| scholarly article | Q13442814 |
| P2093 | author name string | Ron R Kopito | |
| Melissa A Harrington | |||
| P2860 | cites work | Structure of a voltage-dependent K+ channel beta subunit | Q27618988 |
| Structure of the cytoplasmic beta subunit-T1 assembly of voltage-dependent K+ channels | Q27625246 | ||
| Site-directed mutagenesis by overlap extension using the polymerase chain reaction | Q27860503 | ||
| Accessory protein facilitated CFTR-CFTR interaction, a molecular mechanism to potentiate the chloride channel activity | Q28142263 | ||
| ATPase activity of the cystic fibrosis transmembrane conductance regulator | Q28854569 | ||
| The "megaprimer" method of site-directed mutagenesis | Q29620742 | ||
| Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR) | Q33970197 | ||
| Slow conversions among subconductance states of cystic fibrosis transmembrane conductance regulator chloride channel | Q34017151 | ||
| CFTR channels in immortalized human airway cells | Q34208228 | ||
| Regulation of the gating of cystic fibrosis transmembrane conductance regulator C1 channels by phosphorylation and ATP hydrolysis | Q35269834 | ||
| ATP-dependent bacterial transporters and cystic fibrosis: analogy between channels and transporters | Q35323989 | ||
| Gating of cystic fibrosis transmembrane conductance regulator chloride channels by adenosine triphosphate hydrolysis. Quantitative analysis of a cyclic gating scheme | Q36412100 | ||
| Regulation of CFTR Cl- channel gating by ATP binding and hydrolysis | Q37238263 | ||
| Interdomain but not intermolecular interactions observed in CFTR channels | Q40771268 | ||
| The two halves of CFTR form a dual-pore ion channel | Q40890137 | ||
| Redox reagents and divalent cations alter the kinetics of cystic fibrosis transmembrane conductance regulator channel gating | Q40928853 | ||
| A single conductance pore for chloride ions formed by two cystic fibrosis transmembrane conductance regulator molecules | Q40967502 | ||
| Novel pore-lining residues in CFTR that govern permeation and open-channel block | Q41022138 | ||
| Block by MOPS reveals a conformation change in the CFTR pore produced by ATP hydrolysis. | Q41081260 | ||
| Intracellular loop between transmembrane segments IV and V of cystic fibrosis transmembrane conductance regulator is involved in regulation of chloride channel conductance state | Q41269444 | ||
| Membrane topology of a cysteine-less mutant of human P-glycoprotein | Q41380800 | ||
| Defective regulation of outwardly rectifying Cl- channels by protein kinase A corrected by insertion of CFTR | Q41608893 | ||
| Phosphorylation-regulated CI− channel in CHO cells stably expressing the cystic fibrosis gene | Q41669744 | ||
| Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis | Q41714520 | ||
| Nucleoside triphosphates are required to open the CFTR chloride channel. | Q41769807 | ||
| Pyridine nucleotide redox potential modulates cystic fibrosis transmembrane conductance regulator Cl- conductance | Q42068756 | ||
| Effects of pyrophosphate and nucleotide analogs suggest a role for ATP hydrolysis in cystic fibrosis transmembrane regulator channel gating. | Q42674364 | ||
| Demonstration That CFTR Is a Chloride Channel by Alteration of Its Anion Selectivity | Q43847410 | ||
| Phosphorylation of the R domain by cAMP-dependent protein kinase regulates the CFTR chloride channel | Q43911618 | ||
| Transformation of rat cells by DNA of human adenovirus 5 | Q44464709 | ||
| Conformational states of CFTR associated with channel gating: the role ATP binding and hydrolysis. | Q46017118 | ||
| Intracellular turnover of cystic fibrosis transmembrane conductance regulator. Inefficient processing and rapid degradation of wild-type and mutant proteins | Q46621436 | ||
| Coupling of CFTR Cl- channel gating to an ATP hydrolysis cycle | Q46797528 | ||
| N-Acetyl-L-cysteine and its derivatives activate a Cl- conductance in epithelial cells | Q49021235 | ||
| NO+, NO, and NO- donation by S-nitrosothiols: implications for regulation of physiological functions by S-nitrosylation and acceleration of disulfide formation. | Q51605840 | ||
| Control of CFTR channel gating by phosphorylation and nucleotide hydrolysis. | Q53938455 | ||
| Regulation of CFTR channel gating | Q58112756 | ||
| Effect of Deleting the R Domain on CFTR-Generated Chloride Channels | Q67694895 | ||
| Inhibition of vacuolar H(+)-ATPase by disulfide bond formation between cysteine 254 and cysteine 532 in subunit A | Q72403613 | ||
| Covalent inhibitors of P-glycoprotein ATPase activity | Q72671369 | ||
| Covalent modification of the regulatory domain irreversibly stimulates cystic fibrosis transmembrane conductance regulator | Q73770423 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1278-1292 | |
| P577 | publication date | 2002-03-01 | |
| P1433 | published in | Biophysical Journal | Q2032955 |
| P1476 | title | Cysteine residues in the nucleotide binding domains regulate the conductance state of CFTR channels | |
| P478 | volume | 82 |
| Q30445827 | Activation of chloride transport in CF airway epithelial cell lines and primary CF nasal epithelial cells by S-nitrosoglutathione. |
| Q36981796 | Impaired Ca2+-dependent activation of large-conductance Ca2+-activated K+ channels in the coronary artery smooth muscle cells of Zucker Diabetic Fatty rats |
| Q36379776 | Insight in eukaryotic ABC transporter function by mutation analysis |
| Q45204993 | Intracellular thiol-mediated modulation of epithelial sodium channel activity |
| Q41466794 | Modulation of cystic fibrosis transmembrane conductance regulator (CFTR) activity and genistein binding by cytosolic pH. |
| Q34989488 | Multicenter intestinal current measurements in rectal biopsies from CF and non-CF subjects to monitor CFTR function |
| Q38035816 | Overview of pyridine nucleotides review series. |
| Q41888706 | Oxidative stress caused by pyocyanin impairs CFTR Cl(-) transport in human bronchial epithelial cells |
| Q57282398 | Oxidative stress, autophagy and airway ion transport |
| Q42670820 | State-dependent chemical reactivity of an engineered cysteine reveals conformational changes in the outer vestibule of the cystic fibrosis transmembrane conductance regulator |
| Q45199722 | Stimulation of colonic anion secretion by monochloramine: action sites |
| Q33750252 | The H-loop in the second nucleotide-binding domain of the cystic fibrosis transmembrane conductance regulator is required for efficient chloride channel closing |
| Q43249070 | The yin and yang of cystic fibrosis transmembrane conductance regulator function: implications for chronic lung disease |
| Q38913048 | Trafficking and function of the cystic fibrosis transmembrane conductance regulator: a complex network of posttranslational modifications |
| Q24633363 | Vitamin C controls the cystic fibrosis transmembrane conductance regulator chloride channel |
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