∆F508 CFTR interactome remodelling promotes rescue of cystic fibrosis

Author:

Pankow Sandra,Bamberger Casimir,Calzolari Diego,Martínez-Bartolomé Salvador,Lavallée-Adam Mathieu,Balch William E.,Yates John R.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Reference55 articles.

1. Dalemans, W. et al. Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutation. Nature 354, 526–528 (1991)

2. Collins, F. S. Cystic fibrosis: molecular biology and therapeutic implications. Science 256, 774–779 (1992)

3. Watson, M. S. et al. Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel. Genet. Med. 6, 387–391 (2004)

4. World Health Organization. The Molecular Genetic Epidemiology of Cystic Fibrosis http://www.who.int/genomics/publications/en/HGN_WB_04.02_report.pdf (World Health Organization, 2004)

5. Lukacs, G. L. et al. The ΔF508 mutation decreases the stability of cystic fibrosis transmembrane conductance regulator in the plasma membrane. Determination of functional half-lives on transfected cells. J. Biol. Chem. 268, 21592–21598 (1993)

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