Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Anion Binding as a Probe of the Pore

Author:

Mansoura Monique K.,Smith Stephen S.,Choi Anne D.,Richards Neil W.,Strong Theresa V.,Drumm Mitchell L.,Collins Francis S.,Dawson David C.

Publisher

Elsevier BV

Subject

Biophysics

Reference61 articles.

1. Identification of channel-lining residues in the M6 membrane-spanning segment of CFTR and the position of the anion-selectivity filter;Akabas;Biophys. J.,1996

2. Amino acid residues lining the chloride channel of the cystic fibrosis transmembrane conductance regulator;Akabas;J. Biol. Chem.,1994

3. Demonstration that CFTR is a chloride channel by alteration of its anion selectivity;Anderson;Science,1991

4. Cl− channel activity in Xenopus oocytes expressing the cystic fibrosis gene;Bear;J. Biol. Chem.,1991

5. Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR);Bear;Cell,1992

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