Mucin glycosylation changes in cystic fibrosis lung disease are not manifest in submucosal gland secretions

SMG (submucosal gland) secretions are a major component of the airway surface liquid, are associated with innate immunity in the lung, and have been reported to be altered in lung disease. Changes in lung mucosal glycosylation have been reported in CF (cystic fibrosis), which may be responsible for...

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Main Authors: Schulz, Benjamin L., Sloane, Andrew J., Robinson, Leanne J., Sebastian, Lucille T., Glanville, Allan R., Song, Yuanlin, Verkman, Alan S., Harry, Jenny L., Packer, Nicolle H., Karlsson, Niclas G.
Formato: Artigo
Idioma:Inglês
Publicado: Portland Press Ltd. 2005
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Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC1135025/
https://ncbi.nlm.nih.gov/pubmed/15563276
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BJ20041641
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