抄録
Defective HCO3- and fluid secretion are hallmarks of the pathophysiology of the pancreas of cystic fibrosis patients. Recently, impaired HCO3- secretion has been shown in most tissues known to express the cystic fibrosis transmembrane conductance regulator (CFTR). New results suggest that CFTR plays an important role in the transcellular secretion of HCO3-.
本文言語 | English |
---|---|
ページ(範囲) | 38-42 |
ページ数 | 5 |
ジャーナル | News in Physiological Sciences |
巻 | 18 |
号 | 1 |
DOI | |
出版ステータス | Published - 2003 2 |
外部発表 | はい |
ASJC Scopus subject areas
- Physiology