Pharmacological characterization of the apparent splice variants of the murine 5-HT3 R-A subunit expressed in Xenopus laevis oocytes

Author:

Downie D.L.,Hope A.G.,Lambert J.J.,Peters J.A.,Blackburn T.P.,Jones B.J.

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Pharmacology

Reference34 articles.

1. Molecular properties of 5-hydroxytryptamine3 receptor-type binding sites purified from NG 108-15 cells;Boess;J. Neurochem.,1992

2. 5-HT3 receptors in NG 108-15 neuroblastoma × glioma cells: effect of the novel agonist 1-(m-chlorophenyl)-biguanide;Boess;Neuropharmacology,1992

3. Pharmacological characterization of 5-HT3 receptors in murine brain and ileum by the novel radioligand [3H] RS 42358-197;Bonhaus;J. Neurochem,1994

4. 5-HT3 receptors are membrane ion channels;Derkach;Nature,1989

5. Enhancement by trichloroethanol of agonist-induced currents mediated by a cloned murine 5-HT3 receptor subunit (5-HT3 R-A) expressed in Xenopus oocytes;Downie;Br. J. Pharmac.,1993

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