(Q35749944)

English

Molecular basis for the chloride channel activity of cystic fibrosis transmembrane conductance regulator and the consequences of disease-causing mutations

scientific article published on January 2004

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

1 reference

Europe PubMed Central

Molecular basis for the chloride channel activity of cystic fibrosis transmembrane conductance regulator and the consequences of disease-causing mutations (English)

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

cystic fibrosis

0 references

transmembrane protein

0 references

author name string

Jackie F Kidd

1

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Ilana Kogan

2

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Christine E Bear

3

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

publication date

1 January 2004

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Current Topics in Developmental Biology

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

60

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

215-249

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Regulatory interaction between the cystic fibrosis transmembrane conductance regulator and HCO3- salvage mechanisms in model systems and the mouse pancreatic duct

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Nucleoside triphosphate pentose ring impact on CFTR gating and hydrolysis

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

The non-hydrolytic pathway of cystic fibrosis transmembrane conductance regulator ion channel gating

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Differential interactions of nucleotides at the two nucleotide binding domains of the cystic fibrosis transmembrane conductance regulator

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

The age-related incidence of meconium ileus equivalent in a cystic fibrosis population: the impact of high-energy intake.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Nucleoside triphosphates are required to open the CFTR chloride channel.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Demonstration That CFTR Is a Chloride Channel by Alteration of Its Anion Selectivity

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Regulation by ATP and ADP of CFTR chloride channels that contain mutant nucleotide-binding domains

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Monitoring of ligand-independent dimerization and ligand-induced conformational changes of melatonin receptors in living cells by bioluminescence resonance energy transfer

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Prolonged nonhydrolytic interaction of nucleotide with CFTR's NH2-terminal nucleotide binding domain and its role in channel gating

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Coupling of CFTR Cl- channel gating to an ATP hydrolysis cycle

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Coupling of ATP hydrolysis with channel gating by purified, reconstituted CFTR.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR)

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

COOH-terminal truncations promote proteasome-dependent degradation of mature cystic fibrosis transmembrane conductance regulator from post-Golgi compartments

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

An overview of the pathogenesis of cystic fibrosis lung disease

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Strategies for correcting the delta F508 CFTR protein-folding defect

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Genistein modifies the activation kinetics and magnitude of phosphorylated wild-type and G551D-CFTR chloride currents.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

The two nucleotide-binding domains of cystic fibrosis transmembrane conductance regulator (CFTR) have distinct functions in controlling channel activity

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Severed molecules functionally define the boundaries of the cystic fibrosis transmembrane conductance regulator's NH(2)-terminal nucleotide binding domain

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Structure of MsbA from Vibrio cholera: a multidrug resistance ABC transporter homolog in a closed conformation

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

RETRACTED: Structure of MsbA from E. coli: a homolog of the multidrug resistance ATP binding cassette (ABC) transporters

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Phosphorylation of protein kinase C sites in NBD1 and the R domain control CFTR channel activation by PKA.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

CFTR is a monomer: biochemical and functional evidence

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of cystic fibrosis transmembrane conductance regulator channel-lining residues in and flanking the M6 membrane-spanning segment.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Locating the anion-selectivity filter of the cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

The role of inflammation in the pathophysiology of CF lung disease

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Aberrant CFTR-dependent HCO3- transport in mutations associated with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Effect of cystic fibrosis-associated mutations in the fourth intracellular loop of cystic fibrosis transmembrane conductance regulator.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

CFTR: mechanism of anion conduction

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the nucleotide binding domain 1 signature motif region rescue processing and functional defects of cystic fibrosis transmembrane conductance regulator delta f508.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

The cystic fibrosis mutation G551D alters the non-Michaelis-Menten behavior of the cystic fibrosis transmembrane conductance regulator (CFTR) channel and abolishes the inhibitory Genistein binding site.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

The second half of the cystic fibrosis transmembrane conductance regulator forms a functional chloride channel

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Activation of NF-kappaB by adherent Pseudomonas aeruginosa in normal and cystic fibrosis respiratory epithelial cells

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Update on pathogenesis of cystic fibrosis lung disease

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

The pathophysiology of the pancreatic defect in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Pancreatic aspects of cystic fibrosis and other inherited causes of pancreatic dysfunction

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

X-ray structure of a ClC chloride channel at 3.0 A reveals the molecular basis of anion selectivity

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Gating the selectivity filter in ClC chloride channels

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Vanadate-catalyzed photocleavage of the signature motif of an ATP-binding cassette (ABC) transporter

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Ten years with CFTR

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

G-protein-coupled receptor oligomerization and its potential for drug discovery

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Pathophysiology and Management of Pulmonary Infections in Cystic Fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular determinants and role of an anion binding site in the external mouth of the CFTR chloride channel pore

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Conformational states of CFTR associated with channel gating: the role ATP binding and hydrolysis.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Asymmetric structure of the cystic fibrosis transmembrane conductance regulator chloride channel pore suggested by mutagenesis of the twelfth transmembrane region

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Non-CFTR chloride channels likely contribute to secretion in the murine small intestine

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Amelioration of intestinal disease severity in cystic fibrosis mice is associated with improved chloride secretory capacity

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Inhibition of cystic fibrosis transmembrane conductance regulator by novel interaction with the metabolic sensor AMP-activated protein kinase

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

The ABC of channel regulation

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

ABC transporters: physiology, structure and mechanism--an overview

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Structural biology. The xyz of ABC transporters

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Structural biology of Rad50 ATPase: ATP-driven conformational control in DNA double-strand break repair and the ABC-ATPase superfamily

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Structural biochemistry and interaction architecture of the DNA double-strand break repair Mre11 nuclease and Rad50-ATPase

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Rad50/SMC proteins and ABC transporters: unifying concepts from high-resolution structures.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Protein kinase A regulates ATP hydrolysis and dimerization by a CFTR (cystic fibrosis transmembrane conductance regulator) domain.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Rethinking cystic fibrosis pathology: the critical role of abnormal reduced glutathione (GSH) transport caused by CFTR mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

The perplexing challenges of a pump turned channel

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular pharmacology of the CFTR Cl- channel

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Genistein potentiates wild-type and delta F508-CFTR channel activity

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Single molecule imaging of green fluorescent proteins in living cells: E-cadherin forms oligomers on the free cell surface.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Regulation of CFTR Cl- channel gating by ATP binding and hydrolysis

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Membrane potential and bicarbonate secretion in isolated interlobular ducts from guinea-pig pancreas

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Simultaneous observation of individual ATPase and mechanical events by a single myosin molecule during interaction with actin.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

From membrane to molecule to the third amino acid from the left with a membrane transport protein

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Mislocalization of ΔF508 CFTR in cystic fibrosis sweat gland

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductance

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Gluthathione: in defence of the lung

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

A molecular mechanism for aberrant CFTR-dependent HCO(3)(-) transport in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Perturbation of the pore of the cystic fibrosis transmembrane conductance regulator (CFTR) inhibits its atpase activity

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

CFTR directly mediates nucleotide-regulated glutathione flux.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Pancreatic fluid secretion and protein hyperconcentration in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

MOLSCRIPT: a program to produce both detailed and schematic plots of protein structures

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Evidence that CFTR channels can regulate the open duration of other CFTR channels: cooperativity

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Two mechanisms of genistein inhibition of cystic fibrosis transmembrane conductance regulator Cl- channels expressed in murine cell line

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Projection structure of P-glycoprotein by electron microscopy. Evidence for a closed conformation of the nucleotide binding domains

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

D2 dopamine receptor homodimerization is mediated by multiple sites of interaction, including an intermolecular interaction involving transmembrane domain 4.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Sweat testing for the diagnosis of cystic fibrosis: practical considerations

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

The cystic fibrosis mutation (delta F508) does not influence the chloride channel activity of CFTR.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

ATPase activity of the cystic fibrosis transmembrane conductance regulator

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Possible transition-state analogs for ribonuclease. Complexes of uridine with oxovanadium(IV) ion and vanadium(V) ion

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Direct block of the cystic fibrosis transmembrane conductance regulator Cl(-) channel by butyrate and phenylbutyrate

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Relationship between anion binding and anion permeability revealed by mutagenesis within the cystic fibrosis transmembrane conductance regulator chloride channel pore

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular determinants of anion selectivity in the cystic fibrosis transmembrane conductance regulator chloride channel pore

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Disulphonic stilbene block of cystic fibrosis transmembrane conductance regulator Cl- channels expressed in a mammalian cell line and its regulation by a critical pore residue

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Permeability of wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels to polyatomic anions

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

The E. coli BtuCD structure: a framework for ABC transporter architecture and mechanism

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

The "LSGGQ" motif in each nucleotide-binding domain of human P-glycoprotein is adjacent to the opposing walker A sequence

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Cystic fibrosis transmembrane conductance regulator: the purified NBF1+R protein interacts with the purified NBF2 domain to form a stable NBF1+R/NBF2 complex while inducing a conformational change transmitted to the C-terminal region

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Constitutive internalization of cystic fibrosis transmembrane conductance regulator occurs via clathrin-dependent endocytosis and is regulated by protein phosphorylation

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

High-affinity activators of cystic fibrosis transmembrane conductance regulator (CFTR) chloride conductance identified by high-throughput screening

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Dibasic protein kinase A sites regulate bursting rate and nucleotide sensitivity of the cystic fibrosis transmembrane conductance regulator chloride channel.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

The CFTR chloride channel: nucleotide interactions and temperature-dependent gating

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

The Hsc70 co-chaperone CHIP targets immature CFTR for proteasomal degradation

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Raster3D: photorealistic molecular graphics

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

A macromolecular complex of beta 2 adrenergic receptor, CFTR, and ezrin/radixin/moesin-binding phosphoprotein 50 is regulated by PKA

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

A functional R domain from cystic fibrosis transmembrane conductance regulator is predominantly unstructured in solution

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Effects of C-terminal deletions on cystic fibrosis transmembrane conductance regulator function in cystic fibrosis airway epithelia

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

CFTR mutations and host susceptibility to Pseudomonas aeruginosa lung infection.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Role of CFTR in airway disease

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutation of Walker-A lysine 464 in cystic fibrosis transmembrane conductance regulator reveals functional interaction between its nucleotide-binding domains

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Physiological basis of cystic fibrosis: a historical perspective

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

The neglected ion: HCO3-

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Pulmonary infections in patients with cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Dimeric cystic fibrosis transmembrane conductance regulator exists in the plasma membrane

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Walker mutations reveal loose relationship between catalytic and channel-gating activities of purified CFTR (cystic fibrosis transmembrane conductance regulator)

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

A monomer is the minimum functional unit required for channel and ATPase activity of the cystic fibrosis transmembrane conductance regulator

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Stable dimeric assembly of the second membrane-spanning domain of CFTR (cystic fibrosis transmembrane conductance regulator) reconstitutes a chloride-selective pore

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Activation of the epithelial Na+ channel (ENaC) requires CFTR Cl- channel function

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Control of dynamic CFTR selectivity by glutamate and ATP in epithelial cells

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

cAMP-inducible chloride conductance in mouse fibroblast lines stably expressing the human cystic fibrosis transmembrane conductance regulator

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of the cystic fibrosis gene: chromosome walking and jumping

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

The ATPase and ATP-binding functions of P-glycoprotein--modulation by interaction with defined phospholipids

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Repacking of the transmembrane domains of P-glycoprotein during the transport ATPase cycle

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

The GxxxG motif: a framework for transmembrane helix-helix association

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Lack of conventional ATPase properties in CFTR chloride channel gating

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Influence of phosphorylation by protein kinase A on CFTR at the cell surface and endoplasmic reticulum

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Disease-Associated Mutations in Cytoplasmic Loops 1 and 2 of Cystic Fibrosis Transmembrane Conductance Regulator Impede Processing or Opening of the Channel†

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Disease-associated mutations in the fourth cytoplasmic loop of cystic fibrosis transmembrane conductance regulator compromise biosynthetic processing and chloride channel activity.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Cystic fibrosis: channel, catalytic, and folding properties of the CFTR protein.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

cAMP-dependent protein kinase-mediated phosphorylation of cystic fibrosis transmembrane conductance regulator residue Ser-753 and its role in channel activation

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

The amino-terminal portion of CFTR forms a regulated Cl- channel.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Structure and function of the CFTR chloride channel

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

A FRET-based sensor reveals large ATP hydrolysis-induced conformational changes and three distinct states of the molecular motor myosin

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

ATP binding to the motor domain from an ABC transporter drives formation of a nucleotide sandwich dimer

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

CFTR: covalent and noncovalent modification suggests a role for fixed charges in anion conduction

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Cystic fibrosis transmembrane conductance regulator. Physical basis for lyotropic anion selectivity patterns

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Oligomerization of Dopamine Transporters Visualized in Living Cells by Fluorescence Resonance Energy Transfer Microscopy

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Cystic fibrosis transmembrane conductance regulator inverts protein kinase A-mediated regulation of epithelial sodium channel single channel kinetics

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

CFTR Cl- channel and CFTR-associated ATP channel: distinct pores regulated by common gates.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

E3KARP mediates the association of ezrin and protein kinase A with the cystic fibrosis transmembrane conductance regulator in airway cells

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Nucleotide occlusion in the human cystic fibrosis transmembrane conductance regulator. Different patterns in the two nucleotide binding domains

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Phosphorylation-regulated CI− channel in CHO cells stably expressing the cystic fibrosis gene

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Halide permeation in wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Antioxidant imbalance in the lungs of cystic fibrosis transmembrane conductance regulator protein mutant mice

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

On the mechanism of MgATP-dependent gating of CFTR Cl- channels

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Deletion of phenylalanine 508 causes attenuated phosphorylation-dependent activation of CFTR chloride channels

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Accessory protein facilitated CFTR-CFTR interaction, a molecular mechanism to potentiate the chloride channel activity

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Degradation of CFTR by the ubiquitin-proteasome pathway

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Rules of conduct for the cystic fibrosis anion channel

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Stimulation of CFTR activity by its phosphorylated R domain.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

A short segment of the R domain of cystic fibrosis transmembrane conductance regulator contains channel stimulatory and inhibitory activities that are separable by sequence modification

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Binding of Pseudomonas aeruginosa to respiratory epithelial cells from patients with various mutations in the cystic fibrosis transmembrane regulator

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Correction of G551D-CFTR transport defect in epithelial monolayers by genistein but not by CPX or MPB-07.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Pharmacologic restoration of delta F508 CFTR-mediated chloride current.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

A new ER trafficking signal regulates the subunit stoichiometry of plasma membrane K(ATP) channels

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Limited proteolysis as a probe for arrested conformational maturation of delta F508 CFTR

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Gating rearrangements in cyclic nucleotide-gated channels revealed by patch-clamp fluorometry.

1 reference

https://api.crossref.org/works/10.1016%2FS0070-2153%2804%2960007-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0070-2153(04)60007-X

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q35749944&oldid=1585144888"