http://www.cnr.it/ontology/cnr/individuo/prodotto/ID38903
Stable expression and functional characterization of a human nicotinic acetylcholine receptor with alpha 6 beta 2 properties: discovery of selective antagonists (Articolo in rivista)
- Type
- Label
- Stable expression and functional characterization of a human nicotinic acetylcholine receptor with alpha 6 beta 2 properties: discovery of selective antagonists (Articolo in rivista) (literal)
- Anno
- 2011-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1111/j.1476-5381.2011.01213.x (literal)
- Alternative label
Capelli, Anna Maria; Castelletti, Laura; Chen, Yu Hua; Van der Keyl, Harjeet; Pucci, Luca; Oliosi, Beatrice; Salvagno, Cristian; Bertani, Barbara; Gotti, Cecilia; Powell, Andrew; Mugnaini, Manolo (2011)
Stable expression and functional characterization of a human nicotinic acetylcholine receptor with alpha 6 beta 2 properties: discovery of selective antagonists
in British journal of pharmacology
(literal)
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- Capelli, Anna Maria; Castelletti, Laura; Chen, Yu Hua; Van der Keyl, Harjeet; Pucci, Luca; Oliosi, Beatrice; Salvagno, Cristian; Bertani, Barbara; Gotti, Cecilia; Powell, Andrew; Mugnaini, Manolo (literal)
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- ISI Web of Science (WOS) (literal)
- ISI Web of Science (WoS) (literal)
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- GlaxoSmithKline; GlaxoSmithKline; GlaxoSmithKline; Consiglio Nazionale delle Ricerche (CNR) (literal)
- Titolo
- Stable expression and functional characterization of a human nicotinic acetylcholine receptor with alpha 6 beta 2 properties: discovery of selective antagonists (literal)
- Abstract
- Despite growing evidence that inhibition of alpha 6 beta 2-containing (alpha 6 beta 2*) nicotinic acetylcholine receptors (nAChRs) may be beneficial for the therapy of tobacco addiction, the lack of good sources of alpha 6 beta 2*-nAChRs has delayed the discovery of alpha 6 beta 2-selective antagonists. Our aim was to generate a cell line stably expressing functional nAChRs with alpha 6 beta 2 properties, to enable pharmacological characterization and the identification of novel alpha 6 beta 2-selective antagonists. (literal)
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