Cystic fibrosis is a fatal disease caused by a defective gene which codes for cystic fibrosis transmembrane conductance regulator (CFTR), a glycoprotein important in chloride transport. Approximately 75% of patients with CF carry a deletion of phenylalanine from position 508 (F508) of the coding sequence for CFTR. This mutant CFTR is incompletely processed within the endoplasmic reticulum with limited transport of nonfunctional CFTR to the surface of airway epithelial cells, thereby causing defective chloride secretion via the protein.

Project Start
1997-12-01
Project End
1998-11-30
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
38
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Washington
Department
Type
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
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