Regulation of Cl-/ HCO3- exchange by cystic fibrosis transmembrane conductance regulator expressed in NIH 3T3 and HEK 293 cells (Q40977592)

25 September 2017

title

Regulation of Cl-/ HCO3- exchange by cystic fibrosis transmembrane conductance regulator expressed in NIH 3T3 and HEK 293 cells (English)

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25 September 2017

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transmembrane protein

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25 September 2017

Wigley WC

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25 September 2017

Zeng W

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25 September 2017

Noel LE

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25 September 2017

Marino CR

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25 September 2017

Thomas PJ

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25 September 2017

Muallem S

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25 September 2017

language of work or name

English

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publication date

1 February 1999

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Journal of Biological Chemistry

25 September 2017

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inferred from page(s)

published in

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25 September 2017

volume

274

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25 September 2017

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25 September 2017

page(s)

3414-3421

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Cl- conductance and acid secretion in the human sweat duct

25 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3414

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.274.6.3414

Chloride impermeability in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3414

Generation of cAMP-Activated Chloride Currents by Expression of CFTR

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3414

Understanding how cystic fibrosis mutations cause a loss of Cl- channel function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3414

cAMP stimulates bicarbonate secretion across normal, but not cystic fibrosis airway epithelia

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3414

A functional CFTR protein is required for mouse intestinal cAMP-, cGMP- and Ca(2+)-dependent HCO3- secretion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3414

Membrane localization of H+ and HCO3- transporters in the rat pancreatic duct

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3414

Chloride channels and cystic fibrosis of the pancreas

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3414

Acid-stimulated duodenal bicarbonate secretion involves a CFTR-mediated transport pathway in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3414

A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3414

Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3414

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3414

Defective protein folding as a basis of human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3414

Degradation of CFTR by the ubiquitin-proteasome pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3414

Intracellular Ca2+ stores in chicken Purkinje neurons: differential distribution of the low affinity-high capacity Ca2+ binding protein, calsequestrin, of Ca2+ ATPase and of the ER lumenal protein, Bip

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3414

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3414

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3414

Regulation of KATP channel activity by diazoxide and MgADP. Distinct functions of the two nucleotide binding folds of the sulfonylurea receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3414

CFTR as a cAMP-dependent regulator of sodium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3414

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.274.6.3414

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.274.6.3414

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3414

Cystic fibrosis transmembrane conductance regulator activates water conductance in Xenopus oocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3414

Characterization and Localization of P2Receptors in Rat Submandibular Gland Acinar and Duct Cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.6.3414

21 January 2018

Identifiers

DOI

10.1074/JBC.274.6.3414

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25 September 2017

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