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Items: 1 to 20 of 733

1.

Identification of amino acid residues responsible for the alpha5 subunit binding selectivity of L-655,708, a benzodiazepine binding site ligand at the GABA(A) receptor.

Casula MA, Bromidge FA, Pillai GV, Wingrove PB, Martin K, Maubach K, Seabrook GR, Whiting PJ, Hadingham KL.

J Neurochem. 2001 Apr;77(2):445-51.

2.

Structural elements of the gamma-aminobutyric acid type A receptor conferring subtype selectivity for benzodiazepine site ligands.

Renard S, Olivier A, Granger P, Avenet P, Graham D, Sevrin M, George P, Besnard F.

J Biol Chem. 1999 May 7;274(19):13370-4.

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In vivo labelling of alpha5 subunit-containing GABA(A) receptors using the selective radioligand [(3)H]L-655,708.

Atack JR, Alder L, Cook SM, Smith AJ, McKernan RM.

Neuropharmacology. 2005 Aug;49(2):220-9. Epub 2005 Apr 26.

PMID:
15996568
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Role of the histidine residue at position 105 in the human alpha 5 containing GABA(A) receptor on the affinity and efficacy of benzodiazepine site ligands.

Kelly MD, Smith A, Banks G, Wingrove P, Whiting PW, Atack J, Seabrook GR, Maubach KA.

Br J Pharmacol. 2002 Jan;135(1):248-56.

13.

Mechanism of alpha-subunit selectivity of benzodiazepine pharmacology at gamma-aminobutyric acid type A receptors.

Wingrove PB, Safo P, Wheat L, Thompson SA, Wafford KA, Whiting PJ.

Eur J Pharmacol. 2002 Feb 15;437(1-2):31-9.

PMID:
11864636
14.

Expression and pharmacology of human GABAA receptors containing gamma 3 subunits.

Hadingham KL, Wafford KA, Thompson SA, Palmer KJ, Whiting PJ.

Eur J Pharmacol. 1995 Nov 30;291(3):301-9.

PMID:
8719414
16.

Residues in transmembrane domains I and II determine gamma-aminobutyric acid type AA receptor subtype-selective antagonism by furosemide.

Thompson SA, Arden SA, Marshall G, Wingrove PB, Whiting PJ, Wafford KA.

Mol Pharmacol. 1999 Jun;55(6):993-9.

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