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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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Detalhes bibliográficos
Main Authors: Cho, Do-Yeon, Hwang, Peter H., Illek, Beate, Fischer, Horst
Formato: Artigo
Idioma:Inglês
Publicado em: 2011
Assuntos:
Acesso em linha: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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