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Effect of ATP-sensitive K+ channel regulators on cystic fibrosis transmembrane conductance regulator chloride currents

The cystic fibrosis transmembrane conductance regulator (CFTR) is a Cl- channel that is regulated by cAMP-dependent phosphorylation and by intracellular ATP. Intracellular ATP also regulates a class of K+ channels that have a distinct pharmacology: they are inhibited by sulfonylureas and activated b...

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Bibliografiset tiedot
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: The Rockefeller University Press 1992
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2229110/
https://ncbi.nlm.nih.gov/pubmed/1281220
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