Is Cystic Fibrosis Lung Disease Caused by Abnormal Ion Composition or Abnormal Volume?

Por Krouse, Mauri E.
Publicado em 2001

Inhibition of airway surface fluid absorption by cholinergic stimulation

Por Joo, Nam Soo, Krouse, Mauri E., Choi, Jae Young, Cho, Hyung-Ju, Wine, Jeffrey J.
Publicado no Sci Rep (2016)

Substance P stimulates human airway submucosal gland secretion mainly via a CFTR-dependent process

Por Choi, Jae Young, Khansaheb, Monal, Joo, Nam Soo, Krouse, Mauri E., Robbins, Robert C., Weill, David, Wine, Jeffrey J.
Publicado em 2009

Substance P stimulates human airway submucosal gland secretion mainly via a CFTR-dependent process

Por Choi, Jae Young, Khansaheb, Monal, Joo, Nam Soo, Krouse, Mauri E., Robbins, Robert C., Weill, David, Wine, Jeffrey J.
Publicado em 2010

Synergistic airway gland mucus secretion in response to vasoactive intestinal peptide and carbachol is lost in cystic fibrosis

Por Choi, Jae Young, Joo, Nam Soo, Krouse, Mauri E., Wu, Jin V., Robbins, Robert C., Ianowski, Juan P., Hanrahan, John W., Wine, Jeffrey J.
Publicado em 2007