Cl−transport by cystic fibrosis transmembrane conductance regulator (CFTR) contributes to the inhibition of epithelial Na+channels (ENaCs) inXenopusoocytes co-expressing CFTR and ENaC-Reference-Cited by-同舟云学术

Cl−transport by cystic fibrosis transmembrane conductance regulator (CFTR) contributes to the inhibition of epithelial Na+channels (ENaCs) inXenopusoocytes co-expressing CFTR and ENaC

Published:1998-05 Issue:3 Volume:508 Page:825-836
ISSN:0022-3751
Container-title:The Journal of Physiology
language:en
Short-container-title:

Author:

Briel M.,Greger R.,Kunzelmann K.

Publisher

Wiley

Subject

Physiology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-7793.1998.825bp.x/fullpdf

Reference38 articles.

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3. Regulation of epithelial sodium channels by short actin filaments;Berdiev;Journal of Biological Chemistry,1996

4. Cystic fibrosis transmembrane conductance regulator activation stimulates endosome fusion in vivo.;Biwersi;Proceedings of the National Academy of Sciences of the USA,1996

5. Regulation of plasma membrane recycling by CFTR;Bradbury;Science,1992

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