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The 5‐HT4 receptor agonist, tegaserod, is a potent 5‐HT2B receptor antagonist in vitro and in vivo

British journal of pharmacology, 2004-11, Vol.143 (5), p.549-560

2004

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The 5‐HT 4 receptor agonist, tegaserod, is a potent 5‐HT 2B receptor antagonist in vitro and in vivo

British journal of pharmacology, 2009-02, Vol.143 (5), p.549-560

2009

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Evidence for a Multivalent Interaction of Symmetrical, N-Linked, Lidocaine Dimers with Voltage-Gated Na+ Channels

Molecular pharmacology, 2006-03, Vol.69 (3), p.921-931

2006

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A comparison of the pharmacological properties of guinea‐pig and human recombinant 5‐HT4 receptors

British journal of pharmacology, 2007-03, Vol.150 (6), p.782-791

2007

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Distinct Dynamin-Dependent and -Independent Mechanisms Target Structurally Homologous Dopamine Receptors to Different Endocytic Membranes

The Journal of cell biology, 1999-01, Vol.144 (1), p.31-43

1999

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A comparison of the pharmacological properties of guinea‐pig and human recombinant 5‐HT 4 receptors

British journal of pharmacology, 2009-01, Vol.150 (6), p.782-791

2009

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Dexmedetomidine diminishes halothane anesthetic requirements in rats through a postsynaptic alpha2 adrenergic receptor

Anesthesiology (Philadelphia), 1988-12, Vol.69 (6), p.818-823

1988

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Clonidine reduces halothane MAC in rats

Anesthesiology (Philadelphia), 1987-11, Vol.67 (5), p.868-868

1987

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An in vitro investigation of the cardiovascular effects of the 5-HT4 receptor selective agonists, velusetrag and TD-8954

Vascular pharmacology, 2013-01, Vol.58 (1), p.150-156

2013

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Mechanism of halothane-induced inhibition of isoproterenol-stimulated lipolysis in isolated rat adipocytes

Molecular pharmacology, 1988-03, Vol.33 (3), p.338-343

1988

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Anesthetic and hemodynamic effects of the stereoisomers of medetomidine, an α2-adrenergic agonist, in halothane-anesthetized dogs

Anesthesia and analgesia, 1988, Vol.67 (7), p.611-615

1988

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Dexmedetomidine diminishes halothane anesthetic requirements in rats through a postsynaptic alpha 2 adrenergic receptor

Anesthesiology (Philadelphia), 1988-12, Vol.69 (6), p.818-823

1988

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Action of the stereoisomers of medetomidine, in halothane-anesthetized dogs

Acta veterinaria Scandinavica. Supplementum, 1989, Vol.85, p.71

1989

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The in vitro pharmacological profile of TD-5108, a selective 5-HT4 receptor agonist with high intrinsic activity

Naunyn-Schmiedeberg's archives of pharmacology, 2008-07, Vol.378 (1), p.125-137

2008

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Anesthetic and hemodynamic effects of the stereoisomers of medetomidine, an alpha 2-adrenergic agonist, in halothane-anesthetized dogs

Anesthesia and analgesia, 1988-07, Vol.67 (7), p.611-615

1988

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Molecular identification of SqKv1A. A candidate for the delayed rectifier K channel in squid giant axon

The Journal of general physiology, 1996-09, Vol.108 (3), p.207-219

1996

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Dexmedetomidine decreases halothane anesthetic requirements in rats

Acta veterinaria Scandinavica. Supplementum, 1989, Vol.85, p.55

1989

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L-phenylisopropyladenosine (L-PIA) diminishes halothane anesthetic requirements and decreases noradrenergic neurotransmission in rats

Life sciences (1973), 1988, Vol.42 (14), p.1355-1360

1988

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Mechanism for desensitization of β-adrenergic receptor-stimulated lipolysis in adipocytes from rats harboring pheochromocytoma

Endocrinology (Philadelphia), 1988-07, Vol.123 (1), p.528-533

1988

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A Multivalent Approach to the Design and Discovery of Orally Efficacious 5-HT4 Receptor Agonists

Journal of medicinal chemistry, 2009-09, Vol.52 (17), p.5330-5343

2009

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A comparison of the pharmacological properties of guinea-pig and human recombinant 5-HT sub(4) receptors

British journal of pharmacology, 2007-03, Vol.150 (6), p.782-791

2007

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The in vitro pharmacological profile of TD-5108, a selective 5-HT(4) receptor agonist with high intrinsic activity

Naunyn-Schmiedeberg's archives of pharmacology, 2008-07, Vol.378 (1), p.125-137

2008

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An in vitro investigation of the cardiovascular effects of the 5-HT(4) receptor selective agonists, velusetrag and TD-8954

Vascular pharmacology, 2013-01, Vol.58 (1-2), p.150-156

2013

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Comparison of the pharmacological properties of rat Na(V)1.8 with rat Na(V)1.2a and human Na(V)1.5 voltage-gated sodium channel subtypes using a membrane potential sensitive dye and FLIPR

Receptors & channels, 2004, Vol.10 (1), p.11-23

2004

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Anesthetic and Hemodynamic Effects of the Alpha2-adrenergic Agonist, Azepexole, in Isoflurane-anesthetized Dogs

Anesthesiology (Philadelphia), 1988, Vol.68 (5), p.689-694

1988

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The 5‐HT4 receptor agonist, tegaserod, is a potent 5‐HT2B receptor antagonist in vitro and in vivo

The 5‐HT 4 receptor agonist, tegaserod, is a potent 5‐HT 2B receptor antagonist in vitro and in vivo

Evidence for a Multivalent Interaction of Symmetrical, N-Linked, Lidocaine Dimers with Voltage-Gated Na+ Channels

A comparison of the pharmacological properties of guinea‐pig and human recombinant 5‐HT4 receptors

Distinct Dynamin-Dependent and -Independent Mechanisms Target Structurally Homologous Dopamine Receptors to Different Endocytic Membranes

A comparison of the pharmacological properties of guinea‐pig and human recombinant 5‐HT 4 receptors

Dexmedetomidine diminishes halothane anesthetic requirements in rats through a postsynaptic alpha2 adrenergic receptor

Clonidine reduces halothane MAC in rats

An in vitro investigation of the cardiovascular effects of the 5-HT4 receptor selective agonists, velusetrag and TD-8954

Mechanism of halothane-induced inhibition of isoproterenol-stimulated lipolysis in isolated rat adipocytes

Anesthetic and hemodynamic effects of the stereoisomers of medetomidine, an α2-adrenergic agonist, in halothane-anesthetized dogs

Dexmedetomidine diminishes halothane anesthetic requirements in rats through a postsynaptic alpha 2 adrenergic receptor

Action of the stereoisomers of medetomidine, in halothane-anesthetized dogs

The in vitro pharmacological profile of TD-5108, a selective 5-HT4 receptor agonist with high intrinsic activity

Anesthetic and hemodynamic effects of the stereoisomers of medetomidine, an alpha 2-adrenergic agonist, in halothane-anesthetized dogs

Molecular identification of SqKv1A. A candidate for the delayed rectifier K channel in squid giant axon

Dexmedetomidine decreases halothane anesthetic requirements in rats

L-phenylisopropyladenosine (L-PIA) diminishes halothane anesthetic requirements and decreases noradrenergic neurotransmission in rats

Mechanism for desensitization of β-adrenergic receptor-stimulated lipolysis in adipocytes from rats harboring pheochromocytoma

A Multivalent Approach to the Design and Discovery of Orally Efficacious 5-HT4 Receptor Agonists

A comparison of the pharmacological properties of guinea-pig and human recombinant 5-HT sub(4) receptors

The in vitro pharmacological profile of TD-5108, a selective 5-HT(4) receptor agonist with high intrinsic activity

An in vitro investigation of the cardiovascular effects of the 5-HT(4) receptor selective agonists, velusetrag and TD-8954

Comparison of the pharmacological properties of rat Na(V)1.8 with rat Na(V)1.2a and human Na(V)1.5 voltage-gated sodium channel subtypes using a membrane potential sensitive dye and FLIPR

Anesthetic and Hemodynamic Effects of the Alpha2-adrenergic Agonist, Azepexole, in Isoflurane-anesthetized Dogs

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