(Q45200858)

10 December 2017

title

The effect of varying tonicity on nasal epithelial ion transport in cystic fibrosis (English)

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10 December 2017

Michael G Davies

1

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10 December 2017

Duncan M Geddes

series ordinal

2

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10 December 2017

Eric W F W Alton

series ordinal

3

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10 December 2017

language of work or name

English

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publication date

23 December 2004

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American Journal of Respiratory and Critical Care Medicine

10 December 2017

published in

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10 December 2017

volume

171

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10 December 2017

issue

7

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10 December 2017

page(s)

760-763

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Ion composition of airway surface liquid of patients with cystic fibrosis as compared with normal and disease-control subjects

10 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200310-1423OC

Harvesting airway surface liquid: a comparison of two techniques

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200310-1423OC

Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200310-1423OC

Sodium and chloride concentrations, pH, and depth of airway surface liquid in distal airways

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200310-1423OC

Loss of CFTR chloride channels alters salt absorption by cystic fibrosis airway epithelia in vitro.

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200310-1423OC

The genesis of cystic fibrosis lung disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200310-1423OC

Cystic fibrosis airway epithelia fail to kill bacteria because of abnormal airway surface fluid.

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200310-1423OC

Hyperventilation with dry air increases airway surface fluid osmolality in canine peripheral airways.

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200310-1423OC

Effect of exercise on the nasal transmucosal potential difference in patients with cystic fibrosis and normal subjects

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200310-1423OC

Exercise inhibits epithelial sodium channels in patients with cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200310-1423OC

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200310-1423OC

Expression and characterization of the cystic fibrosis transmembrane conductance regulator.

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200310-1423OC

Cystic fibrosis transmembrane conductance regulator-associated ATP release is controlled by a chloride sensor

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200310-1423OC

Selective response of human airway epithelia to luminal but not serosal solution hypertonicity. Possible role for proximal airway epithelia as an osmolality transducer

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200310-1423OC

Defective regulatory volume decrease in human cystic fibrosis tracheal cells because of altered regulation of intermediate conductance Ca2+-dependent potassium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200310-1423OC

Nasal application of the cationic liposome DC-Chol:DOPE does not alter ion transport, lung function or bacterial growth

21 January 2018

1 reference

https://api.crossref.org/works/10.1164%2FRCCM.200310-1423OC

10.1164/RCCM.200310-1423OC

21 January 2018

Identifiers

DOI

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10 December 2017

1 reference