Article
A new model of cystic fibrosis pathology: lack of transport of glutathione and its thiocyanate conjugates.
Medical hypotheses - 1 Jan 2007
Childers Melanie, Eckel George, Himmel Alan, Caldwell Jim
Abstract excerpt
Many of the symptoms of cystic fibrosis are not explained by the current disease mechanisms. Therefore, the authors conducted an extensive literature review and present a new model of cystic fibrosis pathology, which is the culmination of this research. Understanding that the cystic fibrosis transmembrane conductance regulator (CFTR) is responsible for glutathione (GSH) transport, the authors hypothesize that...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
