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Cloning, localisation and functional expression of the human orthologue of the TREK-1 potassium channel

Pflügers Archiv, 2000-04, Vol.439 (6), p.714-722

2000

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Differential effects of acute and repeat dosing with the H3 antagonist GSK189254 on the sleep–wake cycle and narcoleptic episodes in Ox−/− mice

British journal of pharmacology, 2009-05, Vol.157 (1), p.104-117

2009

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Nonpeptide tachykinin receptor antagonists. II. Pharmacological and pharmacokinetic profile of SB-222200, a central nervous system penetrant, potent and selective NK-3 receptor antagonist

The Journal of pharmacology and experimental therapeutics, 2000-10, Vol.295 (1), p.373

2000

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Quantitative mRNA analysis of five C-terminal splice variants of the human 5-HT4 receptor in the central nervous system by TaqMan real time RT-PCR

Brain research. Molecular brain research., 2001-06, Vol.90 (2), p.125-134

2001

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Cloning and Characterization of Human NTT5 and v7-3: Two Orphan Transporters of the Na+/Cl−-Dependent Neurotransmitter Transporter Gene Family

Genomics (San Diego, Calif.), 2000-12, Vol.70 (2), p.241-252

2000

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Simultaneous measurement of [3H]noradrenaline release and neurogenic contraction under identical conditions, to determine the prejunctional inhibitory effects of SKF 99101H and BRL 56905 in dog saphenous vein

Naunyn-Schmiedeberg's archives of pharmacology, 1997-04, Vol.355 (4), p.475-482

1997

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hrIL-8-Induced Hyperresponsiveness in Guinea Pig Perfused Lungs

Annals of the New York Academy of Sciences, 1991-07, Vol.629 (1), p.419-421

1991

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Characterization of the 5‐HT4 receptor mediating tachycardia in piglet isolated right atrium

British journal of pharmacology, 1993-11, Vol.110 (3), p.1023-1030

1993

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Pharmacological and immunohistochemical characterization of the APJ receptor and its endogenous ligand apelin

Journal of neurochemistry, 2003-03, Vol.84 (5), p.1162-1172

2003

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Differences in the Central Nervous System Distribution and Pharmacology of the Mouse 5-Hydroxytryptamine-6 Receptor Compared with Rat and Human Receptors Investigated by Radioligand Binding, Site-Directed Mutagenesis, and Molecular Modeling

Molecular pharmacology, 2003-12, Vol.64 (6), p.1295-1308

2003

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Kinetic modification of the α1I subunit‐mediated T‐type Ca2+ channel by a human neuronal Ca2+ channel γ subunit

The Journal of physiology, 2001-06, Vol.533 (2), p.467-478

2001

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(.+-.)-3-Amino-6-carboxamido-1,2,3,4-tetrahydrocarbazole: a conformationally restricted analog of 5-carboxamidotryptamine with selectivity for the serotonin 5-HT1D receptor

Journal of medicinal chemistry, 1993-06, Vol.36 (13), p.1918-1919

1993

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Nitric oxide synthase inhibitors 7- and 6-nitroindazole relax smooth muscle in vitro

European journal of pharmacology, 1994-04, Vol.256 (1), p.R5-R6

1994

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Cloning and functional expression of a human orthologue of rat vanilloid receptor-1

Pain (Amsterdam), 2000-11, Vol.88 (2), p.205-215

2000

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Cloning and Functional Expression of Human Short TRP7, a Candidate Protein for Store-operated Ca2+ Influx

The Journal of biological chemistry, 2002-04, Vol.277 (14), p.12302-12309

2002

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mRNA distribution analysis of human TRPC family in CNS and peripheral tissues

Brain research. Molecular brain research., 2002-12, Vol.109 (1), p.95-104

2002

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Cloning, localisation and functional expression of the human orthologue of the TREK-1 potassium channel

Pflügers Archiv, 2000-04, Vol.439 (6), p.714-722

2000

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Characterization of histamine H3 receptors in Alzheimer's Disease brain and amyloid over-expressing TASTPM mice: Histamine

British journal of pharmacology, 2009, Vol.157 (1), p.130-138

2009

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Modulation of hippocampal excitability by 5-HT 4 receptor agonists persists in a transgenic model of Alzheimer's disease

Neuroscience, 2004, Vol.129 (1), p.49-54

2004

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Nonpeptide tachykinin receptor antagonists: I. Pharmacological and pharmacokinetic characterization of SB 223412, a novel, potent and selective neurokinin-3 receptor antagonist

The Journal of pharmacology and experimental therapeutics, 1997-06, Vol.281 (3), p.1303

1997

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The PPAR[gamma] agonist pioglitazone is effective in the MPTP mouse model of Parkinson's disease through inhibition of monoamine oxidase B

British journal of pharmacology, 2008-05, Vol.154 (1), p.226

2008

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The PPARgamma agonist pioglitazone is effective in the MPTP mouse model of Parkinson's disease through inhibition of monoamine oxidase B

British journal of pharmacology, 2008-05, Vol.154 (1), p.226

2008

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Differential effects of acute and repeat dosing with the H3antagonist GSK189254 on the sleep-wake cycle and narcoleptic episodes in Ox-/-mice: Histamine

British journal of pharmacology, 2009, Vol.157 (1), p.104-117

2009

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Protection but maintained dysfunction of nigral dopaminergic nerve cell bodies and striatal dopaminergic terminals in MPTP-lesioned mice after acute treatment with the mGluR5 antagonist MPEP

Brain research, 2005-02, Vol.1033 (2), p.216-220

2005

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Bicyclic heteroarylpiperazines as selective brain penetrant 5-HT6 receptor antagonists

Bioorganic & medicinal chemistry letters, 2005-11, Vol.15 (21), p.4867-4871

2005

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Cloning, localisation and functional expression of the human orthologue of the TREK-1 potassium channel

Differential effects of acute and repeat dosing with the H3 antagonist GSK189254 on the sleep–wake cycle and narcoleptic episodes in Ox−/− mice

Nonpeptide tachykinin receptor antagonists. II. Pharmacological and pharmacokinetic profile of SB-222200, a central nervous system penetrant, potent and selective NK-3 receptor antagonist

Quantitative mRNA analysis of five C-terminal splice variants of the human 5-HT4 receptor in the central nervous system by TaqMan real time RT-PCR

Cloning and Characterization of Human NTT5 and v7-3: Two Orphan Transporters of the Na+/Cl−-Dependent Neurotransmitter Transporter Gene Family

Simultaneous measurement of [3H]noradrenaline release and neurogenic contraction under identical conditions, to determine the prejunctional inhibitory effects of SKF 99101H and BRL 56905 in dog saphenous vein

hrIL-8-Induced Hyperresponsiveness in Guinea Pig Perfused Lungs

Characterization of the 5‐HT4 receptor mediating tachycardia in piglet isolated right atrium

Pharmacological and immunohistochemical characterization of the APJ receptor and its endogenous ligand apelin

Differences in the Central Nervous System Distribution and Pharmacology of the Mouse 5-Hydroxytryptamine-6 Receptor Compared with Rat and Human Receptors Investigated by Radioligand Binding, Site-Directed Mutagenesis, and Molecular Modeling

Kinetic modification of the α1I subunit‐mediated T‐type Ca2+ channel by a human neuronal Ca2+ channel γ subunit

(.+-.)-3-Amino-6-carboxamido-1,2,3,4-tetrahydrocarbazole: a conformationally restricted analog of 5-carboxamidotryptamine with selectivity for the serotonin 5-HT1D receptor

Nitric oxide synthase inhibitors 7- and 6-nitroindazole relax smooth muscle in vitro

Cloning and functional expression of a human orthologue of rat vanilloid receptor-1

Cloning and Functional Expression of Human Short TRP7, a Candidate Protein for Store-operated Ca2+ Influx

mRNA distribution analysis of human TRPC family in CNS and peripheral tissues

Cloning, localisation and functional expression of the human orthologue of the TREK-1 potassium channel

Characterization of histamine H3 receptors in Alzheimer's Disease brain and amyloid over-expressing TASTPM mice: Histamine

Modulation of hippocampal excitability by 5-HT 4 receptor agonists persists in a transgenic model of Alzheimer's disease

Nonpeptide tachykinin receptor antagonists: I. Pharmacological and pharmacokinetic characterization of SB 223412, a novel, potent and selective neurokinin-3 receptor antagonist

The PPAR[gamma] agonist pioglitazone is effective in the MPTP mouse model of Parkinson's disease through inhibition of monoamine oxidase B

The PPARgamma agonist pioglitazone is effective in the MPTP mouse model of Parkinson's disease through inhibition of monoamine oxidase B

Differential effects of acute and repeat dosing with the H3antagonist GSK189254 on the sleep-wake cycle and narcoleptic episodes in Ox-/-mice: Histamine

Protection but maintained dysfunction of nigral dopaminergic nerve cell bodies and striatal dopaminergic terminals in MPTP-lesioned mice after acute treatment with the mGluR5 antagonist MPEP

Bicyclic heteroarylpiperazines as selective brain penetrant 5-HT6 receptor antagonists

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