Airways in cystic fibrosis are acidified: detection by exhaled breath condensate (Q35534919)

8 August 2017

title

Airways in cystic fibrosis are acidified: detection by exhaled breath condensate (English)

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8 August 2017

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Tate S

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8 August 2017

MacGregor G

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8 August 2017

Davis M

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8 August 2017

Innes JA

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8 August 2017

Greening AP

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8 August 2017

language of work or name

English

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publication date

1 November 2002

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8 August 2017

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8 August 2017

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8 August 2017

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8 August 2017

page(s)

926-929

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Submucosal gland secretions in airways from cystic fibrosis patients have normal [Na(+)] and pH but elevated viscosity

8 August 2017

cites work

1 reference

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Acid exposure stimulates the adherence of Streptococcus pneumoniae to cultured human airway epithelial cells: effects on platelet-activating factor receptor expression

27 July 2018

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CFTR induces the expression of DRA along with Cl(-)/HCO(3)(-) exchange activity in tracheal epithelial cells

27 July 2018

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Endogenous airway acidification. Implications for asthma pathophysiology

27 July 2018

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Cystic fibrosis transmembrane conductance regulator regulates luminal Cl-/HCO3- exchange in mouse submandibular and pancreatic ducts

27 July 2018

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Nitrite levels in breath condensate of patients with cystic fibrosis is elevated in contrast to exhaled nitric oxide

27 July 2018

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HCO3-dependent pHi regulation in tracheal epithelial cells

27 July 2018

1 reference

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

27 July 2018

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Characterization of binding of Escherichia coli strains which are enteropathogens to small-bowel mucin

27 July 2018

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

27 July 2018

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Aberrant CFTR-dependent HCO3- transport in mutations associated with cystic fibrosis

27 July 2018

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Exhaled 8-isoprostane as a new non-invasive biomarker of oxidative stress in cystic fibrosis.

26 September 2018

1 reference

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Bicarbonate and chloride secretion in Calu-3 human airway epithelial cells

26 September 2018

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Role of CFTR in airway disease

26 September 2018

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

26 September 2018

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Endobronchial pH. Relevance of aminoglycoside activity in gram-negative bacillary pneumonia

26 September 2018

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12 December 2020

Impaired chloride secretion, as well as bicarbonate secretion, underlies the fluid secretory defect in the cystic fibrosis pancreas

1 reference

12 December 2020

Origins of chloride and bicarbonate secretory defects in the cystic fibrosis pancreas, as suggested by pancreatic function studies on control and CF subjects with preserved pancreatic function

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12 December 2020

Viscosity of human salivary mucins: effect of pH and ionic strength and role of sialic acid

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12 December 2020

Profound increase in viscosity and aggregation of pig gastric mucin at low pH

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12 December 2020

Influence of external pH on ciliary beat frequency in human bronchi and bronchioles

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12 December 2020

pH-regulated chloride secretion in fetal lung epithelia

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12 December 2020

Hydrogen peroxide and nitric oxide in exhaled air of children with cystic fibrosis during antibiotic treatment

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12 December 2020

Bronchial pH metrics in situ. Effects of hypoxia-hypercapnia

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12 December 2020

Identifiers

DOI

10.1136/THORAX.57.11.926

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8 August 2017

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8 August 2017

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