Stabilizing Rescued Surface-Localized ΔF508 CFTR by Potentiation of Its Interaction with Na+/H+ Exchanger Regulatory Factor 1
Author:
Affiliation:
1. Division of Pulmonary Medicine, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, MLC2021 3333 Burnet Avenue, Cincinnati, Ohio 45229, United States
Publisher
American Chemical Society (ACS)
Subject
Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/bi401263h
Reference45 articles.
1. Cystic Fibrosis
2. Aberrant CFTR-dependent HCO-3 transport in mutations associated with cystic fibrosis
3. The Phenotypic Consequences of CFTR Mutations
4. Identification of the Cystic Fibrosis Gene: Genetic Analysis
5. Cystic fibrosis: A worldwide analysis ofCFTR mutations?correlation with incidence data and application to screening
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