Rauh, Robert <br/><br/>
A mutation of the epithelial sodium channel associated with atypical cystic fibrosis increases channel open probability and reduces Na+ self inhibition.  [electronic resource] 

 -  The Journal of physiology  Apr 2010 
 - 1211-25 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1469-7793 
<br/><br/><label>Standard No.: </label>10.1113/jphysiol.2009.180224  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Cells, Cultured<br/>Chymotrypsin--metabolism<br/>Cystic Fibrosis--physiopathology<br/>Cystic Fibrosis Transmembrane Conductance Regulator--genetics<br/>Epithelial Sodium Channels--genetics<br/>Feedback, Physiological--physiology<br/>Female<br/>Humans<br/>Mutation--genetics<br/>Oocytes--cytology<br/>Patch-Clamp Techniques<br/>Phenotype<br/>Plasmids<br/>Sodium--metabolism<br/>Xenopus laevis