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Expression cloning of GABA(B) receptors uncovers similarity to metabotropic glutamate receptors

Nature (London), 1997-03, Vol.386 (6622), p.239-246

1997

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CGP 37849 and CGP 39551: novel and potent competitive N‐methyl‐d‐aspartate receptor antagonists with oral activity

British journal of pharmacology, 1990-04, Vol.99 (4), p.791-797

1990

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Human γ -aminobutyric Acid Type B Receptors are Differentially Expressed and Regulate Inwardly Rectifying K+Channels

Proceedings of the National Academy of Sciences - PNAS, 1998-12, Vol.95 (25), p.14991-14996

1998

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Synthesis and biochemical studies of spirocyclic amino acids. II. Activity of 2-azaspiro[5.5]undecane-7-carboxylates as GABA-uptake inhibitors

European journal of medicinal chemistry, 1995, Vol.30 (9), p.707-713

1995

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GABA B receptor antagonists: from synthesis to therapeutic applications

Trends in pharmacological sciences (Regular ed.), 1993, Vol.14 (11), p.391-394

1993

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Alteration of central alpha2- and beta-adrenergic receptors in the rat after DSP-4, a selective noradrenergic neurotoxin

Neuroscience, 1983-08, Vol.9 (4), p.889-898

1983

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GABAB receptor antagonists : from synthesis to therapeutic applications

Trends in pharmacological sciences (Regular ed.), 1993-11, Vol.14 (11), p.391-394

1993

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CGP 35348: a centrally active blocker of GABA B receptors

European journal of pharmacology, 1990-10, Vol.187 (1), p.27-38

1990

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In vivo [ 3H]spiperone binding to the rat hippocampal formation: Involvement of dopamine receptors

European journal of pharmacology, 1980-12, Vol.68 (3), p.305-315

1980

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CGP 35348 : a centrally active blocker of GABAB receptors

European journal of pharmacology, 1990-10, Vol.187 (1-2), p.27-38

1990

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Brofaromine : a monoamine oxidase-A and serotonin uptake inhibitor

Clinical neuropharmacology, 1993, Vol.16, p.S19-S24

1993

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CGP 28014, a new inhibitor of cerebral catechol-O-methylation with a non-catechol structure

Naunyn-Schmiedeberg's archives of pharmacology, 1990-09, Vol.342 (3), p.305-311

1990

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GABA and glutamate release affected by GABAB receptor antagonists with similar potency: no evidence for pharmacologically different presynaptic receptors

British journal of pharmacology, 1994-12, Vol.113 (4), p.1515-1521

1994

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CGP 20712 A: a useful tool for quantitating β1- and β2-adrenoceptors

European journal of pharmacology, 1986-10, Vol.130 (1-2), p.137-139

1986

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Simple Radioligand Binding Assay for the Determination of Urinary Scopolamine

Journal of pharmaceutical sciences, 1984-04, Vol.73 (4), p.561-563

1984

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Benzodiazepine interactions with central thyroid-releasing hormone binding sites: characterization and physiological significance

The Journal of pharmacology and experimental therapeutics, 1986-07, Vol.238 (1), p.178

1986

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Substance P depresses neuronal activity in the rat olfactory bulb in vitro and in vivo: possible mediation via γ-aminobutyric acid release

Brain research, 1987-06, Vol.412 (2), p.269-274

1987

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THE SUBCELLULAR DISTRIBUTION OF PARTICLE‐BOUND NEGATIVE CHARGES IN RAT BRAIN

Journal of neurochemistry, 1977-05, Vol.28 (5), p.917-922

1977

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The actions of orally active GABAB receptor antagonists on GABAergic transmission in vivo and in vitro

European journal of pharmacology, 1993-03, Vol.233 (2-3), p.179-186

1993

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Is the estimation of GABA turnover rate in vivo a tool to differentiate between various types of drugs interfering with the GABA/benzodiazepine/ionophore receptor complex?

Neuropharmacology, 1984, Vol.23 (7), p.815-816

1984

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CGP 31358 binds to a site on the NMDA receptor that is coupled to both the transmitter recognition site and the channel domain

Neuroscience letters, 1989-12, Vol.107 (1), p.184-188

1989

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Differential decrease of the central beta-adrenergic receptor in the rat after subchronic infusion of desipramine and clenbuterol

Neurochemistry international, 1983, Vol.5 (3), p.333-338

1983

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Optical rotatory dispersion and circular dichroism of carbanilyl polysaccharides

Biopolymers, 1969-04, Vol.7 (4), p.539-556

1969

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Pharmacological and neurochemical aspects of kindling

Journal of Neural Transmission, 1985-01, Vol.63 (2), p.143-155

1985

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Morpholin-2-yl-phosphinic acids are potent GABA(B) receptor antagonists in rat brain

European journal of pharmacology, 1998-11, Vol.362 (1), p.27-34

1998

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Expression cloning of GABA(B) receptors uncovers similarity to metabotropic glutamate receptors

CGP 37849 and CGP 39551: novel and potent competitive N‐methyl‐d‐aspartate receptor antagonists with oral activity

Human γ -aminobutyric Acid Type B Receptors are Differentially Expressed and Regulate Inwardly Rectifying K+Channels

Synthesis and biochemical studies of spirocyclic amino acids. II. Activity of 2-azaspiro[5.5]undecane-7-carboxylates as GABA-uptake inhibitors

GABA B receptor antagonists: from synthesis to therapeutic applications

Alteration of central alpha2- and beta-adrenergic receptors in the rat after DSP-4, a selective noradrenergic neurotoxin

GABAB receptor antagonists : from synthesis to therapeutic applications

CGP 35348: a centrally active blocker of GABA B receptors

In vivo [ 3H]spiperone binding to the rat hippocampal formation: Involvement of dopamine receptors

CGP 35348 : a centrally active blocker of GABAB receptors

Brofaromine : a monoamine oxidase-A and serotonin uptake inhibitor

CGP 28014, a new inhibitor of cerebral catechol-O-methylation with a non-catechol structure

GABA and glutamate release affected by GABAB receptor antagonists with similar potency: no evidence for pharmacologically different presynaptic receptors

CGP 20712 A: a useful tool for quantitating β1- and β2-adrenoceptors

Simple Radioligand Binding Assay for the Determination of Urinary Scopolamine

Benzodiazepine interactions with central thyroid-releasing hormone binding sites: characterization and physiological significance

Substance P depresses neuronal activity in the rat olfactory bulb in vitro and in vivo: possible mediation via γ-aminobutyric acid release

THE SUBCELLULAR DISTRIBUTION OF PARTICLE‐BOUND NEGATIVE CHARGES IN RAT BRAIN

The actions of orally active GABAB receptor antagonists on GABAergic transmission in vivo and in vitro

Is the estimation of GABA turnover rate in vivo a tool to differentiate between various types of drugs interfering with the GABA/benzodiazepine/ionophore receptor complex?

CGP 31358 binds to a site on the NMDA receptor that is coupled to both the transmitter recognition site and the channel domain

Differential decrease of the central beta-adrenergic receptor in the rat after subchronic infusion of desipramine and clenbuterol

Optical rotatory dispersion and circular dichroism of carbanilyl polysaccharides

Pharmacological and neurochemical aspects of kindling

Morpholin-2-yl-phosphinic acids are potent GABA(B) receptor antagonists in rat brain

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