Chloride channels play important functions in different aspects of cell physiology including volume regulation, transepithelial ion transport and stabilization of membrane potential. In recent years the molecular identity of the chloride channels defective in cystic fibrosis and myotonia congenital has been elucidated, highlighting the importance of anion-selective channels in cell and tissue function. Concurrently, several proteins have been identified as chloride channels along with proteins that possess channel regulatory behavior. Novel interactions with more potent pharmacological compounds have been reported with different chloride channels. This burgeoning field of interest is reviewed.
CITATION STYLE
Valverde, M. A., Hardy, S. P., & Sepúlveda, F. V. (1995). Chloride channels: a state of flux. The FASEB Journal, 9(7), 509–515. https://doi.org/10.1096/fasebj.9.7.7737459
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