Relationship of a non-cystic fibrosis transmembrane conductance regulator-mediated chloride conductance to organ-level disease in Cftr(-/-) mice.

Although loss of cystic fibrosis transmembrane conductance regulator (CFTR)-mediated Cl- channel function is common to all epithelia in cystic fibrosis (CF) patients, the severity of disease varies in different organs. We hypothesized that differences in disease severity in CF relate to the expressi...

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Detalhes bibliográficos
Main Authors: Clarke, L L, Grubb, B R, Yankaskas, J R, Cotton, C U, McKenzie, A, Boucher, R C
Formato: Artigo
Idioma:Inglês
Publicado em: 1994
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC42972/
https://ncbi.nlm.nih.gov/pubmed/7507247
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