Molecular basis for defective glycosylation and Pseudomonas pathogenesis in cystic fibrosis lung
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference41 articles.
1. CFTR Is a Conductance Regulator as well as a Chloride Channel
2. Defective acidification of intracellular organelles in cystic fibrosis
3. Cystic Fibrosis Airway Epithelia Fail to Kill Bacteria Because of Abnormal Airway Surface Fluid
4. Human β-Defensin-1 Is a Salt-Sensitive Antibiotic in Lung That Is Inactivated in Cystic Fibrosis
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