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Effect of the TRPV1 antagonist SB‐705498 on the nasal parasympathetic reflex response in the ovalbumin sensitized guinea pig

British journal of pharmacology, 2013-06, Vol.169 (3), p.580-589

2013

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Antagonism of human CC‐chemokine receptor 4 can be achieved through three distinct binding sites on the receptor

Pharmacology research & perspectives, 2013-12, Vol.1 (2), p.e00019-n/a

2013

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Evidence for an enhancement of excitatory transmission in adult CNS by Wnt signaling pathway modulation

Molecular and cellular neuroscience, 2007-08, Vol.35 (4), p.513-524

2007

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Discovery of Functionally Selective 7,8,9,10-Tetrahydro-7,10-ethano-1,2,4-triazolo[3,4-a]phthalazines as GABAA Receptor Agonists at the α3 Subunit

Journal of medicinal chemistry, 2005-03, Vol.48 (5), p.1367-1383

2005

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Mechanism of action of general anaesthetics — new information from molecular pharmacology

Current Opinion in Pharmacology, 2001-02, Vol.1 (1), p.78-83

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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2,5-Dihydropyrazolo[4,3-c]pyridin-3-ones: functionally selective benzodiazepine binding site ligands on the GABAA receptor

Bioorganic & medicinal chemistry letters, 2004-07, Vol.14 (13), p.3441-3444

2004

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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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Activity of chlormethiazole at human recombinant GABAA and NMDA receptors

British journal of pharmacology, 2003-11, Vol.140 (6), p.1045-1050

2003

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Functional characteristics of recombinant human GABA A receptors containing the ϵ-subunit

Toxicology letters, 1998-11, Vol.100, p.233-238

1998

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N-(indol-3-ylglyoxylyl)piperidines : High affinity agonists of human GABA-A receptors containing the α1 subunit

Bioorganic & medicinal chemistry letters, 2000-06, Vol.10 (12), p.1381-1384

2000

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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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Activity of chlormethiazole at human recombinant GABA(A) and NMDA receptors

British journal of pharmacology, 2003-11, Vol.140 (6), p.1045-1050

2003

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2,5-Dihydropyrazolo[4,3- c]pyridin-3-ones: functionally selective benzodiazepine binding site ligands on the GABA A receptor

Bioorganic & medicinal chemistry letters, 2004-07, Vol.14 (13), p.3441-3444

2004

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ChemInform Abstract: N-(Indol-3-ylglyoxylyl)piperidines: High Affinity Agonists of Human GABA-A Receptors Containing the α1 Subunit

ChemInform, 2000-09, Vol.31 (39), p.no-no

2000

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Tracazolate Reveals a Novel Type of Allosteric Interaction with Recombinant Î³-Aminobutyric AcidA Receptors

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

2002

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Discovery of functionally selective 7,8,9,10-tetrahydro-7,10-ethano-1,2,4-triazolo[3,4-a]phthalazines as GABA A receptor agonists at the alpha3 subunit

Journal of medicinal chemistry, 2005-03, Vol.48 (5), p.1367-1383

2005

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Discovery of Functionally Selective 7,8,9,10-Tetrahydro-7,10-ethano-1,2,4-triazolo[3,4- a ]phthalazines as GABA A Receptor Agonists at the α 3 Subunit

Journal of medicinal chemistry, 2005-03, Vol.48 (5), p.1367-1383

2005

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Pharmacological properties of recombinant human GABAA receptors

Thompson, Sally-Anne

2002

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Pharmacological properties of recombinant human gabaâ†a receptors

Thompson, Sally-Anne

2002

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Functional characteristics of recombinant human GABAA receptors containing the ϵ-subunit

Toxicology letters, 1998-11, Vol.100-101, p.233-238

1998

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N-(Indol-3-ylglyoxylyl)piperidines: high affinity agonists of human GABA-A receptors containing the α 1 subunit

Bioorganic & medicinal chemistry letters, 2000, Vol.10 (12), p.1381-1384

2000

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Trial of Early, Goal-Directed Resuscitation for Septic Shock

The New England journal of medicine, 2015-04, Vol.372 (14), p.1301-1311

2015

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ChemInform Abstract: N‐(Indol‐3‐ylglyoxylyl)piperidines: High Affinity Agonists of Human GABA‐A Receptors Containing the α 1 Subunit

ChemInform, 2000-09, Vol.31 (39)

2000

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The development of a self-help intervention to build social confidence in people living with visible skin conditions or scars: a think-aloud study

Scars, burns & healing, 2019-01, Vol.5, p.2059513118822954-2059513118822954

2019

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Effect of the TRPV1 antagonist SB‐705498 on the nasal parasympathetic reflex response in the ovalbumin sensitized guinea pig

Antagonism of human CC‐chemokine receptor 4 can be achieved through three distinct binding sites on the receptor

Evidence for an enhancement of excitatory transmission in adult CNS by Wnt signaling pathway modulation

Discovery of Functionally Selective 7,8,9,10-Tetrahydro-7,10-ethano-1,2,4-triazolo[3,4-a]phthalazines as GABAA Receptor Agonists at the α3 Subunit

Mechanism of action of general anaesthetics — new information from molecular pharmacology

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

2,5-Dihydropyrazolo[4,3-c]pyridin-3-ones: functionally selective benzodiazepine binding site ligands on the GABAA receptor

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

Activity of chlormethiazole at human recombinant GABAA and NMDA receptors

Functional characteristics of recombinant human GABA A receptors containing the ϵ-subunit

N-(indol-3-ylglyoxylyl)piperidines : High affinity agonists of human GABA-A receptors containing the α1 subunit

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

Activity of chlormethiazole at human recombinant GABA(A) and NMDA receptors

2,5-Dihydropyrazolo[4,3- c]pyridin-3-ones: functionally selective benzodiazepine binding site ligands on the GABA A receptor

ChemInform Abstract: N-(Indol-3-ylglyoxylyl)piperidines: High Affinity Agonists of Human GABA-A Receptors Containing the α1 Subunit

Tracazolate Reveals a Novel Type of Allosteric Interaction with Recombinant Î³-Aminobutyric AcidA Receptors

Discovery of functionally selective 7,8,9,10-tetrahydro-7,10-ethano-1,2,4-triazolo[3,4-a]phthalazines as GABA A receptor agonists at the alpha3 subunit

Discovery of Functionally Selective 7,8,9,10-Tetrahydro-7,10-ethano-1,2,4-triazolo[3,4- a ]phthalazines as GABA A Receptor Agonists at the α 3 Subunit

Pharmacological properties of recombinant human GABAA receptors

Pharmacological properties of recombinant human gabaâ†a receptors

Functional characteristics of recombinant human GABAA receptors containing the ϵ-subunit

N-(Indol-3-ylglyoxylyl)piperidines: high affinity agonists of human GABA-A receptors containing the α 1 subunit

Trial of Early, Goal-Directed Resuscitation for Septic Shock

ChemInform Abstract: N‐(Indol‐3‐ylglyoxylyl)piperidines: High Affinity Agonists of Human GABA‐A Receptors Containing the α 1 Subunit

The development of a self-help intervention to build social confidence in people living with visible skin conditions or scars: a think-aloud study

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