-
1
-
-
0035416126
-
High-throughput docking for lead generation
-
Abagyan, R., and Totrov, M. (2001). High-throughput docking for lead generation. Curr Opin Chem Biol 5, 375-382.
-
(2001)
Curr Opin Chem Biol
, vol.5
, pp. 375-382
-
-
Abagyan, R.1
Totrov, M.2
-
2
-
-
38949184303
-
Arresting serotonin
-
Abbas, A., and Roth, B.L. (2008). Arresting serotonin. Proc Natl Acad Sci USA 105, 831-832. doi: 10.1073/pnas.0711335105.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 831-832
-
-
Abbas, A.1
Roth, B.L.2
-
3
-
-
84864477056
-
Evidence of the importance of the first intracellular loop of prokineticin receptor 2 in receptor function
-
Abreu, A.P., Noel, S.D., Xu, S., Carroll, R.S., Latronico, A.C., and Kaiser, U.B. (2012). Evidence of the importance of the first intracellular loop of prokineticin receptor 2 in receptor function. Mol Endocrinol 26,1417-1427. doi: 10.1210/me.2012-1102 me.2012-1102 [pii].
-
(2012)
Mol Endocrinol
, vol.26
, pp. 1417-1427
-
-
Abreu, A.P.1
Noel, S.D.2
Xu, S.3
Carroll, R.S.4
Latronico, A.C.5
Kaiser, U.B.6
-
4
-
-
84873052698
-
Rational design, efficient syntheses and biological evaluation of N N'-symmetrically bis-substituted butylimidazole analogs as a new class of potent Angiotensin II receptor blockers
-
Agelis, G., Resvani, A., Koukoulitsa, C, Tumova, T., Slaninova, J., Kalavrizioti, D., Spyridaki, K., Afantitis, A., Melagraki, G., Siafaka, A., Gkini, E., Megariotis, G., Grdadolnik, S.G., Papadopoulos, M.G., Vlahakos, D., Maragoudakis, M., Liapakis, G., Mavromoustakos, T., and Matsoukas, J. (2013). Rational design, efficient syntheses and biological evaluation of N, N'-symmetrically bis-substituted butylimidazole analogs as a new class of potent Angiotensin II receptor blockers. Eur J Med Chem 62, 352-370. doi: 10.1016/j.ejmech.2012.12.044.
-
(2013)
Eur J Med Chem
, vol.62
, pp. 352-370
-
-
Agelis, G.1
Resvani, A.2
Koukoulitsa, C.3
Tumova, T.4
Slaninova, J.5
Kalavrizioti, D.6
Spyridaki, K.7
Afantitis, A.8
Melagraki, G.9
Siafaka, A.10
Gkini, E.11
Megariotis, G.12
Grdadolnik, S.G.13
Papadopoulos, M.G.14
Vlahakos, D.15
Maragoudakis, M.16
Liapakis, G.17
Mavromoustakos, T.18
Matsoukas, J.19
-
5
-
-
79951512210
-
Strategies to discover unexpected targets for drugs active at G protein-coupled receptors
-
Allen, J.A., and Roth, B.L. (2011). Strategies to discover unexpected targets for drugs active at G protein-coupled receptors. Annu Rev Pharmacol Toxicol 51, 117-144. doi: 10.1146/annurev-pharmtox-010510-100553.
-
(2011)
Annu Rev Pharmacol Toxicol
, vol.51
, pp. 117-144
-
-
Allen, J.A.1
Roth, B.L.2
-
6
-
-
79960456109
-
Oxycodone-related side effects: impact on degree of bother, adherence, pain relief, satisfaction, and quality of life
-
Anastassopoulos, K.P., Chow, W., Ackerman, S.J., Tapia, C, Benson, C, and Kim, M.S. (2011). Oxycodone-related side effects: impact on degree of bother, adherence, pain relief, satisfaction, and quality of life./Opioid Manag 7, 203-215.
-
(2011)
Opioid Manag
, vol.7
, pp. 203-215
-
-
Anastassopoulos, K.P.1
Chow, W.2
Ackerman, S.J.3
Tapia, C.4
Benson, C.5
Kim, M.S.6
-
7
-
-
84897026211
-
Structure-based and fragmentbased GPCR drug discovery
-
Andrews, S.P., Brown, G.A., and Christopher, J.A. (2014). Structure-based and fragmentbased GPCR drug discovery. Chem Med Chem 9, 256-275. doi: 10.1002/cmdc.201300382.
-
(2014)
Chem Med Chem
, vol.9
, pp. 256-275
-
-
Andrews, S.P.1
Brown, G.A.2
Christopher, J.A.3
-
8
-
-
34247640671
-
Evolving the lock to fit the key to create a family of G protein-coupled receptors potently activated by an inert ligand
-
Armbruster, B.N., Li, X., Pausch, M.H., Herlitze, S., and Roth, B.L. (2007). Evolving the lock to fit the key to create a family of G protein-coupled receptors potently activated by an inert ligand. Proc Natl Acad Sci USA 104, 5163-5168. doi: 0700293104 [pii] 10.1073/pnas.0700293104.
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 5163-5168
-
-
Armbruster, B.N.1
Li, X.2
Pausch, M.H.3
Herlitze, S.4
Roth, B.L.5
-
9
-
-
79952032110
-
The physiology, signaling, and pharmacology of dopamine receptors
-
Beaulieu, J.M., and Gainetdinov, R.R. (2011). The physiology, signaling, and pharmacology of dopamine receptors. Pharmacol Rev 63,182-217. doi: 10.1124/pr.ll0.002642.
-
(2011)
Pharmacol Rev
, vol.63
, pp. 182-217
-
-
Beaulieu, J.M.1
Gainetdinov, R.R.2
-
10
-
-
22744449073
-
An Akt/beta-arrestin 2/PP2A signaling complex mediates dopaminergic neurotransmission and behavior
-
Beaulieu, J.M., Sotnikova, T.D., Marion, S., Lefkowitz, R.J., Gainetdinov, R.R., and Caron, M.G. (2005). An Akt/beta-arrestin 2/PP2A signaling complex mediates dopaminergic neurotransmission and behavior. Cell 122, 261-273. doi: 10.1016/j.cell.2005.05.012.
-
(2005)
Cell
, vol.122
, pp. 261-273
-
-
Beaulieu, J.M.1
Sotnikova, T.D.2
Marion, S.3
Lefkowitz, R.J.4
Gainetdinov, R.R.5
Caron, M.G.6
-
11
-
-
77956896591
-
Angiotensin II revisited: new roles in inflammation, immunology and aging
-
Benigni, A., Cassis, P., and Remuzzi, G. (2010). Angiotensin II revisited: new roles in inflammation, immunology and aging. EMBO Mol Med 2, 247-257. doi: 10.1002/emmm.201000080.
-
(2010)
EMBO Mol Med
, vol.2
, pp. 247-257
-
-
Benigni, A.1
Cassis, P.2
Remuzzi, G.3
-
12
-
-
84867617550
-
The meningococcal minor pilin PilX is responsible for type IV pilus conformational changes associated with signaling to endothelial cells
-
Brissac, T., Mikaty, G., Dumenil, G., Coureuil, M., and Nassif, X. (2012). The meningococcal minor pilin PilX is responsible for type IV pilus conformational changes associated with signaling to endothelial cells. Infect Immun 80, 3297-3306. doi: 10.1128/IAI.00369-12.
-
(2012)
Infect Immun
, vol.80
, pp. 3297-3306
-
-
Brissac, T.1
Mikaty, G.2
Dumenil, G.3
Coureuil, M.4
Nassif, X.5
-
13
-
-
79151478285
-
Three-dimensional quantitative structure-selectivity relationships analysis guided rational design of a highly selective ligand for the cannabinoid receptor 2
-
Brogi, S., Corelli, F., Di Marzo, V., Ligresti, A., Mugnaini, C, Pasquini, S., and Tafi, A. (2011). Three-dimensional quantitative structure-selectivity relationships analysis guided rational design of a highly selective ligand for the cannabinoid receptor 2. EurJ Med Chem 46, 547-555. doi: 10.1016/j.ejmech.2010.11.034.
-
(2011)
EurJ Med Chem
, vol.46
, pp. 547-555
-
-
Brogi, S.1
Corelli, F.2
Di Marzo, V.3
Ligresti, A.4
Mugnaini, C.5
Pasquini, S.6
Tafi, A.7
-
14
-
-
72949120874
-
Pharmacophore modeling for qualitative prediction of antiestrogenic activity
-
Brogi, S., Kladi, M., Vagias, C, Papazafiri, P., Roussis, V., and Tafi, A. (2009). Pharmacophore modeling for qualitative prediction of antiestrogenic activity./Chem Inf Model 49, 2489-2497. doi: 10.1021/ci900254b.
-
(2009)
Chem Inf Model
, vol.49
, pp. 2489-2497
-
-
Brogi, S.1
Kladi, M.2
Vagias, C.3
Papazafiri, P.4
Roussis, V.5
Tafi, A.6
-
15
-
-
84882523749
-
3D-QSAR using pharmacophorebased alignment and virtual screening for discovery of novel MCF-7 cell line inhibitors
-
Brogi, S., Papazafiri, P., Roussis, V., and Tafi, A. (2013). 3D-QSAR using pharmacophorebased alignment and virtual screening for discovery of novel MCF-7 cell line inhibitors. EurJ Med Chem 67, 344-351. doi: 10.1016/j.ejmech.2013.06.048.
-
(2013)
EurJ Med Chem
, vol.67
, pp. 344-351
-
-
Brogi, S.1
Papazafiri, P.2
Roussis, V.3
Tafi, A.4
-
16
-
-
75149183092
-
The dynorphin/kappa opioid system as a modulator of stress-induced and pro-addictive behaviors
-
Bruchas, M.R., Land, B.B., and Chavkin, C. (2010). The dynorphin/kappa opioid system as a modulator of stress-induced and pro-addictive behaviors. Brain Res 1314, 44-55. doi: 10.1016/j.brainres.2009.08.062
-
(2010)
Brain Res
, vol.1314
, pp. 44-55
-
-
Bruchas, M.R.1
Land, B.B.2
Chavkin, C.3
-
17
-
-
79951958713
-
Strategies for the identification of allosteric modulators of G-protein-coupled receptors
-
Burford, N.T., Watson, J., Bertekap, R., and Alt, A. (2011). Strategies for the identification of allosteric modulators of G-protein-coupled receptors. Biochem Pharmacol 81, 691-702. doi: 10.1016/j.bcp.2010.12.012.
-
(2011)
Biochem Pharmacol
, vol.81
, pp. 691-702
-
-
Burford, N.T.1
Watson, J.2
Bertekap, R.3
Alt, A.4
-
18
-
-
84879514548
-
Discovery of positive allosteric modulators and silent allosteric modulators of μ-opioid receptor
-
Burford, N.T., Clark, M.J., Wehrman, T.S., Gerritz, S.W., Banks, M., O'Connell, J, Traynor, J.R., and Alt, A. (2013). Discovery of positive allosteric modulators and silent allosteric modulators of μ-opioid receptor. Proc Natl Acad Sci USA. 110, 10830-5. doi: 10.1073/pnas. 1300393110.
-
(2013)
Proc Natl Acad Sci USA
, vol.110
, pp. 10830-10835
-
-
Burford, N.T.1
Clark, M.J.2
Wehrman, T.S.3
Gerritz, S.W.4
Banks, M.5
O'Connell, J.6
Traynor, J.R.7
Alt, A.8
-
19
-
-
84874415806
-
Synthesis and structure-activity relationship studies in serotonin 5-HT(lA) receptor agonists based on fused pyrrolidone scaffolds
-
Cappelli, A., Manini, M., Valenti, S., Castriconi, F., Giuliani, G., Anzini, M., Brogi, S., Butini, S., Gemma, S., Campiani, G., Giorgi, G., Mennuni, L, Lanza, M., Giordani, A., Caselli, G., Letari, 0., and Makovec, F. (2013). Synthesis and structure-activity relationship studies in serotonin 5-HT(lA) receptor agonists based on fused pyrrolidone scaffolds. EurJ Med Chem 63, 85-94. doi: 10.1016/j.ejmech.2013.01.044.
-
(2013)
EurJ Med Chem
, vol.63
, pp. 85-94
-
-
Cappelli, A.1
Manini, M.2
Valenti, S.3
Castriconi, F.4
Giuliani, G.5
Anzini, M.6
Brogi, S.7
Butini, S.8
Gemma, S.9
Campiani, G.10
Giorgi, G.11
Mennuni, L.12
Lanza, M.13
Giordani, A.14
Caselli, G.15
Letari, 0.16
Makovec, F.17
-
20
-
-
84857272638
-
Characterization of COR627 and COR628, two novel positive allosteric modulators of the GABA(B) receptor
-
Castelli, M.P., Casu, A., Casti, P., Lobina, C, Carai, M.A., Colombo, G., Solinas, M., Giunta, D., Mugnaini, C, Pasquini, S., Tafi, A., Brogi, S., Gessa, G.L., and Corelli, F. (2012). Characterization of COR627 and COR628, two novel positive allosteric modulators of the GABA(B) receptor./Pharmacol Exp Ther 340, 529-538. doi: 10.1124/jpet.lll.l86460.
-
(2012)
Pharmacol Exp Ther
, vol.340
, pp. 529-538
-
-
Castelli, M.P.1
Casu, A.2
Casti, P.3
Lobina, C.4
Carai, M.A.5
Colombo, G.6
Solinas, M.7
Giunta, D.8
Mugnaini, C.9
Pasquini, S.10
Tafi, A.11
Brogi, S.12
Gessa, G.L.13
Corelli, F.14
-
21
-
-
84886532899
-
Structure-activity relationships and discovery of a G protein biased mu opioid receptor ligand, [(3-methoxythiophen-2-yl)methyl]({2-[(9R)-9-(pyridin-2-yl)-6-oxaspiro-[4.5]decan- 9-yl]ethylJ)amine (TRV130), for the treatment of acute severe pain
-
Chen, X.T., Pitis, P., Liu, G., Yuan, C, Gotchev, D., Cowan, C.L., Rominger, D.H., Koblish, M., Dewire, S.M., Crombie, A.L., Violin, J.D., and Yamashita, D.S. (2013). Structure-activity relationships and discovery of a G protein biased mu opioid receptor ligand, [(3-methoxythiophen-2-yl)methyl]({2-[(9R)-9-(pyridin-2-yl)-6-oxaspiro-[4.5]decan- 9-yl]ethylJ)amine (TRV130), for the treatment of acute severe pain./Med Chem 56, 8019-8031. doi: 10.1021/jm4010829.
-
(2013)
Med Chem
, vol.56
, pp. 8019-8031
-
-
Chen, X.T.1
Pitis, P.2
Liu, G.3
Yuan, C.4
Gotchev, D.5
Cowan, C.L.6
Rominger, D.H.7
Koblish, M.8
Dewire, S.M.9
Crombie, A.L.10
Violin, J.D.11
Yamashita, D.S.12
-
22
-
-
9944252602
-
A robotic system for crystallizing membrane and soluble proteins in lipidic mesophases
-
Cherezov, V., Peddi, A., Muthusubramaniam, L., Zheng, Y.F., and Caffrey, M. (2004). A robotic system for crystallizing membrane and soluble proteins in lipidic mesophases. Acta Crystallogr D Biol Crystallogr 60,1795-1807. doi: 10.1107/S0907444904019109
-
(2004)
Acta Crystallogr D Biol Crystallogr
, vol.60
, pp. 1795-1807
-
-
Cherezov, V.1
Peddi, A.2
Muthusubramaniam, L.3
Zheng, Y.F.4
Caffrey, M.5
-
23
-
-
36448995359
-
High-resolution crystal structure of an engineered human beta2-adrenergic G protein-coupled receptor
-
Cherezov, V., Rosenbaum, D.M., Hanson, MA, Rasmussen, S.G., Thian, F.S., Kobilka, T.S., Choi, H.J., Kuhn, P., Weis, W.I., Kobilka, B.K., and Stevens, R.C. (2007). High-resolution crystal structure of an engineered human beta2-adrenergic G protein-coupled receptor. Science 318,1258-1265. doi: 10.1126/science.ll50577.
-
(2007)
Science
, vol.318
, pp. 1258-1265
-
-
Cherezov, V.1
Rosenbaum, D.M.2
Hanson, M.A.3
Rasmussen, S.G.4
Thian, F.S.5
Kobilka, T.S.6
Choi, H.J.7
Kuhn, P.8
Weis, W.I.9
Kobilka, B.K.10
Stevens, R.C.11
-
24
-
-
78449305788
-
Structure of the human dopamine D3 receptor in complex with a D2/D3 selective antagonist
-
Chien, E.Y., Liu, W., Zhao, Q., Katritch, V., Han, G.W., Hanson, M.A., Shi, L, Newman, A.H., Javitch, J.A., Cherezov, V., and Stevens, R.C. (2010). Structure of the human dopamine D3 receptor in complex with a D2/D3 selective antagonist. Science 330, 1091-1095. doi: 10.1126/science.ll97410.
-
(2010)
Science
, vol.330
, pp. 1091-1095
-
-
Chien, E.Y.1
Liu, W.2
Zhao, Q.3
Katritch, V.4
Han, G.W.5
Hanson, M.A.6
Shi, L.7
Newman, A.H.8
Javitch, J.A.9
Cherezov, V.10
Stevens, R.C.11
-
25
-
-
84877716938
-
Biophysical fragment screening of the betal-adrenergic receptor: identification of high affinity arylpiperazine leads using structure-based drug design
-
Christopher, J.A., Brown, J., Dore, A.S., Errey, J.C., Koglin, M., Marshall, F.H., Myszka, D.G., Rich, R.L., Tate, C.G., Tehan, B., Warne, T., and Congreve, M. (2013). Biophysical fragment screening of the betal-adrenergic receptor: identification of high affinity arylpiperazine leads using structure-based drug design. J Med Chem 56, 3446-3455. doi: 10.1021/jm400140q.
-
(2013)
J Med Chem
, vol.56
, pp. 3446-3455
-
-
Christopher, J.A.1
Brown, J.2
Dore, A.S.3
Errey, J.C.4
Koglin, M.5
Marshall, F.H.6
Myszka, D.G.7
Rich, R.L.8
Tate, C.G.9
Tehan, B.10
Warne, T.11
Congreve, M.12
-
26
-
-
0036490942
-
Allosteric binding sites on cell-surface receptors: novel targets for drug discovery
-
Christopoulos, A. (2002). Allosteric binding sites on cell-surface receptors: novel targets for drug discovery. Nat Rev Drug Discov 1,198-210. doi: 10.1038/nrd746.
-
(2002)
Nat Rev Drug Discov
, vol.1
, pp. 198-210
-
-
Christopoulos, A.1
-
27
-
-
84861984672
-
Fusion partner toolchest for the stabilization and crystallization of G protein-coupled receptors
-
Chun, E., Thompson, A.A., Liu, W., Roth, C.B., Griffith, M.T., Katritch, V., Kunken, J., Xu, F., Cherezov, V., Hanson, M.A., and Stevens, R.C. (2012). Fusion partner toolchest for the stabilization and crystallization of G protein-coupled receptors. Structure 20, 967-976. doi: 10.1016/j.str.2012.04.010.
-
(2012)
Structure
, vol.20
, pp. 967-976
-
-
Chun, E.1
Thompson, A.A.2
Liu, W.3
Roth, C.B.4
Griffith, M.T.5
Katritch, V.6
Kunken, J.7
Xu, F.8
Cherezov, V.9
Hanson, M.A.10
Stevens, R.C.11
-
28
-
-
34247274157
-
Respiratory depression with opioids
-
Dahan, A. (2007). Respiratory depression with opioids. J Pain Palliat Care Pharmacother 21, 63-66.
-
(2007)
J Pain Palliat Care Pharmacother
, vol.21
, pp. 63-66
-
-
Dahan, A.1
-
29
-
-
30044442319
-
Opioid-induced tolerance and dependence in mice is modulated by the distance between pharmacophores in a bivalent ligand series
-
Daniels, D.J., Lenard, N.R., Etienne, C.L., Law, P.Y., Roerig, S.C., and Portoghese, P.S. (2005). Opioid-induced tolerance and dependence in mice is modulated by the distance between pharmacophores in a bivalent ligand series. Proc Natl Acad Sci USA 102, 19208-19213. doi: 10.1073/pnas.0506627102.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 19208-19213
-
-
Daniels, D.J.1
Lenard, N.R.2
Etienne, C.L.3
Law, P.Y.4
Roerig, S.C.5
Portoghese, P.S.6
-
30
-
-
33947401068
-
Beta-arrestins and cell signaling
-
Dewire, S.M., Ahn, S., Lefkowitz, R.J., and Shenoy, S.K. (2007). Beta-arrestins and cell signaling. Annu Rev Physiol 69, 483-510. doi: 10.1146/annurev.ph.69.013107.100021.
-
(2007)
Annu Rev Physiol
, vol.69
, pp. 483-510
-
-
Dewire, S.M.1
Ahn, S.2
Lefkowitz, R.J.3
Shenoy, S.K.4
-
31
-
-
79960382104
-
Biased ligands for better cardiovascular drugs: dissecting G-protein-coupled receptor pharmacology
-
Dewire, S.M., and Violin, J.D. (2011). Biased ligands for better cardiovascular drugs: dissecting G-protein-coupled receptor pharmacology. Circ Res 109, 205-216. doi: 10.1161/CIRCRESAHA.110.231308109/2/205 [pii].
-
(2011)
Circ Res
, vol.109
, pp. 205-216
-
-
Dewire, S.M.1
Violin, J.D.2
-
32
-
-
43249100162
-
Targeting the endocannabinoid system: to enhance or reduce?
-
Di Marzo, V. (2008). Targeting the endocannabinoid system: to enhance or reduce? Nat Rev Drug Discov 7, 438-455. doi: 10.1038/nrd2553.
-
(2008)
Nat Rev Drug Discov
, vol.7
, pp. 438-455
-
-
Di Marzo, V.1
-
33
-
-
84904994581
-
Structure of class C GPCR metabotropic glutamate receptor 5 transmembrane domain
-
Dore, A.S., Okrasa, K., Patel, J.C., Serrano-Vega, M., Bennett, K., Cooke, R.M., Errey, J.C., Jazayeri, A., Khan, S., Tehan, B., Weir, M., Wiggin, G.R., and Marshall, F.H. (2014). Structure of class C GPCR metabotropic glutamate receptor 5 transmembrane domain. Nature 511, 557-562. doi: 10.1038/naturel3396.
-
(2014)
Nature
, vol.511
, pp. 557-562
-
-
Dore, A.S.1
Okrasa, K.2
Patel, J.C.3
Serrano-Vega, M.4
Bennett, K.5
Cooke, R.M.6
Errey, J.C.7
Jazayeri, A.8
Khan, S.9
Tehan, B.10
Weir, M.11
Wiggin, G.R.12
Marshall, F.H.13
-
34
-
-
84891693732
-
Prokineticin receptor-1 is a new regulator of endothelial insulin uptake and capillary formation to control insulin sensitivity and cardiovascular and kidney functions
-
jah3343
-
Dormishian, M., Turkeri, G., Urayama, K., Nguyen, T.L., Boulberdaa, M., Messaddeq, N., Renault, G., Henrion, D., and Nebigil, C.G. (2013). Prokineticin receptor-1 is a new regulator of endothelial insulin uptake and capillary formation to control insulin sensitivity and cardiovascular and kidney functions./Am Heart Assoc 2, e000411. doi: 10.1161/JAHA.113.000411 jah3343 [pii].
-
(2013)
Am Heart Assoc
, vol.2
-
-
Dormishian, M.1
Turkeri, G.2
Urayama, K.3
Nguyen, T.L.4
Boulberdaa, M.5
Messaddeq, N.6
Renault, G.7
Henrion, D.8
Nebigil, C.G.9
-
35
-
-
30744447460
-
Efficacy of short-term monotherapy with maraviroc, a new CCR5 antagonist, in patients infected with HIV-1
-
Fatkenheuer, G., Pozniak, A.L., Johnson, M.A., Plettenberg, A., Staszewski, S., Hoepelman, A.I., Saag, M.S., Goebel, F.D., Rockstroh, J.K., Dezube, B.J., Jenkins, T.M., Medhurst, C, Sullivan, J.F., Ridgway, C, Abel, S., James, I.T., Youle, M., and Van Der Ryst, E. (2005). Efficacy of short-term monotherapy with maraviroc, a new CCR5 antagonist, in patients infected with HIV-1. Nat Med 11,1170-1172. doi: 10.1038/nml319.
-
(2005)
Nat Med
, vol.11
, pp. 1170-1172
-
-
Fatkenheuer, G.1
Pozniak, A.L.2
Johnson, M.A.3
Plettenberg, A.4
Staszewski, S.5
Hoepelman, A.I.6
Saag, M.S.7
Goebel, F.D.8
Rockstroh, J.K.9
Dezube, B.J.10
Jenkins, T.M.11
Medhurst, C.12
Sullivan, J.F.13
Ridgway, C.14
Abel, S.15
James, I.T.16
Youle, M.17
Van Der Ryst, E.18
-
36
-
-
84893954062
-
Molecular control of delta-opioid receptor signalling
-
Fenalti, G., Giguere, P.M., Katritch, V., Huang, X.P., Thompson, A.A., Cherezov, V., Roth, B.L., and Stevens, R.C. (2014). Molecular control of delta-opioid receptor signalling. Nature 506,191-196. doi: 10.1038/naturel2944.
-
(2014)
Nature
, vol.506
, pp. 191-196
-
-
Fenalti, G.1
Giguere, P.M.2
Katritch, V.3
Huang, X.P.4
Thompson, A.A.5
Cherezov, V.6
Roth, B.L.7
Stevens, R.C.8
-
37
-
-
35748965848
-
Comparative protein structure modeling by combining multiple templates and optimizing sequence-to-structure alignments
-
btm377
-
Fernandez-Fuentes, N., Rai, B.K., Madrid-Aliste, C.J., Fajardo, J.E., and Fiser, A. (2007). Comparative protein structure modeling by combining multiple templates and optimizing sequence-to-structure alignments. Bioinformatics 23, 2558-2565. doi: btm377 [pii] 10.1093/bioinformatics/btm377.
-
(2007)
Bioinformatics
, vol.23
, pp. 2558-2565
-
-
Fernandez-Fuentes, N.1
Rai, B.K.2
Madrid-Aliste, C.J.3
Fajardo, J.E.4
Fiser, A.5
-
38
-
-
2442709037
-
Chemical function based pharmacophore generation of endothelin-A selective receptor antagonists
-
Funk, O.F., Kettmann, V., Drimal, J., and Langer, T. (2004). Chemical function based pharmacophore generation of endothelin-A selective receptor antagonists./Med Chem 47, 2750-2760. doi: 10.1021/jm031041j.
-
(2004)
Med Chem
, vol.47
, pp. 2750-2760
-
-
Funk, O.F.1
Kettmann, V.2
Drimal, J.3
Langer, T.4
-
39
-
-
84858769326
-
Generation of a synthetic memory trace
-
335/6075/1513
-
Garner, A.R., Rowland, D.C., Hwang, S.Y., Baumgaertel, K., Roth, B.L., Kentros, C, and Mayford, M. (2012). Generation of a synthetic memory trace. Science 335, 1513-1516. doi: 10.1126/science.l214985335/6075/1513 [pii].
-
(2012)
Science
, vol.335
, pp. 1513-1516
-
-
Garner, A.R.1
Rowland, D.C.2
Hwang, S.Y.3
Baumgaertel, K.4
Roth, B.L.5
Kentros, C.6
Mayford, M.7
-
40
-
-
84896260151
-
HCV-targeted antivirals: current status and future challenges
-
Gemma, S., Brogi, S., Novellino, E., Campiani, G., Maga, G., Brindisi, M., and Butini, S. (2014a). HCV-targeted antivirals: current status and future challenges. Curr Pharm Des 20, 3445-3464.
-
(2014)
Curr Pharm Des
, vol.20
, pp. 3445-3464
-
-
Gemma, S.1
Brogi, S.2
Novellino, E.3
Campiani, G.4
Maga, G.5
Brindisi, M.6
Butini, S.7
-
41
-
-
84891458817
-
From (+)-epigallocatechin gallate to a simplified synthetic analogue as a cytoadherence inhibitor for P. falciparum
-
Gemma, S., Brogi, S., Patil, P.R., Giovani, S., Lamponi, S., Cappelli, A., Novellino, E., Brown, A., Higgins, M.K., Mustafa, K., Szestak, T., Craig, A.G., Campiani, G., Butini, S., and Brindisi, M. (2014b). From (+)-epigallocatechin gallate to a simplified synthetic analogue as a cytoadherence inhibitor for P. falciparum. RSC Advances 4, 4769-4781. doi: 10.1039/c3ra45933k.
-
(2014)
RSC Advances
, vol.4
, pp. 4769-4781
-
-
Gemma, S.1
Brogi, S.2
Patil, P.R.3
Giovani, S.4
Lamponi, S.5
Cappelli, A.6
Novellino, E.7
Brown, A.8
Higgins, M.K.9
Mustafa, K.10
Szestak, T.11
Craig, A.G.12
Campiani, G.13
Butini, S.14
Brindisi, M.15
-
42
-
-
73949084919
-
A beta-arrestin-biased agonist of the parathyroid hormone receptor (PTH1R) promotes bone formation independent of G protein activation
-
lral
-
Gesty-Palmer, D., Flannery, P., Yuan, L, Corsino, L, Spurney, R., Lefkowitz, R.J., and Luttrell, L.M. (2009). A beta-arrestin-biased agonist of the parathyroid hormone receptor (PTH1R) promotes bone formation independent of G protein activation. Sci Transl Med 1, l r a l. doi: 10.1126/scitranslmed.3000071.
-
(2009)
Sci Transl Med
, vol.1
-
-
Gesty-Palmer, D.1
Flannery, P.2
Yuan, L.3
Corsino, L.4
Spurney, R.5
Lefkowitz, R.J.6
Luttrell, L.M.7
-
43
-
-
84903957340
-
Rational design of the first difluorostatonebased PfSUBl inhibitors
-
Giovani, S., Penzo, M., Brogi, S., Brindisi, M., Gemma, S., Novellino, E., Savini, L, Blackman, M.J., Campiani, G., and Butini, S. (2014). Rational design of the first difluorostatonebased PfSUBl inhibitors. Bioorg Med Chem Lett 24, 3582-3586. doi: 10.1016/j.bmcl.2014.05.044.
-
(2014)
Bioorg Med Chem Lett
, vol.24
, pp. 3582-3586
-
-
Giovani, S.1
Penzo, M.2
Brogi, S.3
Brindisi, M.4
Gemma, S.5
Novellino, E.6
Savini, L.7
Blackman, M.J.8
Campiani, G.9
Butini, S.10
-
44
-
-
0030594604
-
Angiotensin receptors and their antagonists
-
Goodfriend, T.L., Elliott, M.E., and Catt, K.J. (1996). Angiotensin receptors and their antagonists. NEnglJMed 334,1649-1654. doi: 10.1056/NEJM199606203342507.
-
(1996)
NEnglJMed
, vol.334
, pp. 1649-1654
-
-
Goodfriend, T.L.1
Elliott, M.E.2
Catt, K.J.3
-
45
-
-
84861075468
-
Structure of the delta-opioid receptor bound to naltrindole
-
Granier, S., Manglik, A., Kruse, A.C., Kobilka, T.S., Thian, F.S., Weis, W.I., and Kobilka, B.K. (2012). Structure of the delta-opioid receptor bound to naltrindole. Nature 485, 400-404. doi: 10.1038/naturelllll.
-
(2012)
Nature
, vol.485
, pp. 400-404
-
-
Granier, S.1
Manglik, A.2
Kruse, A.C.3
Kobilka, T.S.4
Thian, F.S.5
Weis, W.I.6
Kobilka, B.K.7
-
46
-
-
34447134181
-
A familial thyrotropin (TSH) receptor mutation provides in vivo evidence that the inositol phosphates/Ca2+ cascade mediates TSH action on thyroid hormone synthesis
-
Grasberger, H., Van Sande, J., Hag-Dahood Mahameed, A., Tenenbaum-Rakover, Y., and Refetoff, S. (2007). A familial thyrotropin (TSH) receptor mutation provides in vivo evidence that the inositol phosphates/Ca2+ cascade mediates TSH action on thyroid hormone synthesis./Clin Endocrinol Metab 92, 2816-2820. doi: jc.2007-0366 [pii] 10.1210/JC.2007-0366.
-
(2007)
Clin Endocrinol Metab
, vol.92
, pp. 2816-2820
-
-
Grasberger, H.1
Van Sande, J.2
Hag-Dahood Mahameed, A.3
Tenenbaum-Rakover, Y.4
Refetoff, S.5
-
47
-
-
72649084796
-
A chemical-genetic approach to study G protein regulation of beta cell function in vivo
-
Guettier, J.M., Gautam, D., Scarselli, M., Ruiz De Azua, I., Li, J.H., Rosemond, E., Ma, X., Gonzalez, F.J., Armbruster, B.N., Lu, H., Roth, B.L., and Wess, J. (2009). A chemical-genetic approach to study G protein regulation of beta cell function in vivo. Proc Natl Acad Sci USA 106, 19197-19202. doi: 10.1073/pnas.0906593106 0906593106 [pii].
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 19197-19202
-
-
Guettier, J.M.1
Gautam, D.2
Scarselli, M.3
Ruiz De Azua, I.4
Li, J.H.5
Rosemond, E.6
Ma, X.7
Gonzalez, F.J.8
Armbruster, B.N.9
Lu, H.10
Roth, B.L.11
Wess, J.12
-
48
-
-
84862777405
-
Structure of the human M2 muscarinic acetylcholine receptor bound to an antagonist
-
Haga, K., Kruse, A.C., Asada, H., Yurugi-Kobayashi, T., Shiroishi, M., Zhang, C, Weis, W.I., Okada, T., Kobilka, B.K., Haga, T., and Kobayashi, T. (2012). Structure of the human M2 muscarinic acetylcholine receptor bound to an antagonist. Nature 482, 547-551. doi: 10.1038/naturel0753.
-
(2012)
Nature
, vol.482
, pp. 547-551
-
-
Haga, K.1
Kruse, A.C.2
Asada, H.3
Yurugi-Kobayashi, T.4
Shiroishi, M.5
Zhang, C.6
Weis, W.I.7
Okada, T.8
Kobilka, B.K.9
Haga, T.10
Kobayashi, T.11
-
49
-
-
44649172481
-
A specific cholesterol binding site is established by the 2 8 A structure of the human beta2-adrenergic receptor
-
Hanson, M.A., Cherezov, V., Griffith, M.T., Roth, C.B., Jaakola, V.P., Chien, E.Y., Velasquez, J., Kuhn, P., and Stevens, R.C. (2008). A specific cholesterol binding site is established by the 2.8 A structure of the human beta2-adrenergic receptor. Structure 16, 897-905. doi: 10.1016/j.str.2008.05.001.
-
(2008)
Structure
, vol.16
, pp. 897-905
-
-
Hanson, M.A.1
Cherezov, V.2
Griffith, M.T.3
Roth, C.B.4
Jaakola, V.P.5
Chien, E.Y.6
Velasquez, J.7
Kuhn, P.8
Stevens, R.C.9
-
50
-
-
84857254248
-
Crystal structure of a lipid G protein-coupled receptor
-
Hanson, M.A., Roth, C.B., Jo, E., Griffith, M.T., Scott, F.L., Reinhart, G., Desale, H., Clemons, B., Cahalan, S.M., Schuerer, S.C., Sanna, M.G., Han, G.W., Kuhn, P., Rosen, H., and Stevens, R.C. (2012). Crystal structure of a lipid G protein-coupled receptor. Science 335, 851-855. doi: 10.1126/science.l215904.
-
(2012)
Science
, vol.335
, pp. 851-855
-
-
Hanson, M.A.1
Roth, C.B.2
Jo, E.3
Griffith, M.T.4
Scott, F.L.5
Reinhart, G.6
Desale, H.7
Clemons, B.8
Cahalan, S.M.9
Schuerer, S.C.10
Sanna, M.G.11
Han, G.W.12
Kuhn, P.13
Rosen, H.14
Stevens, R.C.15
-
51
-
-
84881173408
-
Structure of class B GPCR corticotropin-releasing factor receptor 1
-
Hollenstein, K., Kean, J., Bortolato, A., Cheng, R.K., Dore, A.S., Jazayeri, A., Cooke, R.M., Weir, M., and Marshall, F.H. (2013). Structure of class B GPCR corticotropin-releasing factor receptor 1. Nature 499, 438-443. doi: 10.1038/naturel2357.
-
(2013)
Nature
, vol.499
, pp. 438-443
-
-
Hollenstein, K.1
Kean, J.2
Bortolato, A.3
Cheng, R.K.4
Dore, A.S.5
Jazayeri, A.6
Cooke, R.M.7
Weir, M.8
Marshall, F.H.9
-
52
-
-
56749103466
-
The 2 6 angstrom crystal structure of a human A2A adenosine receptor bound to an antagonist
-
Jaakola, V.P., Griffith, M.T., Hanson, M.A., Cherezov, V., Chien, E.Y., Lane, J.R., Ijzerman, A.P., and Stevens, R.C. (2008). The 2.6 angstrom crystal structure of a human A2A adenosine receptor bound to an antagonist. Science 322, 1211-1217. doi: 10.1126/science.ll64772.
-
(2008)
Science
, vol.322
, pp. 1211-1217
-
-
Jaakola, V.P.1
Griffith, M.T.2
Hanson, M.A.3
Cherezov, V.4
Chien, E.Y.5
Lane, J.R.6
Ijzerman, A.P.7
Stevens, R.C.8
-
53
-
-
84905443315
-
Allosteric and biased g protein-coupled receptor signaling regulation: potentials for new therapeutics
-
Khoury, E., Clement, S., and Laporte, S.A. (2014). Allosteric and biased g protein-coupled receptor signaling regulation: potentials for new therapeutics. Front Endocrinol (Lausanne) 5, 68. doi: 10.3389/fendo.2014.00068.
-
(2014)
Front Endocrinol (Lausanne)
, vol.5
, pp. 68
-
-
Khoury, E.1
Clement, S.2
Laporte, S.A.3
-
54
-
-
66149149851
-
Structure-based discovery of beta2-adrenergic receptor ligands
-
Kolb, P., Rosenbaum, D.M., Irwin, J.J., Fung, J.J., Kobilka, B.K., and Shoichet, B.K. (2009). Structure-based discovery of beta2-adrenergic receptor ligands. Proc Natl Acad Sci U SA 106, 6843-6848. doi: 10.1073/pnas.0812657106.
-
(2009)
Proc Natl Acad Sci U SA
, vol.106
, pp. 6843-6848
-
-
Kolb, P.1
Rosenbaum, D.M.2
Irwin, J.J.3
Fung, J.J.4
Kobilka, B.K.5
Shoichet, B.K.6
-
55
-
-
84868012864
-
GABAergic RIP-Cre neurons in the arcuate nucleus selectively regulate energy expenditure
-
Kong, D., Tong, Q., Ye, C, Koda, S., Fuller, P.M., Krashes, M.J., Vong, L, Ray, R.S., Olson, D.P., and Lowell, B.B. (2012). GABAergic RIP-Cre neurons in the arcuate nucleus selectively regulate energy expenditure. Cell 151, 645-657. doi: 10.1016/j.cell.2012.09.020 S0092-8674(12)01127-0 [pii].
-
(2012)
Cell
, vol.151
, pp. 645-657
-
-
Kong, D.1
Tong, Q.2
Ye, C.3
Koda, S.4
Fuller, P.M.5
Krashes, M.J.6
Vong, L.7
Ray, R.S.8
Olson, D.P.9
Lowell, B.B.10
-
56
-
-
84873344962
-
From heptahelical bundle to hits from the Haystack: structure-based virtual screening for GPCR ligands
-
Kooistra, A.J., Roumen, L., Leurs, R., De Esch, I.J., and De Graaf, C. (2013). From heptahelical bundle to hits from the Haystack: structure-based virtual screening for GPCR ligands. Methods Enzymol 522, 279-336. doi: 10.1016/B978-0-12-407865-9.00015-7.
-
(2013)
Methods Enzymol
, vol.522
, pp. 279-336
-
-
Kooistra, A.J.1
Roumen, L.2
Leurs, R.3
De Esch, I.J.4
De Graaf, C.5
-
57
-
-
33749263335
-
Effect of beta blockers, particularly carvedilol, on reducing the risk of events after acute myocardial infarction
-
Kopecky, S.L. (2006). Effect of beta blockers, particularly carvedilol, on reducing the risk of events after acute myocardial infarction. Am] Cardiol 98, 1115-1119. doi: S0002-9149(06)01295-1 [pii] 10.1016/j.amjcard.2006.05.039.
-
(2006)
Am] Cardiol
, vol.98
, pp. 1115-1119
-
-
Kopecky, S.L.1
-
58
-
-
84863115467
-
Structure and dynamics of the M3 muscarinic acetylcholine receptor
-
Kruse, A.C., Hu, J., Pan, A.C., Arlow, D.H., Rosenbaum, D.M., Rosemond, E., Green, H.F., Liu, T., Chae, P.S., Dror, R.O., Shaw, D.E., Weis, W.I., Wess, J., and Kobilka, B.K. (2012). Structure and dynamics of the M3 muscarinic acetylcholine receptor. Nature 482, 552-556. doi: 10.1038/naturel0867.
-
(2012)
Nature
, vol.482
, pp. 552-556
-
-
Kruse, A.C.1
Hu, J.2
Pan, A.C.3
Arlow, D.H.4
Rosenbaum, D.M.5
Rosemond, E.6
Green, H.F.7
Liu, T.8
Chae, P.S.9
Dror, R.O.10
Shaw, D.E.11
Weis, W.I.12
Wess, J.13
Kobilka, B.K.14
-
59
-
-
84884685355
-
Muscarinic receptors as model targets and antitargets for structure-based ligand discovery
-
Kruse, A.C., Weiss, D.R., Rossi, M., Hu, J., Hu, K., Eitel, K., Gmeiner, P., Wess, J., Kobilka, B.K., and Shoichet, B.K. (2013). Muscarinic receptors as model targets and antitargets for structure-based ligand discovery. Mol Pharmacol 84, 528-540. doi: 10.1124/mol.ll3.087551.
-
(2013)
Mol Pharmacol
, vol.84
, pp. 528-540
-
-
Kruse, A.C.1
Weiss, D.R.2
Rossi, M.3
Hu, J.4
Hu, K.5
Eitel, K.6
Gmeiner, P.7
Wess, J.8
Kobilka, B.K.9
Shoichet, B.K.10
-
60
-
-
84888883269
-
Structure-based ligand discovery targeting orthosteric and allosteric pockets of dopamine receptors
-
Lane, J.R., Chubukov, P., Liu, W., Canals, M., Cherezov, V., Abagyan, R., Stevens, R.C., and Katritch, V. (2013). Structure-based ligand discovery targeting orthosteric and allosteric pockets of dopamine receptors. Mol Pharmacol 84, 794-807. doi: 10.1124/mol.ll3.088054.
-
(2013)
Mol Pharmacol
, vol.84
, pp. 794-807
-
-
Lane, J.R.1
Chubukov, P.2
Liu, W.3
Canals, M.4
Cherezov, V.5
Abagyan, R.6
Stevens, R.C.7
Katritch, V.8
-
61
-
-
84865441831
-
Identification of molecular phenotypes and biased signaling induced by naturally occurring mutations of the human calcium-sensing receptor
-
Leach, K., Wen, A., Davey, A.E., Sexton, P.M., Conigrave, A.D., and Christopoulos, A. (2012). Identification of molecular phenotypes and biased signaling induced by naturally occurring mutations of the human calcium-sensing receptor. Endocrinology 153, 4304-4316. doi: 10.1210/en.2012-1449 en.2012-1449 [pii].
-
(2012)
Endocrinology
, vol.153
, pp. 4304-4316
-
-
Leach, K.1
Wen, A.2
Davey, A.E.3
Sexton, P.M.4
Conigrave, A.D.5
Christopoulos, A.6
-
62
-
-
17644402459
-
Transduction of receptor signals by beta-arrestins
-
Lefkowitz, R.J., and Shenoy, S.K. (2005). Transduction of receptor signals by beta-arrestins. Science 308, 512-517. doi: 10.1126/science.ll09237.
-
(2005)
Science
, vol.308
, pp. 512-517
-
-
Lefkowitz, R.J.1
Shenoy, S.K.2
-
63
-
-
77950638605
-
Computational modeling of structurefunction of g protein-coupled receptors with applications for drug design
-
Li, Y.Y., Hou, T.J., and Goddard, W.A., 3rd (2010). Computational modeling of structurefunction of g protein-coupled receptors with applications for drug design. Curr Med Chem 17,1167-1180.
-
(2010)
Curr Med Chem
, vol.17
, pp. 1167-1180
-
-
Li, Y.Y.1
Hou, T.J.2
Goddard III, W.A.3
-
64
-
-
0033613938
-
Betaarrestin-dependent formation of beta2 adrenergic receptor-Src protein kinase complexes
-
Luttrell, L.M., Ferguson, S.S., Daaka, Y., Miller, W.E., Maudsley, S., Delia Rocca, G.J., Lin, F., Kawakatsu, H., Owada, K., Luttrell, D.K., Caron, M.G., and Lefkowitz, R.J. (1999). Betaarrestin-dependent formation of beta2 adrenergic receptor-Src protein kinase complexes. Science 283, 655-661.
-
(1999)
Science
, vol.283
, pp. 655-661
-
-
Luttrell, L.M.1
Ferguson, S.S.2
Daaka, Y.3
Miller, W.E.4
Maudsley, S.5
Delia Rocca, G.J.6
Lin, F.7
Kawakatsu, H.8
Owada, K.9
Luttrell, D.K.10
Caron, M.G.11
Lefkowitz, R.J.12
-
65
-
-
77949458560
-
Third generation antipsychotic drugs: partial agonism or receptor functional selectivity?
-
CPD-Richard B. Mailman (Albert Adell) [pii]
-
Mailman, R.B., and Murthy, V. (2010). Third generation antipsychotic drugs: partial agonism or receptor functional selectivity? Curr Pharm Des 16, 488-501. doi: CPD-Richard B. Mailman (Albert Adell) [pii].
-
(2010)
Curr Pharm Des
, vol.16
, pp. 488-501
-
-
Mailman, R.B.1
Murthy, V.2
-
66
-
-
84861096654
-
Crystal structure of the micro-opioid receptor bound to a morphinan antagonist
-
Manglik, A., Kruse, A.C., Kobilka, T.S., Thian, F.S., Mathiesen, J.M., Sunahara, R.K., Pardo, L, Weis, W.I., Kobilka, B.K., and Granier, S. (2012). Crystal structure of the micro-opioid receptor bound to a morphinan antagonist. Nature 485, 321-326. doi: 10.1038/naturel0954.
-
(2012)
Nature
, vol.485
, pp. 321-326
-
-
Manglik, A.1
Kruse, A.C.2
Kobilka, T.S.3
Thian, F.S.4
Mathiesen, J.M.5
Sunahara, R.K.6
Pardo, L.7
Weis, W.I.8
Kobilka, B.K.9
Granier, S.10
-
67
-
-
51649084026
-
Antagonism of dopamine D2receptor/beta-arrestin 2 interaction is a common property of clinically effective antipsychotics
-
Masri, B., Salahpour, A., Didriksen, M., Ghisi, V., Beaulieu, J.M., Gainetdinov, R.R., and Caron, M.G. (2008). Antagonism of dopamine D2receptor/beta-arrestin 2 interaction is a common property of clinically effective antipsychotics. Proc Natl Acad Sci USA 105, 13656-13661. doi: 10.1073/pnas.0803522105 0803522105 [pii].
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 13656-13661
-
-
Masri, B.1
Salahpour, A.2
Didriksen, M.3
Ghisi, V.4
Beaulieu, J.M.5
Gainetdinov, R.R.6
Caron, M.G.7
-
68
-
-
0025325535
-
Structure of a cannabinoid receptor and functional expression of the cloned cDNA
-
Matsuda, LA, Lolait, S.J., Brownstein, M.J., Young, A.C., and Bonner, T.I. (1990). Structure of a cannabinoid receptor and functional expression of the cloned cDNA. Nature 346, 561-564. doi: 10.1038/346561a0.
-
(1990)
Nature
, vol.346
, pp. 561-564
-
-
Matsuda, L.A.1
Lolait, S.J.2
Brownstein, M.J.3
Young, A.C.4
Bonner, T.I.5
-
69
-
-
75849150801
-
Discovery of benzhydrylpiperazine derivatives as CB1 receptor inverse agonists via privileged structure-based approach
-
Meng, T., Wang, J., Peng, H., Fang, G., Li, M., Xiong, B., Xie, X., Zhang, Y., Wang, X., and Shen, J. (2010). Discovery of benzhydrylpiperazine derivatives as CB1 receptor inverse agonists via privileged structure-based approach. EurJ Med Chem 45, 1133-1139. doi: 10.1016/j.ejmech.2009.12.018.
-
(2010)
Eur J Med Chem
, vol.45
, pp. 1133-1139
-
-
Meng, T.1
Wang, J.2
Peng, H.3
Fang, G.4
Li, M.5
Xiong, B.6
Xie, X.7
Zhang, Y.8
Wang, X.9
Shen, J.10
-
70
-
-
69049108756
-
Modern homology modeling of G-protein coupled receptors: which structural template to use?
-
Mobarec, J.C., Sanchez, R., and Filizola, M. (2009). Modern homology modeling of G-protein coupled receptors: which structural template to use?/Med Chem 52, 5207-5216. doi: 10.1021/jm9005252.
-
(2009)
Med Chem
, vol.52
, pp. 5207-5216
-
-
Mobarec, J.C.1
Sanchez, R.2
Filizola, M.3
-
71
-
-
84871980480
-
Molecular alliance -From orthosteric and allosteric ligands to dualsteric/bitopic agonists at G protein coupled receptors
-
Mohr, K., Schmitz, J., Schrage, R., Trannkle, C, and Holzgrabe, U. (2013). Molecular alliance -From orthosteric and allosteric ligands to dualsteric/bitopic agonists at G protein coupled receptors. Angewandte Chemie - International Edition 52, 508-516.
-
(2013)
Angewandte Chemie - International Edition
, vol.52
, pp. 508-516
-
-
Mohr, K.1
Schmitz, J.2
Schrage, R.3
Trannkle, C.4
Holzgrabe, U.5
-
72
-
-
84884409614
-
The beta-arrestin-biased ligand TRV120023 inhibits angiotensin II-induced cardiac hypertrophy while preserving enhanced myofilament response to calcium
-
Monasky, M.M., Taglieri, D.M., Henze, M., Warren, CM., Utter, M.S., Soergel, D.G., Violin, J.D., and Solaro, R.J. (2013). The beta-arrestin-biased ligand TRV120023 inhibits angiotensin II-induced cardiac hypertrophy while preserving enhanced myofilament response to calcium. Am J Physiol Heart Circ Physiol 305, H856-866. doi: 10.1152/ajpheart.00327.2013 ajpheart.00327.2013 [pii].
-
(2013)
Am J Physiol Heart Circ Physiol
, vol.305
, pp. H856-866
-
-
Monasky, M.M.1
Taglieri, D.M.2
Henze, M.3
Warren, C.M.4
Utter, M.S.5
Soergel, D.G.6
Violin, J.D.7
Solaro, R.J.8
-
73
-
-
67649424757
-
Prokineticin receptors in cardiovascular function: foe or friend?
-
Nebigil, C.G. (2009). Prokineticin receptors in cardiovascular function: foe or friend? Trends Cardiovasc Med 19, 55-60. doi: 10.1016/j.tcm.2009.04.007 S1050-1738(09)00065-6 [pii].
-
(2009)
Trends Cardiovasc Med
, vol.19
, pp. 55-60
-
-
Nebigil, C.G.1
-
74
-
-
84875475404
-
Discovery of a novel selective kappa-opioid receptor agonist using crystal structurebased virtual screening
-
Negri, A., Rives, M.L., Caspers, M.J., Prisinzano, T.E., Javitch, J.A., and Filizola, M. (2013). Discovery of a novel selective kappa-opioid receptor agonist using crystal structurebased virtual screening./Chem Inf Model 53, 521-526. doi: 10.1021/ci400019t.
-
(2013)
Chem Inf Model
, vol.53
, pp. 521-526
-
-
Negri, A.1
Rives, M.L.2
Caspers, M.J.3
Prisinzano, T.E.4
Javitch, J.A.5
Filizola, M.6
-
75
-
-
84873298278
-
The dynamic process of beta(2)-adrenergic receptor activation
-
Nygaard, R., Zou, Y., Dror, R.O., Mildorf, T.J., Arlow, D.H., Manglik, A., Pan, A.C., Liu, C.W., Fung, J.J., Bokoch, M.P., Thian, F.S., Kobilka, T.S., Shaw, D.E., Mueller, L, Prosser, R.S., and Kobilka, B.K. (2013). The dynamic process of beta(2)-adrenergic receptor activation. Cell 152, 532-542. doi: 10.1016/j.cell.2013.01.008 S0092-8674(13)00011-l [pii].
-
(2013)
Cell
, vol.152
, pp. 532-542
-
-
Nygaard, R.1
Zou, Y.2
Dror, R.O.3
Mildorf, T.J.4
Arlow, D.H.5
Manglik, A.6
Pan, A.C.7
Liu, C.W.8
Fung, J.J.9
Bokoch, M.P.10
Thian, F.S.11
Kobilka, T.S.12
Shaw, D.E.13
Mueller, L.14
Prosser, R.S.15
Kobilka, B.K.16
-
76
-
-
34248591811
-
The angiotensin II ATI receptor structure-activity correlations in the light of rhodopsin structure
-
87/2/565
-
Oliveira, L, Costa-Neto, CM., Nakaie, C.R., Schreier, S., Shimuta, S.I., and Paiva, A.C. (2007). The angiotensin II ATI receptor structure-activity correlations in the light of rhodopsin structure. Physiol Rev 87, 565-592. doi: 87/2/565 [pii] 10.1152/physrev.00040.2005.
-
(2007)
Physiol Rev
, vol.87
, pp. 565-592
-
-
Oliveira, L.1
Costa-Neto, C.M.2
Nakaie, C.R.3
Schreier, S.4
Shimuta, S.I.5
Paiva, A.C.6
-
77
-
-
84886920785
-
In silico identification of novel lead compounds with ATI receptor antagonist activity: successful application of chemical database screening protocol
-
Pal, M., and Paliwal, S. (2012). In silico identification of novel lead compounds with ATI receptor antagonist activity: successful application of chemical database screening protocol. Org Med Chem Lett 2, 7. doi: 10.1186/2191-2858-2-7.
-
(2012)
Org Med Chem Lett
, vol.2
, pp. 7
-
-
Pal, M.1
Paliwal, S.2
-
78
-
-
0034604451
-
Crystal structure of rhodopsin: A G protein-coupled receptor
-
Palczewski, K., Kumasaka, T., Hori, T., Behnke, C.A., Motoshima, H., Fox, B.A., Le Trong, I., Teller, D.C, Okada, T., Stenkamp, R.E., Yamamoto, M., and Miyano, M. (2000). Crystal structure of rhodopsin: A G protein-coupled receptor. Science 289, 739-745.
-
(2000)
Science
, vol.289
, pp. 739-745
-
-
Palczewski, K.1
Kumasaka, T.2
Hori, T.3
Behnke, C.A.4
Motoshima, H.5
Fox, B.A.6
Le Trong, I.7
Teller, D.C.8
Okada, T.9
Stenkamp, R.E.10
Yamamoto, M.11
Miyano, M.12
-
79
-
-
84910664637
-
Search for cannabinoid receptor 1 antagonists using structure-based virtual screening: identification of natural product hits
-
Pandey, P., Roy, K.K., Liu, H., Elokely, K.M., Pettaway, S., Cutler, S.J., and Doerksen, R.J. (2014). Search for cannabinoid receptor 1 antagonists using structure-based virtual screening: identification of natural product hits. Planta Med 80, PF11. doi: 10.1055/S-0034-1382589.
-
(2014)
Planta Med
, vol.80
, pp. PF11
-
-
Pandey, P.1
Roy, K.K.2
Liu, H.3
Elokely, K.M.4
Pettaway, S.5
Cutler, S.J.6
Doerksen, R.J.7
-
80
-
-
47049130668
-
Crystal structure of the ligand-free G-protein-coupled receptor opsin
-
Park, J.H., Scheerer, P., Hofmann, K.P., Choe, H.W., and Ernst, O.P. (2008). Crystal structure of the ligand-free G-protein-coupled receptor opsin. Nature 454, 183-187. doi: 10.1038/nature07063.
-
(2008)
Nature
, vol.454
, pp. 183-187
-
-
Park, J.H.1
Scheerer, P.2
Hofmann, K.P.3
Choe, H.W.4
Ernst, O.P.5
-
81
-
-
84870290491
-
Structure of the chemokine receptor CXCR1 in phospholipid bilayers
-
Park, S.H., Das, B.B., Casagrande, F., Tian, Y., Nothnagel, H.J., Chu, M., Kiefer, H., Maier, K., De Angelis, A.A., Marassi, F.M., and Opella, S.J. (2012). Structure of the chemokine receptor CXCR1 in phospholipid bilayers. Nature 491, 779-783. doi: 10.1038/naturell580.
-
(2012)
Nature
, vol.491
, pp. 779-783
-
-
Park, S.H.1
Das, B.B.2
Casagrande, F.3
Tian, Y.4
Nothnagel, H.J.5
Chu, M.6
Kiefer, H.7
Maier, K.8
De Angelis, A.A.9
Marassi, F.M.10
Opella, S.J.11
-
82
-
-
84862270531
-
Design, synthesis, and pharmacological characterization of indol-3-ylacetamides, indol-3-yloxoacetamides, and indol-3-ylcarboxamides: potent and selective CB2 cannabinoid receptor inverse agonists
-
Pasquini, S., Mugnaini, C, Ligresti, A., Tafi, A., Brogi, S., Falciani, C, Pedani, V., Pesco, N., Guida, F., Luongo, L., Varani, K., Borea, P.A., Maione, S., Di Marzo, V., and Corelli, F. (2012). Design, synthesis, and pharmacological characterization of indol-3-ylacetamides, indol-3-yloxoacetamides, and indol-3-ylcarboxamides: potent and selective CB2 cannabinoid receptor inverse agonists. J Med Chem 55, 5391-5402. doi: 10.1021/jm3003334.
-
(2012)
J Med Chem
, vol.55
, pp. 5391-5402
-
-
Pasquini, S.1
Mugnaini, C.2
Ligresti, A.3
Tafi, A.4
Brogi, S.5
Falciani, C.6
Pedani, V.7
Pesco, N.8
Guida, F.9
Luongo, L.10
Varani, K.11
Borea, P.A.12
Maione, S.13
Di Marzo, V.14
Corelli, F.15
-
83
-
-
15444377047
-
Bioluminescence resonance energy transfer reveals ligand-induced conformational changes in CXCR4 homo- and heterodimers
-
M411151200
-
Percherancier, Y., Berchiche, Y.A., Slight, I., Volkmer-Engert, R., Tamamura, H., Fujii, N., Bouvier, M., and Heveker, N. (2005). Bioluminescence resonance energy transfer reveals ligand-induced conformational changes in CXCR4 homo- and heterodimers./BiolChem 280, 9895-9903. doi: M411151200 [pii] 10.1074/jbc. M411151200.
-
(2005)
BiolChem
, vol.280
, pp. 9895-9903
-
-
Percherancier, Y.1
Berchiche, Y.A.2
Slight, I.3
Volkmer-Engert, R.4
Tamamura, H.5
Fujii, N.6
Bouvier, M.7
Heveker, N.8
-
84
-
-
0032539780
-
Dimerization of sumatriptan as an efficient way to design a potent, centrally and orally active 5-HT1B agonist
-
Perez, M., Pauwels, P.J., Fourrier, C, Chopin, P., Valentin, J.P., John, G.W., Marien, M., and Halazy, S. (1998). Dimerization of sumatriptan as an efficient way to design a potent, centrally and orally active 5-HT1B agonist. Bioorg Med Chem Lett 8, 675-680.
-
(1998)
Bioorg Med Chem Lett
, vol.8
, pp. 675-680
-
-
Perez, M.1
Pauwels, P.J.2
Fourrier, C.3
Chopin, P.4
Valentin, J.P.5
John, G.W.6
Marien, M.7
Halazy, S.8
-
85
-
-
34248997811
-
Novel insights in dopamine receptor physiology
-
Pivonello, R., Ferone, D., Lombardi, G., Colao, A., Lamberts, S.W., and Hofland, L.J. (2007). Novel insights in dopamine receptor physiology. EurJ Endocrinol 156 Suppl 1, S13-21. doi: 10.1530/eje.l.02353.
-
(2007)
Eur J Endocrinol 156 Suppl
, vol.1
, pp. S13-S21
-
-
Pivonello, R.1
Ferone, D.2
Lombardi, G.3
Colao, A.4
Lamberts, S.W.5
Hofland, L.J.6
-
86
-
-
0029091082
-
Endothelin receptors and calcium signaling
-
Pollock, D.M., Keith, T.L., and Highsmith, R.F. (1995). Endothelin receptors and calcium signaling. FASEBJ9,1196-1204.
-
(1995)
FASEBJ9
, pp. 1196-1204
-
-
Pollock, D.M.1
Keith, T.L.2
Highsmith, R.F.3
-
87
-
-
3142776467
-
Comparison of carvedilol and metoprolol on clinical outcomes in patients with chronic heart failure in the Carvedilol Or Metoprolol European Trial (COMET): randomised controlled trial
-
Carvedilol or Metoprolol European Trial I.
-
Poole-Wilson, PA, Swedberg, K., Cleland, J.G., Di Lenarda, A., Hanrath, P., Komajda, M., Lubsen, J., Lutiger, B., Metra, M., Remme, W.J., Torp-Pedersen, C, Scherhag, A., Skene, A., and Carvedilol or Metoprolol European Trial, I. (2003). Comparison of carvedilol and metoprolol on clinical outcomes in patients with chronic heart failure in the Carvedilol Or Metoprolol European Trial (COMET): randomised controlled trial. lancet 362, 7-13. doi: S0140-6736(03)13800-7 [pii] 10.1016/S0140-6736(03)13800-7.
-
(2003)
lancet
, vol.362
, pp. 7-13
-
-
Poole-Wilson, P.A.1
Swedberg, K.2
Cleland, J.G.3
Di Lenarda, A.4
Hanrath, P.5
Komajda, M.6
Lubsen, J.7
Lutiger, B.8
Metra, M.9
Remme, W.J.10
Torp-Pedersen, C.11
Scherhag, A.12
Skene, A.13
-
88
-
-
77951844975
-
Teaching old receptors new tricks: biasing seven-transmembrane receptors
-
nrd3024
-
Rajagopal, S., Rajagopal, K., and Lefkowitz, R.J. (2010). Teaching old receptors new tricks: biasing seven-transmembrane receptors. Nat Rev Drug Discov 9, 373-386. doi: 10.1038/nrd3024 nrd3024 [pii].
-
(2010)
Nat Rev Drug Discov
, vol.9
, pp. 373-386
-
-
Rajagopal, S.1
Rajagopal, K.2
Lefkowitz, R.J.3
-
89
-
-
35649005909
-
Neuronal Gq/11-coupled dopamine receptors: an uncharted role for dopamine
-
Rashid, A.J., O'dowd, B.F., Verma, V., and George, S.R. (2007). Neuronal Gq/11-coupled dopamine receptors: an uncharted role for dopamine. Trends Pharmacol Sci 28, 551-555. doi: 10.1016/j.tips.2007.10.001.
-
(2007)
Trends Pharmacol Sci
, vol.28
, pp. 551-555
-
-
Rashid, A.J.1
O'dowd, B.F.2
Verma, V.3
George, S.R.4
-
90
-
-
36248970132
-
Crystal structure of the human beta2 adrenergic G-proteincoupled receptor
-
Rasmussen, S.G., Choi, H.J., Rosenbaum, D.M., Kobilka, T.S., Thian, F.S., Edwards, P.C., Burghammer, M., Ratnala, V.R., Sanishvili, R., Fischetti, R.F., Schertler, G.F., Weis, W.I., and Kobilka, B.K. (2007). Crystal structure of the human beta2 adrenergic G-proteincoupled receptor. Nature 450, 383-387. doi: 10.1038/nature06325.
-
(2007)
Nature
, vol.450
, pp. 383-387
-
-
Rasmussen, S.G.1
Choi, H.J.2
Rosenbaum, D.M.3
Kobilka, T.S.4
Thian, F.S.5
Edwards, P.C.6
Burghammer, M.7
Ratnala, V.R.8
Sanishvili, R.9
Fischetti, R.F.10
Schertler, G.F.11
Weis, W.I.12
Kobilka, B.K.13
-
91
-
-
84875640243
-
Virtual screening of CB(2) receptor agonists from bayesian network and high-throughput docking: structural insights into agonist-modulated GPCR features
-
Renault, N., Laurent, X., Farce, A., El Bakali, J., Mansouri, R., Gervois, P., Millet, R., Desreumaux, P., Furman, C, and Chavatte, P. (2013). Virtual screening of CB(2) receptor agonists from bayesian network and high-throughput docking: structural insights into agonist-modulated GPCR features. Chem Biol Drug Des 81, 442-454. doi: 10.1111/cbdd.l2095.
-
(2013)
Chem Biol Drug Des
, vol.81
, pp. 442-454
-
-
Renault, N.1
Laurent, X.2
Farce, A.3
El Bakali, J.4
Mansouri, R.5
Gervois, P.6
Millet, R.7
Desreumaux, P.8
Furman, C.9
Chavatte, P.10
-
92
-
-
84900498728
-
Biased ligands: pathway validation for novel GPCR therapeutics
-
Rominger, D.H., Cowan, C.L., Gowen-Macdonald, W., and Violin, J.D. (2014). Biased ligands: pathway validation for novel GPCR therapeutics. Curr Opin Pharmacol 16, 108-115. doi: 10.1016/j.coph.2014.04.002 S1471-4892(14)00041-l [pii].
-
(2014)
Curr Opin Pharmacol
, vol.16
, pp. 108-115
-
-
Rominger, D.H.1
Cowan, C.L.2
Gowen-Macdonald, W.3
Violin, J.D.4
-
93
-
-
36448978229
-
GPCR engineering yields high-resolution structural insights into beta2-adrenergic receptor function
-
(New York, N Y)
-
Rosenbaum, D.M., Cherezov, V., Hanson, M.A., Rasmussen, S.G., Thian, F.S., Kobilka, T.S., Choi, H.J., Yao, X.J., Weis, W.I., Stevens, R.C., and Kobilka, B.K. (2007). GPCR engineering yields high-resolution structural insights into beta2-adrenergic receptor function. Science (New York, N Y) 318,1266-1273. doi: 10.1126/science.ll50609.
-
(2007)
Science
, vol.318
, pp. 1266-1273
-
-
Rosenbaum, D.M.1
Cherezov, V.2
Hanson, M.A.3
Rasmussen, S.G.4
Thian, F.S.5
Kobilka, T.S.6
Choi, H.J.7
Yao, X.J.8
Weis, W.I.9
Stevens, R.C.10
Kobilka, B.K.11
-
94
-
-
53349102957
-
Use of the X-ray structure of the beta2-adrenergic receptor for drug discovery. Part 2 Identification of active compounds
-
Sabio, M., Jones, K., and Topiol, S. (2008). Use of the X-ray structure of the beta2-adrenergic receptor for drug discovery. Part 2: Identification of active compounds. Bioorg Med Chem Lett 18, 5391-5395. doi: 10.1016/j.bmcl.2008.09.046
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 5391-5395
-
-
Sabio, M.1
Jones, K.2
Topiol, S.3
-
95
-
-
0035146135
-
Transactivation: a novel signaling pathway from angiotensin II to tyrosine kinase receptors
-
Saito, Y., and Berk, B.C. (2001). Transactivation: a novel signaling pathway from angiotensin II to tyrosine kinase receptors./Mol Cell Cardiol 33, 3-7. doi: 10.1006/jmcc.2000.1272 S0022-2828(00)91272-0 [pii].
-
(2001)
Mol Cell Cardiol
, vol.33
, pp. 3-7
-
-
Saito, Y.1
Berk, B.C.2
-
96
-
-
84905227323
-
Biased signaling through G-protein-coupled PROKR2 receptors harboring missense mutations
-
Sbai, 0., Monnier, C, Dode, C, Pin, J.P., Hardelin, J.P., and Rondard, P. (2014). Biased signaling through G-protein-coupled PROKR2 receptors harboring missense mutations. FASEBJ 28, 3734-3744. doi: 10.1096/fj.13-243402 fj.13-243402 [pii].
-
(2014)
FASEBJ
, vol.28
, pp. 3734-3744
-
-
Sbai, 0.1
Monnier, C.2
Dode, C.3
Pin, J.P.4
Hardelin, J.P.5
Rondard, P.6
-
97
-
-
52949102889
-
Crystal structure of opsin in its G-protein-interacting conformation
-
Scheerer, P., Park, J.H., Hildebrand, P.W., Kim, Y.J., Krauss, N., Choe, H.W., Hofmann, K.P., and Ernst, O.P. (2008). Crystal structure of opsin in its G-protein-interacting conformation. Nature 455, 497-502. doi: 10.1038/nature07330.
-
(2008)
Nature
, vol.455
, pp. 497-502
-
-
Scheerer, P.1
Park, J.H.2
Hildebrand, P.W.3
Kim, Y.J.4
Krauss, N.5
Choe, H.W.6
Hofmann, K.P.7
Ernst, O.P.8
-
98
-
-
66749154689
-
Dissociation of the opioid receptor mechanisms that control mechanical and heat pain
-
Scherrer, G., Imamachi, N., Cao, Y.Q., Contet, C, Mennicken, F., O'donnell, D., Kieffer, B.L., and Basbaum, A.I. (2009). Dissociation of the opioid receptor mechanisms that control mechanical and heat pain. Cell 137,1148-1159. doi: 10.1016/j.cell.2009.04.019.
-
(2009)
Cell
, vol.137
, pp. 1148-1159
-
-
Scherrer, G.1
Imamachi, N.2
Cao, Y.Q.3
Contet, C.4
Mennicken, F.5
O'donnell, D.6
Kieffer, B.L.7
Basbaum, A.I.8
-
99
-
-
81555213635
-
Pharmacological modulation of chemokine receptor function
-
Scholten, D.J., Canals, M., Maussang, D., Roumen, L, Smit, M.J., Wijtmans, M., De Graaf, C, Vischer, H.F., and Leurs, R. (2012). Pharmacological modulation of chemokine receptor function. Br J Pharmacol 165, 1617-1643. doi: lO.llll/j.1476-5381.2011.01551.x.
-
(2012)
Br J Pharmacol
, vol.165
, pp. 1617-1643
-
-
Scholten, D.J.1
Canals, M.2
Maussang, D.3
Roumen, L.4
Smit, M.J.5
Wijtmans, M.6
De Graaf, C.7
Vischer, H.F.8
Leurs, R.9
-
100
-
-
38949158505
-
Conformational thermostabilization of the betal-adrenergic receptor in a detergent-resistant form
-
Serrano-Vega, M.J., Magnani, F., Shibata, Y., and Tate, C.G. (2008). Conformational thermostabilization of the betal-adrenergic receptor in a detergent-resistant form. Proc Natl Acad Sci US A 105, 877-882. doi: 10.1073/pnas.0711253105.
-
(2008)
Proc Natl Acad Sci US A
, vol.105
, pp. 877-882
-
-
Serrano-Vega, M.J.1
Magnani, F.2
Shibata, Y.3
Tate, C.G.4
-
101
-
-
0042887023
-
Aripiprazole, a novel atypical antipsychotic drug with a unique and robust pharmacology
-
1300203
-
Shapiro, D.A., Renock, S., Arrington, E., Chiodo, L.A., Liu, L.X., Sibley, D.R., Roth, B.L., and Mailman, R. (2003). Aripiprazole, a novel atypical antipsychotic drug with a unique and robust pharmacology. Neuropsychopharmacology 28, 1400-1411. doi: 10.1038/sj.npp.l300203 1300203 [pii].
-
(2003)
Neuropsychopharmacology
, vol.28
, 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
-
102
-
-
79960070651
-
Structure of the human histamine HI receptor complex with doxepin
-
Shimamura, T., Shiroishi, M., Weyand, S., Tsujimoto, H., Winter, G., Katritch, V., Abagyan, R., Cherezov, V., Liu, W., Han, G.W., Kobayashi, T., Stevens, R.C., and Iwata, S. (2011). Structure of the human histamine HI receptor complex with doxepin. Nature 475, 65-70. doi: 10.1038/naturel0236.
-
(2011)
Nature
, vol.475
, pp. 65-70
-
-
Shimamura, T.1
Shiroishi, M.2
Weyand, S.3
Tsujimoto, H.4
Winter, G.5
Katritch, V.6
Abagyan, R.7
Cherezov, V.8
Liu, W.9
Han, G.W.10
Kobayashi, T.11
Stevens, R.C.12
Iwata, S.13
-
103
-
-
84861224187
-
"Monovalent" ligands that trigger TLR-4 and TCR are not necessarily truly monovalent
-
Sigalov, A.B. (2012). "Monovalent" ligands that trigger TLR-4 and TCR are not necessarily truly monovalent. Mol Immunol 51, 356-362. doi: 10.1016/j.molimm.2012.03.031 S0161-5890(12)00220-9 [pii].
-
(2012)
Mol Immunol
, vol.51
, pp. 356-362
-
-
Sigalov, A.B.1
-
104
-
-
52449133904
-
Homozygous mutation in the prokineticinreceptor2 gene (Val274Asp) presenting as reversible Kallmann syndrome and persistent oligozoospermia: case report
-
den247
-
Sinisi, A.A., Asci, R., Bellastella, G., Maione, L., Esposito, D., Elefante, A., De Bellis, A., Bellastella, A., and Iolascon, A. (2008). Homozygous mutation in the prokineticinreceptor2 gene (Val274Asp) presenting as reversible Kallmann syndrome and persistent oligozoospermia: case report. Hum Reprod 23, 2380-2384. doi: 10.1093/humrep/den247 den247 [pii].
-
(2008)
Hum Reprod
, vol.23
, pp. 2380-2384
-
-
Sinisi, A.A.1
Asci, R.2
Bellastella, G.3
Maione, L.4
Esposito, D.5
Elefante, A.6
De Bellis, A.7
Bellastella, A.8
Iolascon, A.9
-
105
-
-
84881193006
-
Structure of the human glucagon class B G-protein-coupled receptor
-
Siu, F.Y., He, M., De Graaf, C, Han, G.W., Yang, D., Zhang, Z., Zhou, C, Xu, Q., Wacker, D., Joseph, J.S., Liu, W., Lau, J., Cherezov, V., Katritch, V., Wang, M.W., and Stevens, R.C. (2013). Structure of the human glucagon class B G-protein-coupled receptor. Nature 499, 444-449. doi: 10.1038/naturel2393.
-
(2013)
Nature
, vol.499
, pp. 444-449
-
-
Siu, F.Y.1
He, M.2
De Graaf, C.3
Han, G.W.4
Yang, D.5
Zhang, Z.6
Zhou, C.7
Xu, Q.8
Wacker, D.9
Joseph, J.S.10
Liu, W.11
Lau, J.12
Cherezov, V.13
Katritch, V.14
Wang, M.W.15
Stevens, R.C.16
-
106
-
-
84898655082
-
First clinical experience with TRV130: pharmacokinetics and pharmacodynamics in healthy volunteers
-
Soergel, D.G., Subach, R.A., Sadler, B., Connell, J., Marion, A.S., Cowan, C.L., Violin, J.D., and Lark, M.W. (2014). First clinical experience with TRV130: pharmacokinetics and pharmacodynamics in healthy volunteers./Clin Pharmacol 54, 351-357. doi: 10.1002/jcph.207.
-
(2014)
Clin Pharmacol
, vol.54
, pp. 351-357
-
-
Soergel, D.G.1
Subach, R.A.2
Sadler, B.3
Connell, J.4
Marion, A.S.5
Cowan, C.L.6
Violin, J.D.7
Lark, M.W.8
-
107
-
-
80051784951
-
Multiple templates-based homology modeling enhances structure quality of ATI receptor: validation by molecular dynamics and antagonist docking
-
Sokkar, P., Mohandass, S., and Ramachandran, M. (2011). Multiple templates-based homology modeling enhances structure quality of ATI receptor: validation by molecular dynamics and antagonist docking./Mol Model 17, 1565-1577. doi: 10.1007/s00894-010-0860-z.
-
(2011)
Mol Model
, vol.17
, pp. 1565-1577
-
-
Sokkar, P.1
Mohandass, S.2
Ramachandran, M.3
-
108
-
-
84891873565
-
Prokineticin receptor 1 as a novel suppressor of preadipocyte proliferation and differentiation to control obesity
-
Szatkowski, C, Vallet, J., Dormishian, M., Messaddeq, N., Valet, P., Boulberdaa, M., Metzger, D., Chambon, P., and Nebigil, C.G. (2013). Prokineticin receptor 1 as a novel suppressor of preadipocyte proliferation and differentiation to control obesity. PLoS One 8, e81175. doi: 10.1371/journal.pone.0081175 PONE-D-13-25805 [pii].
-
(2013)
PLoS One
, vol.8
-
-
Szatkowski, C.1
Vallet, J.2
Dormishian, M.3
Messaddeq, N.4
Valet, P.5
Boulberdaa, M.6
Metzger, D.7
Chambon, P.8
Nebigil, C.G.9
-
109
-
-
84884673669
-
Structure of the CCR5 chemokine receptor-HIV entry inhibitor maraviroc complex
-
Tan, Q., Zhu, Y., Li, J., Chen, Z., Han, G.W., Kufareva, I., Li, T., Ma, L, Fenalti, G., Zhang, W., Xie, X., Yang, H., Jiang, H., Cherezov, V., Liu, H., Stevens, R.C., Zhao, Q., and Wu, B. (2013). Structure of the CCR5 chemokine receptor-HIV entry inhibitor maraviroc complex. Science 341,1387-1390. doi: 10.1126/science.l241475.
-
(2013)
Science
, vol.341
, pp. 1387-1390
-
-
Tan, Q.1
Zhu, Y.2
Li, J.3
Chen, Z.4
Han, G.W.5
Kufareva, I.6
Li, T.7
Ma, L.8
Fenalti, G.9
Zhang, W.10
Xie, X.11
Yang, H.12
Jiang, H.13
Cherezov, V.14
Liu, H.15
Stevens, R.C.16
Zhao, Q.17
Wu, B.18
-
110
-
-
84861019261
-
Structure of the nociceptin/orphanin FQ receptor in complex with a peptide mimetic
-
Thompson, A.A., Liu, W., Chun, E., Katritch, V., Wu, H., Vardy, E., Huang, X.P., Trapella, C, Guerrini, R., Calo, G., Roth, B.L., Cherezov, V., and Stevens, R.C. (2012). Structure of the nociceptin/orphanin FQ receptor in complex with a peptide mimetic. Nature 485, 395-399. doi: 10.1038/naturell085.
-
(2012)
Nature
, vol.485
, pp. 395-399
-
-
Thompson, A.A.1
Liu, W.2
Chun, E.3
Katritch, V.4
Wu, H.5
Vardy, E.6
Huang, X.P.7
Trapella, C.8
Guerrini, R.9
Calo, G.10
Roth, B.L.11
Cherezov, V.12
Stevens, R.C.13
-
111
-
-
39849101195
-
Use of the X-ray structure of the Beta2-adrenergic receptor for drug discovery
-
Topiol, S., and Sabio, M. (2008). Use of the X-ray structure of the Beta2-adrenergic receptor for drug discovery. Bioorg Med Chem Lett 18, 1598-1602. doi: 10.1016/j.bmcl.2008.01.063.
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 1598-1602
-
-
Topiol, S.1
Sabio, M.2
-
112
-
-
33745699190
-
Cinacalcet HC1: a novel treatment for secondary hyperparathyroidism caused by chronic kidney disease
-
Torres, P.U. (2006). Cinacalcet HC1: a novel treatment for secondary hyperparathyroidism caused by chronic kidney disease./Ren Nutr 16, 253-258. doi: 10.1053/j.jrn.2006.04.010.
-
(2006)
Ren Nutr
, vol.16
, pp. 253-258
-
-
Torres, P.U.1
-
113
-
-
33845718611
-
Aripiprazole has functionally selective actions at dopamine D2 receptor-mediated signaling pathways
-
Urban, J.D., Vargas, G.A., Von Zastrow, M., and Mailman, R.B. (2007). Aripiprazole has functionally selective actions at dopamine D2 receptor-mediated signaling pathways. Neuropsychopharmacology 32, 67-77. doi: 10.1038/sj.npp.l301071.
-
(2007)
Neuropsychopharmacology
, vol.32
, pp. 67-77
-
-
Urban, J.D.1
Vargas, G.A.2
Von Zastrow, M.3
Mailman, R.B.4
-
114
-
-
84896987724
-
Separation of on-target efficacy from adverse effects through rational design of a bitopic adenosine receptor agonist
-
Valant, C, May, L.T., Aurelio, L, Chuo, C.H., White, P.J., Baltos, J.A., Sexton, P.M., Scammells, P.J., and Christopoulos, A. (2014). Separation of on-target efficacy from adverse effects through rational design of a bitopic adenosine receptor agonist. Proc Natl AcadSci USA 111, 4614-4619. doi: 10.1073/pnas.l320962111.
-
(2014)
Proc Natl AcadSci USA
, vol.111
, pp. 4614-4619
-
-
Valant, C.1
May, L.T.2
Aurelio, L.3
Chuo, C.H.4
White, P.J.5
Baltos, J.A.6
Sexton, P.M.7
Scammells, P.J.8
Christopoulos, A.9
-
115
-
-
0033957873
-
Structure and function of dopamine receptors
-
Vallone, D., Picetti, R., and Borrelli, E. (2000). Structure and function of dopamine receptors. Neurosci BiobehavRev 24,125-132. doi: S0149-7634(99)00063-9 [pii].
-
(2000)
Neurosci BiobehavRev
, vol.24
, pp. 125-132
-
-
Vallone, D.1
Picetti, R.2
Borrelli, E.3
-
116
-
-
84895811180
-
Virtual fragment screening on GPCRs: a case study on dopamine D3 and histamine H4 receptors
-
Vass, M., Schmidt, E., Horti, F., and Keseru, G.M. (2014). Virtual fragment screening on GPCRs: a case study on dopamine D3 and histamine H4 receptors. EurJ Med Chem 77, 38-46. doi: 10.1016/j.ejmech.2014.02.034.
-
(2014)
Eur J Med Chem
, vol.77
, pp. 38-46
-
-
Vass, M.1
Schmidt, E.2
Horti, F.3
Keseru, G.M.4
-
117
-
-
76249121106
-
Ligand and structure-based models for the prediction of ligand-receptor affinities and virtual screenings: Development and application to the beta(2)-adrenergic receptor
-
Vilar, S., Karpiak, J., and Costanzi, S. (2010). Ligand and structure-based models for the prediction of ligand-receptor affinities and virtual screenings: Development and application to the beta(2)-adrenergic receptor. J Comput Chem 31, 707-720. doi: 10.1002/jcc.21346.
-
(2010)
J Comput Chem
, vol.31
, pp. 707-720
-
-
Vilar, S.1
Karpiak, J.2
Costanzi, S.3
-
118
-
-
84903387265
-
Biased ligands at G-proteincoupled receptors: promise and progress
-
Violin, J.D., Crombie, A.L., Soergel, D.G., and Lark, M.W. (2014). Biased ligands at G-proteincoupled receptors: promise and progress. Trends Pharmacol Sci 35, 308-316. doi: 10.1016/j.tips.2014.04.007 S0165-6147(14)00069-8 [pii].
-
(2014)
Trends Pharmacol Sci
, vol.35
, pp. 308-316
-
-
Violin, J.D.1
Crombie, A.L.2
Soergel, D.G.3
Lark, M.W.4
-
119
-
-
34447649922
-
Beta-arrestin-biased ligands at seventransmembrane receptors
-
Violin, J.D., and Lefkowitz, R.J. (2007). Beta-arrestin-biased ligands at seventransmembrane receptors. Trends Pharmacol Sci 28, 416-422. doi: 10.1016/j.tips.2007.06.006.
-
(2007)
Trends Pharmacol Sci
, vol.28
, pp. 416-422
-
-
Violin, J.D.1
Lefkowitz, R.J.2
-
120
-
-
84877631485
-
Structural features for functional selectivity at serotonin receptors
-
Wacker, D., Wang, C, Katritch, V., Han, G.W., Huang, X.P., Vardy, E., Mccorvy, J.D., Jiang, Y., Chu, M., Siu, F.Y., Liu, W., Xu, H.E., Cherezov, V., Roth, B.L., and Stevens, R.C. (2013). Structural features for functional selectivity at serotonin receptors. Science 340, 615-619. doi: 10.1126/science.l232808.
-
(2013)
Science
, vol.340
, pp. 615-619
-
-
Wacker, D.1
Wang, C.2
Katritch, V.3
Han, G.W.4
Huang, X.P.5
Vardy, E.6
Mccorvy, J.D.7
Jiang, Y.8
Chu, M.9
Siu, F.Y.10
Liu, W.11
Xu, H.E.12
Cherezov, V.13
Roth, B.L.14
Stevens, R.C.15
-
121
-
-
21144446486
-
A heterodimer-selective agonist shows in vivo relevance of G protein-coupled receptor dimers
-
Waldhoer, M., Fong, J., Jones, R.M., Lunzer, M.M., Sharma, S.K., Kostenis, E., Portoghese, P.S., and Whistler, J.L. (2005). A heterodimer-selective agonist shows in vivo relevance of G protein-coupled receptor dimers. Proc Natl Acad Sci USA 102, 9050-9055. doi: 10.1073/pnas.0501112102.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 9050-9055
-
-
Waldhoer, M.1
Fong, J.2
Jones, R.M.3
Lunzer, M.M.4
Sharma, S.K.5
Kostenis, E.6
Portoghese, P.S.7
Whistler, J.L.8
-
122
-
-
84877607189
-
Structural basis for molecular recognition at serotonin receptors
-
Wang, C, Jiang, Y., Ma, J., Wu, H., Wacker, D., Katritch, V., Han, G.W., Liu, W., Huang, X.P., Vardy, E., Mccorvy, J.D., Gao, X., Zhou, X.E., Melcher, K., Zhang, C, Bai, F., Yang, H., Yang, L., Jiang, H., Roth, B.L., Cherezov, V., Stevens, R.C, and Xu, H.E. (2013a). Structural basis for molecular recognition at serotonin receptors. Science 340, 610-614. doi: 10.1126/science.l232807.
-
(2013)
Science
, vol.340
, pp. 610-614
-
-
Wang, C.1
Jiang, Y.2
Ma, J.3
Wu, H.4
Wacker, D.5
Katritch, V.6
Han, G.W.7
Liu, W.8
Huang, X.P.9
Vardy, E.10
Mccorvy, J.D.11
Gao, X.12
Zhou, X.E.13
Melcher, K.14
Zhang, C.15
Bai, F.16
Yang, H.17
Yang, L.18
Jiang, H.19
Roth, B.L.20
Cherezov, V.21
Stevens, R.C.22
Xu, H.E.23
more..
-
123
-
-
84878112106
-
Structure of the human smoothened receptor bound to an antitumour agent
-
Wang, C, Wu, H., Katritch, V., Han, G.W., Huang, X.P., Liu, W., Siu, F.Y., Roth, B.L., Cherezov, V., and Stevens, R.C. (2013b). Structure of the human smoothened receptor bound to an antitumour agent. Nature 497, 338-343. doi: 10.1038/naturel2167.
-
(2013)
Nature
, vol.497
, pp. 338-343
-
-
Wang, C.1
Wu, H.2
Katritch, V.3
Han, G.W.4
Huang, X.P.5
Liu, W.6
Siu, F.Y.7
Roth, B.L.8
Cherezov, V.9
Stevens, R.C.10
-
124
-
-
43049151814
-
Identification of novel cannabinoid CB1 receptor antagonists by using virtual screening with a pharmacophore model
-
Wang, H., Duffy, R.A., Boykow, G.C., Chackalamannil, S., and Madison, V.S. (2008). Identification of novel cannabinoid CB1 receptor antagonists by using virtual screening with a pharmacophore model./Med Chem 51, 2439-2446. doi: 10.1021/jm701519h.
-
(2008)
Med Chem
, vol.51
, pp. 2439-2446
-
-
Wang, H.1
Duffy, R.A.2
Boykow, G.C.3
Chackalamannil, S.4
Madison, V.S.5
-
125
-
-
47949129742
-
Structure of a betal-adrenergic G-protein-coupled receptor
-
Warne, T., Serrano-Vega, M.J., Baker, J.G., Moukhametzianov, R., Edwards, P.C., Henderson, R., Leslie, A.G., Tate, C.G., and Schertler, G.F. (2008). Structure of a betal-adrenergic G-protein-coupled receptor. Nature 454, 486-491. doi: 10.1038/nature07101.
-
(2008)
Nature
, vol.454
, pp. 486-491
-
-
Warne, T.1
Serrano-Vega, M.J.2
Baker, J.G.3
Moukhametzianov, R.4
Edwards, P.C.5
Henderson, R.6
Leslie, A.G.7
Tate, C.G.8
Schertler, G.F.9
-
126
-
-
0141703263
-
Independent beta-arrestin 2 and G protein-mediated pathways for angiotensin II activation of extracellular signal-regulated kinases 1 and 2
-
Wei, H., Ahn, S., Shenoy, S.K., Karnik, S.S., Hunyady, L, Luttrell, L.M., and Lefkowitz, R.J. (2003). Independent beta-arrestin 2 and G protein-mediated pathways for angiotensin II activation of extracellular signal-regulated kinases 1 and 2. Proc Natl Acad Sci USA 100, 10782-10787. doi: 10.1073/pnas.l834556100 1834556100 [pii].
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 10782-10787
-
-
Wei, H.1
Ahn, S.2
Shenoy, S.K.3
Karnik, S.S.4
Hunyady, L.5
Luttrell, L.M.6
Lefkowitz, R.J.7
-
127
-
-
84875807317
-
Conformation guides molecular efficacy in docking screens of activated beta-2 adrenergic G protein coupled receptor
-
Weiss, D.R., Ahn, S., Sassano, M.F., Kleist, A., Zhu, X., Strachan, R., Roth, B.L., Lefkowitz, R.J., and Shoichet, B.K. (2013). Conformation guides molecular efficacy in docking screens of activated beta-2 adrenergic G protein coupled receptor. ACS Chem Biol 8, 1018-1026. doi: 10.1021/cb400103f.
-
(2013)
ACS Chem Biol
, vol.8
, pp. 1018-1026
-
-
Weiss, D.R.1
Ahn, S.2
Sassano, M.F.3
Kleist, A.4
Zhu, X.5
Strachan, R.6
Roth, B.L.7
Lefkowitz, R.J.8
Shoichet, B.K.9
-
128
-
-
79952488185
-
Therapeutic potential of beta-arrestinand G protein-biased agonists
-
Whalen, E.J., Rajagopal, S., and Lefkowitz, R.J. (2011). Therapeutic potential of beta-arrestinand G protein-biased agonists. Trends Mol Med 17, 126-139. doi: 10.1016/j.molmed.2010.11.004 S1471-4914(10)00182-6 [pii].
-
(2011)
Trends Mol Med
, vol.17
, pp. 126-139
-
-
Whalen, E.J.1
Rajagopal, S.2
Lefkowitz, R.J.3
-
129
-
-
84867840947
-
Structure of the agonist-bound neurotensin receptor
-
White, J.F., Noinaj, N., Shibata, Y., Love, J., Kloss, B., Xu, F., Gvozdenovic-Jeremic, J., Shah, P., Shiloach, J., Tate, C.G., and Grisshammer, R. (2012). Structure of the agonist-bound neurotensin receptor. Nature 490, 508-513. doi: 10.1038/naturell558.
-
(2012)
Nature
, vol.490
, pp. 508-513
-
-
White, J.F.1
Noinaj, N.2
Shibata, Y.3
Love, J.4
Kloss, B.5
Xu, F.6
Gvozdenovic-Jeremic, J.7
Shah, P.8
Shiloach, J.9
Tate, C.G.10
Grisshammer, R.11
-
130
-
-
77953661232
-
Re-exploration of the PHCCC Scaffold: Discovery of Improved Positive Allosteric Modulators of mGluR4
-
Williams, R., Zhou, Y., Niswender, CM., Luo, Q., Conn, P.J., Lindsley, C.W., and Hopkins, C.R. (2010). Re-exploration of the PHCCC Scaffold: Discovery of Improved Positive Allosteric Modulators of mGluR4. ACS Chem Neurosci 1, 411-419. doi: 10.1021/cn9000318.
-
(2010)
ACS Chem Neurosci
, vol.1
, pp. 411-419
-
-
Williams, R.1
Zhou, Y.2
Niswender, C.M.3
Luo, Q.4
Conn, P.J.5
Lindsley, C.W.6
Hopkins, C.R.7
-
131
-
-
85027927015
-
Structures of the CXCR4 chemokine GPCR with small-molecule and cyclic peptide antagonists
-
Wu, B., Chien, E.Y., Mol, CD., Fenalti, G., Liu, W., Katritch, V., Abagyan, R., Brooun, A., Wells, P., Bi, F.C., Hamel, D.J., Kuhn, P., Handel, T.M., Cherezov, V., and Stevens, R.C. (2010). Structures of the CXCR4 chemokine GPCR with small-molecule and cyclic peptide antagonists. Science 330,1066-1071. doi: 10.1126/science.ll94396.
-
(2010)
Science
, vol.330
, pp. 1066-1071
-
-
Wu, B.1
Chien, E.Y.2
Mol, C.D.3
Fenalti, G.4
Liu, W.5
Katritch, V.6
Abagyan, R.7
Brooun, A.8
Wells, P.9
Bi, F.C.10
Hamel, D.J.11
Kuhn, P.12
Handel, T.M.13
Cherezov, V.14
Stevens, R.C.15
-
132
-
-
84862777742
-
Structure of the human kappa-opioid receptor in complex with JDTic
-
Wu, H., Wacker, D., Mileni, M., Katritch, V., Han, G.W., Vardy, E., Liu, W., Thompson, A.A., Huang, X.P., Carroll, F.I., Mascarella, S.W., Westkaemper, R.B., Mosier, P.D., Roth, B.L., Cherezov, V., and Stevens, R.C. (2012). Structure of the human kappa-opioid receptor in complex with JDTic. Nature 485, 327-332. doi: 10.1038/naturel0939.
-
(2012)
Nature
, vol.485
, pp. 327-332
-
-
Wu, H.1
Wacker, D.2
Mileni, M.3
Katritch, V.4
Han, G.W.5
Vardy, E.6
Liu, W.7
Thompson, A.A.8
Huang, X.P.9
Carroll, F.I.10
Mascarella, S.W.11
Westkaemper, R.B.12
Mosier, P.D.13
Roth, B.L.14
Cherezov, V.15
Stevens, R.C.16
-
133
-
-
73349140520
-
A Selective Pharmacophore Model for beta(2)-Adrenoceptor Agonists
-
Xing, R.J., Wang, J., Pan, L., and Cheng, M.S. (2009). A Selective Pharmacophore Model for beta(2)-Adrenoceptor Agonists. Molecules 14, 4486-4496. doi: 10.3390/moleculesl4114486.
-
(2009)
Molecules
, vol.14
, pp. 4486-4496
-
-
Xing, R.J.1
Wang, J.2
Pan, L.3
Cheng, M.S.4
-
134
-
-
79953191134
-
N-naphthoyl-beta-naltrexamine (NNTA), a highly selective and potent activator of mu/kappa-opioid heteromers
-
Yekkirala, A.S., Lunzer, M.M., Mccurdy, C.R., Powers, M.D., Kalyuzhny, A.E., Roerig, S.C., and Portoghese, P.S. (2011). N-naphthoyl-beta-naltrexamine (NNTA), a highly selective and potent activator of mu/kappa-opioid heteromers. Proc Natl Acad Sci USA 108, 5098-5103. doi: 10.1073/pnas.l016277108.
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, pp. 5098-5103
-
-
Yekkirala, A.S.1
Lunzer, M.M.2
Mccurdy, C.R.3
Powers, M.D.4
Kalyuzhny, A.E.5
Roerig, S.C.6
Portoghese, P.S.7
-
135
-
-
84871411930
-
Highresolution crystal structure of human protease-activated receptor 1
-
Zhang, C, Srinivasan, Y., Arlow, D.H., Fung, J.J., Palmer, D., Zheng, Y., Green, H.F., Pandey, A., Dror, R.O., Shaw, D.E., Weis, W.I., Coughlin, S.R., and Kobilka, B.K. (2012). Highresolution crystal structure of human protease-activated receptor 1. Nature 492, 387-392. doi: 10.1038/naturell701.
-
(2012)
Nature
, vol.492
, pp. 387-392
-
-
Zhang, C.1
Srinivasan, Y.2
Arlow, D.H.3
Fung, J.J.4
Palmer, D.5
Zheng, Y.6
Green, H.F.7
Pandey, A.8
Dror, R.O.9
Shaw, D.E.10
Weis, W.I.11
Coughlin, S.R.12
Kobilka, B.K.13
-
136
-
-
84899751079
-
Agonist-bound structure of the human P2Y12 receptor
-
Zhang, J., Zhang, K., Gao, Z.G., Paoletta, S., Zhang, D., Han, G.W., Li, T., Ma, L, Zhang, W., Muller, C.E., Yang, H., Jiang, H., Cherezov, V., Katritch, V., Jacobson, K.A., Stevens, R.C, Wu, B., and Zhao, Q. (2014). Agonist-bound structure of the human P2Y12 receptor. Nature 509,119-122. doi: 10.1038/naturel3288.
-
(2014)
Nature
, vol.509
, pp. 119-122
-
-
Zhang, J.1
Zhang, K.2
Gao, Z.G.3
Paoletta, S.4
Zhang, D.5
Han, G.W.6
Li, T.7
Ma, L.8
Zhang, W.9
Muller, C.E.10
Yang, H.11
Jiang, H.12
Cherezov, V.13
Katritch, V.14
Jacobson, K.A.15
Stevens, R.C.16
Wu, B.17
Zhao, Q.18
-
137
-
-
77957908601
-
Synthesis and biological evaluation of bivalent ligands for the cannabinoid 1 receptor
-
Zhang, Y., Gilliam, A., Maitra, R., Damaj, M.I., Tajuba, J.M., Seltzman, H.H., and Thomas, B.F. (2010). Synthesis and biological evaluation of bivalent ligands for the cannabinoid 1 receptor. J Med Chem 53, 7048-7060. doi: 10.1021/jml006676
-
(2010)
J Med Chem
, vol.53
, pp. 7048-7060
-
-
Zhang, Y.1
Gilliam, A.2
Maitra, R.3
Damaj, M.I.4
Tajuba, J.M.5
Seltzman, H.H.6
Thomas, B.F.7
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