| Title | Date | PubMed ID |
|---|
| Cystic Fibrosis Transmembrane Conductance Regulator (CFTR): CLOSED AND OPEN STATE CHANNEL MODELS. | 2015 Sep 18 | 26229102 |
| The Fifth Transmembrane Segment of Cystic Fibrosis Transmembrane Conductance Regulator Contributes to Its Anion Permeation Pathway. | 2015 Jun 23 | 26024338 |
| Impact of the F508del mutation on ovine CFTR, a Cl- channel with enhanced conductance and ATP-dependent gating. | 2015 Jun 1 | 25763566 |
| Mutating the Conserved Q-loop Glutamine 1291 Selectively Disrupts Adenylate Kinase-dependent Channel Gating of the ATP-binding Cassette (ABC) Adenylate Kinase Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) and Reduces Channel Function in Primary Human Airway Epithelia. | 2015 May 29 | 25887396 |
| Molecular Basis for Fe(III)-Independent Curcumin Potentiation of Cystic Fibrosis Transmembrane Conductance Regulator Activity. | 2015 May 12 | 25867080 |
| Localizing a gate in CFTR. | 2015 Feb 24 | 25675504 |
| A single amino acid substitution in CFTR converts ATP to an inhibitory ligand. | 2014 Oct | 25225552 |
| Conserved allosteric hot spots in the transmembrane domains of cystic fibrosis transmembrane conductance regulator (CFTR) channels and multidrug resistance protein (MRP) pumps. | 2014 Jul 18 | 24876383 |
| ATP and AMP mutually influence their interaction with the ATP-binding cassette (ABC) adenylate kinase cystic fibrosis transmembrane conductance regulator (CFTR) at separate binding sites. | 2013 Sep 20 | 23921386 |
| Two salt bridges differentially contribute to the maintenance of cystic fibrosis transmembrane conductance regulator (CFTR) channel function. | 2013 Jul 12 | 23709221 |