-
1
-
-
0035914406
-
A receptors characterized by fluorescence resonance energy transfer-derived measurements of membrane potential
-
A receptors characterized by fluorescence resonance energy transfer-derived measurements of membrane potential. J Biol Chem 276:38934-38939.
-
(2001)
J Biol Chem
, vol.276
, pp. 38934-38939
-
-
Adkins, C.E.1
Pillai, G.V.2
Kerby, J.3
Bonnert, T.P.4
Haldon, C.5
McKernan, R.M.6
Gonzalez, J.E.7
Oades, K.8
Whiting, P.J.9
Simpson, P.B.10
-
2
-
-
0024554279
-
Clinical pharmacokinetics of nonsteroidal anti-inflammatory drugs in the cerebrospinal fluid
-
Bannwarth B, Netter P, Pourel J, Royer RJ, and Gaucher A (1989) Clinical pharmacokinetics of nonsteroidal anti-inflammatory drugs in the cerebrospinal fluid. Biomed Pharmacother 43:121-126.
-
(1989)
Biomed Pharmacother
, vol.43
, pp. 121-126
-
-
Bannwarth, B.1
Netter, P.2
Pourel, J.3
Royer, R.J.4
Gaucher, A.5
-
3
-
-
0030922807
-
The interaction of the general anesthetic etomidate with the γ-aminobutyric acid type A receptor is influenced by a single amino acid
-
Belleli D, Lambert JL, Peters JA, Wafford K, and Whiting PJ (1997) The interaction of the general anesthetic etomidate with the γ-aminobutyric acid type A receptor is influenced by a single amino acid. Proc Natl Acad Sci USA 94:11031-11036.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 11031-11036
-
-
Belleli, D.1
Lambert, J.L.2
Peters, J.A.3
Wafford, K.4
Whiting, P.J.5
-
5
-
-
0034006474
-
A single glycine residue at the entrance to the first membrane-spanning domain of the γ-aminobutyric acid type A receptor β2 subunit affects allosteric sensitivity to GABA and anesthetics
-
Carlson BX, Engblom AC, Kristiansen U, Schousboe A, and Olsen RW (2000) A single glycine residue at the entrance to the first membrane-spanning domain of the γ-aminobutyric acid type A receptor β2 subunit affects allosteric sensitivity to GABA and anesthetics. Mol Pharmacol 57:474-484.
-
(2000)
Mol Pharmacol
, vol.57
, pp. 474-484
-
-
Carlson, B.X.1
Engblom, A.C.2
Kristiansen, U.3
Schousboe, A.4
Olsen, R.W.5
-
8
-
-
0031452190
-
Differences in agonist/antagonist binding affinity and receptor transduction using recombinant human γ-aminobutyric acid type A receptors, cells
-
Ebert B, Thompson SA, Saounatsou K, McKernan R, Krogsgaard-Larsen P, and Wafford K (1997) Differences in agonist/antagonist binding affinity and receptor transduction using recombinant human γ-aminobutyric acid type A receptors, cells. Mol Pharmacol 52:1150-1156.
-
(1997)
Mol Pharmacol
, vol.52
, pp. 1150-1156
-
-
Ebert, B.1
Thompson, S.A.2
Saounatsou, K.3
McKernan, R.4
Krogsgaard-Larsen, P.5
Wafford, K.6
-
10
-
-
0033537884
-
Stoichiometry of a ligand-gated ion channel determined by fluorescence energy transfer
-
Farrar SJ, Whiting PJ, Bonnert TP, and McKernan RM (1999) Stoichiometry of a ligand-gated ion channel determined by fluorescence energy transfer. J Biol Chem 274:10100-10104.
-
(1999)
J Biol Chem
, vol.274
, pp. 10100-10104
-
-
Farrar, S.J.1
Whiting, P.J.2
Bonnert, T.P.3
McKernan, R.M.4
-
11
-
-
0028977843
-
A receptor heterogeneity in the adult rat brain: Differential regional and cellular distribution of seven major subunits
-
A receptor heterogeneity in the adult rat brain: differential regional and cellular distribution of seven major subunits. J Comp Neurol 359:154-194.
-
(1995)
J Comp Neurol
, vol.359
, pp. 154-194
-
-
Fritschy, J.-M.1
Mohler, H.2
-
12
-
-
0344500746
-
Cell-based assays and instrumentation for screening ion channel targets
-
Gonzalez JE, Oades K, Leychkis Y, Harootunian A, and Negulescu PA (1999) Cell-based assays and instrumentation for screening ion channel targets. Drug Discov Today 4:431-439.
-
(1999)
Drug Discov Today
, vol.4
, pp. 431-439
-
-
Gonzalez, J.E.1
Oades, K.2
Leychkis, Y.3
Harootunian, A.4
Negulescu, P.A.5
-
13
-
-
0028801324
-
Comparison of the effects of fenamates on Ca-activated chloride and potassium currents in rabbit portal vein smooth muscle cells
-
Greenwood IA and Large WA (1995) Comparison of the effects of fenamates on Ca-activated chloride and potassium currents in rabbit portal vein smooth muscle cells. Br J Pharmacol 116:2939-2948.
-
(1995)
Br J Pharmacol
, vol.116
, pp. 2939-2948
-
-
Greenwood, I.A.1
Large, W.A.2
-
14
-
-
0027761396
-
Role of the β subunit in determining the pharmacology of human γ-aminobutyric acid type A receptors
-
Hadingham KL, Wingrove PB, Wafford KA, Bain C, Kemp JA, Palmer KJ, Wilson AW, Wilcox AS, Sikela JM, Ragan CI, et al. (1993) Role of the β subunit in determining the pharmacology of human γ-aminobutyric acid type A receptors. Mol Pharmacol 44:1211-1218.
-
(1993)
Mol Pharmacol
, vol.44
, pp. 1211-1218
-
-
Hadingham, K.L.1
Wingrove, P.B.2
Wafford, K.A.3
Bain, C.4
Kemp, J.A.5
Palmer, K.J.6
Wilson, A.W.7
Wilcox, A.S.8
Sikela, J.M.9
Ragan, C.I.10
-
15
-
-
0032866803
-
A receptors by the non-steroidal anti-inflammatory agent, mefenamic acid
-
A receptors by the non-steroidal anti-inflammatory agent, mefenamic acid. Eur J Neurosci 11:2897-2905.
-
(1999)
Eur J Neurosci
, vol.11
, pp. 2897-2905
-
-
Halliwell, R.F.1
Thomas, P.2
Patten, D.3
James, C.H.4
Martinez-Torres, A.5
Miledi, R.6
Smart, T.G.7
-
16
-
-
17944397975
-
Substituted 3β-phenylethynyl derivatives of 3α-hydroxy- 5α-pregnan-20-one: Remarkably potent neuroactive steroid modulators of γ-aminobutyric acid type A receptors
-
Hawkinson JE, Acosta-Burruel M, Yang KC, Hogenkamp DJ, Chen J-S, Lan NC, Drewe JA, Whittemore ER, Woodward RM, Carter RB, et al. (1998) Substituted 3β-phenylethynyl derivatives of 3α-hydroxy-5α-pregnan-20-one: remarkably potent neuroactive steroid modulators of γ-aminobutyric acid type A receptors. J Pharmacol Exp Ther 287:198-207.
-
(1998)
J Pharmacol Exp Ther
, vol.287
, pp. 198-207
-
-
Hawkinson, J.E.1
Acosta-Burruel, M.2
Yang, K.C.3
Hogenkamp, D.J.4
Chen, J.-S.5
Lan, N.C.6
Drewe, J.A.7
Whittemore, E.R.8
Woodward, R.M.9
Carter, R.B.10
-
19
-
-
0037064306
-
Fenamate-induced enhancement of heterologously expressed HERG currents in Xenopus oocytes
-
Malykhina AP, Shoeb F, and Akbarali HI (2002) Fenamate-induced enhancement of heterologously expressed HERG currents in Xenopus oocytes. Eur J Pharmacol 452:269-277.
-
(2002)
Eur J Pharmacol
, vol.452
, pp. 269-277
-
-
Malykhina, A.P.1
Shoeb, F.2
Akbarali, H.I.3
-
20
-
-
0034108997
-
A receptor α1 subtype
-
A receptor α1 subtype. Nat Neurosci 3:587-592.
-
(2000)
Nat Neurosci
, vol.3
, pp. 587-592
-
-
McKernan, R.M.1
Rosahl, T.W.2
Reynolds, D.S.3
Sur, C.4
Wafford, K.A.5
Atack, J.R.6
Farrar, S.7
Myers, J.8
Cook, G.9
Ferris, P.10
-
27
-
-
0041353559
-
A receptor function by niflumic acid, a nonsteroidal anti-inflammatory drug
-
A receptor function by niflumic acid, a nonsteroidal anti-inflammatory drug. Mol Pharmacol 64:753-763.
-
(2003)
Mol Pharmacol
, vol.64
, pp. 753-763
-
-
Sinkkonen, S.T.1
Mansikkamaki, S.2
Moykkynen, T.3
Luddens, H.4
Uusi-Oukari, M.5
Korpi, E.R.6
-
28
-
-
0035039871
-
36Cl ion flux
-
36Cl ion flux. Mol Pharmacol 59:1108-1118.
-
(2001)
Mol Pharmacol
, vol.59
, pp. 1108-1118
-
-
Smith, A.J.1
Alder, L.2
Silk, J.3
Adkins, C.4
Fletcher, A.E.5
Scales, T.6
Kerby, J.7
Marshall, G.8
Wafford, K.A.9
McKernan, R.M.10
-
29
-
-
0029417325
-
β-Carboline γ-aminobutyric acid A receptor inverse agonists modulate γ-aminobutyric acid via the loreclezole binding site as well as the benzodiazepine site
-
Stevenson A, Wingrove PB, Whiting PJ, and Wafford KA (1995) β-Carboline γ-aminobutyric acid A receptor inverse agonists modulate γ-aminobutyric acid via the loreclezole binding site as well as the benzodiazepine site. Mol Pharmacol 48:965-969.
-
(1995)
Mol Pharmacol
, vol.48
, pp. 965-969
-
-
Stevenson, A.1
Wingrove, P.B.2
Whiting, P.J.3
Wafford, K.A.4
-
30
-
-
2542547342
-
A receptors
-
A receptors. Br J Pharmacol 142:97-106.
-
(2004)
Br J Pharmacol
, vol.142
, pp. 97-106
-
-
Thompson, S.A.1
Wheat, L.2
Brown, N.A.3
Wingrove, P.B.4
Pillai, G.V.5
Whiting, P.J.6
Adkins, C.7
Woodward, C.H.8
Smith, A.J.9
Simpson, P.B.10
-
33
-
-
0025904922
-
Attenuation of epileptogenesis by non-steroidal anti-inflammatory drugs in the rat
-
Wallenstein MC (1991) Attenuation of epileptogenesis by non-steroidal anti-inflammatory drugs in the rat. Neuropharmacology 30:657-663.
-
(1991)
Neuropharmacology
, vol.30
, pp. 657-663
-
-
Wallenstein, M.C.1
-
34
-
-
0033009936
-
A receptor gene family
-
A receptor gene family. Ann NY Acad Sci 868:645-653.
-
(1999)
Ann NY Acad Sci
, vol.868
, pp. 645-653
-
-
Whiting, P.J.1
Bonnert, T.P.2
McKernan, R.M.3
Farrar, S.4
Bourdelles, B.L.5
Heavens, R.P.6
Smith, D.W.7
Hewson, L.8
Rigby, M.R.9
Sirinathsmghji, D.J.10
-
35
-
-
0029807606
-
Pharmacology of the human γ-aminobutyric acid A receptor α4 subunit expressed in Xenopus laevis oocytes
-
Whittemore ER, Yang W, Drewe JA, and Woodward RM (1996) Pharmacology of the human γ-aminobutyric acid A receptor α4 subunit expressed in Xenopus laevis oocytes. Mol Pharmacol 50:1364-1375.
-
(1996)
Mol Pharmacol
, vol.50
, pp. 1364-1375
-
-
Whittemore, E.R.1
Yang, W.2
Drewe, J.A.3
Woodward, R.M.4
-
37
-
-
0028257965
-
The modulatory action of loreclezole at the γ-aminobutyric acid type A receptor is determined by a single amino acid in the β2 and β3 subunit
-
Wingrove PB, Wafford KA, Bain C, and Whiting PJ (1994) The modulatory action of loreclezole at the γ-aminobutyric acid type A receptor is determined by a single amino acid in the β2 and β3 subunit. Proc Natl Acad Sci USA 91:4569-4573.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 4569-4573
-
-
Wingrove, P.B.1
Wafford, K.A.2
Bain, C.3
Whiting, P.J.4
-
38
-
-
0026612363
-
A receptor subunit mRNAs in the rat brain: I. Telencephalon, diencephalon, mesencephalon
-
A receptor subunit mRNAs in the rat brain: I. Telencephalon, diencephalon, mesencephalon. J Neurosci 12:1040-1062.
-
(1992)
J Neurosci
, vol.12
, pp. 1040-1062
-
-
Wisden, W.1
Laurie, D.J.2
Monyer, H.3
Seeburg, P.H.4
|