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Increased sulfation of glycoconjugates by cultured nasal epithelial cells from patients with cystic fibrosis.

Cystic fibrosis (CF) respiratory epithelia exhibit abnormal anion transport that may be linked to abnormal lung defense. In these studies, we investigated whether primary cultures of CF respiratory epithelial cells regulate abnormally the sulfate content of high molecular weight glycoconjugates (HMG...

Ausführliche Beschreibung

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Bibliographische Detailangaben
Hauptverfasser: Cheng, P W, Boat, T F, Cranfill, K, Yankaskas, J R, Boucher, R C
Format: Artigo
Sprache:Inglês
Veröffentlicht: 1989
Schlagworte:
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC303954/
https://ncbi.nlm.nih.gov/pubmed/2738159
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