(Q30630605)

25 June 2017

title

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

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25 June 2017

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transmembrane protein

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author name string

Schreiber R

1

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25 June 2017

Nitschke R

2

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25 June 2017

Greger R

3

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25 June 2017

Kunzelmann K

4

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25 June 2017

language of work or name

English

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publication date

1 April 1999

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Journal of Biological Chemistry

25 June 2017

published in

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25 June 2017

volume

274

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25 June 2017

issue

17

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25 June 2017

page(s)

11811-11816

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CFTR as a cAMP-dependent regulator of sodium channels

25 June 2017

cites work

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https://api.crossref.org/works/10.1074%2FJBC.274.17.11811

The cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.11811

Regulation of epithelial ion channels by the cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.11811

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.11811

Cystic fibrosis: gastrointestinal complications

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.11811

Evidence for reduced Cl- and increased Na+ permeability in cystic fibrosis human primary cell cultures.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.11811

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/10.1074%2FJBC.274.17.11811

A Multifunctional Aqueous Channel Formed by CFTR

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.11811

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.11811

CFTR expression and chloride secretion in polarized immortal human bronchial epithelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.11811

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.11811

Effect of intracellular pH on agonist-induced [Ca2+]i transients in HT29 cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.11811

Heteromultimeric CLC chloride channels with novel properties

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.11811

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/10.1074%2FJBC.274.17.11811

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/10.1074%2FJBC.274.17.11811

Pathophysiology of the aquaporin water channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.11811

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/10.1074%2FJBC.274.17.11811

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/10.1074%2FJBC.274.17.11811

Structure and chromosomal localization of a human water channel (AQP3) gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.11811

Regulation of human airway surface liquid

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.11811

Fluid transport across cultures of human tracheal glands is altered in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.11811

Expression of the cystic fibrosis gene in adult human lung

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.11811

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/10.1074%2FJBC.274.17.11811

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/10.1074%2FJBC.274.17.11811

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/10.1074%2FJBC.274.17.11811

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/10.1074%2FJBC.274.17.11811

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/10.1074%2FJBC.274.17.11811

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.11811

Na+ and Cl? conductances in airway epithelial cells: increased Na+ conductance in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.17.11811

21 January 2018

Identifiers

DOI

10.1074/JBC.274.17.11811

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25 June 2017

1 reference