Use of an α3β4 nicotinic acetylcholine receptor subunit concatamer to characterize ganglionic receptor subtypes with specific subunit composition reveals species-specific pharmacologic properties (Q41817415)

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scientific article published on 11 May 2012

Language	Label	Description	Also known as
English	Use of an α3β4 nicotinic acetylcholine receptor subunit concatamer to characterize ganglionic receptor subtypes with specific subunit composition reveals species-specific pharmacologic properties	scientific article published on 11 May 2012

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

Use of an α3β4 nicotinic acetylcholine receptor subunit concatamer to characterize ganglionic receptor subtypes with specific subunit composition reveals species-specific pharmacologic properties (English)

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

author name string

Clare Stokes

1

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

Roger L Papke

2

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

publication date

11 May 2012

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

Neuropharmacology

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

63

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

4

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

538-546

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

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Rodent habenulo-interpeduncular pathway expresses a large variety of uncommon nAChR subtypes, but only the alpha3beta4* and alpha3beta3beta4* subtypes mediate acetylcholine release

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Multiple pharmacophores for the selective activation of nicotinic alpha7-type acetylcholine receptors

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Varenicline is a partial agonist at alpha4beta2 and a full agonist at alpha7 neuronal nicotinic receptors

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Heterologous expression of human {alpha}6{beta}4{beta}3{alpha}5 nicotinic acetylcholine receptors: binding properties consistent with their natural expression require quaternary subunit assembly including the {alpha}5 subunit

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Identifiers

10.1016/J.NEUROPHARM.2012.04.035

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Europe PubMed Central

PMC publication ID

12 October 2017

release_rlmocc2hrnaojntvkuquxgjlda

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PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

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