Bioelectric Characterization of Epithelia from Neonatal CFTR Knockout Ferrets

Cystic fibrosis (CF) is a life-shortening, recessive, multiorgan genetic disorder caused by the loss of CF transmembrane conductance regulator (CFTR) chloride channel function found in many types of epithelia. Animal models that recapitulate the human disease phenotype are critical to understanding...

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Detalhes bibliográficos
Main Authors: Fisher, John T., Tyler, Scott R., Zhang, Yulong, Lee, Ben J., Liu, Xiaoming, Sun, Xingshen, Sui, Hongshu, Liang, Bo, Luo, Meihui, Xie, Weiliang, Yi, Yaling, Zhou, Weihong, Song, Yi, Keiser, Nicholas, Wang, Kai, de Jonge, Hugo R., Engelhardt, John F.
Formato: Artigo
Idioma:Inglês
Publicado em: American Thoracic Society 2013
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3931095/
https://ncbi.nlm.nih.gov/pubmed/23782101
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1165/rcmb.2012-0433OC
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