Rules of conduct for the cystic fibrosis anion channel
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Biochemistry, Genetics and Molecular Biology,General Medicine
Link
http://www.nature.com/articles/nm0703-827.pdf
Reference9 articles.
1. Reddy, M.M. & Quinton, P.M. Control of dynamic CFTR selectivity by glutamate & ATPin epithelial cells. Nature 423, 757–760 (2003).
2. Choi, J.Y. et al. Aberrant CFTR-dependent HCO3− transport in mutations associated with cystic fibrosis. Nature 410, 94–97 (2001).
3. Ko, S.B. et al. A molecular mechanism for aberrant CFTR-dependent HCO3− transport in cystic fibrosis. EMBO J. 21, 5662–5672 (2002).
4. Vergani, P., Nairn, A.C. & Gadsby, D.C. On the mechanism of MgATP-dependent gating of CFTR Cl− channels. J. Gen. Physiol. 121, 17–36 (2003).
5. Aleksandrov, A.A., Chang, X., Aleksandrov, L. & Riordan, J.R. The non-hydrolytic pathway of cystic fibrosis transmembrane conductance regulator ion channel gating. J. Physiol. 528, 259–265 (2000).
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