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Role of nitric oxide in the regulation of CFTR trafficking in intestinal epithelial cells

✍ Scribed by Skinn, Andrew C.; Macnaughton, Wallace K.

Book ID
122338300
Publisher
Elsevier Science
Year
2003
Tongue
English
Weight
362 KB
Volume
124
Category
Article
ISSN
0016-5085

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## Abstract Cystic fibrosis transmembrane conductance regulator (CFTR) is an apical membrane chloride channel critical to the regulation of fluid, chloride, and bicarbonate transport in epithelia and other cell types. The most common cause of cystic fibrosis (CF) is the abnormal trafficking of CFTR