Persistence of Abnormal Chloride Conductance Regulation in Transformed Cystic Fibrosis Epithelia
Author:
Affiliation:
1. National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709.
2. Department of Medicine, University of North Carolina, Chapel Hill, NC 27514.
Publisher
American Association for the Advancement of Science (AAAS)
Subject
Multidisciplinary
Reference33 articles.
1. BOUCHER, R.C., EVIDENCE FOR REDUCED CL- AND INCREASED NA+ PERMEABILITY IN CYSTIC-FIBROSIS HUMAN PRIMARY-CELL CULTURES, JOURNAL OF PHYSIOLOGY-LONDON 405: 77 (1988).
2. CARSON, J.L., ULTRASTRUCTURAL CHARACTERIZATION OF EPITHELIAL-CELL MEMBRANES IN NORMAL HUMAN CONDUCTING AIRWAY EPITHELIUM - A FREEZE-FRACTURE STUDY, AMERICAN JOURNAL OF ANATOMY 173: 257 (1985).
3. CEPKO, C.L., CONSTRUCTION AND APPLICATIONS OF A HIGHLY TRANSMISSIBLE MURINE RETROVIRUS SHUTTLE VECTOR, CELL 37: 1053 (1984).
4. COTTON, C.U., ABNORMAL APICAL CELL-MEMBRANE IN CYSTIC-FIBROSIS RESPIRATORY EPITHELIUM - AN INVITRO ELECTROPHYSIOLOGIC ANALYSIS, JOURNAL OF CLINICAL INVESTIGATION 79: 80 (1987).
5. Altered Regulation of Airway Epithelial Cell Chloride Channels in Cystic Fibrosis
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