(Q42809539)

7 November 2017

CFTR and outward rectifying chloride channels are distinct proteins with a regulatory relationship (English)

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7 November 2017

Gabriel SE

1

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7 November 2017

Clarke LL

series ordinal

2

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7 November 2017

Boucher RC

series ordinal

3

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7 November 2017

Stutts MJ

series ordinal

4

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7 November 2017

language of work or name

English

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publication date

1 May 1993

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7 November 2017

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7 November 2017

363

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7 November 2017

263-268

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7 November 2017

6426

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https://scigraph.springernature.com/pub.10.1038/363263a0

7 November 2017

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cites work

Abnormal Ion Permeation Through Cystic Fibrosis Respiratory Epithelium

1 reference

7 January 2021

Increased sulfation of glycoconjugates by cultured nasal epithelial cells from patients with cystic fibrosis

1 reference

7 January 2021

Cystic fibrosis: a disease in electrolyte transport.

1 reference

7 January 2021

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

1 reference

7 January 2021

Generation of cAMP-Activated Chloride Currents by Expression of CFTR

1 reference

7 January 2021

Identification and regulation of the cystic fibrosis transmembrane conductance regulator-generated chloride channel

1 reference

7 January 2021

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

1 reference

7 January 2021

Defective regulation of outwardly rectifying Cl- channels by protein kinase A corrected by insertion of CFTR

1 reference

7 January 2021

Altered regulation of airway epithelial cell chloride channels in cystic fibrosis

1 reference

7 January 2021

Regulation of chloride channels by protein kinase C in normal and cystic fibrosis airway epithelia

1 reference

7 January 2021

A cAMP-regulated chloride channel in lymphocytes that is affected in cystic fibrosis

1 reference

7 January 2021

Phosphorylation fails to activate chloride channels from cystic fibrosis airway cells

1 reference

7 January 2021

Cl- channels in CF: lack of activation by protein kinase C and cAMP-dependent protein kinase

1 reference

7 January 2021

(Dys)regulation of epithelial chloride channels

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7 January 2021

Persistence of abnormal chloride conductance regulation in transformed cystic fibrosis epithelia.

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7 January 2021

An animal model for cystic fibrosis made by gene targeting

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7 January 2021

Defective epithelial chloride transport in a gene-targeted mouse model of cystic fibrosis

1 reference

7 January 2021

Cystic fibrosis gene expression is not correlated with rectifying Cl- channels

1 reference

7 January 2021

Low-conductance chloride channel activated by cAMP in the epithelial cell line T84

1 reference

7 January 2021

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

1 reference

7 January 2021

Small linear chloride channels are endogenous to nonepithelial cells

1 reference

7 January 2021

Regulation of plasma membrane recycling by CFTR.

1 reference

7 January 2021

Regulation of Cl- channels in normal and cystic fibrosis airway epithelial cells by extracellular ATP

1 reference

7 January 2021

Identifiers

DOI

10.1038/363263A0

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Dimensions Publication ID

7 November 2017

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1 reference