-
2
-
-
33748671369
-
The 7 TM G-protein-coupled receptor target family
-
Jacoby E., et al. The 7 TM G-protein-coupled receptor target family. ChemMedChem 1 (2006) 761-782
-
(2006)
ChemMedChem
, vol.1
, pp. 761-782
-
-
Jacoby, E.1
-
3
-
-
17844400914
-
The repertoire of G-protein-coupled receptors in fully sequenced genomes
-
Fredriksson R., and Schiöth H.B. The repertoire of G-protein-coupled receptors in fully sequenced genomes. Mol. Pharmacol. 67 (2005) 1414-1425
-
(2005)
Mol. Pharmacol.
, vol.67
, pp. 1414-1425
-
-
Fredriksson, R.1
Schiöth, H.B.2
-
4
-
-
31144473816
-
Pharmacological and clinical properties of calcimimetics: calcium receptor activators that afford an innovative approach to controlling hyperparathyroidism
-
Nagano N. Pharmacological and clinical properties of calcimimetics: calcium receptor activators that afford an innovative approach to controlling hyperparathyroidism. Pharmacol. Ther. 109 (2006) 339-365
-
(2006)
Pharmacol. Ther.
, vol.109
, pp. 339-365
-
-
Nagano, N.1
-
5
-
-
33845973375
-
Structure, pharmacology and therapeutic prospects of family C G-protein coupled receptors
-
Brauner-Osborne H., et al. Structure, pharmacology and therapeutic prospects of family C G-protein coupled receptors. Curr. Drug Targets 8 (2007) 169-184
-
(2007)
Curr. Drug Targets
, vol.8
, pp. 169-184
-
-
Brauner-Osborne, H.1
-
6
-
-
34249711352
-
Access denied? The status of co-receptor inhibition to counter HIV entry
-
Biswas P., et al. Access denied? The status of co-receptor inhibition to counter HIV entry. Expert Opin. Pharmacother. 8 (2007) 923-933
-
(2007)
Expert Opin. Pharmacother.
, vol.8
, pp. 923-933
-
-
Biswas, P.1
-
7
-
-
27644510382
-
Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type 1 activity
-
Dorr P., et al. Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type 1 activity. Antimicrob. Agents Chemother. 49 (2005) 4721-4732
-
(2005)
Antimicrob. Agents Chemother.
, vol.49
, pp. 4721-4732
-
-
Dorr, P.1
-
8
-
-
33645360875
-
Keynote review: allosterism in membrane receptors
-
Gao Z.G., and Jacobson K.A. Keynote review: allosterism in membrane receptors. Drug Discov. Today 11 (2006) 191-202
-
(2006)
Drug Discov. Today
, vol.11
, pp. 191-202
-
-
Gao, Z.G.1
Jacobson, K.A.2
-
9
-
-
33747181100
-
Allosteric agonists of 7TM receptors: expanding the pharmacological toolbox
-
Langmead C.J., and Christopoulos A. Allosteric agonists of 7TM receptors: expanding the pharmacological toolbox. Trends Pharmacol. Sci. 27 (2006) 475-481
-
(2006)
Trends Pharmacol. Sci.
, vol.27
, pp. 475-481
-
-
Langmead, C.J.1
Christopoulos, A.2
-
11
-
-
6344260294
-
The power of two: protein dimerization in biology
-
Marianayagam N.J., et al. The power of two: protein dimerization in biology. Trends Biochem. Sci. 29 (2004) 618-625
-
(2004)
Trends Biochem. Sci.
, vol.29
, pp. 618-625
-
-
Marianayagam, N.J.1
-
12
-
-
33947369500
-
G protein-coupled receptor dimerisation: molecular basis and relevance to function
-
Milligan G. G protein-coupled receptor dimerisation: molecular basis and relevance to function. Biochim. Biophys. Acta 1768 (2007) 825-835
-
(2007)
Biochim. Biophys. Acta
, vol.1768
, pp. 825-835
-
-
Milligan, G.1
-
13
-
-
33646526069
-
GPCR hetero-dimers: pharmacology, function and relevance to drug discovery
-
Milligan G. GPCR hetero-dimers: pharmacology, function and relevance to drug discovery. Drug Discov. Today 11 (2006) 541-549
-
(2006)
Drug Discov. Today
, vol.11
, pp. 541-549
-
-
Milligan, G.1
-
14
-
-
21744445403
-
Dimer-based model for heptaspanning membrane receptors
-
Franco R., et al. Dimer-based model for heptaspanning membrane receptors. Trends Biochem. Sci. 30 (2005) 360-366
-
(2005)
Trends Biochem. Sci.
, vol.30
, pp. 360-366
-
-
Franco, R.1
-
15
-
-
33745127060
-
The two-state dimer receptor model: a general model for receptor dimers
-
Franco R., et al. The two-state dimer receptor model: a general model for receptor dimers. Mol. Pharmacol. 69 (2006) 1905-1912
-
(2006)
Mol. Pharmacol.
, vol.69
, pp. 1905-1912
-
-
Franco, R.1
-
16
-
-
34447562579
-
2-adrenoceptor
-
2-adrenoceptor. Cell. Signal. 19 (2007) 1928-1938
-
(2007)
Cell. Signal.
, vol.19
, pp. 1928-1938
-
-
Sartania, N.1
-
17
-
-
0038606535
-
Hypersensitization of the Orexin 1 receptor by the CB1 receptor: evidence for cross-talk blocked by the specific CB1 antagonist, SR141716
-
Hilairet S., et al. Hypersensitization of the Orexin 1 receptor by the CB1 receptor: evidence for cross-talk blocked by the specific CB1 antagonist, SR141716. J. Biol. Chem. 278 (2003) 23731-23737
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 23731-23737
-
-
Hilairet, S.1
-
18
-
-
33846030175
-
Orexin-1 receptor-cannabinoid CB1 receptor hetero-dimerization results in both ligand-dependent and -independent co-ordinated alterations of receptor localization and function
-
Ellis J., et al. Orexin-1 receptor-cannabinoid CB1 receptor hetero-dimerization results in both ligand-dependent and -independent co-ordinated alterations of receptor localization and function. J. Biol. Chem. 281 (2006) 38812-38824
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 38812-38824
-
-
Ellis, J.1
-
19
-
-
13444274883
-
Evidence for negative binding cooperativity within CCR5-CCR2b heterodimers
-
El-Asmar L., et al. Evidence for negative binding cooperativity within CCR5-CCR2b heterodimers. Mol. Pharmacol. 67 (2005) 460-469
-
(2005)
Mol. Pharmacol.
, vol.67
, pp. 460-469
-
-
El-Asmar, L.1
-
20
-
-
33645802812
-
Allosteric modulation of binding properties between units of chemokine receptor homo- and hetero-oligomers
-
Springael J.Y., et al. Allosteric modulation of binding properties between units of chemokine receptor homo- and hetero-oligomers. Mol. Pharmacol. 69 (2006) 1652-1666
-
(2006)
Mol. Pharmacol.
, vol.69
, pp. 1652-1666
-
-
Springael, J.Y.1
-
21
-
-
0034714335
-
Oligomerization of mu and delta-opioid receptors. Generation of novel functional properties
-
George S.R., et al. Oligomerization of mu and delta-opioid receptors. Generation of novel functional properties. J. Biol. Chem. 275 (2000) 26128-26135
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 26128-26135
-
-
George, S.R.1
-
22
-
-
34548188312
-
Computational studies of family A and family B GPCRs
-
Vohra S., et al. Computational studies of family A and family B GPCRs. Biochem. Soc. Trans. 35 (2007) 749-754
-
(2007)
Biochem. Soc. Trans.
, vol.35
, pp. 749-754
-
-
Vohra, S.1
-
23
-
-
21144446486
-
A heterodimer-selective agonist shows in vivo relevance of G protein-coupled receptor dimers
-
Waldhoer M., et al. A heterodimer-selective agonist shows in vivo relevance of G protein-coupled receptor dimers. Proc. Natl. Acad. Sci. U. S. A. 102 (2005) 9050-9055
-
(2005)
Proc. Natl. Acad. Sci. U. S. A.
, vol.102
, pp. 9050-9055
-
-
Waldhoer, M.1
-
24
-
-
27144434813
-
Techniques: promiscuous Galpha proteins in basic research and drug discovery
-
Kostenis E., et al. Techniques: promiscuous Galpha proteins in basic research and drug discovery. Trends Pharmacol. Sci. 26 (2005) 595-602
-
(2005)
Trends Pharmacol. Sci.
, vol.26
, pp. 595-602
-
-
Kostenis, E.1
-
25
-
-
33846328669
-
D1-D2 dopamine receptor heterooligomers with unique pharmacology are coupled to rapid activation of Gq/11 in the striatum
-
Rashid A.J., et al. D1-D2 dopamine receptor heterooligomers with unique pharmacology are coupled to rapid activation of Gq/11 in the striatum. Proc. Natl. Acad. Sci. U. S. A. 104 (2007) 654-659
-
(2007)
Proc. Natl. Acad. Sci. U. S. A.
, vol.104
, pp. 654-659
-
-
Rashid, A.J.1
-
26
-
-
17844410926
-
Concurrent stimulation of cannabinoid CB1 and dopamine D2 receptors enhances heterodimer formation: a mechanism for receptor cross-talk?
-
Kearn C.S., et al. Concurrent stimulation of cannabinoid CB1 and dopamine D2 receptors enhances heterodimer formation: a mechanism for receptor cross-talk?. Mol. Pharmacol. 67 (2005) 1697-1704
-
(2005)
Mol. Pharmacol.
, vol.67
, pp. 1697-1704
-
-
Kearn, C.S.1
-
27
-
-
30444435782
-
Hetero-trimeric G proteins: a short history
-
Milligan G., and Kostenis E. Hetero-trimeric G proteins: a short history. Br. J. Pharmacol. 147 S1 (2006) S46-S55
-
(2006)
Br. J. Pharmacol.
, vol.147
, Issue.SUPPL.1
-
-
Milligan, G.1
Kostenis, E.2
-
28
-
-
33845720603
-
Asymmetric conformational changes in a GPCR dimer controlled by G-proteins
-
Damian M., et al. Asymmetric conformational changes in a GPCR dimer controlled by G-proteins. EMBO J. 25 (2006) 5693-5702
-
(2006)
EMBO J.
, vol.25
, pp. 5693-5702
-
-
Damian, M.1
-
29
-
-
4644308014
-
Different functional roles of T1R subunits in the heteromeric taste receptors
-
Xu H., et al. Different functional roles of T1R subunits in the heteromeric taste receptors. Proc. Natl. Acad. Sci. U. S. A. 101 (2004) 14258-14263
-
(2004)
Proc. Natl. Acad. Sci. U. S. A.
, vol.101
, pp. 14258-14263
-
-
Xu, H.1
-
30
-
-
33847419390
-
International Union of Basic and Clinical Pharmacology. LXVII. Recommendations for the recognition and nomenclature of G protein-coupled receptor heteromultimers
-
Pin J.P., et al. International Union of Basic and Clinical Pharmacology. LXVII. Recommendations for the recognition and nomenclature of G protein-coupled receptor heteromultimers. Pharmacol. Rev. 59 (2007) 5-13
-
(2007)
Pharmacol. Rev.
, vol.59
, pp. 5-13
-
-
Pin, J.P.1
-
31
-
-
3142685557
-
The heptahelical domain of GABA(B2) is activated directly by CGP7930, a positive allosteric modulator of the GABA(B) receptor
-
Binet V., 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. 279 (2004) 29085-29091
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 29085-29091
-
-
Binet, V.1
-
32
-
-
33845874637
-
Drug treatments for obesity: orlistat, sibutramine, and rimonabant
-
Padwal R.S., and Mujumdar S.R. Drug treatments for obesity: orlistat, sibutramine, and rimonabant. Lancet 369 (2007) 71-77
-
(2007)
Lancet
, vol.369
, pp. 71-77
-
-
Padwal, R.S.1
Mujumdar, S.R.2
-
33
-
-
0030826705
-
A selective inverse agonist for central cannabinoid receptor inhibits mitogen-activated protein kinase activation stimulated by insulin or insulin-like growth factor 1. Evidence for a new model of receptor/ligand interactions
-
Bouaboula M., et al. A selective inverse agonist for central cannabinoid receptor inhibits mitogen-activated protein kinase activation stimulated by insulin or insulin-like growth factor 1. Evidence for a new model of receptor/ligand interactions. J. Biol. Chem. 272 (1997) 22330-22339
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 22330-22339
-
-
Bouaboula, M.1
-
34
-
-
33646526072
-
I want a new drug: G-protein-coupled receptors in drug development
-
Schlyer S., and Horuk R. I want a new drug: G-protein-coupled receptors in drug development. Drug Discov. Today 11 (2006) 481-493
-
(2006)
Drug Discov. Today
, vol.11
, pp. 481-493
-
-
Schlyer, S.1
Horuk, R.2
-
36
-
-
33746290412
-
The orphan GPR50 receptor specifically inhibits MT1 melatonin receptor function through heterodimerization
-
Levoye A., et al. The orphan GPR50 receptor specifically inhibits MT1 melatonin receptor function through heterodimerization. EMBO J. 25 (2006) 3012-3023
-
(2006)
EMBO J.
, vol.25
, pp. 3012-3023
-
-
Levoye, A.1
-
37
-
-
20244388129
-
G-protein-coupled receptor Mas is a physiological antagonist of the angiotensin II type 1 receptor
-
Kostenis E., et al. G-protein-coupled receptor Mas is a physiological antagonist of the angiotensin II type 1 receptor. Circulation 111 (2005) 1806-1813
-
(2005)
Circulation
, vol.111
, pp. 1806-1813
-
-
Kostenis, E.1
-
38
-
-
34248374907
-
Protease-activated receptor-3 (PAR3) regulates PAR1 signaling by receptor dimerization
-
McLaughlin J.N., et al. Protease-activated receptor-3 (PAR3) regulates PAR1 signaling by receptor dimerization. Proc. Natl. Acad. Sci. U. S. A. 104 (2007) 5662-5667
-
(2007)
Proc. Natl. Acad. Sci. U. S. A.
, vol.104
, pp. 5662-5667
-
-
McLaughlin, J.N.1
-
39
-
-
33644551294
-
Presynaptic control of striatal glutamateric neurotranmission by adenosine A1-A2a receptor heteromers
-
Ciruela F., et al. Presynaptic control of striatal glutamateric neurotranmission by adenosine A1-A2a receptor heteromers. J. Neurosci. 26 (2006) 2080-2087
-
(2006)
J. Neurosci.
, vol.26
, pp. 2080-2087
-
-
Ciruela, F.1
|