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Acid and Base Secretion in Freshly Excised Nasal Tissue From Cystic Fibrosis Patients with ΔF508 Mutation

Cystic fibrosis (CF) is caused by a misfunctional CFTR protein, which is believed to contributes to the regulation of the airway surface liquid (ASL) pH. This study investigated acid and base secretion in freshly excised human nasal tissues from CF patients homozygous for the ΔF508 mutation. Human n...

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Autores principales: Cho, Do-Yeon, Hwang, Peter H., Illek, Beate, Fischer, Horst
Formato: Artigo
Lenguaje:Inglês
Publicado: 2011
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3199580/
https://ncbi.nlm.nih.gov/pubmed/22034590
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/alr.20028
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