(Q48887641)

16 February 2018

title

Aquaporin 3 cloned from Xenopus laevis is regulated by the cystic fibrosis transmembrane conductance regulator. (English)

1 reference

16 February 2018

main subject

cystic fibrosis

0 references

transmembrane protein

0 references

1 reference

4

1 reference

16 February 2018

author name string

Schreiber R

series ordinal

1

1 reference

16 February 2018

Pavenstädt H

series ordinal

2

1 reference

16 February 2018

Greger R

series ordinal

3

1 reference

16 February 2018

language of work or name

English

0 references

publication date

1 June 2000

1 reference

16 February 2018

published in

FEBS Letters

1 reference

16 February 2018

volume

475

1 reference

16 February 2018

page(s)

291-295

1 reference

16 February 2018

issue

3

1 reference

16 February 2018

CFTR as a cAMP-dependent regulator of sodium channels

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

cAMP stimulation of CFTR-expressing Xenopus oocytes activates a chromanol-inhibitable K+ conductance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

An apical PDZ protein anchors the cystic fibrosis transmembrane conductance regulator to the cytoskeleton

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

The first-nucleotide binding domain of the cystic-fibrosis transmembrane conductance regulator is important for inhibition of the epithelial Na+ channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

Cystic fibrosis transmembrane conductance regulator activates water conductance in Xenopus oocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

The cystic fibrosis transmembrane conductance regulator activates aquaporin 3 in airway epithelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

The cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

A Multifunctional Aqueous Channel Formed by CFTR

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

Heteromultimeric CLC chloride channels with novel properties

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

Inhibition of epithelial Na+ currents by intracellular domains of the cystic fibrosis transmembrane conductance regulator.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

Expression of multiple water channel activities in Xenopus oocytes injected with mRNA from rat kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

Molecular cloning and expression of a member of the aquaporin family with permeability to glycerol and urea in addition to water expressed at the basolateral membrane of kidney collecting duct cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

Cloning and expression of AQP3, a water channel from the medullary collecting duct of rat kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

Chloride channel and chloride conductance regulator domains of CFTR, the cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

Regulation of human airway surface liquid

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

Wild type but not deltaF508 CFTR inhibits Na+ conductance when coexpressed in Xenopus oocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

Sensitivity of a renal K+ channel (ROMK2) to the inhibitory sulfonylurea compound glibenclamide is enhanced by coexpression with the ATP-binding cassette transporter cystic fibrosis transmembrane regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

Novel subunit composition of a renal epithelial KATP channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

Cystic fibrosis transmembrane conductance regulator mediates sulphonylurea block of the inwardly rectifying K+ channel Kir6.1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

Cl- transport by cystic fibrosis transmembrane conductance regulator (CFTR) contributes to the inhibition of epithelial Na+ channels (ENaCs) in Xenopus oocytes co-expressing CFTR and ENaC.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

CFTR, a regulator of channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

Regulation of epithelial sodium channels by the cystic fibrosis transmembrane conductance regulator.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

Peptide binding consensus of the NHE-RF-PDZ1 domain matches the C-terminal sequence of cystic fibrosis transmembrane conductance regulator (CFTR)

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

Intrinsic anion channel activity of the recombinant first nucleotide binding fold domain of the cystic fibrosis transmembrane regulator protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

The amiloride-inhibitable Na+ conductance is reduced by the cystic fibrosis transmembrane conductance regulator in normal but not in cystic fibrosis airways.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

Aquaporin water channels in gastrointestinal physiology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

Sequence homologies between nucleotide binding regions of CFTR and G-proteins suggest structural and functional similarities

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

CFTR is a conductance regulator as well as a chloride channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

Mechanisms of renal tubular cell hypertrophy: mitogen-induced suppression of proteolysis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

Triple-barrel organization of ENaC, a cloned epithelial Na+ channel.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

Localization of Aquaporin-3 mRNA and protein along the gastrointestinal tract of Wistar rats

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901689-6

10.1016/S0014-5793(00)01689-6

7 January 2021

Identifiers

DOI

1 reference

16 February 2018

release_6nrqb2orlzflje4kcr36f7tzoe

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/6nrqb2orlzflje4kcr36f7tzoe

mapped directly with Wikidata item

24 November 2022

based on heuristic

PubMed ID

10869574

1 reference

16 February 2018