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A transcription factor network represses CFTR gene expression in airway epithelial cells.

Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene cause the inherited disorder cystic fibrosis (CF). Lung disease is the major cause of CF morbidity, though CFTR expression levels are substantially lower in the airway epithelium than in pancreatic duct and intestinal e...

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Dettagli Bibliografici
Pubblicato in:Biochem J
Autori principali: Mutolo, Michael J., Leir, Shih-Hsing, Fossum, Sara L, Browne, James A, Harris, Ann
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2018
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6380350/
https://ncbi.nlm.nih.gov/pubmed/29572268
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BCJ20180044
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