Amino acid residues lining the chloride channel of the cystic fibrosis transmembrane conductance regulator.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference31 articles.
1. The Cystic Fibrosis Transmembrane Conductance Regulator
2. Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis
3. Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA
4. Effect of Deleting the R Domain on CFTR-Generated Chloride Channels
5. Nucleoside triphosphates are required to open the CFTR chloride channel
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2. Cysteine Scanning of CFTR’s First Transmembrane Segment Reveals Its Plausible Roles in Gating and Permeation;Biophysical Journal;2013-02
3. Mutation p.E92K is the primary cause of cystic fibrosis in Chuvashes;Russian Journal of Genetics;2012-07
4. Functional arrangement of the 12th transmembrane region in the CFTR chloride channel pore based on functional investigation of a cysteine-less CFTR variant;Pflügers Archiv - European Journal of Physiology;2011-07-28
5. Alignment of transmembrane regions in the cystic fibrosis transmembrane conductance regulator chloride channel pore;Journal of General Physiology;2011-07-11
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