adrenergic receptor mutants display different phosphorylation and internalization features. Mol Pharmacol 1999;55:339-47
-
(1999)
Mol Pharmacol
, vol.55
, pp. 339-347
-
-
Mhaouty-Kodja, S.1
Barak, L.2
Scheer, A.3
-
58
-
-
0032895241
-
Receptor selectivity of the cloned opossum G protein-coupled receptor kinase 2 (GRK2) in intact opossum kidney cells: Role in desensitization of endogenous alpha2C-adrenergic but not serotonin 1B receptors
-
Lembo P, Ghahremani M, Albert P. Receptor selectivity of the cloned opossum G protein-coupled receptor kinase 2 (GRK2) in intact opossum kidney cells: role in desensitization of endogenous alpha2C-adrenergic but not serotonin 1B receptors. Mol Endocrinol 1999;13:138-47
-
(1999)
Mol Endocrinol
, vol.13
, pp. 138-147
-
-
Lembo, P.1
Ghahremani, M.2
Albert, P.3
-
59
-
-
0034815178
-
Kinase-inactive G protein-coupled receptor kinases are able to attenuate follicle-stimulating hormone-induced signaling
-
Reiter E, Marion S, Robert F, et al. Kinase-inactive G protein-coupled receptor kinases are able to attenuate follicle-stimulating hormone-induced signaling. Biochem Biophys Res Commun 2001;282:71-8
-
(2001)
Biochem Biophys Res Commun
, vol.282
, pp. 71-78
-
-
Reiter, E.1
Marion, S.2
Robert, F.3
-
60
-
-
0037067705
-
Phosphorylation-independent regulation of metabotropic glutamate receptor signaling by G protein-coupled receptor kinase 2
-
Dhami G, Anborgh P, Dale L, et al. Phosphorylation-independent regulation of metabotropic glutamate receptor signaling by G protein-coupled receptor kinase 2. J Biol Chem 2002;277:25266-72
-
(2002)
J Biol Chem
, vol.277
, pp. 25266-25272
-
-
Dhami, G.1
Anborgh, P.2
Dale, L.3
-
61
-
-
0042575596
-
Phosphorylation-independent desensitization of GABA(B) receptor by GRK4
-
Perroy J, Adam L, Qanbar R, et al. Phosphorylation-independent desensitization of GABA(B) receptor by GRK4. EMBO J 2003;22:3816-24
-
(2003)
EMBO J
, vol.22
, pp. 3816-3824
-
-
Perroy, J.1
Adam, L.2
Qanbar, R.3
-
62
-
-
33947314576
-
Regulation of receptor trafficking by GRKs and arrestins
-
Moore C, Milano S, Benovic J. Regulation of receptor trafficking by GRKs and arrestins. Ann Rev Physiol 2007;69:451-82
-
(2007)
Ann Rev Physiol
, vol.69
, pp. 451-482
-
-
Moore, C.1
Milano, S.2
Benovic, J.3
-
63
-
-
0036765857
-
D2 and D3 dopamine receptor cell surface localization mediated by interaction with protein 4.1N
-
Binda A, Kabbani N, Lin R, et al. D2 and D3 dopamine receptor cell surface localization mediated by interaction with protein 4.1N. Mol Pharmacol 2002;62:507-13
-
(2002)
Mol Pharmacol
, vol.62
, pp. 507-513
-
-
Binda, A.1
Kabbani, N.2
Lin, R.3
-
64
-
-
33747075228
-
Interaction of the amyloid precursor like protein 1 with the alpha2A-adrenergic receptor increases agonist-mediated inhibition of adenylyl cyclase
-
Weber B, Schaper C, Scholz J, et al. Interaction of the amyloid precursor like protein 1 with the alpha2A-adrenergic receptor increases agonist-mediated inhibition of adenylyl cyclase. Cell Signal 2006;18:1748-57
-
(2006)
Cell Signal
, vol.18
, pp. 1748-1757
-
-
Weber, B.1
Schaper, C.2
Scholz, J.3
-
65
-
-
0034731494
-
ATRAP, novel AT1 receptor associated protein, enhances internalization of AT1 receptor and inhibits vascular smooth muscle cell growth
-
Cui T, Nakagami H, Iwai M, et al. ATRAP, novel AT1 receptor associated protein, enhances internalization of AT1 receptor and inhibits vascular smooth muscle cell growth. Biochem Biophys Res Commun 2000;279:938-41
-
(2000)
Biochem Biophys Res Commun
, vol.279
, pp. 938-941
-
-
Cui, T.1
Nakagami, H.2
Iwai, M.3
-
66
-
-
0034048720
-
Dual signaling regulated by calcyon, a D1 dopamine receptor interacting protein
-
Lezcano N, Mrzljak L, Eubanks S, et al. Dual signaling regulated by calcyon, a D1 dopamine receptor interacting protein. Science 2000;287:1660-4
-
(2000)
Science
, vol.287
, pp. 1660-1664
-
-
Lezcano, N.1
Mrzljak, L.2
Eubanks, S.3
-
67
-
-
18044377786
-
Regulation of dense core vesicle release from PC12 cells by interaction between the D2 dopamine receptor and calcium-dependent activator protein for secretion (CAPS)
-
Binda A, Kabbani N, Levenson R. Regulation of dense core vesicle release from PC12 cells by interaction between the D2 dopamine receptor and calcium-dependent activator protein for secretion (CAPS). Biochem Pharmacol 2005;69:1451-61
-
(2005)
Biochem Pharmacol
, vol.69
, pp. 1451-1461
-
-
Binda, A.1
Kabbani, N.2
Levenson, R.3
-
68
-
-
2442626676
-
Nm23-H2 interacts with a G protein-coupled receptor to regulate its endocytosis through an Rac1-dependent mechanism
-
Rochdi M, Laroche G, Dupre E, et al. Nm23-H2 interacts with a G protein-coupled receptor to regulate its endocytosis through an Rac1-dependent mechanism. J Biol Chem 2004;279:18981-9
-
(2004)
J Biol Chem
, vol.279
, pp. 18981-18989
-
-
Rochdi, M.1
Laroche, G.2
Dupre, E.3
-
69
-
-
0038505967
-
GIPC interacts with the beta1-adrenergic receptor and regulates beta1-adrenergic receptor-mediated ERK activation
-
Hu L, Chen W, Martin N, et al. GIPC interacts with the beta1-adrenergic receptor and regulates beta1-adrenergic receptor-mediated ERK activation. J Biol Chem 2003;278:26295-301
-
(2003)
J Biol Chem
, vol.278
, pp. 26295-26301
-
-
Hu, L.1
Chen, W.2
Martin, N.3
-
70
-
-
0034764182
-
The carboxyl terminus of the prolactin-releasing peptide receptor interacts with PDZ domain proteins involved in alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid receptor clustering
-
Lin S, Arai A, Wang Z, et al. The carboxyl terminus of the prolactin-releasing peptide receptor interacts with PDZ domain proteins involved in alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid receptor clustering. Mol Pharmacol 2001;60:916-23
-
(2001)
Mol Pharmacol
, vol.60
, pp. 916-923
-
-
Lin, S.1
Arai, A.2
Wang, Z.3
-
71
-
-
0037178754
-
Modulation of postendocytic sorting of G protein-coupled receptors
-
Whistler J, Enquist J, Marley A, et al. Modulation of postendocytic sorting of G protein-coupled receptors. Science 2002;297:615-20
-
(2002)
Science
, vol.297
, pp. 615-620
-
-
Whistler, J.1
Enquist, J.2
Marley, A.3
-
72
-
-
0742270638
-
Interactions of GIPC with dopamine D2, D3 but not D4 receptors define a novel mode of regulation of G protein-coupled receptors
-
Jeanneteau F, Diaz J, Sokoloff P, et al. Interactions of GIPC with dopamine D2, D3 but not D4 receptors define a novel mode of regulation of G protein-coupled receptors. Mol Biol Cell 2004;15:696-705
-
(2004)
Mol Biol Cell
, vol.15
, pp. 696-705
-
-
Jeanneteau, F.1
Diaz, J.2
Sokoloff, P.3
-
73
-
-
0141783682
-
CLIC6, a member of the intracellular chloride channel family, interacts with dopamine D(2)-like receptors
-
Griffon N, Jeanneteau F, Prieur F, et al. CLIC6, a member of the intracellular chloride channel family, interacts with dopamine D(2)-like receptors. Brain Res Mol Brain Res 2003;117:47-57
-
(2003)
Brain Res Mol Brain Res
, vol.117
, pp. 47-57
-
-
Griffon, N.1
Jeanneteau, F.2
Prieur, F.3
-
74
-
-
0036813090
-
Interaction with neuronal calcium sensor NCS-1 mediates desensitization of the D2 dopamine receptor
-
Kabbani N, Negyessy L, Lin R, et al. Interaction with neuronal calcium sensor NCS-1 mediates desensitization of the D2 dopamine receptor. J Neurosci 2002;22:8476-86
-
(2002)
J Neurosci
, vol.22
, pp. 8476-8486
-
-
Kabbani, N.1
Negyessy, L.2
Lin, R.3
-
75
-
-
0242384770
-
Activation-independent parathyroid hormone receptor internalization is regulated by NHERF1 (EBP50)
-
Sneddon W, Syme C, Bisello A, et al. Activation-independent parathyroid hormone receptor internalization is regulated by NHERF1 (EBP50). J Biol Chem 2003;278:43787-96
-
(2003)
J Biol Chem
, vol.278
, pp. 43787-43796
-
-
Sneddon, W.1
Syme, C.2
Bisello, A.3
-
76
-
-
27144523294
-
Inhibition of metabotropic glutamate receptor signaling by the huntingtin-binding protein optineurin
-
Anborgh P, Godin C, Pampillo M, et al. Inhibition of metabotropic glutamate receptor signaling by the huntingtin-binding protein optineurin. J Biol Chem 2005;280:34840-8
-
(2005)
J Biol Chem
, vol.280
, pp. 34840-34848
-
-
Anborgh, P.1
Godin, C.2
Pampillo, M.3
-
77
-
-
0037016681
-
Rab5 association with the angiotensin II type 1A receptor promotes Rab5 GTP binding and vesicular fusion
-
Seachrist J, Laporte S, Dale L, et al. Rab5 association with the angiotensin II type 1A receptor promotes Rab5 GTP binding and vesicular fusion. J Biol Chem 2002;277:679-85
-
(2002)
J Biol Chem
, vol.277
, pp. 679-685
-
-
Seachrist, J.1
Laporte, S.2
Dale, L.3
-
78
-
-
30944451158
-
RGS proteins have a signaling complex: Interactions between RGS proteins and GPCRs, effectors, and auxiliary proteins
-
Abramow-Newerly M, Roy A, Nunn C, et al. RGS proteins have a signaling complex: interactions between RGS proteins and GPCRs, effectors, and auxiliary proteins. Cell Signal 2006;18:579-91
-
(2006)
Cell Signal
, vol.18
, pp. 579-591
-
-
Abramow-Newerly, M.1
Roy, A.2
Nunn, C.3
-
79
-
-
5444265165
-
Ral and phospholipase D2-dependent pathway for constitutive metabotropic glutamate receptor endocytosis
-
Bhattacharya M, Babwah A, Godin C, et al. Ral and phospholipase D2-dependent pathway for constitutive metabotropic glutamate receptor endocytosis. J Neurosci 2004;24:8752-61
-
(2004)
J Neurosci
, vol.24
, pp. 8752-8761
-
-
Bhattacharya, M.1
Babwah, A.2
Godin, C.3
-
80
-
-
34548496035
-
The neuronal Ca(2+)-binding protein 2 (NECAB2) interacts with the adenosine A(2A) receptor and modulates the cell surface expression and function of the receptor
-
Canela L, Lujan R, Lluis C, et al. The neuronal Ca(2+)-binding protein 2 (NECAB2) interacts with the adenosine A(2A) receptor and modulates the cell surface expression and function of the receptor. Mol Cell Neurosci 2007;36:1-12
-
(2007)
Mol Cell Neurosci
, vol.36
, pp. 1-12
-
-
Canela, L.1
Lujan, R.2
Lluis, C.3
-
81
-
-
35549009435
-
Involvement of HSP-90 in CB2 cannabinoid receptor-mediated cell migration - a new role of HSP-90 in migration signaling of a G protein-coupled receptor
-
Epub ahead of print
-
He F, Qiao Z, Cai J, et al. Involvement of HSP-90 in CB2 cannabinoid receptor-mediated cell migration - a new role of HSP-90 in migration signaling of a G protein-coupled receptor. Mol Pharmacol 2007 [Epub ahead of print]
-
(2007)
Mol Pharmacol
-
-
He, F.1
Qiao, Z.2
Cai, J.3
-
82
-
-
34548789127
-
A proteomic approach to receptor signaling: Molecular mechanisms and therapeutic implications derived from discovery of the dopamine D(2) receptor signalplex
-
Epub ahead of print
-
Kabbani N, Levenson R. A proteomic approach to receptor signaling: molecular mechanisms and therapeutic implications derived from discovery of the dopamine D(2) receptor signalplex. Eur J Pharmacol 2007 [Epub ahead of print]
-
(2007)
Eur J Pharmacol
-
-
Kabbani, N.1
Levenson, R.2
-
83
-
-
33747181100
-
Allosteric agonists of 7TM receptors: Expanding the pharmacological toolbox
-
Langmead C, Christopoulos A. Allosteric agonists of 7TM receptors: expanding the pharmacological toolbox. Trends Pharmacol Sci 2006;27:475-81
-
(2006)
Trends Pharmacol Sci
, vol.27
, pp. 475-481
-
-
Langmead, C.1
Christopoulos, A.2
-
84
-
-
0036258990
-
G protein-coupled receptor allosterism and complexing
-
Christopoulos A, Kenakin T. G protein-coupled receptor allosterism and complexing. Pharmacol Rev 2002;54:323-74
-
(2002)
Pharmacol Rev
, vol.54
, pp. 323-374
-
-
Christopoulos, A.1
Kenakin, T.2
-
85
-
-
0036490942
-
Allosteric binding sites on cell-surface receptors: Novel targets for drug discovery
-
Christopoulos A. Allosteric binding sites on cell-surface receptors: novel targets for drug discovery. Nat Rev Drug Discov 2002;1:198-210
-
(2002)
Nat Rev Drug Discov
, vol.1
, pp. 198-210
-
-
Christopoulos, A.1
-
86
-
-
34250743762
-
Allosteric approaches to the targeting of G protein-coupled receptors for novel drug discovery: A critical assessment
-
Raddatz R, Schaffhauser H, Marino M. Allosteric approaches to the targeting of G protein-coupled receptors for novel drug discovery: a critical assessment. Biochem Pharmacol 2007;74:383-91
-
(2007)
Biochem Pharmacol
, vol.74
, pp. 383-391
-
-
Raddatz, R.1
Schaffhauser, H.2
Marino, M.3
-
87
-
-
0141869933
-
Allosteric modulators of G protein-coupled receptors
-
May L, Christopoulos A. Allosteric modulators of G protein-coupled receptors. Curr Opin Pharmacol 2003;3:551-6
-
(2003)
Curr Opin Pharmacol
, vol.3
, pp. 551-556
-
-
May, L.1
Christopoulos, A.2
-
88
-
-
33644547054
-
The 'allosteric modulator' SCH-202676 disrupts G protein-coupled receptor function via sulfhydryl-sensitive mechanisms
-
Lewandowicz A, Vepsalainen J, Laitinen J. The 'allosteric modulator' SCH-202676 disrupts G protein-coupled receptor function via sulfhydryl-sensitive mechanisms. Br J Pharmacol 2006;147:422-9
-
(2006)
Br J Pharmacol
, vol.147
, pp. 422-429
-
-
Lewandowicz, A.1
Vepsalainen, J.2
Laitinen, J.3
-
89
-
-
0029776693
-
Activation of muscarinic acetylcholine receptors via their allosteric binding sites
-
Jakubik J, Bacakova L, Lisa V, et al. Activation of muscarinic acetylcholine receptors via their allosteric binding sites. Proc Natl Acad Sci USA 1996;93:8705-9
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 8705-8709
-
-
Jakubik, J.1
Bacakova, L.2
Lisa, V.3
-
90
-
-
0031443549
-
Unique allosteric regulation of 5-hydroxytryptamine receptor-mediated signal transduction by oleamide
-
Thomas E, Carson M, Neal M, et al. Unique allosteric regulation of 5-hydroxytryptamine receptor-mediated signal transduction by oleamide. Proc Natl Acad Sci USA 1997;94:14115-9
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 14115-14119
-
-
Thomas, E.1
Carson, M.2
Neal, M.3
-
91
-
-
20144381462
-
A novel selective positive allosteric modulator of metabotropic glutamate receptor subtype 5 has in vivo activity and antipsychotic-like effects in rat behavioral models
-
Kinney G, O'Brien J, Lemaire W, et al. A novel selective positive allosteric modulator of metabotropic glutamate receptor subtype 5 has in vivo activity and antipsychotic-like effects in rat behavioral models. J Pharmacol Exp Ther 2005;313:199-206
-
(2005)
J Pharmacol Exp Ther
, vol.313
, pp. 199-206
-
-
Kinney, G.1
O'Brien, J.2
Lemaire, W.3
-
92
-
-
0346259943
-
Metal ion-mediated agonism and agonist enhancement in melanocortin MC1 and MC4 receptors
-
Holst B, Elling C, Schwartz T. Metal ion-mediated agonism and agonist enhancement in melanocortin MC1 and MC4 receptors. J Biol Chem 2002;277:47662-70
-
(2002)
J Biol Chem
, vol.277
, pp. 47662-47670
-
-
Holst, B.1
Elling, C.2
Schwartz, T.3
-
93
-
-
24344479915
-
Nonpeptide and peptide growth hormone secretagogues act both as ghrelin receptor agonist and as positive or negative allosteric modulators of ghrelin signaling
-
Holst B, Brandt E, Bach A, et al. Nonpeptide and peptide growth hormone secretagogues act both as ghrelin receptor agonist and as positive or negative allosteric modulators of ghrelin signaling. Mol Endocrinol 2005;19:2400-11
-
(2005)
Mol Endocrinol
, vol.19
, pp. 2400-2411
-
-
Holst, B.1
Brandt, E.2
Bach, A.3
-
94
-
-
3142685557
-
The heptahelical domain of GABA(B2) is activated directly by CGP7930, a positive allosteric modulator of the GABA(B) receptor
-
Binet V, Brajon C, Le Corre L, et al. The heptahelical domain of GABA(B2) is activated directly by CGP7930, a positive allosteric modulator of the GABA(B) receptor. J Biol Chem 2004;279:29085-91
-
(2004)
J Biol Chem
, vol.279
, pp. 29085-29091
-
-
Binet, V.1
Brajon, C.2
Le Corre, L.3
-
95
-
-
33846477446
-
Small-molecule agonists for the glucagon-like peptide 1 receptor
-
Knudsen L, Kiel D, Teng M, et al. Small-molecule agonists for the glucagon-like peptide 1 receptor. Proc Natl Acad Sci USA 2007;104:937-42
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 937-942
-
-
Knudsen, L.1
Kiel, D.2
Teng, M.3
-
96
-
-
33645796458
-
Ago-allosteric modulation and other types of allostery in dimeric 7TM receptors
-
Schwartz T, Holst B. Ago-allosteric modulation and other types of allostery in dimeric 7TM receptors. J Recept Signal Transduct Res 2006;26:107-28
-
(2006)
J Recept Signal Transduct Res
, vol.26
, pp. 107-128
-
-
Schwartz, T.1
Holst, B.2
-
97
-
-
0141702358
-
Protean agonism at histamine H3 receptors in vitro and in vivo
-
Gbahou F, Rouleau A, Morisset S, et al. Protean agonism at histamine H3 receptors in vitro and in vivo. Proc Natl Acad Sci USA 2003;100:11086-91
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 11086-11091
-
-
Gbahou, F.1
Rouleau, A.2
Morisset, S.3
-
98
-
-
0037305047
-
Principles: Extending the utility of [35S]GTP gamma S binding assays
-
Milligan G. Principles: extending the utility of [35S]GTP gamma S binding assays. Trends Pharmacol Sci 2003;24:87-90
-
(2003)
Trends Pharmacol Sci
, vol.24
, pp. 87-90
-
-
Milligan, G.1
-
99
-
-
0033782021
-
Advantages of heterologous expression of human D2long dopamine receptors in human neuroblastoma SH-SY5Y over human embryonic kidney 293 cells
-
Alberts G, Pregenzer J, Im W. Advantages of heterologous expression of human D2long dopamine receptors in human neuroblastoma SH-SY5Y over human embryonic kidney 293 cells. Br J Pharmacol 2000;131:514-20
-
(2000)
Br J Pharmacol
, vol.131
, pp. 514-520
-
-
Alberts, G.1
Pregenzer, J.2
Im, W.3
-
100
-
-
38149064653
-
Functional complementation of high-efficiency resonance energy transfer: A new tool for the study of protein binding interactions in living cells
-
Molinari P, Casella I, Costa T. Functional complementation of high-efficiency resonance energy transfer: a new tool for the study of protein binding interactions in living cells. Biochem J 2008;409:251-61
-
(2008)
Biochem J
, vol.409
, pp. 251-261
-
-
Molinari, P.1
Casella, I.2
Costa, T.3
-
101
-
-
18744376919
-
Real-time monitoring of receptor and G protein interactions in living cells
-
Galés C, Rebois R, Hogue M, et al. Real-time monitoring of receptor and G protein interactions in living cells. Nat Methods 2005; 2:177-84
-
(2005)
Nat Methods
, vol.2
, pp. 177-184
-
-
Galés, C.1
Rebois, R.2
Hogue, M.3
-
102
-
-
29444446964
-
Heterotrimeric G proteins precouple with G protein-coupled receptors in living cells
-
Nobles M, Benians A, Tinker A. Heterotrimeric G proteins precouple with G protein-coupled receptors in living cells. Proc Natl Acad Sci USA 2005;102:18706-11
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 18706-18711
-
-
Nobles, M.1
Benians, A.2
Tinker, A.3
-
103
-
-
34548433883
-
Kinetic analysis of G protein-coupled receptor signaling using fluorescence resonance energy transfer in living cells
-
Lohse M, Hoffmann C, Nikolaev V, et al. Kinetic analysis of G protein-coupled receptor signaling using fluorescence resonance energy transfer in living cells. Adv Protein Chem 2007;74:167-88
-
(2007)
Adv Protein Chem
, vol.74
, pp. 167-188
-
-
Lohse, M.1
Hoffmann, C.2
Nikolaev, V.3
-
104
-
-
36448965981
-
Pharmacology under the microscope: The use of fluorescence correlation spectroscopy to determine the properties of ligand-receptor complexes
-
Briddon S, Hill S. Pharmacology under the microscope: the use of fluorescence correlation spectroscopy to determine the properties of ligand-receptor complexes. Trends Pharmacol Sci 2007;28:637-45
-
(2007)
Trends Pharmacol Sci
, vol.28
, pp. 637-645
-
-
Briddon, S.1
Hill, S.2
-
105
-
-
0019137579
-
A ternary complex model explains the agonist-specific binding properties of the adenylyl cyclase-coupled beta-adrenergic receptor
-
De Lean A, Stadel J, Lefkowitz R. A ternary complex model explains the agonist-specific binding properties of the adenylyl cyclase-coupled beta-adrenergic receptor. J Biol Chem 1980;255:7108-17
-
(1980)
J Biol Chem
, vol.255
, pp. 7108-7117
-
-
De Lean, A.1
Stadel, J.2
Lefkowitz, R.3
-
106
-
-
0242552831
-
The [35S] GTPgammaS binding assay: Approaches and applications in pharmacology
-
Harrison C, Traynor J. The [35S] GTPgammaS binding assay: approaches and applications in pharmacology. Life Sci 2003;74:489-508
-
(2003)
Life Sci
, vol.74
, pp. 489-508
-
-
Harrison, C.1
Traynor, J.2
-
107
-
-
3242792519
-
The antibody-capture [(35)S] GTPgammaS scintillation proximity assay: A powerful emerging technique for analysis of GPCR pharmacology
-
DeLapp N. The antibody-capture [(35)S] GTPgammaS scintillation proximity assay: a powerful emerging technique for analysis of GPCR pharmacology. Trends Pharmacol Sci 2004;25:400-1
-
(2004)
Trends Pharmacol Sci
, vol.25
, pp. 400-401
-
-
DeLapp, N.1
-
108
-
-
0028588656
-
Cellular signaling by an agonist-activated receptor/Gs alpha fusion protein
-
Bertin B, Freissmuth M, Jockers R, et al. Cellular signaling by an agonist-activated receptor/Gs alpha fusion protein. Proc Natl Acad Sci USA 1994;91:8827-31
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 8827-8831
-
-
Bertin, B.1
Freissmuth, M.2
Jockers, R.3
-
109
-
-
35248877040
-
Novel pharmacological applications of G protein-coupled receptor-G protein fusions
-
Epub ahead of print
-
Milligan G, Parenty G, Stoddart L, et al. Novel pharmacological applications of G protein-coupled receptor-G protein fusions. Curr Opin Pharmacol 2007 [Epub ahead of print]
-
(2007)
Curr Opin Pharmacol
-
-
Milligan, G.1
Parenty, G.2
Stoddart, L.3
-
110
-
-
0038521270
-
Promiscuous coupling at receptor-Galpha fusion proteins. The receptor of one covalent complex interacts with the alpha-subunit of another
-
Molinari P, Ambrosio C, Riitano D, et al. Promiscuous coupling at receptor-Galpha fusion proteins. The receptor of one covalent complex interacts with the alpha-subunit of another. J Biol Chem 2003;278:15778-88
-
(2003)
J Biol Chem
, vol.278
, pp. 15778-15788
-
-
Molinari, P.1
Ambrosio, C.2
Riitano, D.3
-
111
-
-
34547471030
-
Ligand screening system using fusion proteins of G protein-coupled receptors with G protein alpha subunits
-
Suga H, Haga T. Ligand screening system using fusion proteins of G protein-coupled receptors with G protein alpha subunits. Neurochem Int 2007;51:140-64
-
(2007)
Neurochem Int
, vol.51
, pp. 140-164
-
-
Suga, H.1
Haga, T.2
-
112
-
-
0021759089
-
ADP-ribosylation of transducin by pertussis toxin blocks the light-stimulated hydrolysis of GTP and cGMP in retinal photoreceptors
-
Van Dop C, Yamanaka G, Steinberg F, et al. ADP-ribosylation of transducin by pertussis toxin blocks the light-stimulated hydrolysis of GTP and cGMP in retinal photoreceptors. J Biol Chem 1984;259:23-6
-
(1984)
J Biol Chem
, vol.259
, pp. 23-26
-
-
Van Dop, C.1
Yamanaka, G.2
Steinberg, F.3
-
113
-
-
0030810745
-
Activation of the G protein Gq/11 through tyrosine phosphorylation of the alpha subunit
-
Umemori H, Inoue T, Kume S, et al. Activation of the G protein Gq/11 through tyrosine phosphorylation of the alpha subunit. Science 1997;276:1878-81
-
(1997)
Science
, vol.276
, pp. 1878-1881
-
-
Umemori, H.1
Inoue, T.2
Kume, S.3
-
114
-
-
0028672388
-
Injection of antisera into cells to study G protein regulation of channel function
-
McFadzean I, Caulfield M, Vallis Y, et al. Injection of antisera into cells to study G protein regulation of channel function. Methods Enzymol 1994;238:357-64
-
(1994)
Methods Enzymol
, vol.238
, pp. 357-364
-
-
McFadzean, I.1
Caulfield, M.2
Vallis, Y.3
-
115
-
-
0023716027
-
Site of G protein binding to rhodopson mapped with synthetic peptides from the α subunit
-
Hamm HE, Deretic D, Arendt A, et al. Site of G protein binding to rhodopson mapped with synthetic peptides from the α subunit. Science 1988;241:832-5
-
(1988)
Science
, vol.241
, pp. 832-835
-
-
Hamm, H.E.1
Deretic, D.2
Arendt, A.3
-
116
-
-
0028101036
-
Synthetic peptides as probes for G protein function. Carboxyl-terminal G alpha s peptides mimic Gs and evoke high affinity agonist binding to beta-adrenergic receptors
-
Rasenick M, Watanabe M, Lazarevic M, et al. Synthetic peptides as probes for G protein function. Carboxyl-terminal G alpha s peptides mimic Gs and evoke high affinity agonist binding to beta-adrenergic receptors. J Biol Chem 1994;269:21519-25
-
(1994)
J Biol Chem
, vol.269
, pp. 21519-21525
-
-
Rasenick, M.1
Watanabe, M.2
Lazarevic, M.3
-
117
-
-
0032510948
-
Antagonists of the receptor-G protein interface block Gi-coupled signal transduction
-
Gilchrist A, Mazzoni M, Dineen B, et al. Antagonists of the receptor-G protein interface block Gi-coupled signal transduction. J Biol Chem 1998;273:14912-9
-
(1998)
J Biol Chem
, vol.273
, pp. 14912-14919
-
-
Gilchrist, A.1
Mazzoni, M.2
Dineen, B.3
-
118
-
-
33644843243
-
A membrane-permeable peptide containing the last 21 residues of the G alpha(s) carboxyl terminus inhibits G(s)-coupled receptor signaling in intact cells: Correlations between peptide structure and biological activity
-
D'Ursi A, Giusti L, Albrizio S, et al. A membrane-permeable peptide containing the last 21 residues of the G alpha(s) carboxyl terminus inhibits G(s)-coupled receptor signaling in intact cells: correlations between peptide structure and biological activity. Mol Pharmacol 2006;69:727-36
-
(2006)
Mol Pharmacol
, vol.69
, pp. 727-736
-
-
D'Ursi, A.1
Giusti, L.2
Albrizio, S.3
-
119
-
-
0027245830
-
Substitution of three amino acids switches receptor specificity of Gq alpha to that of Gi alpha
-
Conklin B, Farfel Z, Lustig K, et al. Substitution of three amino acids switches receptor specificity of Gq alpha to that of Gi alpha. Nature 1993;363:274-6
-
(1993)
Nature
, vol.363
, pp. 274-276
-
-
Conklin, B.1
Farfel, Z.2
Lustig, K.3
-
120
-
-
0031016906
-
Molecular basis of receptor/G protein coupling selectivity studied by coexpression of wild type and mutant m2 muscarinic receptors with mutant G alpha(q) subunits
-
Kostenis E, Conklin B, Wess J. Molecular basis of receptor/G protein coupling selectivity studied by coexpression of wild type and mutant m2 muscarinic receptors with mutant G alpha(q) subunits. Biochemistry 1997;36:1487-95
-
(1997)
Biochemistry
, vol.36
, pp. 1487-1495
-
-
Kostenis, E.1
Conklin, B.2
Wess, J.3
-
121
-
-
0032475966
-
Extreme C terminus of G protein α-subunits contains a site that discriminates between Gi-coupled metabotropic glutamate receptors
-
Blahos Jn, Mary S, Perroy J, et al. Extreme C terminus of G protein α-subunits contains a site that discriminates between Gi-coupled metabotropic glutamate receptors. J Biol Chem 1998;273:25765-9
-
(1998)
J Biol Chem
, vol.273
, pp. 25765-25769
-
-
Blahos, J.1
Mary, S.2
Perroy, J.3
-
122
-
-
0029957669
-
Carboxyl-terminal mutations of Gq alpha and Gs alpha that alter the fidelity of receptor activation
-
Conklin B, Herzmark P, Ishida S, et al. Carboxyl-terminal mutations of Gq alpha and Gs alpha that alter the fidelity of receptor activation. Mol Pharmacol 1996;50:885-90
-
(1996)
Mol Pharmacol
, vol.50
, pp. 885-890
-
-
Conklin, B.1
Herzmark, P.2
Ishida, S.3
-
123
-
-
0344609797
-
A dominant-negative strategy for studying roles of G proteins in vivo
-
Gilchrist A, Bunemann M, Li A, et al. A dominant-negative strategy for studying roles of G proteins in vivo. J Biol Chem 1999;274:6610-6
-
(1999)
J Biol Chem
, vol.274
, pp. 6610-6616
-
-
Gilchrist, A.1
Bunemann, M.2
Li, A.3
-
124
-
-
0035854829
-
G alpha minigenes expressing C-terminal peptides serve as specific inhibitors of thrombin-mediated endothelial activation
-
Gilchrist A, Vanhauwe J, Li A, et al. G alpha minigenes expressing C-terminal peptides serve as specific inhibitors of thrombin-mediated endothelial activation. J Biol Chem 2001;276:25672-9
-
(2001)
J Biol Chem
, vol.276
, pp. 25672-25679
-
-
Gilchrist, A.1
Vanhauwe, J.2
Li, A.3
-
125
-
-
0037022438
-
G alpha COOH-terminal minigene vectors dissect heterotrimeric G protein signaling
-
Gilchrist A, Li A, Hamm H. G alpha COOH-terminal minigene vectors dissect heterotrimeric G protein signaling. Sci STKE 2002;5:PL1
-
(2002)
Sci STKE
, vol.5
-
-
Gilchrist, A.1
Li, A.2
Hamm, H.3
-
126
-
-
21344451993
-
Essential roles of G{alpha} 12/13 signaling in distinct cell behaviors driving zebrafish convergence and extension gastrulation movements
-
Lin F, Sepich D, Chen S, et al. Essential roles of G{alpha} 12/13 signaling in distinct cell behaviors driving zebrafish convergence and extension gastrulation movements. J Cell Biol 2005;169:777-87
-
(2005)
J Cell Biol
, vol.169
, pp. 777-787
-
-
Lin, F.1
Sepich, D.2
Chen, S.3
-
127
-
-
17744388606
-
G alpha 12/G alpha13 subunits of heterotrimeric G proteins mediate parathyroid hormone activation of phospholipase D in UMR-106 osteoblastic cells
-
Singh A, Gilchrist A, Voyno-Yasenetskaya T, et al. G alpha 12/G alpha13 subunits of heterotrimeric G proteins mediate parathyroid hormone activation of phospholipase D in UMR-106 osteoblastic cells. Endocrinology 2005;146:2171-5
-
(2005)
Endocrinology
, vol.146
, pp. 2171-2175
-
-
Singh, A.1
Gilchrist, A.2
Voyno-Yasenetskaya, T.3
-
128
-
-
33947529532
-
LPA(4)/GPR23 is a lysophosphatidic acid (LPA) receptor utilizing G(s)-, G(q)/G(i)-mediated calcium signaling and G(12/13)-mediated Rho activation
-
Lee C, Rivera R, Dubin A, et al. LPA(4)/GPR23 is a lysophosphatidic acid (LPA) receptor utilizing G(s)-, G(q)/G(i)-mediated calcium signaling and G(12/13)-mediated Rho activation. J Biol Chem 2007;282:4310-7
-
(2007)
J Biol Chem
, vol.282
, pp. 4310-4317
-
-
Lee, C.1
Rivera, R.2
Dubin, A.3
-
129
-
-
16644369067
-
Galpha13 mediates a signal that is essential for proliferation and survival of thymocyte progenitors
-
Coffield V, Helms W, Jiang Q, et al. Galpha13 mediates a signal that is essential for proliferation and survival of thymocyte progenitors. J Exp Med 2004;200:1315-24
-
(2004)
J Exp Med
, vol.200
, pp. 1315-1324
-
-
Coffield, V.1
Helms, W.2
Jiang, Q.3
-
130
-
-
0033151694
-
Chimeric G proteins allow a high-throughput signaling assay of Gi-coupled receptors
-
Coward P, Chan S, Wada H, et al. Chimeric G proteins allow a high-throughput signaling assay of Gi-coupled receptors. Anal Biochem 1999;270:242-8
-
(1999)
Anal Biochem
, vol.270
, pp. 242-248
-
-
Coward, P.1
Chan, S.2
Wada, H.3
-
131
-
-
0034509508
-
A fluorescent reporter assay for the detection of ligands acting through Gi protein-coupled receptors
-
Xing H, Tran H, Knapp T, et al. A fluorescent reporter assay for the detection of ligands acting through Gi protein-coupled receptors. J Recept Signal Transduct Res 2000;20:189-210
-
(2000)
J Recept Signal Transduct Res
, vol.20
, pp. 189-210
-
-
Xing, H.1
Tran, H.2
Knapp, T.3
-
132
-
-
0041428225
-
Functional calcium coupling with the human metabotropic glutamate receptor subtypes 2 and 4 by stable co-expression with a calcium pathway facilitating G protein chimera in Chinese hamster ovary cells
-
Kowal D, Nawoschik S, Ochalski R, et al. Functional calcium coupling with the human metabotropic glutamate receptor subtypes 2 and 4 by stable co-expression with a calcium pathway facilitating G protein chimera in Chinese hamster ovary cells. Biochem Pharmacol 2003;66:785-90
-
(2003)
Biochem Pharmacol
, vol.66
, pp. 785-790
-
-
Kowal, D.1
Nawoschik, S.2
Ochalski, R.3
-
133
-
-
12444319927
-
A cell-based microarrayed compound screening format for identifying agonists of G protein-coupled receptors
-
Gopalakrishnan S, Moreland R, Kofron J, et al. A cell-based microarrayed compound screening format for identifying agonists of G protein-coupled receptors. Anal Biochem 2003;321:192-201
-
(2003)
Anal Biochem
, vol.321
, pp. 192-201
-
-
Gopalakrishnan, S.1
Moreland, R.2
Kofron, J.3
-
134
-
-
4043133236
-
Characterization of CHO cells stably expressing a G alpha 16/z chimera for high-throughput screening of GPCRs
-
New D, Wong Y. Characterization of CHO cells stably expressing a G alpha 16/z chimera for high-throughput screening of GPCRs. Assay Drug Dev Technol 2004;2:269-80
-
(2004)
Assay Drug Dev Technol
, vol.2
, pp. 269-280
-
-
New, D.1
Wong, Y.2
-
135
-
-
0242289449
-
Replacement of the alpha5 helix of Galpha16 with Galphas-specific sequences enhances promiscuity of Galpha16 toward Gs-coupled receptors
-
Hazari A, Lowes V, Chan J, et al. Replacement of the alpha5 helix of Galpha16 with Galphas-specific sequences enhances promiscuity of Galpha16 toward Gs-coupled receptors. Cell Signal 2004;16:51-62
-
(2004)
Cell Signal
, vol.16
, pp. 51-62
-
-
Hazari, A.1
Lowes, V.2
Chan, J.3
-
136
-
-
3042711567
-
The receptor-Galpha fusion protein as a tool for ligand screening: A model study using a nociceptin receptor-Galphai2 fusion protein
-
Takeda S, Okada T, Okamura M, et al. The receptor-Galpha fusion protein as a tool for ligand screening: a model study using a nociceptin receptor-Galphai2 fusion protein. J Biochem (Tokyo) 2004;135:597-604
-
(2004)
J Biochem (Tokyo)
, vol.135
, pp. 597-604
-
-
Takeda, S.1
Okada, T.2
Okamura, M.3
-
137
-
-
42949173856
-
-
US Patent, 7,208,279
-
US Patent # 7,208,279
-
-
-
-
138
-
-
33646008247
-
Differential targeting of Gbetagamma-subunit signaling with small molecules
-
Bonacci T, Mathews J, Yuan C, et al. Differential targeting of Gbetagamma-subunit signaling with small molecules. Science 2006;312:443-6
-
(2006)
Science
, vol.312
, pp. 443-446
-
-
Bonacci, T.1
Mathews, J.2
Yuan, C.3
-
140
-
-
33845301393
-
Identification of small-molecule inhibitors of RGS4 using a high-throughput flow cytometry protein interaction assay
-
Roman D, Talbot J, Roof R, et al. Identification of small-molecule inhibitors of RGS4 using a high-throughput flow cytometry protein interaction assay. Mol Pharmacol 2007;71:169-75
-
(2007)
Mol Pharmacol
, vol.71
, pp. 169-175
-
-
Roman, D.1
Talbot, J.2
Roof, R.3
-
141
-
-
33751162165
-
Distinct signaling profiles of beta1 and beta2 adrenergic receptor ligands toward adenylyl cyclase and mitogen-activated protein kinase reveals the pluridimensionality of efficacy
-
Galandrin S, Bouvier M. Distinct signaling profiles of beta1 and beta2 adrenergic receptor ligands toward adenylyl cyclase and mitogen-activated protein kinase reveals the pluridimensionality of efficacy. Mol Pharmacol 2006;70:1575-84
-
(2006)
Mol Pharmacol
, vol.70
, pp. 1575-1584
-
-
Galandrin, S.1
Bouvier, M.2
-
142
-
-
0030843863
-
Examination of the effects of increasing Gs protein on beta2-adrenergic receptor, Gs, and adenylyl cyclase interactions
-
Krumins A, Barber R. Examination of the effects of increasing Gs protein on beta2-adrenergic receptor, Gs, and adenylyl cyclase interactions. Biochem Pharmacol 1997;54:61-72
-
(1997)
Biochem Pharmacol
, vol.54
, pp. 61-72
-
-
Krumins, A.1
Barber, R.2
-
143
-
-
0035064796
-
Activation of guanosine 5′-[gamma-(35)S]thio-triphosphate binding through M(1) muscarinic receptors in transfected Chinese hamster ovary cell membranes; 1. Mathematical analysis of catalytic G protein activation
-
Waelbroeck M. Activation of guanosine 5′-[gamma-(35)S]thio-triphosphate binding through M(1) muscarinic receptors in transfected Chinese hamster ovary cell membranes; 1. Mathematical analysis of catalytic G protein activation. Mol Pharmacol 2001;59:875-85
-
(2001)
Mol Pharmacol
, vol.59
, pp. 875-885
-
-
Waelbroeck, M.1
-
144
-
-
0038540318
-
Biochemical and pharmacological control of the multiplicity of coupling at G protein-coupled receptors
-
Hermans E. Biochemical and pharmacological control of the multiplicity of coupling at G protein-coupled receptors. Pharmacol Ther 2003;99:25-44
-
(2003)
Pharmacol Ther
, vol.99
, pp. 25-44
-
-
Hermans, E.1
-
145
-
-
0031815337
-
Effector pathway-dependent relative efficacy at serotonin type 2A and 2C receptors: Evidence for agonist-directed trafficking of receptor stimulus
-
Berg K, Maayani S, Goldfarb J, et al. Effector pathway-dependent relative efficacy at serotonin type 2A and 2C receptors: evidence for agonist-directed trafficking of receptor stimulus. Mol Pharmacol 1998;54:94-104
-
(1998)
Mol Pharmacol
, vol.54
, pp. 94-104
-
-
Berg, K.1
Maayani, S.2
Goldfarb, J.3
-
146
-
-
0032579002
-
D-Arg1,D-Phe5,D-Trp7,9,Leu11] Substance P acts as a biased agonist toward neuropeptide and chemokine receptors
-
Jarpe M, Knall C, Mitchell F, et al. [D-Arg1,D-Phe5,D-Trp7,9,Leu11] Substance P acts as a biased agonist toward neuropeptide and chemokine receptors. J Biol Chem 1998;273:3097-104
-
(1998)
J Biol Chem
, vol.273
, pp. 3097-3104
-
-
Jarpe, M.1
Knall, C.2
Mitchell, F.3
-
147
-
-
22944487986
-
Multiple signaling states of G protein-coupled receptors
-
Perez D, Karnik S. Multiple signaling states of G protein-coupled receptors. Pharmacol Rev 2005;57:147-61
-
(2005)
Pharmacol Rev
, vol.57
, pp. 147-161
-
-
Perez, D.1
Karnik, S.2
-
148
-
-
33845311870
-
Ligand-specific receptor states: Implications for opiate receptor signaling and regulation
-
Pineyro G, Archer-Lahlou E. Ligand-specific receptor states: implications for opiate receptor signaling and regulation. Cell Signal 2007;19:8-19
-
(2007)
Cell Signal
, vol.19
, pp. 8-19
-
-
Pineyro, G.1
Archer-Lahlou, E.2
-
149
-
-
34447633368
-
Conformational complexity of G protein-coupled receptors
-
Kobilka B, Deupi X. Conformational complexity of G protein-coupled receptors. Trends Pharmacol Sci 2007;28:397-406
-
(2007)
Trends Pharmacol Sci
, vol.28
, pp. 397-406
-
-
Kobilka, B.1
Deupi, X.2
-
150
-
-
0037794320
-
Predicting therapeutic value in the lead optimization phase of drug discovery
-
Kenakin T. Predicting therapeutic value in the lead optimization phase of drug discovery. Nat Rev Drug Discov 2003;2:429-38
-
(2003)
Nat Rev Drug Discov
, vol.2
, pp. 429-438
-
-
Kenakin, T.1
-
151
-
-
33744460736
-
Role of beta-adrenergic receptor signaling and desensitization in heart failure: New concepts and prospects for treatment
-
Tilley D, Rockman H. Role of beta-adrenergic receptor signaling and desensitization in heart failure: new concepts and prospects for treatment. Expert Rev Cardiovasc Ther 2006;4:417-32
-
(2006)
Expert Rev Cardiovasc Ther
, vol.4
, pp. 417-432
-
-
Tilley, D.1
Rockman, H.2
-
152
-
-
0141618295
-
Enhanced G(i) signaling selectively negates beta2-adrenergic receptor (AR)-but not beta1-AR-mediated positive inotropic effect in myocytes from failing rat hearts
-
Xiao R, Zhang S, Chakir K, et al. Enhanced G(i) signaling selectively negates beta2-adrenergic receptor (AR)-but not beta1-AR-mediated positive inotropic effect in myocytes from failing rat hearts. Circulation 2003;108:1633-9
-
(2003)
Circulation
, vol.108
, pp. 1633-1639
-
-
Xiao, R.1
Zhang, S.2
Chakir, K.3
-
153
-
-
0345735773
-
Agonist and inverse agonist actions of beta-blockers at the human beta 2-adrenoceptor provide evidence for agonist-directed signaling
-
Baker J, Hall I, Hill S. Agonist and inverse agonist actions of beta-blockers at the human beta 2-adrenoceptor provide evidence for agonist-directed signaling. Mol Pharmacol 2003;64:1357-69
-
(2003)
Mol Pharmacol
, vol.64
, pp. 1357-1369
-
-
Baker, J.1
Hall, I.2
Hill, S.3
-
154
-
-
33645534801
-
Agonist-specific activation of the beta2-adrenoceptor/Gs-protein and beta2-adrenoceptor/ Gi-protein pathway in adult rat ventricular cardiomyocytes
-
Ponicke K, Groner F, Heinroth-Hoffmann I, et al. Agonist-specific activation of the beta2-adrenoceptor/Gs-protein and beta2-adrenoceptor/ Gi-protein pathway in adult rat ventricular cardiomyocytes. Br J Pharmacol 2006;147:714-9
-
(2006)
Br J Pharmacol
, vol.147
, pp. 714-719
-
-
Ponicke, K.1
Groner, F.2
Heinroth-Hoffmann, I.3
-
155
-
-
33847045132
-
Aberrant GPCR expression is a sufficient genetic event to trigger adrenocortical tumorigenesis
-
Mazzuco T, Chabre O, Feige J, et al. Aberrant GPCR expression is a sufficient genetic event to trigger adrenocortical tumorigenesis. Mol Cell Endocrinol 2007;265-266:23-8
-
(2007)
Mol Cell Endocrinol
-
-
Mazzuco, T.1
Chabre, O.2
Feige, J.3
-
156
-
-
33644662506
-
Overexpression of G protein-coupled receptors in cancer cells: Involvement in tumor progression
-
Li S, Huang S, Peng S. Overexpression of G protein-coupled receptors in cancer cells: involvement in tumor progression. Int J Oncol 2005;27:1329-39
-
(2005)
Int J Oncol
, vol.27
, pp. 1329-1339
-
-
Li, S.1
Huang, S.2
Peng, S.3
-
157
-
-
34247388037
-
Protease-activated receptor signaling, endocytic sorting and dysregulation in cancer
-
Arora P, Ricks T, Trejo J. Protease-activated receptor signaling, endocytic sorting and dysregulation in cancer. J Cell Sci 2007;120:921-8
-
(2007)
J Cell Sci
, vol.120
, pp. 921-928
-
-
Arora, P.1
Ricks, T.2
Trejo, J.3
-
158
-
-
33747149560
-
Protease-activated receptor-2 simultaneously directs beta-arrestin-1-dependent inhibition and Galphaq-dependent activation of phosphatidylinositol 3-kinase
-
Wang P, DeFea K. Protease-activated receptor-2 simultaneously directs beta-arrestin-1-dependent inhibition and Galphaq-dependent activation of phosphatidylinositol 3-kinase. Biochemistry 2006;45:9374-85
-
(2006)
Biochemistry
, vol.45
, pp. 9374-9385
-
-
Wang, P.1
DeFea, K.2
-
159
-
-
30144437010
-
Emerging concepts in GPCR function-the influence of cell phenotype on GPCR pharmacology
-
Eglen R. Emerging concepts in GPCR function-the influence of cell phenotype on GPCR pharmacology. Proc West Pharmacol Soc 2005;48:31-4
-
(2005)
Proc West Pharmacol Soc
, vol.48
, pp. 31-34
-
-
Eglen, R.1
-
160
-
-
33846909764
-
Phenotypic' pharmacology: The influence of cellular environment on G protein-coupled receptor antagonist and inverse agonist pharmacology
-
Nelson C, Challiss R. 'Phenotypic' pharmacology: the influence of cellular environment on G protein-coupled receptor antagonist and inverse agonist pharmacology. Biochem Pharmacol 2007;73:737-51
-
(2007)
Biochem Pharmacol
, vol.73
, pp. 737-751
-
-
Nelson, C.1
Challiss, R.2
-
161
-
-
34247120946
-
Phosphorylation and regulation of a G protein-coupled receptor by protein kinase CK2
-
Torrecilla I, Spragg E, Poulin B, et al. Phosphorylation and regulation of a G protein-coupled receptor by protein kinase CK2. J Cell Biol 2007;177:127-37
-
(2007)
J Cell Biol
, vol.177
, pp. 127-137
-
-
Torrecilla, I.1
Spragg, E.2
Poulin, B.3
-
162
-
-
0031434924
-
Differences between natural and recombinant G protein-coupled receptor systems with varying receptor/G protein stoichiometry
-
Kenakin T. Differences between natural and recombinant G protein-coupled receptor systems with varying receptor/G protein stoichiometry. Trends Pharmacol Sci 1997;18:456-64
-
(1997)
Trends Pharmacol Sci
, vol.18
, pp. 456-464
-
-
Kenakin, T.1
-
163
-
-
0037183742
-
Quantitative stoichiometry of G proteins activated by mu-opioid receptors in postmortem human brain
-
Gonzalez-Maeso J, Rodriguez-Puertas R, Meana J. Quantitative stoichiometry of G proteins activated by mu-opioid receptors in postmortem human brain. Eur J Pharmacol 2002;452:21-33
-
(2002)
Eur J Pharmacol
, vol.452
, pp. 21-33
-
-
Gonzalez-Maeso, J.1
Rodriguez-Puertas, R.2
Meana, J.3
-
164
-
-
34547434085
-
Monomeric G protein-coupled receptor rhodopsin in solution activates its G protein transducin at the diffusion limit
-
Ernst O, Gramse V, Kolbe M, et al. Monomeric G protein-coupled receptor rhodopsin in solution activates its G protein transducin at the diffusion limit. Proc Natl Acad Sci USA 2007;104:10859-64
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 10859-10864
-
-
Ernst, O.1
Gramse, V.2
Kolbe, M.3
-
165
-
-
34547124343
-
Signaling through a G protein-coupled receptor and its corresponding G protein follows a stoichiometrically limited model
-
Philip F, Sengupta P, Scarlata S. Signaling through a G protein-coupled receptor and its corresponding G protein follows a stoichiometrically limited model. J Biol Chem 2007;282:19203-16
-
(2007)
J Biol Chem
, vol.282
, pp. 19203-19216
-
-
Philip, F.1
Sengupta, P.2
Scarlata, S.3
-
166
-
-
0032714409
-
Efficient functional coupling of the human D3 dopamine receptor to G(o) subtype of G proteins in SH-SY5Y cells
-
Zaworski P, Alberts G, Pregenzer J, et al. Efficient functional coupling of the human D3 dopamine receptor to G(o) subtype of G proteins in SH-SY5Y cells. Br J Pharmacol 1999;128:1181-8
-
(1999)
Br J Pharmacol
, vol.128
, pp. 1181-1188
-
-
Zaworski, P.1
Alberts, G.2
Pregenzer, J.3
-
167
-
-
0029787046
-
Agonist-induced modulation of inverse agonist efficacy at the beta 2-adrenergic receptor
-
Chidiac P, Nouet S, Bouvier M. Agonist-induced modulation of inverse agonist efficacy at the beta 2-adrenergic receptor. Mol Pharmacol 1996;50:662-9
-
(1996)
Mol Pharmacol
, vol.50
, pp. 662-669
-
-
Chidiac, P.1
Nouet, S.2
Bouvier, M.3
-
168
-
-
11244352269
-
Reciprocal regulation of agonist and inverse agonist signaling efficacy upon short-term treatment of the human delta-opioid receptor with an inverse agonist
-
Pineyro G, Azzi M, deLean A, et al. Reciprocal regulation of agonist and inverse agonist signaling efficacy upon short-term treatment of the human delta-opioid receptor with an inverse agonist. Mol Pharmacol 2005;67:336-48
-
(2005)
Mol Pharmacol
, vol.67
, pp. 336-348
-
-
Pineyro, G.1
Azzi, M.2
deLean, A.3
-
169
-
-
34247507644
-
Protean agonism at the dopamine D2 receptor: (S)-3-(3-hydroxyphenyl)-N-propylpiperidine is an agonist for activation of Go1 but an antagonist/inverse agonist for Gi1,Gi2, and Gi3
-
Lane J, Powney B, Wise A, et al. Protean agonism at the dopamine D2 receptor: (S)-3-(3-hydroxyphenyl)-N-propylpiperidine is an agonist for activation of Go1 but an antagonist/inverse agonist for Gi1,Gi2, and Gi3. Mol Pharmacol 2007;71:1349-59
-
(2007)
Mol Pharmacol
, vol.71
, pp. 1349-1359
-
-
Lane, J.1
Powney, B.2
Wise, A.3
-
170
-
-
33744957160
-
Distinct beta-arrestin- and G protein-dependent pathways for parathyroid hormone receptor-stimulated ERK1/2 activation
-
Gesty-Palmer D, Chen M, Reiter E, et al. Distinct beta-arrestin- and G protein-dependent pathways for parathyroid hormone receptor-stimulated ERK1/2 activation. J Biol Chem 2006;281:10856-64
-
(2006)
J Biol Chem
, vol.281
, pp. 10856-10864
-
-
Gesty-Palmer, D.1
Chen, M.2
Reiter, E.3
-
171
-
-
0035958925
-
Bombesin and substance P analogs differentially regulate G protein coupling to the bombesin receptor. Direct evidence for biased agonism
-
MacKinnon A, Waters C, Jodrell D, et al. Bombesin and substance P analogs differentially regulate G protein coupling to the bombesin receptor. Direct evidence for biased agonism. J Biol Chem 2001;276:28083-91
-
(2001)
J Biol Chem
, vol.276
, pp. 28083-28091
-
-
MacKinnon, A.1
Waters, C.2
Jodrell, D.3
-
172
-
-
34250714898
-
Oxyntomodulin differentially affects glucagon-like peptide-1 receptor beta-arrestin recruitment and signaling through Galpha(s)
-
Jorgensen R, Kubale V, Vrecl M, et al. Oxyntomodulin differentially affects glucagon-like peptide-1 receptor beta-arrestin recruitment and signaling through Galpha(s). J Pharmacol Exp Ther 2007;322:148-54
-
(2007)
J Pharmacol Exp Ther
, vol.322
, pp. 148-154
-
-
Jorgensen, R.1
Kubale, V.2
Vrecl, M.3
-
173
-
-
33846456218
-
An opioid agonist that does not induce micro-opioid receptor-arrestin interactions or receptor internalization
-
Groer C, Tidgewell K, Moyer R, et al. An opioid agonist that does not induce micro-opioid receptor-arrestin interactions or receptor internalization. Mol Pharmacol 2007;71:549-57
-
(2007)
Mol Pharmacol
, vol.71
, pp. 549-557
-
-
Groer, C.1
Tidgewell, K.2
Moyer, R.3
-
174
-
-
19944426642
-
Comparison of pharmacological activities of three distinct ligands (Salvinorin A, TRK-820 and 3FLB) on opioid receptors in vitro and their antipruritic and antinociceptive activities in vivo
-
Wang Y, Tang K, Inan S, et al. Comparison of pharmacological activities of three distinct ligands (Salvinorin A, TRK-820 and 3FLB) on opioid receptors in vitro and their antipruritic and antinociceptive activities in vivo. J Pharmacol Exp Ther 2005;312:220-30
-
(2005)
J Pharmacol Exp Ther
, vol.312
, pp. 220-230
-
-
Wang, Y.1
Tang, K.2
Inan, S.3
-
175
-
-
34247351122
-
The angiotensin type 1 receptor activates extracellular signal-regulated kinases 1 and 2 by G protein-dependent and -independent pathways in cardiac myocytes and langendorff-perfused hearts
-
Aplin M, Christensen G, Schneider M, et al. The angiotensin type 1 receptor activates extracellular signal-regulated kinases 1 and 2 by G protein-dependent and -independent pathways in cardiac myocytes and langendorff-perfused hearts. Basic Clin Pharmacol Toxicol 2007;100:289-95
-
(2007)
Basic Clin Pharmacol Toxicol
, vol.100
, pp. 289-295
-
-
Aplin, M.1
Christensen, G.2
Schneider, M.3
-
177
-
-
0033663775
-
The use of stimulus-biased assay systems to detect agonist-specific receptor active states: Implications for the trafficking of receptor stimulus by agonists
-
Watson C, Chen G, Irving P, et al. The use of stimulus-biased assay systems to detect agonist-specific receptor active states: implications for the trafficking of receptor stimulus by agonists. Mol Pharmacol 2000;58:1230-8
-
(2000)
Mol Pharmacol
, vol.58
, pp. 1230-1238
-
-
Watson, C.1
Chen, G.2
Irving, P.3
-
178
-
-
21744437960
-
Chemically distinct ligands promote differential CB1 cannabinoid receptor-Gi protein interactions
-
Mukhopadhyay S, Howlett A. Chemically distinct ligands promote differential CB1 cannabinoid receptor-Gi protein interactions. Mol Pharmacol 2005;67:2016-24
-
(2005)
Mol Pharmacol
, vol.67
, pp. 2016-2024
-
-
Mukhopadhyay, S.1
Howlett, A.2
-
179
-
-
18144422077
-
The oxytocin receptor antagonist atosiban inhibits cell growth via a 'biased agonist' mechanism
-
Reversi A, Rimoldi V, Marrocco T, et al. The oxytocin receptor antagonist atosiban inhibits cell growth via a 'biased agonist' mechanism. J Biol Chem 2005;280:16311-8
-
(2005)
J Biol Chem
, vol.280
, pp. 16311-16318
-
-
Reversi, A.1
Rimoldi, V.2
Marrocco, T.3
-
180
-
-
34447566050
-
Achieving signaling selectivity of ligands for the corticotropin-releasing factor type 1 receptor by modifying the agonist's signaling domain
-
Beyermann M, Heinrich N, Fechner K, et al. Achieving signaling selectivity of ligands for the corticotropin-releasing factor type 1 receptor by modifying the agonist's signaling domain. Br J Pharmacol 2007;151:851-9
-
(2007)
Br J Pharmacol
, vol.151
, pp. 851-859
-
-
Beyermann, M.1
Heinrich, N.2
Fechner, K.3
-
181
-
-
0035070287
-
-
Kukkonen J, Jansson C, Akerman K. Agonist trafficking of G(i/o)-mediated alpha(2A)-adrenoceptor responses in HEL 92.1.7 cells. Br J Pharmacol 2001;132:1477-84
-
Kukkonen J, Jansson C, Akerman K. Agonist trafficking of G(i/o)-mediated alpha(2A)-adrenoceptor responses in HEL 92.1.7 cells. Br J Pharmacol 2001;132:1477-84
-
-
-
-
182
-
-
0038069031
-
Regulation of activator protein-1 by 8-iso-prostaglandin E2 in a thromboxane A2 receptor-dependent and -independent manner
-
Weber T, Markillie L. Regulation of activator protein-1 by 8-iso-prostaglandin E2 in a thromboxane A2 receptor-dependent and -independent manner. Mol Pharmacol 2003;63:1075-81
-
(2003)
Mol Pharmacol
, vol.63
, pp. 1075-1081
-
-
Weber, T.1
Markillie, L.2
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