Terminal glycosylation in cystic fibrosis (CF): A review emphasizing the airway epithelial cell Andrew D. RhimLydia StoykovaThomas F. Scanlin OriginalPaper Pages: 649 - 659
Human airway mucin glycosylation: A combinatory of carbohydrate determinants which vary in cystic fibrosis Geneviève LamblinSophie DegrootePhilippe Rousse OriginalPaper Pages: 661 - 684
Biosynthesis of mucin type O-glycans: Lack of correlation between glycosyltransferase and sulfotransferase activities and CFTR expression Inka BrockhausenFabienne VavasseurXiaojing Yang OriginalPaper Pages: 685 - 697
FAB-MS characterization of sialyl Lewisx determinants on polylactosamine chains of human airway mucins secreted by patients suffering from cystic fibrosis or chronic bronchitis Willy MorelleMark Sutton-SmithAnne Dell OriginalPaper Pages: 699 - 708
Recognition of mucin components by Pseudomonas aeruginosa Reuben RamphalShiwani K. Arora OriginalPaper Pages: 709 - 713
Signaling networks controlling mucin production in response to Gram-positive and Gram-negative bacteria Nancy McNamaraCarol Basbaum OriginalPaper Pages: 715 - 722
Gene therapy of cystic fibrosis: The glycofection approach Isabelle FajacPascale BriandMichel Monsigny OriginalPaper Pages: 723 - 729
Gene therapy of cystic fibrosis (CF) airways: A review emphasizing targeting with lactose Daniel T. KlinkMary Catherine GlickThomas F. Scanlin OriginalPaper Pages: 731 - 740