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Role of the beta subunit in determining the pharmacology of human gamma-aminobutyric acid type A receptors

Molecular pharmacology, 1993-12, Vol.44 (6), p.1211-1218

1993

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The modulatory action of loreclezole at the gamma-aminobutyric acid type A receptor is determined by a single amino acid in the beta 2 and beta 3 subunit

Proceedings of the National Academy of Sciences - PNAS, 1994-05, Vol.91 (10), p.4569-4573

1994

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beta-Carboline gamma-aminobutyric acidA receptor inverse agonists modulate gamma-aminobutyric acid via the loreclezole binding site as well as the benzodiazepine site

Molecular pharmacology, 1995-12, Vol.48 (6), p.965

1995

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Salicylidene salicylhydrazide, a selective inhibitor of β 1‐containing GABA A receptors

British journal of pharmacology, 2009-01, Vol.142 (1), p.97-106

2009

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Generation and Characterisation of Stable Cell Lines Expressing Recombinant Human N‐Methyl‐d‐Aspartate Receptor Subtypes

Journal of neurochemistry, 1996-06, Vol.66 (6), p.2239-2247

1996

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A novel allosteric modulatory site on the GABAA receptor beta subunit

Neuron (Cambridge, Mass.), 1994-04, Vol.12 (4), p.775-782

1994

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The non‐peptidyl fungal metabolite L‐783,281 activates TRK neurotrophin receptors

Journal of neurochemistry, 2001-09, Vol.78 (5), p.1135-1145

2001

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Mutation at the putative GABA(A) ion-channel gate reveals changes in allosteric modulation

British journal of pharmacology, 1999-07, Vol.127 (6), p.1349-1358

1999

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Characterisation of N‐Methyl‐D‐Aspartate Receptor‐Specific [3H]Ifenprodil Binding to Recombinant Human NR1a/NR2B Receptors Compared with Native Receptors in Rodent Brain Membranes

Journal of neurochemistry, 2000-12, Vol.75 (6), p.2455-2463

2000

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Residues in Transmembrane Domains I and II Determine γ-Aminobutyric Acid Type A A Receptor Subtype-Selective Antagonism by Furosemide

Molecular pharmacology, 1999-06, Vol.55 (6), p.993-999

1999

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Salicylidene salicylhydrazide, a selective inhibitor of β1‐containing GABAA receptors

British journal of pharmacology, 2004-05, Vol.142 (1), p.97-106

2004

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Tracazolate reveals a novel type of allosteric interaction with recombinant gamma-aminobutyric acid(A) receptors

Molecular pharmacology, 2002-04, Vol.61 (4), p.861-869

2002

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A genetically modified mouse model probing the selective action of ifenprodil at the N-methyl-d-aspartate type 2B receptor

Molecular and cellular neuroscience, 2006-09, Vol.33 (1), p.47-56

2006

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Key Amino Acids in the γ Subunit of the γ-Aminobutyric Acid A Receptor that Determine Ligand Binding and Modulation at the Benzodiazepine Site

Molecular pharmacology, 1997-11, Vol.52 (5), p.874-881

1997

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A novel allosteric modulatory site on the GABA A receptor β subunit

Neuron (Cambridge, Mass.), 1994-04, Vol.12 (4), p.775-782

1994

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Mechanism of α-subunit selectivity of benzodiazepine pharmacology at γ-aminobutyric acid type A receptors

European journal of pharmacology, 2002-02, Vol.437 (1), p.31-39

2002

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Salicylidene salicylhydrazide, a selective inhibitor of beta 1-containing GABAA receptors

British journal of pharmacology, 2004-05, Vol.142 (1), p.97-106

2004

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Salicylidene salicylhydrazide, a selective inhibitor of [beta]1-containing GABAA receptors

British journal of pharmacology, 2004-05, Vol.142 (1), p.97

2004

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Mutation at the putative GABA sub(A) ion-channel gate reveals changes in allosteric modulation

British journal of pharmacology, 1999-07, Vol.127 (6), p.1349-1358

1999

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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

Journal of neurochemistry, 2001-04, Vol.77 (2), p.445

2001

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Identification of amino acid residues responsible for the alpha 5 subunit binding selectivity of L-655,708, a benzodiazepine binding site ligand at the GABA sub(A) receptor

Journal of neurochemistry, 2001-04, Vol.77 (2), p.445-451

2001

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Mutation at the putative GABAA ion‐channel gate reveals changes in allosteric modulation

British journal of pharmacology, 1999-07, Vol.127 (6), p.1349-1358

1999

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

Molecular pharmacology, 1999-06, Vol.55 (6), p.993-999

1999

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Key amino acids in the gamma subunit of the gamma-aminobutyric acidA receptor that determine ligand binding and modulation at the benzodiazepine site

Molecular pharmacology, 1997-11, Vol.52 (5), p.874

1997

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The modulatory action of loreclezole at the gamma -aminobutyric acid type A receptor is determined by a single amino acid in the beta sub(2) and beta sub(3) subunit

Proceedings of the National Academy of Sciences - PNAS, 1994-01, Vol.91 (10), p.4569-4573

1994

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Role of the beta subunit in determining the pharmacology of human gamma-aminobutyric acid type A receptors

The modulatory action of loreclezole at the gamma-aminobutyric acid type A receptor is determined by a single amino acid in the beta 2 and beta 3 subunit

beta-Carboline gamma-aminobutyric acidA receptor inverse agonists modulate gamma-aminobutyric acid via the loreclezole binding site as well as the benzodiazepine site

Salicylidene salicylhydrazide, a selective inhibitor of β 1‐containing GABA A receptors

Generation and Characterisation of Stable Cell Lines Expressing Recombinant Human N‐Methyl‐d‐Aspartate Receptor Subtypes

A novel allosteric modulatory site on the GABAA receptor beta subunit

The non‐peptidyl fungal metabolite L‐783,281 activates TRK neurotrophin receptors

Mutation at the putative GABA(A) ion-channel gate reveals changes in allosteric modulation

Characterisation of N‐Methyl‐D‐Aspartate Receptor‐Specific [3H]Ifenprodil Binding to Recombinant Human NR1a/NR2B Receptors Compared with Native Receptors in Rodent Brain Membranes

Residues in Transmembrane Domains I and II Determine γ-Aminobutyric Acid Type A A Receptor Subtype-Selective Antagonism by Furosemide

Salicylidene salicylhydrazide, a selective inhibitor of β1‐containing GABAA receptors

Tracazolate reveals a novel type of allosteric interaction with recombinant gamma-aminobutyric acid(A) receptors

A genetically modified mouse model probing the selective action of ifenprodil at the N-methyl-d-aspartate type 2B receptor

Key Amino Acids in the γ Subunit of the γ-Aminobutyric Acid A Receptor that Determine Ligand Binding and Modulation at the Benzodiazepine Site

A novel allosteric modulatory site on the GABA A receptor β subunit

Mechanism of α-subunit selectivity of benzodiazepine pharmacology at γ-aminobutyric acid type A receptors

Salicylidene salicylhydrazide, a selective inhibitor of beta 1-containing GABAA receptors

Salicylidene salicylhydrazide, a selective inhibitor of [beta]1-containing GABAA receptors

Mutation at the putative GABA sub(A) ion-channel gate reveals changes in allosteric modulation

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

Identification of amino acid residues responsible for the alpha 5 subunit binding selectivity of L-655,708, a benzodiazepine binding site ligand at the GABA sub(A) receptor

Mutation at the putative GABAA ion‐channel gate reveals changes in allosteric modulation

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

Key amino acids in the gamma subunit of the gamma-aminobutyric acidA receptor that determine ligand binding and modulation at the benzodiazepine site

The modulatory action of loreclezole at the gamma -aminobutyric acid type A receptor is determined by a single amino acid in the beta sub(2) and beta sub(3) subunit

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