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Airways in cystic fibrosis are acidified: detection by exhaled breath condensate
Background: The loss of cystic fibrosis transmembrane conductance regulator (CFTR) mediated chloride conductance does not fully explain the diverse pathologies evident in patients with cystic fibrosis (CF). Bicarbonate (HCO(3)(-)) secretion is also impaired in CFTR expressing tissues and CFTR is tho...
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| Autors principals: | , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BMJ Group
2002
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1746233/ https://ncbi.nlm.nih.gov/pubmed/12403872 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/thorax.57.11.926 |
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