Molecular Basis of the Charge Selectivity of Nicotinic Acetylcholine Receptor and Related Ligand-Gated Ion Channels-Reference-Cited by-同舟云学术

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Molecular Basis of the Charge Selectivity of Nicotinic Acetylcholine Receptor and Related Ligand-Gated Ion Channels

Published:2007-09-28 Issue: Volume: Page:215-230
ISSN:1935-4657
Container-title:Novartis Foundation Symposium 225 - Gramicidin and Related Ion Channel-Forming Peptides
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Author:

Corringer Pierre-Jean,Bertrand Sonia,Galzi Jean-Luc,Devillers-Thiéry Anne,Changeux Jean-Pierre,Bertrand Daniel

Publisher

John Wiley & Sons, Ltd.

Reference39 articles.

1. Unconventional pharmacology of a neuronal nicotinic receptor mutated in the channel domain;Bertrand;Proc Natl Acad Sci USA,1992

2. Paradoxical allosteric effects of competitive inhibitors on neuronal alpha7 nicotinic receptor mutants;Bertrand;Neuroreport,1997

3. Allosteric receptors after 30 years;Changeux;Neuron,1998

4. Tris+/Na+ permeability ratios of nicotinic acetylcholine receptors are reduced by mutations near the intracellular end of the M2 region;Cohen;J Gen Physiol,1992

5. Mutational analysis of the charge selectivity filter of the α nicotinic acetylcholine receptor;Corringer;Neuron,1999

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Pharmacological profile of Ascaris suum ACR‐16, a new homomeric nicotinic acetylcholine receptor widely distributed in Ascaris tissues;British Journal of Pharmacology;2016-07-18

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