-
1
-
-
0027456415
-
Receptor reserve masks partial agonist activity of drugs in a cloned rat 5-hydroxytryptaminelb receptor expression system
-
Adham N, Ellerbrock B, Hartig P, Weinshank RL, and Branchek T (1993) Receptor reserve masks partial agonist activity of drugs in a cloned rat 5-hydroxytryptaminelb receptor expression system. Mol Pharmacol 43:427-433.
-
(1993)
Mol Pharmacol
, vol.43
, pp. 427-433
-
-
Adham, N.1
Ellerbrock, B.2
Hartig, P.3
Weinshank, R.L.4
Branchek, T.5
-
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.
-
(1998)
Mol Pharmacol
, vol.54
, pp. 94-104
-
-
Berg, K.A.1
Maayani, S.2
Goldfarb, J.3
Scaramellini, C.4
Leff, P.5
Clarke, W.P.6
-
3
-
-
0029072492
-
Evaluation of cis- and trans-9- and 11-hydroxy-5,6,6a,7,8,12b- hexahydrobenzo[a]phenanthridines as structurally rigid, selective D1 dopamine receptor ligands
-
Brewster WK, Nichols DE, Watts VJ, Riggs RM, Mottola D, and Mailman RB (1995) Evaluation of cis- and trans-9- and 11-hydroxy-5,6,6a,7,8,12b- hexahydrobenzo[a]phenanthridines as structurally rigid, selective D1 dopamine receptor ligands. J Med Chem 38:318-327.
-
(1995)
J Med Chem
, vol.38
, pp. 318-327
-
-
Brewster, W.K.1
Nichols, D.E.2
Watts, V.J.3
Riggs, R.M.4
Mottola, D.5
Mailman, R.B.6
-
5
-
-
0034003405
-
Regulation of adenylyl cyclase in the central nervous system
-
Chern YJ (2000) Regulation of adenylyl cyclase in the central nervous system. Cell Signal 12:195-204.
-
(2000)
Cell Signal
, vol.12
, pp. 195-204
-
-
Chern, Y.J.1
-
6
-
-
0033525899
-
G protein-mediated mitogen-activated protein kinase activation by two dopamine D2 receptors
-
Choi EY, Jeong D, Won K, Park, and Baik JH (1999) G protein-mediated mitogen-activated protein kinase activation by two dopamine D2 receptors. Biochem Biophys Res Commun 256:33-40.
-
(1999)
Biochem Biophys Res Commun
, vol.256
, pp. 33-40
-
-
Choi, E.Y.1
Jeong, D.2
Won, K.3
Park4
Baik, J.H.5
-
7
-
-
0023743186
-
Effects of N-n-propylnorapomorphine enantiomers on single unit activity of substantia nigra pars compacta and ventral tegmental area dopamine neurons
-
Cox RF, Neumeyer JL, and Waszczak BL (1988) Effects of N-n-propylnorapomorphine enantiomers on single unit activity of substantia nigra pars compacta and ventral tegmental area dopamine neurons. J Pharmacol Exp Ther 247:355-362.
-
(1988)
J Pharmacol Exp Ther
, vol.247
, pp. 355-362
-
-
Cox, R.F.1
Neumeyer, J.L.2
Waszczak, B.L.3
-
8
-
-
0037350667
-
o G proteins: Evidence for agonist regulation of G protein selectivity
-
o G proteins: evidence for agonist regulation of G protein selectivity. Br J Pharmacol 138:775-786.
-
(2003)
Br J Pharmacol
, vol.138
, pp. 775-786
-
-
Gazi, L.1
Nickolls, S.A.2
Strange, P.G.3
-
10
-
-
0029664618
-
9-Dihydroxy-2,3,7,11b-tetrahydro-1H-naph[1,2,3-de]isoquinoline: A potent full dopamine D1 agonist containing a rigid-beta-phenyldopamine pharmacophore
-
Ghosh D, Snyder 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.
-
(1996)
J Med Chem
, vol.39
, pp. 549-555
-
-
Ghosh, D.1
Snyder, S.E.2
Watts, V.J.3
Mailman, R.B.4
Nichols, D.E.5
-
11
-
-
1542301679
-
8,9-Dihydro-1,2,3,11b-tetrahydrochromeno[4,3,2,-de]isoquinoline (dinoxyline), a high affinity and potent agonist at all dopamine receptor isoforms
-
Grubbs RA, Lewis MM, Owens-Vance C, Gay EA, Jassen AK, Mailman RB, and Nichols DE (2004) 8,9-Dihydro-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.
-
(2004)
Bioorg Med Chem
, vol.12
, pp. 1403-1412
-
-
Grubbs, R.A.1
Lewis, M.M.2
Owens-Vance, C.3
Gay, E.A.4
Jassen, A.K.5
Mailman, R.B.6
Nichols, D.E.7
-
12
-
-
0347480490
-
Ligand-selective signaling and high-content screening for GPCR drugs
-
Gurwitz D and Haring R (2003) Ligand-selective signaling and high-content screening for GPCR drugs. Drug Discov Today 8:1108-1109.
-
(2003)
Drug Discov Today
, vol.8
, pp. 1108-1109
-
-
Gurwitz, D.1
Haring, R.2
-
13
-
-
0027950411
-
Discrete activation of transduction pathways associated with acetylcholine M1 receptor by several muscarinic ligands
-
Gurwitz D, Haring R, Heldman E, Fraser CM, Manor D, and Fisher A (1994) Discrete activation of transduction pathways associated with acetylcholine M1 receptor by several muscarinic ligands. Eur J Pharmacol 267:21-31.
-
(1994)
Eur J Pharmacol
, vol.267
, pp. 21-31
-
-
Gurwitz, D.1
Haring, R.2
Heldman, E.3
Fraser, C.M.4
Manor, D.5
Fisher, A.6
-
14
-
-
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
-
15
-
-
0038540318
-
Biochemical and pharmacological control of the multiplicity of coupling at G-protein-coupled receptors
-
Hermans E (2003) Biochemical and pharmacological control of the multiplicity of coupling at G-protein-coupled receptors. Pharmacol Ther 99:25-44.
-
(2003)
Pharmacol Ther
, vol.99
, pp. 25-44
-
-
Hermans, E.1
-
17
-
-
0029061611
-
Agonist-receptor efficacy. I: Mechanisms of efficacy and receptor promiscuity
-
Kenakin T (1995) Agonist-receptor efficacy. I: mechanisms of efficacy and receptor promiscuity. Trends Pharmacol Sci 16:188-192.
-
(1995)
Trends Pharmacol Sci
, vol.16
, pp. 188-192
-
-
Kenakin, T.1
-
19
-
-
0036177114
-
Drug efficacy at G protein-coupled receptors
-
Kenakin T (2002) Drug efficacy at G protein-coupled receptors. Ann Rev Pharmacol Toxicol 42:349-379.
-
(2002)
Ann Rev Pharmacol Toxicol
, vol.42
, pp. 349-379
-
-
Kenakin, T.1
-
20
-
-
0036267278
-
Functional selectivity of dopamine receptor agonists. II. Actions of dihydrexidine in D2L receptor-transfected MN9D cells and pituitary lactotrophs
-
Kilts JD, Connery HS, Arrington EG, Lewis MM, Lawler CP, Oxford GS, O'Malley KL, Todd RD, Blake BL, Nichols DE, and Mailman RB (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.
-
(2002)
J Pharmacol Exp Ther
, vol.301
, 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
-
21
-
-
0028132875
-
Dopaminergic benzo[a]phenanthridines: Resolution and pharmacological evaluation of the enantiomers of dihydrexidine, the full efficacy D1 dopamine receptor agonist
-
Knoerzer TA, Nichols DE, Brewster WK, Watts VJ, Mottola D, and Mailman RB (1994) Dopaminergic benzo[a]phenanthridines: resolution and pharmacological evaluation of the enantiomers of dihydrexidine, the full efficacy D1 dopamine receptor agonist. J Med Chem 37:2453-2460.
-
(1994)
J Med Chem
, vol.37
, pp. 2453-2460
-
-
Knoerzer, T.A.1
Nichols, D.E.2
Brewster, W.K.3
Watts, V.J.4
Mottola, D.5
Mailman, R.B.6
-
22
-
-
0036137644
-
Biased inhibition by a suramin analogue of A1-adenosine receptor/G protein coupling in fused receptor/G protein tandems: The A1-adenosine receptor is predominantly coupled to Goalpha in human brain
-
Kudlacek O, Waldhoer M, Kassack MU, Nickel P, Salmi JI, Freissmuth M, and Nanoff C (2002) Biased inhibition by a suramin analogue of A1-adenosine receptor/G protein coupling in fused receptor/G protein tandems: the A1-adenosine receptor is predominantly coupled to Goalpha in human brain. Naunyn Schmiedeberg's Arch Pharmacol 365:8-16.
-
(2002)
Naunyn Schmiedeberg's Arch Pharmacol
, vol.365
, pp. 8-16
-
-
Kudlacek, O.1
Waldhoer, M.2
Kassack, M.U.3
Nickel, P.4
Salmi, J.I.5
Freissmuth, M.6
Nanoff, C.7
-
24
-
-
0034130116
-
Dominant-negative mutants identify a role for GIRK channels in D3 dopamine receptor-mediated regulation of spontaneous secretory activity
-
Kuzhikandathil EV and Oxford GS (2000) Dominant-negative mutants identify a role for GIRK channels in D3 dopamine receptor-mediated regulation of spontaneous secretory activity. J Gen Physiol 115:697-706.
-
(2000)
J Gen Physiol
, vol.115
, pp. 697-706
-
-
Kuzhikandathil, E.V.1
Oxford, G.S.2
-
25
-
-
0032419907
-
2L receptors couple to inward rectifier potassium channels in mammalian cell lines
-
2L receptors couple to inward rectifier potassium channels in mammalian cell lines. Mol Cell Neurosci 12:390-402.
-
(1998)
Mol Cell Neurosci
, vol.12
, pp. 390-402
-
-
Kuzhikandathil, E.V.1
Yu, W.2
Oxford, G.S.3
-
26
-
-
0033151286
-
Interactions of the novel antipsychotic aripiprazole (OPC-14597) with dopamine and serotonin receptor subtypes
-
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.
-
(1999)
Neuropsychopharmacology
, vol.20
, 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
-
28
-
-
0031714391
-
Signaling from G-protein-coupled receptors to mitogen-activated protein (MAP)-kinase cascades
-
Lopez-Ilasaca M (1998) Signaling From G-protein-coupled receptors to mitogen-activated protein (MAP)-kinase cascades. Biochem Pharmacol 56:269-277.
-
(1998)
Biochem Pharmacol
, vol.56
, pp. 269-277
-
-
Lopez-Ilasaca, M.1
-
29
-
-
0031818357
-
D2 dopamine receptors stimulate mitogenesis through pertussis toxin-sensitive G proteins and Ras-involved ERK and SAP/JNK pathways in rat C6-D2L glioma cells
-
Luo YQ, Kokkonen GC, Wang XT, Neve KA, and Roth GS (1998) D2 dopamine receptors stimulate mitogenesis through pertussis toxin-sensitive G proteins and Ras-involved ERK and SAP/JNK pathways in rat C6-D2L glioma cells. J Neurochem 71:980-990.
-
(1998)
J Neurochem
, vol.71
, pp. 980-990
-
-
Luo, Y.Q.1
Kokkonen, G.C.2
Wang, X.T.3
Neve, K.A.4
Roth, G.S.5
-
31
-
-
0036765585
-
Measures of efficacy using G proteins as endpoints: Differential engagement of G proteins through single receptors
-
Manning DR (2002) Measures of efficacy using G proteins as endpoints: differential engagement of G proteins through single receptors. Mol Pharmacol 62:451-452.
-
(2002)
Mol Pharmacol
, vol.62
, pp. 451-452
-
-
Manning, D.R.1
-
32
-
-
6844250767
-
Dopamine receptors: From structure to function
-
Missale C, Nash SR, Robinson SW, Jaber M, and Caron MG (1998) Dopamine receptors: from structure to function. Physiol Rev 78:189-225.
-
(1998)
Physiol Rev
, vol.78
, pp. 189-225
-
-
Missale, C.1
Nash, S.R.2
Robinson, S.W.3
Jaber, M.4
Caron, M.G.5
-
33
-
-
0036260826
-
Functional selectivity of dopamine receptor agonists. I. Selective activation of postsynaptic dopamine D2 receptors linked to adenylate cyclase
-
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.
-
(2002)
J Pharmacol Exp Ther
, vol.301
, pp. 1166-1178
-
-
Mottola, D.M.1
Kilts, J.D.2
Lewis, M.M.3
Connery, 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
-
34
-
-
0030302494
-
Dopamine D2L receptor couples to GαI2 and GαI3 but not GαI1, leading to the inhibition of adenylate cyclase in transfected cell lines
-
O'Hara CM, Tang L, Taussig R, Todd RD, and O'Malley KL (1996) Dopamine D2L receptor couples to GαI2 and GαI3 but not GαI1, leading to the inhibition of adenylate cyclase in transfected cell lines. J Pharmacol Exp Ther 278:354-360.
-
(1996)
J Pharmacol Exp Ther
, vol.278
, pp. 354-360
-
-
O'Hara, C.M.1
Tang, L.2
Taussig, R.3
Todd, R.D.4
O'Malley, K.L.5
-
35
-
-
0030609104
-
Alpha2-Adrenoceptor regulation of adenylyl cyclase in CHO cells: Dependence on receptor density, receptor subtype and current activity of adenylyl cyclase
-
Pohjanoksa K, Jansson CC, Luomala K, Marjamaki A, Savola JM, and Scheinin M (1997) Alpha2-Adrenoceptor regulation of adenylyl cyclase in CHO cells: dependence on receptor density, receptor subtype and current activity of adenylyl cyclase. Eur J Pharmacol 335:53-63.
-
(1997)
Eur J Pharmacol
, vol.335
, pp. 53-63
-
-
Pohjanoksa, K.1
Jansson, C.C.2
Luomala, K.3
Marjamaki, A.4
Savola, J.M.5
Scheinin, M.6
-
36
-
-
0028128734
-
The D2 dopamine receptor isoforms signal through distinct Gi α proteins to inhibit adenylyl cyclase. A study with site-directed mutant Gi a proteins
-
Senogles SE (1994) The D2 dopamine receptor isoforms signal through distinct Gi α proteins to inhibit adenylyl cyclase. A study with site-directed mutant Gi a proteins. J Biol Chem 269:23120-23127.
-
(1994)
J Biol Chem
, vol.269
, pp. 23120-23127
-
-
Senogles, S.E.1
-
37
-
-
0042887023
-
Aripiprazole, a novel atypical antipsychotic drug with a unique and robust pharmacology
-
Shapiro DA, Renock S, Arrington E, Sibley DR, Chiodo LA, Roth BL, and Mailman RB (2003) Aripiprazole, a novel atypical antipsychotic drug with a unique and robust pharmacology. Neuropsychopharmacology 28:1400-1411.
-
(2003)
Neuropsychopharmacology
, vol.28
, pp. 1400-1411
-
-
Shapiro, D.A.1
Renock, S.2
Arrington, E.3
Sibley, D.R.4
Chiodo, L.A.5
Roth, B.L.6
Mailman, R.B.7
-
38
-
-
0037103298
-
(+)-dinapsoline: An efficient synthesis and pharmacological profile of a novel dopamine agonist
-
Sit SY, Xie K, Jacutin-Porte S, Taber MT, Gulwadi AG, Korpinen CD, Burris KD, Molski TF, Ryan E, Xu C, et al. (2002) (+)-Dinapsoline: an efficient synthesis and pharmacological profile of a novel dopamine agonist. J Med Chem 45:3660-3668.
-
(2002)
J Med Chem
, vol.45
, pp. 3660-3668
-
-
Sit, S.Y.1
Xie, K.2
Jacutin-Porte, S.3
Taber, M.T.4
Gulwadi, A.G.5
Korpinen, C.D.6
Burris, K.D.7
Molski, T.F.8
Ryan, E.9
Xu, C.10
-
39
-
-
0031003929
-
Locomotor inhibition, yawning and vacuous chewing induced by a novel dopamine D2 post-synaptic receptor agonist
-
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.
-
(1997)
Eur J Pharmacol
, vol.323
, pp. 27-36
-
-
Smith, H.P.1
Nichols, D.E.2
Mailman, R.B.3
Lawler, C.P.4
-
40
-
-
0030747146
-
Regulation of the ERK subgroup of MAP kinase cascades through G protein-coupled receptors
-
Sugden PH and Clerk A (1997) Regulation of the ERK subgroup of MAP kinase cascades through G protein-coupled receptors. Cell Signal 9:337-351.
-
(1997)
Cell Signal
, vol.9
, pp. 337-351
-
-
Sugden, P.H.1
Clerk, A.2
-
41
-
-
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 Pt 3:717-722.
-
(2000)
Biochem J
, vol.350
, Issue.PART 3
, 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
-
42
-
-
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, Way J, Chen WJ, and Kenakin T (2000) 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 58:1230-1238.
-
(2000)
Mol Pharmacol
, vol.58
, pp. 1230-1238
-
-
Watson, C.1
Chen, G.2
Irving, P.3
Way, J.4
Chen, W.J.5
Kenakin, T.6
-
43
-
-
0029126707
-
Spare receptors and intrinsic activity: Studies with D1 dopamine receptor agonists
-
Watts VJ, Lawler CP, Gonzales AJ, Zhou QY, Civelli O, Nichols DE, and Mailman RB (1995) Spare receptors and intrinsic activity: studies with D1 dopamine receptor agonists. Synapse 21:177-187.
-
(1995)
Synapse
, vol.21
, pp. 177-187
-
-
Watts, V.J.1
Lawler, C.P.2
Gonzales, A.J.3
Zhou, Q.Y.4
Civelli, O.5
Nichols, D.E.6
Mailman, R.B.7
-
44
-
-
0032194951
-
Selective activation of Galphao by D2L dopamine receptors in NS20Y neuroblastoma cells
-
Watts VJ, Wiens BL, Cumbay MG, Vu MN, Neve RL, and Neve KA (1998) Selective activation of Galphao by D2L dopamine receptors in NS20Y neuroblastoma cells. J Neurosci 18:8692-8699.
-
(1998)
J Neurosci
, vol.18
, pp. 8692-8699
-
-
Watts, V.J.1
Wiens, B.L.2
Cumbay, M.G.3
Vu, M.N.4
Neve, R.L.5
Neve, K.A.6
-
45
-
-
0033179904
-
Functional dissociation of mu opioid receptor signaling and endocytosis: Implications for the biology of opiate tolerance and addiction
-
Whistler JL, Chuang HH, Chu P, Jan LY, and von Zastrow M (1999) Functional dissociation of mu opioid receptor signaling and endocytosis: implications for the biology of opiate tolerance and addiction. Neuron 23:737-746.
-
(1999)
Neuron
, vol.23
, pp. 737-746
-
-
Whistler, J.L.1
Chuang, H.H.2
Chu, P.3
Jan, L.Y.4
Von Zastrow, M.5
-
46
-
-
0028180952
-
Recombinant G-protein beta gamma-subunits activate the muscarinic-gated atrial potassium channel
-
Wickman KD, Iniguez-Lluhl JA, Davenport PA, Taussig R, Krapivinsky GB, Linder ME, Gilman AG, and Clapham DE (1994) Recombinant G-protein beta gamma-subunits activate the muscarinic-gated atrial potassium channel. Nature (Lond) 368:255-257.
-
(1994)
Nature (Lond)
, vol.368
, pp. 255-257
-
-
Wickman, K.D.1
Iniguez-Lluhl, J.A.2
Davenport, P.A.3
Taussig, R.4
Krapivinsky, G.B.5
Linder, M.E.6
Gilman, A.G.7
Clapham, D.E.8
-
47
-
-
0031871997
-
Contribution of serine residues to constitutive and agonist-induced signaling via the D2S 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.
-
(1998)
Mol Pharmacol
, vol.54
, pp. 435-444
-
-
Wiens, B.L.1
Nelson, C.S.2
Neve, K.A.3
-
48
-
-
0034307596
-
Selective regulation of N-type Ca channels by different combinations of G-protein beta/gamma subunits and RGS proteins
-
Zhou JY, Siderovski DP, and Miller RJ (2000) Selective regulation of N-type Ca channels by different combinations of G-protein beta/gamma subunits and RGS proteins. J Neurosci 20:7143-7148.
-
(2000)
J Neurosci
, vol.20
, pp. 7143-7148
-
-
Zhou, J.Y.1
Siderovski, D.P.2
Miller, R.J.3
|