Examining basal chloride transport using the nasal potential difference response in a murine model (Q42511337)

1 November 2017

Examining basal chloride transport using the nasal potential difference response in a murine model (English)

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1 November 2017

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Brady KG

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1 November 2017

Kelley TJ

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2

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1 November 2017

Drumm ML

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3

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1 November 2017

1 November 2001

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American Journal of Physiology - Lung Cellular and Molecular Physiology

1 November 2017

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1 November 2017

281

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1 November 2017

L1173-9

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1 November 2017

5

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Generation of cAMP-Activated Chloride Currents by Expression of CFTR

1 November 2017

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https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

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

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

Characterization of human sweat duct chloride conductance by chloride channel blockers

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

cAMP-stimulated ion currents in Xenopus oocytes expressing CFTR cRNA

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

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

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

Differential expression of ORCC and CFTR induced by low temperature in CF airway epithelial cells

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

Hyperabsorption of Na+ and raised Ca(2+)-mediated Cl- secretion in nasal epithelia of CF mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

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

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

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

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

In vivo alterations of IFN regulatory factor-1 and PIAS1 protein levels in cystic fibrosis epithelium

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

In vivo activation of the cystic fibrosis transmembrane conductance regulator mutant deltaF508 in murine nasal epithelium

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

Identification of the cystic fibrosis gene: genetic analysis

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

Relative ion permeability of normal and cystic fibrosis nasal epithelium

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

In vivo nasal potential difference: techniques and protocols for assessing efficacy of gene transfer in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

Voltage-dependent block of the cystic fibrosis transmembrane conductance regulator Cl- channel by two closely related arylaminobenzoates

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

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/10.1152%2FAJPLUNG.2001.281.5.L1173

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

Identification of the cystic fibrosis gene: chromosome walking and jumping

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

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

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

Colonic Cl channel blockade by three classes of compounds

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

Bioelectric characteristics of exon 10 insertional cystic fibrosis mouse: comparison with humans

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

Cystic fibrosis transmembrane conductance regulator-dependent regulation of epithelial inducible nitric oxide synthase expression

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

CFTR as a cAMP-dependent regulator of sodium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

Cl(-)-channel blockers in the thick ascending limb of the loop of Henle. Structure activity relationship

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

A mouse model for the delta F508 allele of cystic fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

Direct comparison of NPPB and DPC as probes of CFTR expressed in Xenopus oocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPLUNG.2001.281.5.L1173

10.1152/AJPLUNG.2001.281.5.L1173

21 January 2018

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