Expression of cystic fibrosis transmembrane conductance regulator in paracervical ganglia
Expression of cystic fibrosis transmembrane conductance regulator in paracervical ganglia
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Publisher
Canada: NRC Research Press
Journal title
Language
English
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Publisher
Canada: NRC Research Press
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Scope and Contents
Contents
The cystic fibrosis transmembrane conductance regulator (CFTR) is an important protein that acts as a chloride channel and regulates many physiological functions, including salt transport and fluid flow. Mutations in the gene encoding the CFTR protein cause cystic fibrosis. CFTR is expressed in the epithelial cells of the lungs, pancreas, intestine...
Alternative Titles
Full title
Expression of cystic fibrosis transmembrane conductance regulator in paracervical ganglia
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TN_cdi_proquest_miscellaneous_754869721
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_754869721
Other Identifiers
ISSN
0829-8211
E-ISSN
1208-6002
DOI
10.1139/O10-016
