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Histamine H3 receptors modulate the release of [3H]‐acetylcholine from slices of rat entorhinal cortex: evidence for the possible existence of H3 receptor subtypes

British journal of pharmacology, 1992-12, Vol.107 (4), p.919-923

1992

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Orphanin FQ Acts as an Anxiolytic to Attenuate Behavioral Responses to Stress

Proceedings of the National Academy of Sciences - PNAS, 1997-12, Vol.94 (26), p.14854-14858

1997

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Development of a radioligand binding assay for 5‐HT4 receptors in guinea‐pig and rat brain

British journal of pharmacology, 1993-07, Vol.109 (3), p.618-624

1993

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Identification and distribution of 5-HT3 receptors in rat brain using radioligand binding

Nature (London), 1987-12, Vol.330 (6150), p.746-748

1987

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The broad‐spectrum anti‐emetic activity of the novel non‐peptide tachykinin NK1 receptor antagonist GR203040

British journal of pharmacology, 1995-12, Vol.116 (8), p.3158-3163

1995

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Morphine-6-glucuronide: Actions and mechanisms

Medicinal research reviews, 2005-09, Vol.25 (5), p.521-544

2005

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GR205171: a novel antagonist with high affinity for the tachykinin NK1 receptor, and potent broad-spectrum anti-emetic activity

Regulatory peptides, 1996-08, Vol.65 (1), p.45-53

1996

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Labelling of CRF1 and CRF2 receptors using the novel radioligand, [3H]-urocortin

Neuropharmacology, 1997-10, Vol.36 (10), p.1439-1446

1997

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Human CRF2 α and β splice variants : Pharmacological characterization using radioligand binding and a luciferase gene expression assay

Neuropharmacology, 1999-03, Vol.38 (3), p.441-448

1999

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The ligand-selective domains of corticotropin-releasing factor type 1 and type 2 receptor reside in different extracellular domains : Generation of chimeric receptors with a novel ligand-selective profile

Journal of neurochemistry, 1999-08, Vol.73 (2), p.821-829

1999

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The pharmacological characterization of 5‐HT3 receptors in three isolated preparations derived from guinea‐pig tissues

British journal of pharmacology, 1990-11, Vol.101 (3), p.591-598

1990

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5-HT3 receptors

Medicinal research reviews, 1990-10, Vol.10 (4), p.441-475

1990

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1-(m-clorophenyl)-biguanide, a potent high affinity 5-HT3 receptor agonist

European journal of pharmacology, 1990-06, Vol.182 (1), p.193-197

1990

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5‐HT3 receptor antagonists injected into the area postrema inhibit cisplatin‐induced emesis in the ferret

British journal of pharmacology, 1989-05, Vol.97 (1), p.247-255

1989

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Binding of the 5-HT3, ligand, [3H]GR65630, to rat area postrema, vagus nerve and the brains of several species

European journal of pharmacology, 1989-01, Vol.159 (2), p.157-164

1989

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Characterization of histamine‐H3 receptors controlling non‐adrenergic non‐cholinergic contractions of the guinea‐pig isolated ileum

British journal of pharmacology, 1992-03, Vol.105 (3), p.667-674

1992

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Molecular biology of the CRH receptors— in the mood

Peptides (New York, N.Y. : 1980), 2001-05, Vol.22 (5), p.753-760

2001

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Towards understanding the aetiology and pathophysiology of the emetic reflex: novel approaches to antiemetic drugs

Oncology, 1996-01, Vol.53 Suppl 1, p.102

1996

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Pharmacological characterization of the novel nonpeptide orphanin FQ/nociceptin receptor agonist Ro 64-6198: rapid and reversible desensitization of the ORL1 receptor in vitro and lack of tolerance in vivo

The Journal of pharmacology and experimental therapeutics, 2001-08, Vol.298 (2), p.812

2001

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Urocortin: slower dissociation than corticotropin releasing factor from the CRF binding protein

European journal of pharmacology, 1999-07, Vol.376 (3), p.321-324

1999

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Interactions between 5-HT3 receptors and cerebral dopamine function: implications for the treatment of schizophrenia and psychoactive substance abuse

Psychopharmacology, 1993-03, Vol.112 (1 Suppl), p.S68-S75

1993

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Thioperamide, the selective histamine H3 receptor antagonist, attenuates stimulant-induced locomotor activity in the mouse

European journal of pharmacology, 1994-07, Vol.259 (2), p.107-114

1994

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The distribution of specific binding of the 5-HT3 receptor ligand [3H]GR65630 in rat brain using quantitative autoradiography

Neuroscience letters, 1988-11, Vol.94 (1-2), p.156-160

1988

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Pharmacological characterisation of the recombinant human CRF binding protein using a simple assay

Journal of neuroscience methods, 1998-03, Vol.80 (1), p.99-105

1998

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The thermodynamics of agonist and antagonist binding to dopamine D-2 receptors

Molecular pharmacology, 1986-09, Vol.30 (3), p.226-234

1986

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Histamine H3 receptors modulate the release of [3H]‐acetylcholine from slices of rat entorhinal cortex: evidence for the possible existence of H3 receptor subtypes

Orphanin FQ Acts as an Anxiolytic to Attenuate Behavioral Responses to Stress

Development of a radioligand binding assay for 5‐HT4 receptors in guinea‐pig and rat brain

Identification and distribution of 5-HT3 receptors in rat brain using radioligand binding

The broad‐spectrum anti‐emetic activity of the novel non‐peptide tachykinin NK1 receptor antagonist GR203040

Morphine-6-glucuronide: Actions and mechanisms

GR205171: a novel antagonist with high affinity for the tachykinin NK1 receptor, and potent broad-spectrum anti-emetic activity

Labelling of CRF1 and CRF2 receptors using the novel radioligand, [3H]-urocortin

Human CRF2 α and β splice variants : Pharmacological characterization using radioligand binding and a luciferase gene expression assay

The ligand-selective domains of corticotropin-releasing factor type 1 and type 2 receptor reside in different extracellular domains : Generation of chimeric receptors with a novel ligand-selective profile

The pharmacological characterization of 5‐HT3 receptors in three isolated preparations derived from guinea‐pig tissues

5-HT3 receptors

1-(m-clorophenyl)-biguanide, a potent high affinity 5-HT3 receptor agonist

5‐HT3 receptor antagonists injected into the area postrema inhibit cisplatin‐induced emesis in the ferret

Binding of the 5-HT3, ligand, [3H]GR65630, to rat area postrema, vagus nerve and the brains of several species

Characterization of histamine‐H3 receptors controlling non‐adrenergic non‐cholinergic contractions of the guinea‐pig isolated ileum

Molecular biology of the CRH receptors— in the mood

Towards understanding the aetiology and pathophysiology of the emetic reflex: novel approaches to antiemetic drugs

Pharmacological characterization of the novel nonpeptide orphanin FQ/nociceptin receptor agonist Ro 64-6198: rapid and reversible desensitization of the ORL1 receptor in vitro and lack of tolerance in vivo

Urocortin: slower dissociation than corticotropin releasing factor from the CRF binding protein

Interactions between 5-HT3 receptors and cerebral dopamine function: implications for the treatment of schizophrenia and psychoactive substance abuse

Thioperamide, the selective histamine H3 receptor antagonist, attenuates stimulant-induced locomotor activity in the mouse

The distribution of specific binding of the 5-HT3 receptor ligand [3H]GR65630 in rat brain using quantitative autoradiography

Pharmacological characterisation of the recombinant human CRF binding protein using a simple assay

The thermodynamics of agonist and antagonist binding to dopamine D-2 receptors

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