Cystic Fibrosis Transmembrane Conductance Regulator–associated ATP Release Is Controlled by a Chloride Sensor

The cystic fibrosis transmembrane conductance regulator (CFTR) is a chloride channel that is defective in cystic fibrosis, and has also been closely associated with ATP permeability in cells. Using a Xenopus oocyte cRNA expression system, we have evaluated the molecular mechanisms that control CFTR-...

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Detalles Bibliográficos
Autores principales: Jiang, Qinshi, Mak, Daniel, Devidas, Sreenivas, Schwiebert, Erik M., Bragin, Alvina, Zhang, Yulong, Skach, William R., Guggino, William B., Foskett, J. Kevin, Engelhardt, John F.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1998
Materias:
Regular Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2148142/
https://www.ncbi.nlm.nih.gov/pubmed/9813087

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2148142/
https://www.ncbi.nlm.nih.gov/pubmed/9813087

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