Terminal glycosylation of cystic fibrosis airway epithelial cells
Terminal glycosylation of cystic fibrosis airway epithelial cells
About this item
Full title
Author / Creator
Rhim, A D , Kothari, V A , Park, P J , Mulberg, A E , Glick, M C and Scanlin, T F
Publisher
United States: Springer Nature B.V
Journal title
Language
English
Formats
Publication information
Publisher
United States: Springer Nature B.V
Subjects
More information
Scope and Contents
Contents
Cystic fibrosis (CF) has a characteristic glycosylation phenotype usually expressed as a decreased ratio of sialic acid to fucose. The glycosylation phenotype was found in CF/T1 airway epithelial cells (deltaF508/deltaF508). When these cells were transfected and were expressing high amounts of wtCFTR, as detected by Western blot analysis and in sit...
Alternative Titles
Full title
Terminal glycosylation of cystic fibrosis airway epithelial cells
Authors, Artists and Contributors
Author / Creator
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Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_72592683
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_72592683
Other Identifiers
ISSN
0282-0080
E-ISSN
1573-4986
DOI
10.1023/a:1007156014384
