-
1
-
-
84866142212
-
Measuring substrate binding and affinity of purified membrane transport proteins using the scintillation proximity assay
-
COI: 1:CAS:528:DC%2BC38XhtFCrsbfI, PID: 22864198
-
Harder D, Fotiadis D (2012) Measuring substrate binding and affinity of purified membrane transport proteins using the scintillation proximity assay. Nat Protoc 7(9):1569–1578
-
(2012)
Nat Protoc
, vol.7
, Issue.9
, pp. 1569-1578
-
-
Harder, D.1
Fotiadis, D.2
-
2
-
-
51149107449
-
Scintillation proximity assays in high-throughput screening
-
COI: 1:CAS:528:DC%2BD1cXnvFChu7o%3D, PID: 18593378
-
Glickman JF, Schmid A, Ferrand S (2008) Scintillation proximity assays in high-throughput screening. Assay Drug Dev Technol 6(3):433–455
-
(2008)
Assay Drug Dev Technol
, vol.6
, Issue.3
, pp. 433-455
-
-
Glickman, J.F.1
Schmid, A.2
Ferrand, S.3
-
3
-
-
0024969084
-
Scintillation proximity assay
-
COI: 1:STN:280:DyaL1MzosVyktw%3D%3D, PID: 2550824
-
Bosworth N, Towers P (1989) Scintillation proximity assay. Nature 341(6238):167–168
-
(1989)
Nature
, vol.341
, Issue.6238
, pp. 167-168
-
-
Bosworth, N.1
Towers, P.2
-
4
-
-
0018718059
-
Scintillation-proximity assay of antigen—antibody binding kinetics: concise communication
-
COI: 1:STN:280:DyaL3c7jvFamtg%3D%3D, PID: 536756
-
Hart HE, Greenwald EB (1979) Scintillation-proximity assay of antigen—antibody binding kinetics: concise communication. J Nucl Med 20(10):1062–1065
-
(1979)
J Nucl Med
, vol.20
, Issue.10
, pp. 1062-1065
-
-
Hart, H.E.1
Greenwald, E.B.2
-
5
-
-
0001528377
-
Scintillation proximity radioimmunoassay utilizing 125I-labeled ligands
-
COI: 1:CAS:528:DyaL28XmsFSrsw%3D%3D, PID: 3866247
-
Udenfriend S, Gerber LD, Brink L, Spector S (1985) Scintillation proximity radioimmunoassay utilizing 125I-labeled ligands. Proc Natl Acad Sci U S A 82(24):8672–8676
-
(1985)
Proc Natl Acad Sci U S A
, vol.82
, Issue.24
, pp. 8672-8676
-
-
Udenfriend, S.1
Gerber, L.D.2
Brink, L.3
Spector, S.4
-
6
-
-
33847667536
-
Scintillation proximity assay as a high-throughput method to identify slowly dissociating nonpeptide ligand binding to the GnRH receptor
-
COI: 1:CAS:528:DC%2BD2sXktFOhtLY%3D, PID: 17208923
-
Heise CE, Sullivan SK, Crowe PD (2007) Scintillation proximity assay as a high-throughput method to identify slowly dissociating nonpeptide ligand binding to the GnRH receptor. J Biomol Screen 12(2):235–239
-
(2007)
J Biomol Screen
, vol.12
, Issue.2
, pp. 235-239
-
-
Heise, C.E.1
Sullivan, S.K.2
Crowe, P.D.3
-
7
-
-
84903211679
-
A study of the molecular mechanism of binding kinetics and long residence times of human CCR5 receptor small molecule allosteric ligands
-
COI: 1:CAS:528:DC%2BC2cXhtVahtbvK
-
Swinney DC, Beavis P, Chuang K-T, Zheng Y, Lee I, Gee P, Deval J, Rotstein DM, Dioszegi M, Ravendran P, Zhang J, Sankuratri S, Kondru R, Vauquelin G (2014) A study of the molecular mechanism of binding kinetics and long residence times of human CCR5 receptor small molecule allosteric ligands. Brit J Pharmacol 171(14):3364–3375
-
(2014)
Brit J Pharmacol
, vol.171
, Issue.14
, pp. 3364-3375
-
-
Swinney, D.C.1
Beavis, P.2
Chuang, K.-T.3
Zheng, Y.4
Lee, I.5
Gee, P.6
Deval, J.7
Rotstein, D.M.8
Dioszegi, M.9
Ravendran, P.10
Zhang, J.11
Sankuratri, S.12
Kondru, R.13
Vauquelin, G.14
-
8
-
-
34250197581
-
C(4)-alkyl substituted furanyl cyclobutenediones as potent, orally bioavailable CXCR2 and CXCR1 receptor antagonists
-
COI: 1:CAS:528:DC%2BD2sXmsFaiu7s%3D, PID: 17459706
-
Chao J, Taveras AG, Chao J, Aki C, Dwyer M, Yu Y, Purakkattle B, Rindgen D, Jakway J, Hipkin W, Fosetta J, Fan X, Lundell D, Fine J, Minnicozzi M, Phillips J, Merritt JR (2007) C(4)-alkyl substituted furanyl cyclobutenediones as potent, orally bioavailable CXCR2 and CXCR1 receptor antagonists. Bioorg Med Chem Lett 17(13):3778–3783
-
(2007)
Bioorg Med Chem Lett
, vol.17
, Issue.13
, pp. 3778-3783
-
-
Chao, J.1
Taveras, A.G.2
Chao, J.3
Aki, C.4
Dwyer, M.5
Yu, Y.6
Purakkattle, B.7
Rindgen, D.8
Jakway, J.9
Hipkin, W.10
Fosetta, J.11
Fan, X.12
Lundell, D.13
Fine, J.14
Minnicozzi, M.15
Phillips, J.16
Merritt, J.R.17
-
9
-
-
41149180692
-
5-Amino-6-chloro-N-[(1-isobutylpiperidin-4-yl)methyl]-2-methylimidazo[1,2-α]pyridine-8-carboxamide (CJ-033,466), a novel and selective 5-hydroxytryptamine4 receptor partial agonist: pharmacological profile in vitro and gastroprokinetic effect in conscious dogs
-
COI: 1:CAS:528:DC%2BD1cXktFGjtLc%3D, PID: 18198343
-
Mikami T, Ochi Y, Suzuki K, Saito T, Sugie Y, Sakakibara M (2008) 5-Amino-6-chloro-N-[(1-isobutylpiperidin-4-yl)methyl]-2-methylimidazo[1,2-α]pyridine-8-carboxamide (CJ-033,466), a novel and selective 5-hydroxytryptamine4 receptor partial agonist: pharmacological profile in vitro and gastroprokinetic effect in conscious dogs. J Pharmacol Exp Ther 325(1):190–199
-
(2008)
J Pharmacol Exp Ther
, vol.325
, Issue.1
, pp. 190-199
-
-
Mikami, T.1
Ochi, Y.2
Suzuki, K.3
Saito, T.4
Sugie, Y.5
Sakakibara, M.6
-
10
-
-
84921757196
-
-
Assay Guidance Manual [Internet], Eli Lilly & Company and the National Center for Advancing Translational Sciences, Bethesda
-
Auld DS Farmen MW, Kahl SD et al (2012) Receptor binding assays for HTS and drug discovery, Assay Guidance Manual [Internet]. Eli Lilly & Company and the National Center for Advancing Translational Sciences, Bethesda
-
(2012)
Receptor binding assays for HTS and drug discovery
-
-
Auld DS Farmen, M.W.1
Kahl, S.D.2
-
11
-
-
44049103958
-
Residence time of receptor—ligand complexes and its effect on biological function
-
COI: 1:CAS:528:DC%2BD1cXks1Ont7s%3D, PID: 18412369
-
Tummino PJ, Copeland RA (2008) Residence time of receptor—ligand complexes and its effect on biological function. Biochemistry 47(20):5481–5492
-
(2008)
Biochemistry
, vol.47
, Issue.20
, pp. 5481-5492
-
-
Tummino, P.J.1
Copeland, R.A.2
-
12
-
-
84901827515
-
Drug-target residence time—a case for G protein-coupled receptors
-
COI: 1:CAS:528:DC%2BC2cXptVagtbs%3D, PID: 24549504
-
Guo D, Hillger JM, IJzerman AP, Heitman LH (2014) Drug-target residence time—a case for G protein-coupled receptors. Med Res Rev 34(4):856–892
-
(2014)
Med Res Rev
, vol.34
, Issue.4
, pp. 856-892
-
-
Guo, D.1
Hillger, J.M.2
IJzerman, A.P.3
Heitman, L.H.4
-
13
-
-
69549098265
-
Exploring the mechanism of agonist efficacy: a relationship between efficacy and agonist dissociation rate at the muscarinic M3 receptor
-
COI: 1:CAS:528:DC%2BC3cXkvVyrsLg%3D, PID: 19498041
-
Sykes DA, Dowling MR, Charlton SJ (2009) Exploring the mechanism of agonist efficacy: a relationship between efficacy and agonist dissociation rate at the muscarinic M3 receptor. Mol Pharmacol 76(3):543–551
-
(2009)
Mol Pharmacol
, vol.76
, Issue.3
, pp. 543-551
-
-
Sykes, D.A.1
Dowling, M.R.2
Charlton, S.J.3
-
14
-
-
84863228021
-
Functional efficacy of adenosine A(2A) receptor agonists is positively correlated to their receptor residence time
-
COI: 1:CAS:528:DC%2BC38XhtVOku7bL
-
Guo D, Mulder-Krieger T, IJzerman AP, Heitman LH (2012) Functional efficacy of adenosine A(2A) receptor agonists is positively correlated to their receptor residence time. Brit J Pharmacol 166(6):1846–1859
-
(2012)
Brit J Pharmacol
, vol.166
, Issue.6
, pp. 1846-1859
-
-
Guo, D.1
Mulder-Krieger, T.2
IJzerman, A.P.3
Heitman, L.H.4
-
15
-
-
84885615252
-
Structure-kinetic relationships—an overlooked parameter in hit-to-lead optimization: a case of cyclopentylamines as chemokine receptor 2 antagonists
-
COI: 1:CAS:528:DC%2BC3sXhsVeksbvM, PID: 24028535
-
Vilums M, Zweemer AJM, Yu Z, de Vries H, Hillger JM, Wapenaar H, Bollen IAE, Barmare F, Gross R, Clemens J, Krenitsky P, Brussee J, Stamos D, Saunders J, Heitman LH, IJzerman AP (2013) Structure-kinetic relationships—an overlooked parameter in hit-to-lead optimization: a case of cyclopentylamines as chemokine receptor 2 antagonists. J Med Chem 56(19):7706–7714
-
(2013)
J Med Chem
, vol.56
, Issue.19
, pp. 7706-7714
-
-
Vilums, M.1
Zweemer, A.J.M.2
Yu, Z.3
de Vries, H.4
Hillger, J.M.5
Wapenaar, H.6
Bollen, I.A.E.7
Barmare, F.8
Gross, R.9
Clemens, J.10
Krenitsky, P.11
Brussee, J.12
Stamos, D.13
Saunders, J.14
Heitman, L.H.15
IJzerman, A.P.16
-
16
-
-
84897974504
-
Binding kinetics of ZM241385 derivatives at the human adenosine A2A receptor
-
COI: 1:CAS:528:DC%2BC2cXjtlyhtrs%3D, PID: 24591302
-
Guo D, Xia L, van Veldhoven JPD, Hazeu M, Mocking T, Brussee J, IJzerman AP, Heitman LH (2014) Binding kinetics of ZM241385 derivatives at the human adenosine A2A receptor. ChemMedChem 9(4):752–761
-
(2014)
ChemMedChem
, vol.9
, Issue.4
, pp. 752-761
-
-
Guo, D.1
Xia, L.2
van Veldhoven, J.P.D.3
Hazeu, M.4
Mocking, T.5
Brussee, J.6
IJzerman, A.P.7
Heitman, L.H.8
-
17
-
-
84930867254
-
Affinity and kinetics study of anthranilic acids as HCA2 receptor agonists
-
van Veldhoven JPD, Liu R, Thee SA, Wouters Y, Verhoork SJM, Mooiman C, Louvel J, IJzerman AP (2015) Affinity and kinetics study of anthranilic acids as HCA2 receptor agonists. Bioorgan Med Chem 23(14):4013–4025
-
(2015)
Bioorgan Med Chem
, vol.23
, Issue.14
, pp. 4013-4025
-
-
van Veldhoven, J.P.D.1
Liu, R.2
Thee, S.A.3
Wouters, Y.4
Verhoork, S.J.M.5
Mooiman, C.6
Louvel, J.7
IJzerman, A.P.8
-
18
-
-
0021336303
-
The kinetics of competitive radioligand binding predicted by the law of mass action
-
COI: 1:STN:280:DyaL2c7mslOmtQ%3D%3D, PID: 6708928
-
Motulsky HJ, Mahan LC (1984) The kinetics of competitive radioligand binding predicted by the law of mass action. Mol Pharmacol 25(1):1–9
-
(1984)
Mol Pharmacol
, vol.25
, Issue.1
, pp. 1-9
-
-
Motulsky, H.J.1
Mahan, L.C.2
-
19
-
-
77957577496
-
Fused tricyclic pyrrolizinones that exhibit pseudo-irreversible blockade of the NK1 receptor
-
COI: 1:CAS:528:DC%2BC3cXhtFGnt73F, PID: 20729082
-
Morriello GJ, Chicchi G, Johnson T, Mills SG, DeMartino J, Kurtz M, Tsao KLC, Zheng S, Tong X, Carlson E, Townson K, Wheeldon A, Boyce S, Collinson N, Rupniak N, DeVita RJ (2010) Fused tricyclic pyrrolizinones that exhibit pseudo-irreversible blockade of the NK1 receptor. Bioorg Med Chem Lett 20(19):5925–5932
-
(2010)
Bioorg Med Chem Lett
, vol.20
, Issue.19
, pp. 5925-5932
-
-
Morriello, G.J.1
Chicchi, G.2
Johnson, T.3
Mills, S.G.4
DeMartino, J.5
Kurtz, M.6
Tsao, K.L.C.7
Zheng, S.8
Tong, X.9
Carlson, E.10
Townson, K.11
Wheeldon, A.12
Boyce, S.13
Collinson, N.14
Rupniak, N.15
DeVita, R.J.16
-
20
-
-
0019495090
-
Mathematical analysis of the kinetics of competitive inhibition in neurotransmitter receptor binding assays
-
COI: 1:CAS:528:DyaL3MXktlGhtLs%3D, PID: 6267444
-
Ehlert FJ, Roeske WR, Yamamura HI (1981) Mathematical analysis of the kinetics of competitive inhibition in neurotransmitter receptor binding assays. Mol Pharmacol 19(3):367–371
-
(1981)
Mol Pharmacol
, vol.19
, Issue.3
, pp. 367-371
-
-
Ehlert, F.J.1
Roeske, W.R.2
Yamamura, H.I.3
-
21
-
-
84873697000
-
Dual-point competition association assay: a fast and high-throughput kinetic screening method for assessing ligand-receptor binding kinetics
-
COI: 1:CAS:528:DC%2BC2cXhs1Ogtb%2FK, PID: 23093571
-
Guo D, Dorp EJH, Mulder-Krieger T, Veldhoven JPD, Brussee J, IJzerman AP, Heitman LH (2013) Dual-point competition association assay: a fast and high-throughput kinetic screening method for assessing ligand-receptor binding kinetics. J Biomol Screen 18(3):309–320
-
(2013)
J Biomol Screen
, vol.18
, Issue.3
, pp. 309-320
-
-
Guo, D.1
Dorp, E.J.H.2
Mulder-Krieger, T.3
Veldhoven, J.P.D.4
Brussee, J.5
IJzerman, A.P.6
Heitman, L.H.7
-
22
-
-
84867303994
-
Use of scintillation proximity assay to measure radioligand binding to immobilized receptors without separation of bound from free ligand
-
Methods in Molecular Biology, Humana Press
-
Berry J, Price-Jones M, Killian B. (2012) Use of scintillation proximity assay to measure radioligand binding to immobilized receptors without separation of bound from free ligand. In: Davenport AP (Ed.) Receptor Binding Techniques, vol 897. Methods in Molecular Biology. Humana Press, pp 79–94.
-
(2012)
Receptor Binding Techniques
, vol.897
, pp. 79-94
-
-
Berry, J.1
Price-Jones, M.2
Killian, B.3
Davenport, A.P.4
-
23
-
-
0023113567
-
Potent adenosine receptor antagonists that are selective for the A1 receptor subtype
-
COI: 1:CAS:528:DyaL2sXktVSht7c%3D, PID: 3561384
-
Martinson EA, Johnson RA, Wells JN (1987) Potent adenosine receptor antagonists that are selective for the A1 receptor subtype. Mol Pharmacol 31(3):247–252
-
(1987)
Mol Pharmacol
, vol.31
, Issue.3
, pp. 247-252
-
-
Martinson, E.A.1
Johnson, R.A.2
Wells, J.N.3
-
24
-
-
0035953021
-
Synthesis and use of FSCPX, an irreversible adenosine A1 antagonist, as a ‘receptor knock-down’ tool
-
COI: 1:CAS:528:DC%2BD3MXitVOjtb8%3D, PID: 11277527
-
Muijlwijk-Koezen JEV, Timmerman H, der Sluis RP, van de Stolpe AC, Menge WMPB, Beukers MW, van der Graaf PH, de Groote M, IJzerman AP (2001) Synthesis and use of FSCPX, an irreversible adenosine A1 antagonist, as a ‘receptor knock-down’ tool. Bioorg Med Chem Lett 11(6):815–818
-
(2001)
Bioorg Med Chem Lett
, vol.11
, Issue.6
, pp. 815-818
-
-
Muijlwijk-Koezen, J.E.V.1
Timmerman, H.2
der Sluis, R.P.3
van de Stolpe, A.C.4
Menge, W.M.P.B.5
Beukers, M.W.6
van der Graaf, P.H.7
de Groote, M.8
IJzerman, A.P.9
-
25
-
-
0024854587
-
2-Chloro-N6-[3H]cyclopentyladenosine ([3HCCPA)—a high affinity agonist radioligand for A1 adenosine receptors
-
COI: 1:CAS:528:DyaK3cXhtFGhsL8%3D
-
Klotz K-N, Lohse M, Schwabe U, Cristalli G, Vittori S, Grifantini M (1989) 2-Chloro-N6-[3H]cyclopentyladenosine ([3HCCPA)—a high affinity agonist radioligand for A1 adenosine receptors. N-S Arch Pharmacol 340(6):679–683
-
(1989)
N-S Arch Pharmacol
, vol.340
, Issue.6
, pp. 679-683
-
-
Klotz, K.-N.1
Lohse, M.2
Schwabe, U.3
Cristalli, G.4
Vittori, S.5
Grifantini, M.6
-
26
-
-
0019507802
-
5′-N-ethylcarboxamidoadenosine: a potent inhibitor of human platelet aggregation
-
COI: 1:CAS:528:DyaL3MXlt1Grurk%3D
-
Cusack NJ, Hourani SMO (1981) 5′-N-ethylcarboxamidoadenosine: a potent inhibitor of human platelet aggregation. Brit J Pharmacol 72(3):443–447
-
(1981)
Brit J Pharmacol
, vol.72
, Issue.3
, pp. 443-447
-
-
Cusack, N.J.1
Hourani, S.M.O.2
-
27
-
-
3142543178
-
New, non-adenosine, high-potency agonists for the human adenosine A2B receptor with an improved selectivity profile compared to the reference agonist N-ethylcarboxamidoadenosine
-
COI: 1:CAS:528:DC%2BD2cXksl2rtL8%3D, PID: 15239649
-
Beukers MW, Chang LCW, von Frijtag Drabbe Künzel JK, Mulder-Krieger T, Spanjersberg RF, Brussee J, IJzerman AP (2004) New, non-adenosine, high-potency agonists for the human adenosine A2B receptor with an improved selectivity profile compared to the reference agonist N-ethylcarboxamidoadenosine. J Med Chem 47(15):3707–3709
-
(2004)
J Med Chem
, vol.47
, Issue.15
, pp. 3707-3709
-
-
Beukers, M.W.1
Chang, L.C.W.2
von Frijtag Drabbe Künzel, J.K.3
Mulder-Krieger, T.4
Spanjersberg, R.F.5
Brussee, J.6
IJzerman, A.P.7
-
28
-
-
0022186670
-
Measurement of protein using bicinchoninic acid
-
COI: 1:CAS:528:DyaL2MXlsFKksL0%3D, PID: 3843705
-
Smith PK, Krohn RI, Hermanson GT, Mallia AK, Gartner FH, Provenzano MD, Fujimoto EK, Goeke NM, Olson BJ, Klenk DC (1985) Measurement of protein using bicinchoninic acid. Anal Biochem 150(1):76–85
-
(1985)
Anal Biochem
, vol.150
, Issue.1
, pp. 76-85
-
-
Smith, P.K.1
Krohn, R.I.2
Hermanson, G.T.3
Mallia, A.K.4
Gartner, F.H.5
Provenzano, M.D.6
Fujimoto, E.K.7
Goeke, N.M.8
Olson, B.J.9
Klenk, D.C.10
-
29
-
-
0015861774
-
Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 percent inhibition (I50) of an enzymatic reaction
-
COI: 1:CAS:528:DyaE2cXhtVGgs7c%3D, PID: 4202581
-
Cheng Y, Prusoff WH (1973) Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 percent inhibition (I50) of an enzymatic reaction. Biochem Pharmacol 22(23):3099–3108
-
(1973)
Biochem Pharmacol
, vol.22
, Issue.23
, pp. 3099-3108
-
-
Cheng, Y.1
Prusoff, W.H.2
-
30
-
-
84939780109
-
-
Ligand residence time at GPCRs—why we should take our time to study it, Mol Pharmacol
-
Hoffmann C, Castro M, Rinken A, Leurs R, Hill SJ, Vischer HF (2015) Ligand residence time at GPCRs—why we should take our time to study it. Mol Pharmacol. doi:10.1124/mol.115.099671
-
(2015)
Vischer HF
-
-
Hoffmann, C.1
Castro, M.2
Rinken, A.3
Leurs, R.4
Hill, S.J.5
-
32
-
-
84958021501
-
Liquid scintillation counters and multiplier phototubes
-
Academic, New York
-
Horrocks D (1974) Liquid scintillation counters and multiplier phototubes. In: Applications of liquid scintillation counting. Academic, New York, pp 69–89
-
(1974)
Applications of liquid scintillation counting
, pp. 69-89
-
-
Horrocks, D.1
-
34
-
-
84929703379
-
Biosensor-based affinities and binding kinetics of small molecule antagonists to the adenosine A2A receptor reconstituted in HDL like particles
-
COI: 1:CAS:528:DC%2BC2MXns1Omu7s%3D, PID: 25935416
-
Segala E, Errey JC, Fiez-Vandal C, Zhukov A, Cooke RM (2015) Biosensor-based affinities and binding kinetics of small molecule antagonists to the adenosine A2A receptor reconstituted in HDL like particles. FEBS Lett 589(13):1399–1405
-
(2015)
FEBS Lett
, vol.589
, Issue.13
, pp. 1399-1405
-
-
Segala, E.1
Errey, J.C.2
Fiez-Vandal, C.3
Zhukov, A.4
Cooke, R.M.5
-
35
-
-
84924047517
-
Real-time monitoring of binding events on a thermostabilized human A2A receptor embedded in a lipid bilayer by surface plasmon resonance
-
COI: 1:CAS:528:DC%2BC2MXjs1OktL0%3D, PID: 25725488
-
Bocquet N, Kohler J, Hug MN, Kusznir EA, Rufer AC, Dawson RJ, Hennig M, Ruf A, Huber W, Huber S (2015) Real-time monitoring of binding events on a thermostabilized human A2A receptor embedded in a lipid bilayer by surface plasmon resonance. BBA - Biomembranes 1848(5):1224–1233
-
(2015)
BBA - Biomembranes
, vol.1848
, Issue.5
, pp. 1224-1233
-
-
Bocquet, N.1
Kohler, J.2
Hug, M.N.3
Kusznir, E.A.4
Rufer, A.C.5
Dawson, R.J.6
Hennig, M.7
Ruf, A.8
Huber, W.9
Huber, S.10
-
36
-
-
0035869428
-
Miniaturization of a hepatitis C virus RNA polymerase assay using a −102°C cooled CCD camera-based imaging system
-
COI: 1:CAS:528:DC%2BD3MXhsF2is7w%3D, PID: 11237322
-
Zheng W, Carroll SS, Inglese J, Graves R, Howells L, Strulovici B (2001) Miniaturization of a hepatitis C virus RNA polymerase assay using a −102°C cooled CCD camera-based imaging system. Anal Biochem 290(2):214–220
-
(2001)
Anal Biochem
, vol.290
, Issue.2
, pp. 214-220
-
-
Zheng, W.1
Carroll, S.S.2
Inglese, J.3
Graves, R.4
Howells, L.5
Strulovici, B.6
-
37
-
-
4043121932
-
WGA-coated yttrium oxide beads enable an imaging-based adenosine 2a receptor binding scintillation proximity assay suitable for high throughput screening
-
COI: 1:CAS:528:DC%2BD2cXls1Omtbw%3D, PID: 15285910
-
Bryant R, McGuinness D, Turek-Etienne T, Guyer D, Yu L, Howells L, Caravano J, Zhai Y, Lachowicz J (2004) WGA-coated yttrium oxide beads enable an imaging-based adenosine 2a receptor binding scintillation proximity assay suitable for high throughput screening. Assay Drug Dev Technol 2(3):290–299
-
(2004)
Assay Drug Dev Technol
, vol.2
, Issue.3
, pp. 290-299
-
-
Bryant, R.1
McGuinness, D.2
Turek-Etienne, T.3
Guyer, D.4
Yu, L.5
Howells, L.6
Caravano, J.7
Zhai, Y.8
Lachowicz, J.9
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