The biogenesis, traffic, and function of the cystic fibrosis transmembrane conductance regulator. (Q41431313)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9102394%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

review article

1 reference

title

The biogenesis, traffic, and function of the cystic fibrosis transmembrane conductance regulator (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9102394%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

main subject

cystic fibrosis

0 references

transmembrane protein

0 references

author name string

T Jilling

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9102394%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

K L Kirk

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9102394%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

publication date

1 January 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9102394%20AND%20SRC:MED&resulttype=core&format=json

International Review of Cytology

2 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9102394%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

volume

172

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9102394%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

page(s)

193-241

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9102394%20AND%20SRC:MED&resulttype=core&format=json

Cloning of the beta cell high-affinity sulfonylurea receptor: a regulator of insulin secretion

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

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Separate Cl- conductances activated by cAMP and Ca2+ in Cl(-)-secreting epithelial cells

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7 January 2021

cAMP-activated Cl channels in CFTR-transfected cystic fibrosis pancreatic epithelial cells

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7 January 2021

Characterization of the cystic fibrosis transmembrane conductance regulator in a colonocyte cell line

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The genetic advantage hypothesis in cystic fibrosis heterozygotes: a murine study

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A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein

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Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutation

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Induction of mutant dynamin specifically blocks endocytic coated vesicle formation

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Receptor and protein kinase C-mediated regulation of ARF binding to the Golgi complex.

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7 January 2021

Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia

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7 January 2021

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

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7 January 2021

Cystic fibrosis with three mutations in the cystic fibrosis transmembrane conductance regulator gene

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7 January 2021

Heterologous expression of delta F508 CFTR results in decreased sialylation of membrane glycoconjugates

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7 January 2021

Antibodies to clathrin inhibit endocytosis but not recycling to the trans Golgi network in vitro

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7 January 2021

Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer

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7 January 2021

Glycan microheterogeneity of alpha 1-antitrypsin in serum and meconium from normal and cystic fibrosis patients by crossed immunoaffinoelectrophoresis with different lectins (Con A, LCA, WGA)

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7 January 2021

Effect of cholera enterotoxin on ion transport across isolated ileal mucosa

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The actin filament disrupter cytochalasin D activates the recombinant cystic fibrosis transmembrane conductance regulator Cl- channel in mouse 3T3 fibroblasts

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The changing epidemiology of cystic fibrosis

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7 January 2021

Gates of Janus: cystic fibrosis and diarrhea

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7 January 2021

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

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Mutations in the putative pore-forming domain of CFTR do not change anion selectivity of the cAMP activated Cl- conductance.

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7 January 2021

Aminoglycoside antibiotics restore CFTR function by overcoming premature stop mutations

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7 January 2021

Structural model of ATP-binding proteins associated with cystic fibrosis, multidrug resistance and bacterial transport

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7 January 2021

Reconstitution of IKATP: an inward rectifier subunit plus the sulfonylurea receptor

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Genetic complementation in cystic fibrosis pancreatic cells by somatic cell fusion

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Severity of cystic fibrosis in patients homozygous and heterozygous for ΔF508 mutation

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Cystic fibrosis transmembrane conductance regulator is required for protein kinase A activation of an outwardly rectified anion channel purified from bovine tracheal epithelia

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7 January 2021

Interaction between cystic fibrosis transmembrane conductance regulator and outwardly rectified chloride channels

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

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7 January 2021

The first nucleotide binding fold of the cystic fibrosis transmembrane conductance regulator can function as an active ATPase

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Effect of high-dose ibuprofen in patients with cystic fibrosis.

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Constitutive Mucin Secretion Linked to CFTR Expression

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Involvement of microtubule motors in basolateral and apical transport in kidney cells.

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Biosynthetic transport of the asialoglycoprotein receptor H1 to the cell surface occurs via endosomes

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7 January 2021

Cyclic AMP-dependent protein kinase opens chloride channels in normal but not cystic fibrosis airway epithelium

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7 January 2021

Conformational maturation of CFTR but not its mutant counterpart (delta F508) occurs in the endoplasmic reticulum and requires ATP

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Localization of the cystic fibrosis transmembrane conductance regulator in pancreas

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Common signals control low density lipoprotein receptor sorting in endosomes and the Golgi complex of MDCK cells

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7 January 2021

Structure and function of ARF proteins: activators of cholera toxin and critical components of intracellular vesicular transport processes

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7 January 2021

Properties of the luminal membrane of isolated perfused rat pancreatic ducts

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7 January 2021

Calnexin fails to associate with substrate proteins in glucosidase-deficient cell lines

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7 January 2021

Mutant (delta F508) cystic fibrosis transmembrane conductance regulator Cl- channel is functional when retained in endoplasmic reticulum of mammalian cells.

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7 January 2021

Bicarbonate conductance and pH regulatory capability of cystic fibrosis transmembrane conductance regulator

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7 January 2021

Role of mutant CFTR in hypersusceptibility of cystic fibrosis patients to lung infections.

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7 January 2021

ATP and cytosol requirements for transferrin recycling in intact and disrupted MDCK cells.

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7 January 2021

cAMP-independent regulation of CFTR by the actin cytoskeleton

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7 January 2021

Cell surface labeling of CFTR in T84 cells

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Rapid endocytosis of the cystic fibrosis transmembrane conductance regulator chloride channel

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7 January 2021

Differential localization of the cystic fibrosis transmembrane conductance regulator in normal and cystic fibrosis airway epithelium

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7 January 2021

Chloride impermeability in cystic fibrosis

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7 January 2021

Human Genetics: What is good about cystic fibrosis?

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7 January 2021

Effect of serum from normal and cystic fibrosis subjects on mucin secretion from dispersed rat submandibular cells

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7 January 2021

Cl- permeability of human sweat duct cells monitored with fluorescence-digital imaging microscopy: evidence for reduced plasma membrane Cl- permeability in cystic fibrosis

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7 January 2021

Expression and functional properties of the second predicted nucleotide binding fold of the cystic fibrosis transmembrane conductance regulator fused to glutathione-S-transferase.

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7 January 2021

Altered electrical potential profile of human reabsorptive sweat duct cells in cystic fibrosis

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7 January 2021

Failure of the cystic fibrosis transmembrane conductance regulator to conduct ATP.

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7 January 2021

Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells

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7 January 2021

Effect of Deleting the R Domain on CFTR-Generated Chloride Channels

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7 January 2021

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

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7 January 2021

Identification of the cystic fibrosis gene: chromosome walking and jumping

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7 January 2021

Mechanisms of intracellular protein transport

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7 January 2021

Infection in patients with cystic fibrosis

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7 January 2021

Secretory activity of hamster tracheal explants and isolated tracheal epithelial cells and the effects of cystic fibrosis serum.

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7 January 2021

Activation of the cystic fibrosis transmembrane regulator by cyclic AMP is not correlated with inhibition of endocytosis

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7 January 2021

Glycerol reverses the misfolding phenotype of the most common cystic fibrosis mutation.

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7 January 2021

Phosphorylation fails to activate chloride channels from cystic fibrosis airway cells

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7 January 2021

A cystic fibrosis pancreatic adenocarcinoma cell line

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7 January 2021

Both CFTR and outwardly rectifying chloride channels contribute to cAMP-stimulated whole cell chloride currents

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7 January 2021

Heterotrimeric G proteins, vesicle trafficking, and CFTR Cl- channels

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7 January 2021

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

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7 January 2021

Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties.

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7 January 2021

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

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Mechanism of dysfunction of two nucleotide binding domain mutations in cystic fibrosis transmembrane conductance regulator that are associated with pancreatic sufficiency.

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Dissection of GLUT4 recycling pathway into exocytosis and endocytosis in rat adipocytes. Evidence that GTP-binding proteins are involved in both processes

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https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

Polarized sorting in epithelia

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

Mechanism by which Liddle's syndrome mutations increase activity of a human epithelial Na+ channel

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

Inhibition of rab5 GTPase activity stimulates membrane fusion in endocytosis

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

Cystic fibrosis gene mutation in two sisters with mild disease and normal sweat electrolyte levels

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

Expression of an abundant alternatively spliced form of the cystic fibrosis transmembrane conductance regulator (CFTR) gene is not associated with a cAMP-activated chloride conductance.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

CFTR as a cAMP-dependent regulator of sodium channels

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

The synaptic vesicle cycle: a cascade of protein-protein interactions

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

Identification of revertants for the cystic fibrosis delta F508 mutation using STE6-CFTR chimeras in yeast

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

Mechanism of adenylate kinase. Are the essential lysines essential?

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

Chloride channels: a state of flux.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

Exocytosis of vacuolar apical compartment (VAC): a cell-cell contact controlled mechanism for the establishment of the apical plasma membrane domain in epithelial cells

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

ATP alters current fluctuations of cystic fibrosis transmembrane conductance regulator: evidence for a three-state activation mechanism

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

Degradation of CFTR by the ubiquitin-proteasome pathway

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

The molecular chaperone calnexin binds Glc1Man9GlcNAc2 oligosaccharide as an initial step in recognizing unfolded glycoproteins

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

Subcellular localization of CFTR to endosomes in a ductal epithelium

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

CFTR: the nucleotide binding folds regulate the accessibility and stability of the activated state

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

The common variant of cystic fibrosis transmembrane conductance regulator is recognized by hsp70 and degraded in a pre-Golgi nonlysosomal compartment

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

Restoration of inactivation in mutants of Shaker potassium channels by a peptide derived from ShB.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

Intravesicular acidification correlates with binding of ADP-ribosylation factor to microsomal membranes

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

Cystic fibrosis: genotypic and phenotypic variations

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

Defective acidification of the biosynthetic pathway in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

Endosomal pathways for water channel and proton pump recycling in kidney epithelial cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7696%2808%2962361-X

7 January 2021

10.1016/S0074-7696(08)62361-X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9102394%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

1 reference