Using the genome to correct the ion transport defect in cystic fibrosis
Author:
Affiliation:
1. BioISI – Biosystems & Integrative Sciences Institute Faculty of Sciences University of Lisbon Lisbon Portugal
Publisher
Wiley
Subject
Physiology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1113/JP282308
Reference84 articles.
1. Functional Genomics Assays to Study CFTR Traffic and ENaC Function
2. High-Content siRNA Screen Reveals Global ENaC Regulators and Potential Cystic Fibrosis Therapy Targets
3. Therapy through chaperones: Sense or antisense? Cystic fibrosis as a model disease
4. Targeting CFTR: How to Treat Cystic Fibrosis by CFTR-Repairing Therapies
5. Novel personalized therapies for cystic fibrosis: treating the basic defect in all patients
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