(Q40481982)

20 September 2017

title

Erythrocytes of humans with cystic fibrosis fail to stimulate nitric oxide synthesis in isolated rabbit lungs. (English)

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20 September 2017

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Griffith Liang

1

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20 September 2017

Alan H Stephenson

series ordinal

2

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20 September 2017

Andrew J Lonigro

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3

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20 September 2017

Randy S Sprague

series ordinal

4

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20 September 2017

publication date

9 December 2004

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American Journal of Physiology Heart and Circulatory Physiology

20 September 2017

published in

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20 September 2017

volume

288

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20 September 2017

issue

4

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20 September 2017

page(s)

H1580-5

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Erythrocyte membrane ATP binding cassette (ABC) proteins: MRP1 and CFTR as well as CD39 (ecto-apyrase) involved in RBC ATP transport and elevated blood plasma ATP of cystic fibrosis

20 September 2017

cites work

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https://api.crossref.org/works/10.1152%2FAJPHEART.00807.2004

Reduced upper airway nitric oxide in cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00807.2004

Shear stress-induced release of nitric oxide from endothelial cells grown on beads

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00807.2004

Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00807.2004

Ibuprofen inhibits cystic fibrosis transmembrane conductance regulator-mediated Cl- secretion

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00807.2004

Exhaled nitric oxide is reduced in infants with cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00807.2004

The obligatory role of endothelial cells in the relaxation of arterial smooth muscle by acetylcholine

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00807.2004

Tetrodotoxin-sensitive Na+ channels and muscarinic and purinergic receptors identified in human erythroid progenitor cells and red blood cell ghosts

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00807.2004

EDRF generation and release from perfused bovine pulmonary artery and vein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00807.2004

Exhaled nitric oxide in paediatric asthma and cystic fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00807.2004

Nitric oxide release accounts for the biological activity of endothelium-derived relaxing factor

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00807.2004

Failure of the cystic fibrosis transmembrane conductance regulator to conduct ATP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00807.2004

CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00807.2004

Effect of ATP-sensitive K+ channel regulators on cystic fibrosis transmembrane conductance regulator chloride currents

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00807.2004

Inhibition of the cystic fibrosis transmembrane conductance regulator by ATP-sensitive K+ channel regulators

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00807.2004

Extracellular ATP signaling in the rabbit lung: erythrocytes as determinants of vascular resistance

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00807.2004

Effect of L-NAME on pressure-flow relationships in isolated rabbit lungs: role of red blood cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00807.2004

Cystic fibrosis transmembrane conductance regulator in human and mouse red blood cell membranes and its interaction with ecto-apyrase

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00807.2004

Localization of cystic fibrosis transmembrane conductance regulator mRNA in the human gastrointestinal tract by in situ hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00807.2004

Plasmodium falciparum-activated chloride channels are defective in erythrocytes from cystic fibrosis patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPHEART.00807.2004

10.1152/AJPHEART.00807.2004

21 January 2018

Identifiers

DOI

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20 September 2017

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