-
1
-
-
77957055780
-
Integrated methods for the construction of three-dimensional models and computational probing of structure-function relations in G protein-coupled receptors
-
Ballesteros JA and Weinstein H (1995) Integrated methods for the construction of three-dimensional models and computational probing of structure-function relations in G protein-coupled receptors. Methods Neurosci 25:366-428.
-
(1995)
Methods Neurosci
, vol.25
, pp. 366-428
-
-
Ballesteros, J.A.1
Weinstein, H.2
-
2
-
-
0031815337
-
Effector pathway-dependent relative efficacy at serotonin type 2A and 2C receptors: Evidence for agonist-directed trafficking of receptor stimulus
-
Berg KA, Maayani S, Goldfarb J, Scaramellini C, Leff P, and Clarke WP (1998) Effector pathway-dependent relative efficacy at serotonin type 2A and 2C receptors: evidence for agonist-directed trafficking of receptor stimulus. Mol Pharmacol 54:94-104. (Pubitemid 28337591)
-
(1998)
Molecular Pharmacology
, vol.54
, Issue.1
, pp. 94-104
-
-
Berg, K.A.1
Maayani, S.2
Goldfarb, J.3
Scaramellini, C.4
Leff, P.5
Clarke, W.P.6
-
3
-
-
44049086134
-
Ligand-stabilized conformational states of human beta(2) adrenergic receptor: Insight into G-protein-coupled receptor activation
-
Bhattacharya S, Hall SE, Li H, and Vaidehi N (2008a) Ligand-stabilized conformational states of human beta(2) adrenergic receptor: insight into G-protein-coupled receptor activation. Biophys J 94:2027-2042.
-
(2008)
Biophys J
, vol.94
, pp. 2027-2042
-
-
Bhattacharya, S.1
Hall, S.E.2
Li, H.3
Vaidehi, N.4
-
4
-
-
50149116588
-
Agonist-induced conformational changes in bovine rhodopsin: Insight into activation of G-protein-coupled receptors
-
Bhattacharya S, Hall SE, and Vaidehi N (2008b) Agonist-induced conformational changes in bovine rhodopsin: insight into activation of G-protein-coupled receptors. J Mol Biol 382:539-555.
-
(2008)
J Mol Biol
, vol.382
, pp. 539-555
-
-
Bhattacharya, S.1
Hall, S.E.2
Vaidehi, N.3
-
5
-
-
77955662759
-
Allosteric antagonist binding sites in class B GPCRs: Corticotropin receptor 1
-
Bhattacharya S, Subramanian G, Hall S, Lin J, Laoui A, and Vaidehi N (2010) Allosteric antagonist binding sites in class B GPCRs: corticotropin receptor 1. J Comput Aided Mol Des 24:659-674.
-
(2010)
J Comput Aided Mol des
, vol.24
, pp. 659-674
-
-
Bhattacharya, S.1
Subramanian, G.2
Hall, S.3
Lin, J.4
Laoui, A.5
Vaidehi, N.6
-
6
-
-
77950823494
-
Computational mapping of the conformational transitions in agonist selective pathways of a G-protein coupled receptor
-
Bhattacharya S and Vaidehi N (2010) Computational mapping of the conformational transitions in agonist selective pathways of a G-protein coupled receptor. J Am Chem Soc 132:5205-5214.
-
(2010)
J Am Chem Soc
, vol.132
, pp. 5205-5214
-
-
Bhattacharya, S.1
Vaidehi, N.2
-
7
-
-
0025298537
-
1 full agonist
-
DOI 10.1021/jm00168a034
-
Brewster WK, Nichols DE, Riggs RM, Mottola DM, Lovenberg TW, Lewis MH, and Mailman RB (1990) trans-10,11-dihydroxy-5,6,6a,7,8,12b-hexahydrobenzo[a-] phenanthridine: a highly potent selective dopamine D1 full agonist. J Med Chem 33:1756-1764. (Pubitemid 20180639)
-
(1990)
Journal of Medicinal Chemistry
, vol.33
, Issue.6
, pp. 1756-1764
-
-
Brewster, W.K.1
Nichols, D.E.2
Riggs, R.M.3
Mottola, D.M.4
Lovenberg, T.W.5
Lewis, M.H.6
Mailman, R.B.7
-
8
-
-
58149521948
-
Rapid, semi-automated, and inexpensive radioimmunoassay of cAMP: Application in GPCR-mediated adenylate cyclase assays
-
Brown JT, Kant A, and Mailman RB (2009) Rapid, semi-automated, and inexpensive radioimmunoassay of cAMP: application in GPCR-mediated adenylate cyclase assays. J Neurosci Methods 177:261-266.
-
(2009)
J Neurosci Methods
, vol.177
, pp. 261-266
-
-
Brown, J.T.1
Kant, A.2
Mailman, R.B.3
-
9
-
-
0037406075
-
Cyclic coordinate descent: A robotics algorithm for protein loop closure
-
DOI 10.1110/ps.0242703
-
Canutescu AA and Dunbrack RL, Jr. (2003) Cyclic coordinate descent: A robotics algorithm for protein loop closure. Protein Sci 12:963-972. (Pubitemid 36505431)
-
(2003)
Protein Science
, vol.12
, Issue.5
, pp. 963-972
-
-
Canutescu, A.A.1
Dunbrack Jr., R.L.2
-
10
-
-
0024425450
-
1 dopamine receptor ligands
-
Charifson PS, Bowen JP, Wyrick SD, Hoffman AJ, Cory M, McPhail AT, and Mailman RB (1989) Conformational analysis and molecular modeling of 1-phenyl-, 4-phenyl-, and 1-benzyl-1,2,3,4-tetrahydroisoquinolines as D1 dopamine receptor ligands. J Med Chem 32:2050-2058. (Pubitemid 19224165)
-
(1989)
Journal of Medicinal Chemistry
, vol.32
, Issue.9
, pp. 2050-2058
-
-
Charifson, P.S.1
Bowen, J.P.2
Wyrick, S.D.3
Hoffman, A.J.4
Cory, M.5
McPhail, A.T.6
Mailman, R.B.7
-
11
-
-
0015861774
-
Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction
-
Cheng Y and Prusoff WH (1973) Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction. Biochem Pharmacol 22:3099-3108.
-
(1973)
Biochem Pharmacol
, vol.22
, pp. 3099-3108
-
-
Cheng, Y.1
Prusoff, W.H.2
-
13
-
-
0025788143
-
Behavioral effects in the rat of dihydrexidine, a high-potency, full-efficacy D1 dopamine receptor agonist
-
Darney KJ Jr, Lewis MH, Brewster WK, Nichols DE, and Mailman RB (1991) Behavioral effects in the rat of dihydrexidine, a high-potency, full-efficacy D1 dopamine receptor agonist. Neuropsychopharmacology 5:187-195.
-
(1991)
Neuropsychopharmacology
, vol.5
, pp. 187-195
-
-
Darney Jr., K.J.1
Lewis, M.H.2
Brewster, W.K.3
Nichols, D.E.4
Mailman, R.B.5
-
14
-
-
0347383758
-
MODELLER: Generation and Refinement of Homology-Based Protein Structure Models
-
DOI 10.1016/S0076-6879(03)74020-8
-
Fiser A and Sali A (2003) Modeller: generation and refinement of homology-based protein structure models. Methods Enzymol 374:461-491. (Pubitemid 37531821)
-
(2003)
Methods in Enzymology
, vol.374
, pp. 461-491
-
-
Fiser, A.1
Sali, A.2
-
15
-
-
3042630989
-
2L cell line: Evidence for induction of ligand-specific receptor states
-
DOI 10.1124/mol.66.1.97
-
Gay EA, Urban JD, Nichols DE, Oxford GS, and Mailman RB (2004) Functional selectivity of D2 receptor ligands in a Chinese hamster ovary hD2L cell line: evidence for induction of ligand-specific receptor states. Mol Pharmacol 66:97-105. (Pubitemid 38822091)
-
(2004)
Molecular Pharmacology
, vol.66
, Issue.1
, pp. 97-105
-
-
Gay, E.A.1
Urban, J.D.2
Nichols, D.E.3
Oxford, G.S.4
Mailman, R.B.5
-
16
-
-
0035816704
-
Functionally different agonists induce distinct conformations in the G protein coupling domain of the beta 2 adrenergic receptor
-
Ghanouni P, Gryczynski Z, Steenhuis JJ, Lee TW, Farrens DL, Lakowicz JR, and Kobilka BK (2001) Functionally different agonists induce distinct conformations in the G protein coupling domain of the beta 2 adrenergic receptor. J Biol Chem 276:24433-24436.
-
(2001)
J Biol Chem
, vol.276
, pp. 24433-24436
-
-
Ghanouni, P.1
Gryczynski, Z.2
Steenhuis, J.J.3
Lee, T.W.4
Farrens, D.L.5
Lakowicz, J.R.6
Kobilka, B.K.7
-
17
-
-
0029664618
-
1 agonist containing a rigid beta-phenyldopamine pharmacophore
-
DOI 10.1021/jm950707+
-
Ghosh D, Snyder SE, Watts VJ, Mailman RB, and Nichols DE (1996) 9-Dihydroxy-2,3,7,11b-tetrahydro-1H-naph[1,2,3-de]isoquinoline: a potent full dopamine D1 agonist containing a rigid-beta-phenyldopamine pharmacophore. J Med Chem 39:549-555. (Pubitemid 26041467)
-
(1996)
Journal of Medicinal Chemistry
, vol.39
, Issue.2
, pp. 549-555
-
-
Ghosh, D.1
Snyder, S.E.2
Watts, V.J.3
Mailman, R.B.4
Nichols, D.E.5
-
18
-
-
1542301679
-
8,9-Dihydroxy-1,2,3,11b-tetrahydrochromeno[4,3,2,-de]isoquinoline (dinoxyline), a high affinity and potent agonist at all dopamine receptor isoforms
-
DOI 10.1016/j.bmc.2004.01.008, PII S0968089604000410
-
Grubbs RA, Lewis MM, Owens-Vance C, Gay EA, Jassen AK, Mailman RB, and Nichols DE (2004) 8,9-dihydroxy-1,2,3,11b-tetrahydrochromeno[4,3,2,-de] isoquinoline (dinoxyline), a high affinity and potent agonist at all dopamine receptor isoforms. Bioorg Med Chem 12:1403-1412. (Pubitemid 38296531)
-
(2004)
Bioorganic and Medicinal Chemistry
, vol.12
, Issue.6
, pp. 1403-1412
-
-
Grubbs, R.A.1
Lewis, M.M.2
Owens-Vance, C.3
Gay, E.A.4
Jassen, A.K.5
Mailman, R.B.6
Nichols, D.E.7
-
20
-
-
0016820947
-
Femtomole sensitive radioimmunoassay for cyclic AMP and cyclic GMP after 2′0 acetylation by acetic anhydride in aqueous solution
-
Harper JF and Brooker G (1975) Femtomole sensitive radioimmunoassay for cyclic AMP and cyclic GMP after 2′0 acetylation by acetic anhydride in aqueous solution. J Cyclic Nucleotide Res 1:207-218.
-
(1975)
J Cyclic Nucleotide Res
, vol.1
, pp. 207-218
-
-
Harper, J.F.1
Brooker, G.2
-
21
-
-
0029054965
-
Agonist-receptor efficacy. II. Agonist trafficking of receptor signals
-
Kenakin T (1995) Agonist-receptor efficacy. II. Agonist trafficking of receptor signals. Trends Pharmacol Sci 16:232-238.
-
(1995)
Trends Pharmacol Sci
, vol.16
, pp. 232-238
-
-
Kenakin, T.1
-
22
-
-
36348946976
-
Functional Selectivity through Protean and Biased Agonism: Who Steers the Ship?
-
Kenakin TP (2007) Functional Selectivity through Protean and Biased Agonism: Who Steers the Ship? Mol Pharmacol.
-
(2007)
Mol Pharmacol
-
-
Kenakin, T.P.1
-
23
-
-
0036267278
-
2L receptor-transfected MN9D cells and pituitary lactotrophs
-
DOI 10.1124/jpet.301.3.1179
-
Kilts JD, Connery HS, Arrington EG, Lewis MM, Lawler CP, Oxford GS, O'Malley KL, Todd RD, Blake BL, Nichols DE, et al. (2002) Functional selectivity of dopamine receptor agonists. II. Actions of dihydrexidine in D2L receptor-transfected MN9D cells and pituitary lactotrophs. J Pharmacol Exp Ther 301:1179-1189. (Pubitemid 34595112)
-
(2002)
Journal of Pharmacology and Experimental Therapeutics
, vol.301
, Issue.3
, pp. 1179-1189
-
-
Kilts, J.D.1
Connery, H.S.2
Arrington, E.G.3
Lewis, M.M.4
Lawler, C.P.5
Oxford, G.S.6
O'Malley, K.L.7
Todd, R.D.8
Blake, B.L.9
Nichols, D.E.10
Mailman, R.B.11
-
24
-
-
58849164925
-
A dopamine D2 receptor mutant capable of G protein-mediated signaling but deficient in arrestin binding
-
Lan H, Liu Y, Bell MI, Gurevich VV, and Neve KA (2009a) A dopamine D2 receptor mutant capable of G protein-mediated signaling but deficient in arrestin binding. Mol Pharmacol 75:113-123.
-
(2009)
Mol Pharmacol
, vol.75
, pp. 113-123
-
-
Lan, H.1
Liu, Y.2
Bell, M.I.3
Gurevich, V.V.4
Neve, K.A.5
-
25
-
-
58849087235
-
An intracellular loop 2 amino acid residue determines differential binding of arrestin to the dopamine D2 and D3 receptors
-
Lan H, Teeter MM, Gurevich VV, and Neve KA (2009b) An intracellular loop 2 amino acid residue determines differential binding of arrestin to the dopamine D2 and D3 receptors. Mol Pharmacol 75:19-26.
-
(2009)
Mol Pharmacol
, vol.75
, pp. 19-26
-
-
Lan, H.1
Teeter, M.M.2
Gurevich, V.V.3
Neve, K.A.4
-
26
-
-
0033151286
-
Interactions of the novel antipsychotic aripiprazole (OPC-14597) with dopamine and serotonin receptor subtypes
-
DOI 10.1016/S0893-133X(98)00099-2, PII S0893133X98000992
-
Lawler CP, Prioleau C, Lewis MM, Mak C, Jiang D, Schetz JA, Gonzalez AM, Sibley DR, and Mailman RB (1999) Interactions of the novel antipsychotic aripiprazole (OPC-14597) with dopamine and serotonin receptor subtypes. Neuropsychopharmacology 20:612-627. (Pubitemid 29189265)
-
(1999)
Neuropsychopharmacology
, vol.20
, Issue.6
, pp. 612-627
-
-
Lawler, C.P.1
Prioleau, C.2
Lewis, M.M.3
Mak, C.4
Jiang, D.5
Schetz, J.A.6
Gonzalez, A.M.7
Sibley, D.R.8
Mailman, R.B.9
-
27
-
-
0006135337
-
Discrete functional selectivity of drugs: OPC-14597. A selective antagonist for post-synaptic dopamine D2 receptors
-
Abstract
-
Lawler CP, Watts VJ, Booth RG, Southerland SB, and Mailman RB (1994) Discrete functional selectivity of drugs: OPC-14597. A selective antagonist for post-synaptic dopamine D2 receptors (Abstract). Soc Neurosci Abstr 20:525.
-
(1994)
Soc Neurosci Abstr
, vol.20
, pp. 525
-
-
Lawler, C.P.1
Watts, V.J.2
Booth, R.G.3
Southerland, S.B.4
Mailman, R.B.5
-
28
-
-
0024397451
-
Dihydrexidine, a novel selective high potency full dopamine D-1 receptor agonist
-
Lovenberg TW, Brewster WK, Mottola DM, Lee RC, Riggs RM, Nichols DE, Lewis MH, and Mailman RB (1989) Dihydrexidine, a novel selective high potency full dopamine D-1 receptor agonist. Eur J Pharmacol 166:111-113. (Pubitemid 19183821)
-
(1989)
European Journal of Pharmacology
, vol.166
, Issue.1
, pp. 111-113
-
-
Lovenberg, T.W.1
Brewster, W.K.2
Mottola, D.M.3
Lee, R.C.4
Riggs, R.M.5
Nichols, D.E.6
Lewis, M.H.7
Mailman, R.B.8
-
29
-
-
34447626644
-
GPCR functional selectivity has therapeutic impact
-
Mailman RB (2007) GPCR functional selectivity has therapeutic impact. Trends Pharmacol Sci 28:390-396.
-
(2007)
Trends Pharmacol Sci
, vol.28
, pp. 390-396
-
-
Mailman, R.B.1
-
30
-
-
0026940770
-
Site-directed mutagenesis of the human dopamine D2 receptor
-
Mansour A, Meng F, Meador-Woodruff JH, Taylor LP, Civelli O, and Akil H (1992) Site-directed mutagenesis of the human dopamine D2 receptor. Eur J Pharmacol 227:205-214.
-
(1992)
Eur J Pharmacol
, vol.227
, pp. 205-214
-
-
Mansour, A.1
Meng, F.2
Meador-Woodruff, J.H.3
Taylor, L.P.4
Civelli, O.5
Akil, H.6
-
31
-
-
0028304962
-
Satisfying hydrogen bonding potential in proteins
-
DOI 10.1006/jmbi.1994.1334
-
McDonald IK and Thornton JM (1994) Satisfying hydrogen bonding potential in proteins. J Mol Biol 238:777-793. (Pubitemid 24168633)
-
(1994)
Journal of Molecular Biology
, vol.238
, Issue.5
, pp. 777-793
-
-
McDonald, I.K.1
Thornton, J.M.2
-
34
-
-
0036260826
-
2 receptors linked to adenylate cyclase
-
DOI 10.1124/jpet.301.3.1166
-
Mottola DM, Kilts JD, Lewis MM, Connery HS, Walker QD, Jones SR, Booth RG, Hyslop DK, Piercey M, Wightman RM, et al. (2002) Functional selectivity of dopamine receptor agonists. I. Selective activation of postsynaptic dopamine D2 receptors linked to adenylate cyclase. J Pharmacol Exp Ther 301:1166-1178. (Pubitemid 34595111)
-
(2002)
Journal of Pharmacology and Experimental Therapeutics
, vol.301
, Issue.3
, pp. 1166-1178
-
-
Mottola, D.M.1
Kilts, J.D.2
Lewis, M.M.3
Connory, H.S.4
Walker, Q.D.5
Jones, S.R.6
Booth, R.G.7
Hyslop, D.K.8
Piercey, M.9
Wightman, R.M.10
Lawler, C.P.11
Nichols, D.E.12
Mailman, R.B.13
-
35
-
-
0029664313
-
1 dopamine receptor agonists: Pharmacophore assessment and receptor mapping
-
DOI 10.1021/jm9502100
-
Mottola DM, Laiter S, Watts VJ, Tropsha A, Wyrick SD, Nichols DE, and Mailman RB (1996) Conformational analysis of D1 dopamine receptor agonists: pharmacophore assessment and receptor mapping. J Med Chem 39:285-296. (Pubitemid 26027034)
-
(1996)
Journal of Medicinal Chemistry
, vol.39
, Issue.1
, pp. 285-296
-
-
Mottola, D.M.1
Laiter, S.2
Watts, V.J.3
Tropsha, A.4
Wyrick, S.D.5
Nichols, D.E.6
Mailman, R.B.7
-
37
-
-
0000180858
-
The development of novel dopamine agonists
-
Kaiser C and Kebabian JW eds American Chemical Society, Washington DC
-
Nichols DE (1983) The development of novel dopamine agonists, in Dopamine Receptors (Kaiser C and Kebabian JW eds) pp 201-218, American Chemical Society, Washington DC.
-
(1983)
Dopamine Receptors
, pp. 201-218
-
-
Nichols, D.E.1
-
38
-
-
25144499754
-
1 receptor agonists
-
DOI 10.1124/mol.105.012153
-
Ryman-Rasmussen JP, Nichols DE, and Mailman RB (2005) Differential activation of adenylate cyclase and receptor internalization by novel dopamine D1 receptor agonists. Mol Pharmacol 68:1039-1048. (Pubitemid 41345795)
-
(2005)
Molecular Pharmacology
, vol.68
, Issue.4
, pp. 1039-1048
-
-
Ryman-Rasmussen, J.P.1
Nichols, D.E.2
Mailman, R.B.3
-
39
-
-
0042887023
-
Aripiprazole, a novel atypical antipsychotic drug with a unique and robust pharmacology
-
DOI 10.1038/sj.npp.1300203
-
Shapiro DA, Renock S, Arrington E, Chiodo LA, Liu LX, Sibley DR, Roth BL, and Mailman R (2003) Aripiprazole, a novel atypical antipsychotic drug with a unique and robust pharmacology. Neuropsychopharmacology 28:1400-1411. (Pubitemid 41070874)
-
(2003)
Neuropsychopharmacology
, vol.28
, Issue.8
, pp. 1400-1411
-
-
Shapiro, D.A.1
Renock, S.2
Arrington, E.3
Chiodo, L.A.4
Liu, L.-X.5
Sibley, D.R.6
Roth, B.L.7
Mailman, R.8
-
40
-
-
0036169280
-
The binding site of aminergic G protein-coupled receptors: The transmembrane segments and second extracellular loop
-
DOI 10.1146/annurev.pharmtox.42.091101.144224
-
Shi L and Javitch JA (2002) The binding site of aminergic G protein-coupled receptors: the transmembrane segments and second extracellular loop. Annu Rev Pharmacol Toxicol 42:437-467. (Pubitemid 34162546)
-
(2002)
Annual Review of Pharmacology and Toxicology
, vol.42
, pp. 437-467
-
-
Shi, L.1
Javitch, J.A.2
-
41
-
-
0031003929
-
2 post-synaptic receptor agonist
-
DOI 10.1016/S0014-2999(97)00026-5, PII S0014299997000265
-
Smith HP, Nichols DE, Mailman RB, and Lawler CP (1997) Locomotor inhibition, yawning and vacuous chewing induced by a novel dopamine D2 post-synaptic receptor agonist. Eur J Pharmacol 323:27-36. (Pubitemid 27136434)
-
(1997)
European Journal of Pharmacology
, vol.323
, Issue.1
, pp. 27-36
-
-
Smith, H.P.1
Nichols, D.E.2
Mailman, R.B.3
Lawler, C.P.4
-
42
-
-
0024344941
-
Identification of two serine residues involved in agonist activation of the beta-adrenergic receptor
-
Strader CD, Candelore MR, Hill WS, Sigal IS, and Dixon RA (1989) Identification of two serine residues involved in agonist activation of the beta-adrenergic receptor. J Biol Chem 264:13572-13578. (Pubitemid 19198437)
-
(1989)
Journal of Biological Chemistry
, vol.264
, Issue.23
, pp. 13572-13578
-
-
Strader, C.D.1
Candelore, M.R.2
Hill, W.S.3
Sigal, I.S.4
Dixon, R.A.F.5
-
43
-
-
20444499405
-
2 adrenoceptor binding site with catechol reveals differences in binding and activation by agonists and partial agonists
-
DOI 10.1074/jbc.M502352200
-
Swaminath G, Deupi X, Lee TW, Zhu W, Thian FS, Kobilka TS, and Kobilka B (2005) Probing the beta2 adrenoceptor binding site with catechol reveals differences in binding and activation by agonists and partial agonists. J Biol Chem 280:22165-22171. (Pubitemid 40827872)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.23
, pp. 22165-22171
-
-
Swaminath, G.1
Deupi, X.2
Lee, T.W.3
Zhu, W.4
Thian, F.S.5
Kobilka, T.S.6
Kobilka, B.7
-
44
-
-
79951972094
-
Histidine 6.55 is a major determinant of ligand-biased signaling in dopamine D2L receptor
-
Tschammer N, Bollinger S, Kenakin T, and Gmeiner P (2011) Histidine 6.55 is a major determinant of ligand-biased signaling in dopamine D2L receptor. Mol Pharmacol 79:575-585.
-
(2011)
Mol Pharmacol
, vol.79
, pp. 575-585
-
-
Tschammer, N.1
Bollinger, S.2
Kenakin, T.3
Gmeiner, P.4
-
45
-
-
33845903110
-
Functional selectivity and classical concepts of quantitative pharmacology
-
DOI 10.1124/jpet.106.104463
-
Urban JD, Clarke WP, von Zastrow M, Nichols DE, Kobilka B, Weinstein H, Javitch JA, Roth BL, Christopoulos A, Sexton PM, et al. (2007) Functional selectivity and classical concepts of quantitative pharmacology. J Pharmacol Exp Ther 320:1-13. (Pubitemid 46025713)
-
(2007)
Journal of Pharmacology and Experimental Therapeutics
, vol.320
, Issue.1
, pp. 1-13
-
-
Urban, J.D.1
Clarke, W.P.2
Von Zastrow, M.3
Nichols, D.E.4
Kobilka, B.5
Weinstein, H.6
Javitch, J.A.7
Roth, B.L.8
Christopoulos, A.9
Sexton, P.M.10
Miller, K.J.11
Spedding, M.12
Mailman, R.B.13
-
46
-
-
78149496656
-
The role of conformational ensembles of seven transmembrane receptors in functional selectivity
-
Vaidehi N and Kenakin T (2010) The role of conformational ensembles of seven transmembrane receptors in functional selectivity. Curr Opin Pharmacol 10:775-781.
-
(2010)
Curr Opin Pharmacol
, vol.10
, pp. 775-781
-
-
Vaidehi, N.1
Kenakin, T.2
-
47
-
-
0034664960
-
A new phosphospecific cell-based ELISA for p42/p44 mitogen-activated protein kinase (MAPK), p38 MAPK, protein kinase B and cAMP-response-element- binding protein
-
Versteeg HH, Nijhuis E, van den Brink GR, Evertzen M, Pynaert GN, van Deventer SJ, Coffer PJ, and Peppelenbosch MP (2000) A new phosphospecific cell-based ELISA for p42/p44 mitogen-activated protein kinase (MAPK), p38 MAPK, protein kinase B and cAMP-response-element-binding protein. Biochem J 350:717-722.
-
(2000)
Biochem J
, vol.350
, pp. 717-722
-
-
Versteeg, H.H.1
Nijhuis, E.2
Van Den Brink, G.R.3
Evertzen, M.4
Pynaert, G.N.5
Van Deventer, S.J.6
Coffer, P.J.7
Peppelenbosch, M.P.8
-
48
-
-
78651405537
-
The structural basis for agonist and partial agonist action on a beta(1)-adrenergic receptor
-
Warne T, Moukhametzianov R, Baker JG, Nehmé R, Edwards PC, Leslie AG, Schertler GF, and Tate CG (2011) The structural basis for agonist and partial agonist action on a beta(1)-adrenergic receptor. Nature 469:241-244.
-
(2011)
Nature
, vol.469
, pp. 241-244
-
-
Warne, T.1
Moukhametzianov, R.2
Baker, J.G.3
Nehmé, R.4
Edwards, P.C.5
Leslie, A.G.6
Schertler, G.F.7
Tate, C.G.8
-
49
-
-
0029838206
-
2-adrenergic receptor
-
DOI 10.1073/pnas.93.17.9276
-
Wieland K, Zuurmond HM, Krasel C, IJzerman AP, and Lohse MJ (1996) Involvement of Asn-293 in stereospecific agonist recognition and in activation of the beta 2-adrenergic receptor. Proc Natl Acad Sci USA 93:9276-9281. (Pubitemid 26282054)
-
(1996)
Proceedings of the National Academy of Sciences of the United States of America
, vol.93
, Issue.17
, pp. 9276-9281
-
-
Wieland, K.1
Zuurmond, H.M.2
Krasel, C.3
Ijzerman, A.P.4
Lohse, M.J.5
-
50
-
-
0031871997
-
Contribution of serine residues to constitutive and agonist- induced signaling via the D(2S) dopamine receptor: Evidence for multiple, agonist- specific active conformations
-
Wiens BL, Nelson CS, and Neve KA (1998) Contribution of serine residues to constitutive and agonist-induced signaling via the D2S dopamine receptor: evidence for multiple, agonist-specific active conformations. Mol Pharmacol 54:435-444. (Pubitemid 28368834)
-
(1998)
Molecular Pharmacology
, vol.54
, Issue.2
, pp. 435-444
-
-
Wiens, B.L.1
Nelson, C.S.2
Neve, K.A.3
-
51
-
-
0030053844
-
2 dopamine receptor using site-directed mutagenesis
-
Woodward R, Coley C, Daniell S, Naylor LH, and Strange PG (1996) Investigation of the role of conserved serine residues in the long form of the rat D2 dopamine receptor using site-directed mutagenesis. J Neurochem 66:394-402. (Pubitemid 26010805)
-
(1996)
Journal of Neurochemistry
, vol.66
, Issue.1
, pp. 394-402
-
-
Woodward, R.1
Coley, C.2
Daniell, S.3
Naylor, L.H.4
Strange, P.G.5
|