Specific and Slow Inhibition of the Kir2.1 K+ Channel by Gambogic Acid
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference24 articles.
1. Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome
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4. Potassium channel block by cytoplasmic polyamines as the mechanism of intrinsic rectification
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