A single channel mutation alters agonist efficacy at 5‐ HT 3 A and 5‐ HT 3 AB receptors
Author:
Affiliation:
1. Department of Biochemistry University of Cambridge Cambridge UK
Publisher
Wiley
Subject
Pharmacology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/bph.12287
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1. The 5-HT3B subunit affects high-potency inhibition of 5-HT3 receptors by morphine
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3. Structural Basis of Activation of Cys-Loop Receptors: the Extracellular–Transmembrane Interface as a Coupling Region
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5. Unconventional pharmacology of a neuronal nicotinic receptor mutated in the channel domain.
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3. A triad of residues is functionally transferrable between 5-HT3 serotonin receptors and nicotinic acetylcholine receptors;Journal of Biological Chemistry;2018-02
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