-
1
-
-
67649438808
-
International Union of Basic and Clinical Pharmacology. LXXIII. Nomenclature for the formyl peptide receptor (FPR) Family
-
R.D. Ye, F. Boulay, J.M. Wang, C. Dahlgren, C. Gerard, and M. Parmentier International Union of Basic and Clinical Pharmacology. LXXIII. Nomenclature for the formyl peptide receptor (FPR) Family Pharmacol Rev 61 2009 119 161
-
(2009)
Pharmacol Rev
, vol.61
, pp. 119-161
-
-
Ye, R.D.1
Boulay, F.2
Wang, J.M.3
Dahlgren, C.4
Gerard, C.5
Parmentier, M.6
-
3
-
-
0027370126
-
Species and subtype variants of the N-formyl peptide chemotactic receptor reveal multiple important functional domains
-
J.L. Gao, and P.M. Murphy Species and subtype variants of the N-formyl peptide chemotactic receptor reveal multiple important functional domains J Biol Chem 268 1993 25395 25401
-
(1993)
J Biol Chem
, vol.268
, pp. 25395-25401
-
-
Gao, J.L.1
Murphy, P.M.2
-
4
-
-
33751211223
-
Formyl peptide receptors: A promiscuous subfamily of G protein-coupled receptors controlling immune responses
-
I. Migeotte, D. Communi, and M. Parmentier Formyl peptide receptors: a promiscuous subfamily of G protein-coupled receptors controlling immune responses Cytokine Growth Factor Rev 17 2006 501 519
-
(2006)
Cytokine Growth Factor Rev
, vol.17
, pp. 501-519
-
-
Migeotte, I.1
Communi, D.2
Parmentier, M.3
-
5
-
-
77953684206
-
Are formyl peptide receptors novel targets for therapeutic intervention in ischaemia-reperfusion injury
-
F.N. Gavins Are formyl peptide receptors novel targets for therapeutic intervention in ischaemia-reperfusion injury Trends Pharmacol Sci 31 2010 266 276
-
(2010)
Trends Pharmacol Sci
, vol.31
, pp. 266-276
-
-
Gavins, F.N.1
-
7
-
-
6944234939
-
A novel nonpeptide ligand for formyl peptide receptor-like 1
-
M. Nanamori, X. Cheng, J. Mei, H. Sang, Y. Xuan, and C. Zhou A novel nonpeptide ligand for formyl peptide receptor-like 1 Mol Pharmacol 66 2004 1213 1222
-
(2004)
Mol Pharmacol
, vol.66
, pp. 1213-1222
-
-
Nanamori, M.1
Cheng, X.2
Mei, J.3
Sang, H.4
Xuan, Y.5
Zhou, C.6
-
8
-
-
33947423228
-
High-throughput screening for small-molecule activators of neutrophils: Identification of novel N-formyl peptide receptor agonists
-
I.A. Schepetkin, L.N. Kirpotina, A.I. Khlebnikov, and M.T. Quinn High-throughput screening for small-molecule activators of neutrophils: identification of novel N-formyl peptide receptor agonists Mol Pharmacol 71 2007 1061 1074
-
(2007)
Mol Pharmacol
, vol.71
, pp. 1061-1074
-
-
Schepetkin, I.A.1
Kirpotina, L.N.2
Khlebnikov, A.I.3
Quinn, M.T.4
-
9
-
-
35648947871
-
New 'chemical probes' to examine the role of the hFPRL1 (or ALXR) receptor in inflammation
-
M. Frohn, H. Xu, X. Zou, C. Chang, M. McElvaine, and M.H. Plant New 'chemical probes' to examine the role of the hFPRL1 (or ALXR) receptor in inflammation Bioorg Med Chem 17 2007 6633 6637
-
(2007)
Bioorg Med Chem
, vol.17
, pp. 6633-6637
-
-
Frohn, M.1
Xu, H.2
Zou, X.3
Chang, C.4
McElvaine, M.5
Plant, M.H.6
-
10
-
-
69049103120
-
6-Methyl-2,4-disubstituted pyridazin-3(2H)-ones: A novel class of small-molecule agonists for formyl peptide receptors
-
A. Cilibrizzi, M.T. Quinn, L.N. Kirpotina, I.A. Schepetkin, J. Holderness, and R.D. Ye 6-Methyl-2,4-disubstituted pyridazin-3(2H)-ones: a novel class of small-molecule agonists for formyl peptide receptors J Med Chem 52 2009 5054 5057
-
(2009)
J Med Chem
, vol.52
, pp. 5054-5057
-
-
Cilibrizzi, A.1
Quinn, M.T.2
Kirpotina, L.N.3
Schepetkin, I.A.4
Holderness, J.5
Ye, R.D.6
-
11
-
-
74549219527
-
Identification of novel small-molecule agonists for human formyl peptide receptors and pharmacophore models of their recognition
-
L.N. Kirpotina, A.I. Khlebnikov, I.A. Schepetkin, R.D. Ye, M.J. Rabiet, and M.A. Jutila Identification of novel small-molecule agonists for human formyl peptide receptors and pharmacophore models of their recognition Mol Pharmacol 77 2010 159 170
-
(2010)
Mol Pharmacol
, vol.77
, pp. 159-170
-
-
Kirpotina, L.N.1
Khlebnikov, A.I.2
Schepetkin, I.A.3
Ye, R.D.4
Rabiet, M.J.5
Jutila, M.A.6
-
12
-
-
78651298563
-
Gastrin-releasing peptide/neuromedin B receptor antagonists PD176252, PD168368, and related analogs are potent agonists of human formyl-peptide receptors
-
I.A. Schepetkin, L.N. Kirpotina, A.I. Khlebnikov, M.A. Jutila, and M.T. Quinn Gastrin-releasing peptide/neuromedin B receptor antagonists PD176252, PD168368, and related analogs are potent agonists of human formyl-peptide receptors Mol Pharmacol 79 2011 77 90
-
(2011)
Mol Pharmacol
, vol.79
, pp. 77-90
-
-
Schepetkin, I.A.1
Kirpotina, L.N.2
Khlebnikov, A.I.3
Jutila, M.A.4
Quinn, M.T.5
-
13
-
-
78650687885
-
Stable formyl peptide receptor agonists that activate the neutrophil NADPH-oxidase identified through screening of a compound library
-
H. Forsman, C. Kalderen, A. Nordin, E. Nordling, A.J. Jensen, and C. Dahlgren Stable formyl peptide receptor agonists that activate the neutrophil NADPH-oxidase identified through screening of a compound library Biochem Pharmacol 81 2011 402 411
-
(2011)
Biochem Pharmacol
, vol.81
, pp. 402-411
-
-
Forsman, H.1
Kalderen, C.2
Nordin, A.3
Nordling, E.4
Jensen, A.J.5
Dahlgren, C.6
-
14
-
-
84864692002
-
Molecular docking of 2-(benzimidazol-2-ylthio)-N-phenylacetamide-derived small-molecule agonists of human formyl peptide receptor 1
-
A.I. Khlebnikov, I.A. Schepetkin, L.N. Kirpotina, L. Brive, C. Dahlgren, and M.A. Jutila Molecular docking of 2-(benzimidazol-2-ylthio)-N- phenylacetamide-derived small-molecule agonists of human formyl peptide receptor 1 J Mol Model 18 2012 2831 2843
-
(2012)
J Mol Model
, vol.18
, pp. 2831-2843
-
-
Khlebnikov, A.I.1
Schepetkin, I.A.2
Kirpotina, L.N.3
Brive, L.4
Dahlgren, C.5
Jutila, M.A.6
-
15
-
-
84861571323
-
Synthesis enantioresolution, and activity profile of chiral 6-methyl-2,4-disubstituted pyridazin-3(2H)-ones as potent N-formyl peptide receptor agonists
-
A. Cilibrizzi, I.A. Schepetkin, G. Bartolucci, L. Crocetti, P.V. Dal, and M.P. Giovannoni Synthesis enantioresolution, and activity profile of chiral 6-methyl-2,4-disubstituted pyridazin-3(2H)-ones as potent N-formyl peptide receptor agonists Bioorg Med Chem 20 2012 3781 3792
-
(2012)
Bioorg Med Chem
, vol.20
, pp. 3781-3792
-
-
Cilibrizzi, A.1
Schepetkin, I.A.2
Bartolucci, G.3
Crocetti, L.4
Dal, P.V.5
Giovannoni, M.P.6
-
16
-
-
79959769615
-
Characterization of Quin-C1 for its anti-inflammatory property in a mouse model of bleomycin-induced lung injury
-
M. He, N. Cheng, W.W. Gao, M. Zhang, Y.Y. Zhang, and R.D. Ye Characterization of Quin-C1 for its anti-inflammatory property in a mouse model of bleomycin-induced lung injury Acta Pharmacol Sin 32 2011 601 610
-
(2011)
Acta Pharmacol Sin
, vol.32
, pp. 601-610
-
-
He, M.1
Cheng, N.2
Gao, W.W.3
Zhang, M.4
Zhang, Y.Y.5
Ye, R.D.6
-
17
-
-
77958121745
-
The agonists of formyl peptide receptors prevent development of severe sepsis after microbial infection
-
S.D. Kim, Y.K. Kim, H.Y. Lee, Y.S. Kim, S.G. Jeon, and S.H. Baek The agonists of formyl peptide receptors prevent development of severe sepsis after microbial infection J Immunol 185 2010 4302 4310
-
(2010)
J Immunol
, vol.185
, pp. 4302-4310
-
-
Kim, S.D.1
Kim, Y.K.2
Lee, H.Y.3
Kim, Y.S.4
Jeon, S.G.5
Baek, S.H.6
-
18
-
-
77954514553
-
(S)-FTY720-vinylphosphonate, an analogue of the immunosuppressive agent FTY720, is a pan-antagonist of sphingosine 1-phosphate GPCR signaling and inhibits autotaxin activity
-
W.J. Valentine, G.N. Kiss, J.E.S. Liu, M. Gotoh, K. Murakami-Murofushi, and T.C. Pham (S)-FTY720-vinylphosphonate, an analogue of the immunosuppressive agent FTY720, is a pan-antagonist of sphingosine 1-phosphate GPCR signaling and inhibits autotaxin activity Cell Signal 22 2010 1543 1553
-
(2010)
Cell Signal
, vol.22
, pp. 1543-1553
-
-
Valentine, W.J.1
Kiss, G.N.2
Liu, J.E.S.3
Gotoh, M.4
Murakami-Murofushi, K.5
Pham, T.C.6
-
19
-
-
39749136531
-
Analysis of efficacy of chiral adrenergic agonists
-
P.N. Patil, C. Li, V. Kumari, and J.P. Hieble Analysis of efficacy of chiral adrenergic agonists Chirality 20 2008 529 543
-
(2008)
Chirality
, vol.20
, pp. 529-543
-
-
Patil, P.N.1
Li, C.2
Kumari, V.3
Hieble, J.P.4
-
20
-
-
34249791476
-
Chirality - A new era of therapeutics
-
Y.K. Agrawal, H.G. Bhatt, H.G. Raval, P.M. Oza, and P.J. Gogoi Chirality - a new era of therapeutics Mini Rev Med Chem 7 2007 451 460
-
(2007)
Mini Rev Med Chem
, vol.7
, pp. 451-460
-
-
Agrawal, Y.K.1
Bhatt, H.G.2
Raval, H.G.3
Oza, P.M.4
Gogoi, P.J.5
-
21
-
-
37849027041
-
Stereoconfiguration of antiallergic and immunologic drugs
-
L. Bielory, and A. Leonov Stereoconfiguration of antiallergic and immunologic drugs Ann Allergy Asthma Immunol 100 2008 1 8
-
(2008)
Ann Allergy Asthma Immunol
, vol.100
, pp. 1-8
-
-
Bielory, L.1
Leonov, A.2
-
22
-
-
65549171434
-
Stereoselectivity in drug metabolism: Molecular mechanisms and analytical methods
-
V.L. Campo, L.S. Bernardes, and I. Carvalho Stereoselectivity in drug metabolism: molecular mechanisms and analytical methods Curr Drug Metab 10 2009 188 205
-
(2009)
Curr Drug Metab
, vol.10
, pp. 188-205
-
-
Campo, V.L.1
Bernardes, L.S.2
Carvalho, I.3
-
23
-
-
0344230147
-
Cholecystokinin B antagonists. Synthesis and quantitative structure-activity relationships of a series of C-terminal analogues of CI-988
-
C.E. Augelli-Szafran, D.C. Horwell, C. Kneen, D.F. Ortwine, M.C. Pritchard, and T.S. Purchase Cholecystokinin B antagonists. Synthesis and quantitative structure-activity relationships of a series of C-terminal analogues of CI-988 Bioorg Med Chem 4 1996 1733 1745
-
(1996)
Bioorg Med Chem
, vol.4
, pp. 1733-1745
-
-
Augelli-Szafran, C.E.1
Horwell, D.C.2
Kneen, C.3
Ortwine, D.F.4
Pritchard, M.C.5
Purchase, T.S.6
-
24
-
-
77949391413
-
Synthesis and structure-activity correlation of natural-product inspired cyclodepsipeptides stabilizing F-actin
-
R. Tannert, L.G. Milroy, B. Ellinger, T.S. Hu, H.D. Arndt, and H. Waldmann Synthesis and structure-activity correlation of natural-product inspired cyclodepsipeptides stabilizing F-actin J Am Chem Soc 132 2010 3063 3077
-
(2010)
J Am Chem Soc
, vol.132
, pp. 3063-3077
-
-
Tannert, R.1
Milroy, L.G.2
Ellinger, B.3
Hu, T.S.4
Arndt, H.D.5
Waldmann, H.6
-
25
-
-
67650726009
-
Structural assessment and biological evaluation of two N3S bombesin derivatives
-
E. Gourni, P. Bouziotis, D. Benaki, G. Loudos, S. Xanthopoulos, and M. Paravatou-Petsotas Structural assessment and biological evaluation of two N3S bombesin derivatives J Med Chem 52 2009 4234 4246
-
(2009)
J Med Chem
, vol.52
, pp. 4234-4246
-
-
Gourni, E.1
Bouziotis, P.2
Benaki, D.3
Loudos, G.4
Xanthopoulos, S.5
Paravatou-Petsotas, M.6
-
26
-
-
58849083281
-
Characterizing cannabinoid CB2 receptor ligands using DiscoveRx PathHunter b arrestin assay
-
D. McGuinness, A. Malikzay, R. Visconti, K. Lin, M. Bayne, and F. Monsma Characterizing cannabinoid CB2 receptor ligands using DiscoveRx PathHunter b arrestin assay J Biomol Screen 14 2009 49 58
-
(2009)
J Biomol Screen
, vol.14
, pp. 49-58
-
-
McGuinness, D.1
Malikzay, A.2
Visconti, R.3
Lin, K.4
Bayne, M.5
Monsma, F.6
-
27
-
-
33646227896
-
Molecular field extrema as descriptors of biological activity: Definition and validation
-
T. Cheeseright, M. Mackey, S. Rose, and A. Vinter Molecular field extrema as descriptors of biological activity: definition and validation J Chem Inf Model 46 2006 665 676
-
(2006)
J Chem Inf Model
, vol.46
, pp. 665-676
-
-
Cheeseright, T.1
MacKey, M.2
Rose, S.3
Vinter, A.4
-
28
-
-
0028695270
-
Extended electron distributions applied to the molecular mechanics of some intermolecular interactions
-
J.G. Vinter Extended electron distributions applied to the molecular mechanics of some intermolecular interactions J Comput Aided Mol Des 8 1994 653 668
-
(1994)
J Comput Aided Mol des
, vol.8
, pp. 653-668
-
-
Vinter, J.G.1
-
29
-
-
79961081104
-
High content pharmacophores from molecular fields: A biologically relevant method for comparing and understanding ligands
-
T.J. Cheeseright, M.D. Mackey, and R.A. Scoffin High content pharmacophores from molecular fields: a biologically relevant method for comparing and understanding ligands Curr Comput Aided Drug Des 7 2011 190 205
-
(2011)
Curr Comput Aided Drug des
, vol.7
, pp. 190-205
-
-
Cheeseright, T.J.1
MacKey, M.D.2
Scoffin, R.A.3
-
30
-
-
63849246525
-
Protein structure prediction on the Web: A case study using the Phyre server
-
L.A. Kelley, and M.J. Sternberg Protein structure prediction on the Web: a case study using the Phyre server Nat Protoc 4 2009 363 371
-
(2009)
Nat Protoc
, vol.4
, pp. 363-371
-
-
Kelley, L.A.1
Sternberg, M.J.2
-
31
-
-
81755173456
-
Stimulation of human formyl peptide receptors by calpain inhibitors: Homology modeling of receptors and ligand docking simulation
-
H. Fujita, T. Kato, N. Watanabe, T. Takahashi, and S. Kitagawa Stimulation of human formyl peptide receptors by calpain inhibitors: homology modeling of receptors and ligand docking simulation Arch Biochem Biophys 516 2011 121 127
-
(2011)
Arch Biochem Biophys
, vol.516
, pp. 121-127
-
-
Fujita, H.1
Kato, T.2
Watanabe, N.3
Takahashi, T.4
Kitagawa, S.5
-
33
-
-
0035141105
-
Identification of an organic anion transport system in the human colon carcinoma cell line HT29 clone 19A
-
S.L. Abrahamse, and G. Rechkemmer Identification of an organic anion transport system in the human colon carcinoma cell line HT29 clone 19A Pflugers Arch 441 2001 529 537
-
(2001)
Pflugers Arch
, vol.441
, pp. 529-537
-
-
Abrahamse, S.L.1
Rechkemmer, G.2
-
34
-
-
66449113577
-
Formyl peptide receptor-like proteins are a novel family of vomeronasal chemosensors
-
S. Riviere, L. Challet, D. Fluegge, M. Spehr, and I. Rodriguez Formyl peptide receptor-like proteins are a novel family of vomeronasal chemosensors Nature 459 2009 574 577
-
(2009)
Nature
, vol.459
, pp. 574-577
-
-
Riviere, S.1
Challet, L.2
Fluegge, D.3
Spehr, M.4
Rodriguez, I.5
-
35
-
-
67649849919
-
Formyl peptide receptors are candidate chemosensory receptors in the vomeronasal organ
-
S.D. Liberles, L.F. Horowitz, D. Kuang, J.J. Contos, K.L. Wilson, and J. Siltberg-Liberles Formyl peptide receptors are candidate chemosensory receptors in the vomeronasal organ Proc Natl Acad Sci U S A 106 2009 9842 9847
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 9842-9847
-
-
Liberles, S.D.1
Horowitz, L.F.2
Kuang, D.3
Contos, J.J.4
Wilson, K.L.5
Siltberg-Liberles, J.6
-
36
-
-
84866913793
-
Formyl peptide receptors from immune and vomeronasal system exhibit distinct agonist properties
-
B. Bufe, T. Schumann, and F. Zufall Formyl peptide receptors from immune and vomeronasal system exhibit distinct agonist properties J Biol Chem 287 2012 33644 33655
-
(2012)
J Biol Chem
, vol.287
, pp. 33644-33655
-
-
Bufe, B.1
Schumann, T.2
Zufall, F.3
-
37
-
-
0029841440
-
Stereoselective recognition of the enantiomers of phenglutarimide and of six related compounds by four muscarinic receptor subtypes
-
M. Waelbroeck, S. Lazareno, O. Pfaff, T. Friebe, M. Tastenoy, and E. Mutschler Stereoselective recognition of the enantiomers of phenglutarimide and of six related compounds by four muscarinic receptor subtypes Br J Pharmacol 119 1996 1319 1330
-
(1996)
Br J Pharmacol
, vol.119
, pp. 1319-1330
-
-
Waelbroeck, M.1
Lazareno, S.2
Pfaff, O.3
Friebe, T.4
Tastenoy, M.5
Mutschler, E.6
-
38
-
-
70349280467
-
Characterization of an enantioselective odorant receptor in the yellow fever mosquito Aedes aegypti
-
J.D. Bohbot, and J.C. Dickens Characterization of an enantioselective odorant receptor in the yellow fever mosquito Aedes aegypti PLoS ONE 4 2009 e7032
-
(2009)
PLoS ONE
, vol.4
, pp. 7032
-
-
Bohbot, J.D.1
Dickens, J.C.2
-
39
-
-
0042020171
-
Stereoselectivity of drug-receptor interactions
-
W. Soudjin, W.I. van, and A.P. I.Jzerman Stereoselectivity of drug-receptor interactions IDrugs 6 2003 43 56
-
(2003)
IDrugs
, vol.6
, pp. 43-56
-
-
Soudjin, W.1
Van, W.I.2
Jzerman, A.P.I.3
-
41
-
-
0035193671
-
Sanazole as substrate of xanthine oxidase and microsomal NADPH/cytochrome P450 reductase
-
I.A. Schepetkin, N.V. Cherdyntseva, and V.T. Kagiya Sanazole as substrate of xanthine oxidase and microsomal NADPH/cytochrome P450 reductase Pathophysiology 8 2001 119 127
-
(2001)
Pathophysiology
, vol.8
, pp. 119-127
-
-
Schepetkin, I.A.1
Cherdyntseva, N.V.2
Kagiya, V.T.3
-
42
-
-
84860675377
-
Diminished toxicity of C-1748, 4-methyl-9-hydroxyethylamino-1- nitroacridine, compared with its demethyl analog, C-857, corresponds to its resistance to metabolism in HepG2 cells
-
A. Wisniewska, M. Niemira, K. Jagiello, A. Potega, M. Swist, and C. Henderson Diminished toxicity of C-1748, 4-methyl-9-hydroxyethylamino-1- nitroacridine, compared with its demethyl analog, C-857, corresponds to its resistance to metabolism in HepG2 cells Biochem Pharmacol 84 2012 30 42
-
(2012)
Biochem Pharmacol
, vol.84
, pp. 30-42
-
-
Wisniewska, A.1
Niemira, M.2
Jagiello, K.3
Potega, A.4
Swist, M.5
Henderson, C.6
-
43
-
-
33749848054
-
Bombesin receptors as a novel anti-anxiety therapeutic target: BB1 receptor actions on anxiety through alterations of serotonin activity
-
Z. Merali, T. Bedard, N. Andrews, B. Davis, A.T. McKnight, and M.I. Gonzalez Bombesin receptors as a novel anti-anxiety therapeutic target: BB1 receptor actions on anxiety through alterations of serotonin activity J Neurosci 26 2006 10387 10396
-
(2006)
J Neurosci
, vol.26
, pp. 10387-10396
-
-
Merali, Z.1
Bedard, T.2
Andrews, N.3
Davis, B.4
McKnight, A.T.5
Gonzalez, M.I.6
-
44
-
-
80053304908
-
B receptor antagonist suppresses tumor angiogenesis and tumor growth in vitro and in vivo
-
H.J. Park, S.R. Kim, M.K. Kim, K.S. Choi, H.O. Jang, and I. Yun B receptor antagonist suppresses tumor angiogenesis and tumor growth in vitro and in vivo Cancer Lett 312 2011 117 127
-
(2011)
Cancer Lett
, vol.312
, pp. 117-127
-
-
Park, H.J.1
Kim, S.R.2
Kim, M.K.3
Choi, K.S.4
Jang, H.O.5
Yun, I.6
-
45
-
-
84860338928
-
Expression of gastrin-releasing peptide is increased by prolonged stretch of human myometrium, and antagonists of its receptor inhibit contractility
-
M. Tattersall, Y. Cordeaux, D.S. Charnock-Jones, and G.C. Smith Expression of gastrin-releasing peptide is increased by prolonged stretch of human myometrium, and antagonists of its receptor inhibit contractility J Physiol 590 2012 2081 2093
-
(2012)
J Physiol
, vol.590
, pp. 2081-2093
-
-
Tattersall, M.1
Cordeaux, Y.2
Charnock-Jones, D.S.3
Smith, G.C.4
-
46
-
-
34548637630
-
Transient receptor potential V2 expressed in sensory neurons is activated by probenecid
-
S. Bang, K.Y. Kim, S. Yoo, S.H. Lee, and S.W. Hwang Transient receptor potential V2 expressed in sensory neurons is activated by probenecid Neurosci Lett 425 2007 120 125
-
(2007)
Neurosci Lett
, vol.425
, pp. 120-125
-
-
Bang, S.1
Kim, K.Y.2
Yoo, S.3
Lee, S.H.4
Hwang, S.W.5
-
47
-
-
84870953045
-
TRPA1 agonist activity of probenecid desensitizes channel responses: Consequences for screening
-
C. McClenaghan, F. Zeng, and J.M. Verkuyl TRPA1 agonist activity of probenecid desensitizes channel responses: consequences for screening Assay Drug Dev Technol 2012
-
(2012)
Assay Drug Dev Technol
-
-
McClenaghan, C.1
Zeng, F.2
Verkuyl, J.M.3
-
48
-
-
79956347958
-
Probenecid inhibits the human bitter taste receptor TAS2R16 and suppresses bitter perception of salicin
-
T.A. Greene, S. Alarcon, A. Thomas, E. Berdougo, B.J. Doranz, and P.A. Breslin Probenecid inhibits the human bitter taste receptor TAS2R16 and suppresses bitter perception of salicin PLoS ONE 6 2011 e20123
-
(2011)
PLoS ONE
, vol.6
, pp. 20123
-
-
Greene, T.A.1
Alarcon, S.2
Thomas, A.3
Berdougo, E.4
Doranz, B.J.5
Breslin, P.A.6
-
49
-
-
0027428066
-
Signal transducing properties of the N-formyl peptide receptor expressed in undifferentiated HL60 cells
-
E.R. Prossnitz, O. Quehenberger, C.G. Cochrane, and R.D. Ye Signal transducing properties of the N-formyl peptide receptor expressed in undifferentiated HL60 cells J Immunol 151 1993 5704 5715
-
(1993)
J Immunol
, vol.151
, pp. 5704-5715
-
-
Prossnitz, E.R.1
Quehenberger, O.2
Cochrane, C.G.3
Ye, R.D.4
-
51
-
-
0030815543
-
Specific expression of heterotrimeric G proteins G12 and G16 during human myeloid differentiation
-
S. Tenailleau, I. Corre, and S. Hermouet Specific expression of heterotrimeric G proteins G12 and G16 during human myeloid differentiation Exp Hematol 25 1997 927 934
-
(1997)
Exp Hematol
, vol.25
, pp. 927-934
-
-
Tenailleau, S.1
Corre, I.2
Hermouet, S.3
-
52
-
-
0035173647
-
Cyclic ADP-ribose production by CD38 regulates intracellular calcium release, extracellular calcium influx and chemotaxis in neutrophils and is required for bacterial clearance in vivo
-
S. Partida-Sánchez, D.A. Cockayne, S. Monard, E.L. Jacobson, N. Oppenheimer, and B. Garvy Cyclic ADP-ribose production by CD38 regulates intracellular calcium release, extracellular calcium influx and chemotaxis in neutrophils and is required for bacterial clearance in vivo Nat Med 7 2001 1209 1216
-
(2001)
Nat Med
, vol.7
, pp. 1209-1216
-
-
Partida-Sánchez, S.1
Cockayne, D.A.2
Monard, S.3
Jacobson, E.L.4
Oppenheimer, N.5
Garvy, B.6
-
53
-
-
77950644914
-
Functional and physical interactions between formyl-peptide-receptors and scavenger receptor MARCO and their involvement in amyloid beta 1-42-induced signal transduction in glial cells
-
L.O. Brandenburg, M. Konrad, C.J. Wruck, T. Koch, R. Lucius, and T. Pufe Functional and physical interactions between formyl-peptide-receptors and scavenger receptor MARCO and their involvement in amyloid beta 1-42-induced signal transduction in glial cells J Neurochem 113 2010 749 760
-
(2010)
J Neurochem
, vol.113
, pp. 749-760
-
-
Brandenburg, L.O.1
Konrad, M.2
Wruck, C.J.3
Koch, T.4
Lucius, R.5
Pufe, T.6
-
54
-
-
77949721283
-
Agonist-selective signaling of G protein-coupled receptor: Mechanisms and implications
-
H. Zheng, H.H. Loh, and P.Y. Law Agonist-selective signaling of G protein-coupled receptor: mechanisms and implications IUBMB Life 62 2010 112 119
-
(2010)
IUBMB Life
, vol.62
, pp. 112-119
-
-
Zheng, H.1
Loh, H.H.2
Law, P.Y.3
-
55
-
-
33845903110
-
Functional selectivity and classical concepts of quantitative pharmacology
-
J.D. Urban, W.P. Clarke, Z.M. von, D.E. Nichols, B. Kobilka, and H. Weinstein Functional selectivity and classical concepts of quantitative pharmacology J Pharmacol Exp Ther 320 2007 1 13
-
(2007)
J Pharmacol Exp Ther
, vol.320
, pp. 1-13
-
-
Urban, J.D.1
Clarke, W.P.2
Von, Z.M.3
Nichols, D.E.4
Kobilka, B.5
Weinstein, H.6
-
56
-
-
84863798032
-
Annexin A1 interaction with the FPR2/ALX Receptor: Identification of distinct domains and downstream associated signaling
-
S. Bena, V. Brancaleone, J.M. Wang, M. Perretti, and R.J. Flower Annexin A1 interaction with the FPR2/ALX Receptor: identification of distinct domains and downstream associated signaling J Biol Chem 287 2012 24690 24697
-
(2012)
J Biol Chem
, vol.287
, pp. 24690-24697
-
-
Bena, S.1
Brancaleone, V.2
Wang, J.M.3
Perretti, M.4
Flower, R.J.5
-
57
-
-
80051625271
-
Production of a bioengineered G-protein coupled receptor of human formyl peptide receptor 3
-
X. Wang, and S. Zhang Production of a bioengineered G-protein coupled receptor of human formyl peptide receptor 3 PLoS ONE 6 2011 e23076
-
(2011)
PLoS ONE
, vol.6
, pp. 23076
-
-
Wang, X.1
Zhang, S.2
|