Altered O-glycosylation and sulfation of airway mucins associated with cystic fibrosis
Author:
Publisher
Oxford University Press (OUP)
Subject
Biochemistry
Link
http://academic.oup.com/glycob/article-pdf/15/8/747/1787106/cwi061.pdf
Reference91 articles.
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3. Bistrup, A. , Bhakta, S., Lee, J.K., Belov, Y.Y., Gunn, M.D., Zuo, F.R., Huang, C.C., Kannagi, R., Rosen, S.D., and Hemmerich, S. (1999) Sulfotransferases of two specificities function in the reconstitution of high endothelial cell ligands for L-selectin. J. Cell Biol., 145, 899–910.
4. Boat, T.F. and Cheng, P.W. (1989) Epithelial cell dysfunction in cystic fibrosis: implications for airways disease. Acta Paediatr. Scand. Suppl., 363, 25–29; Discussion 29–30.
5. Boat, T.F. , Cheng, P.W., Iyer, R.N., Carlson, D.M., and Polony, I. (1976) Human respiratory tract secretion. Mucous glycoproteins of nonpurulent tracheobronchial secretions, and sputum of patients with bronchitis and cystic fibrosis. Arch. Biochem. Biophys., 177, 95–104.
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