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...

Descripció completa

Dades bibliogràfiques

Publicat a:	Proc Natl Acad Sci U S A
Autors principals:	Clarke, L L, Grubb, B R, Yankaskas, J R, Cotton, C U, McKenzie, A, Boucher, R C
Format:	Artigo
Idioma:	Inglês
Publicat:	National Academy of Sciences 1994
Matèries:	Research Article
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC42972/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7507247/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.91.2.479
Etiquetes:	Afegir etiqueta Sense etiquetes, Sigues el primer a etiquetar aquest registre!