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In vitro Methods for the Development and Analysis of Human Primary Airway Epithelia
Cystic fibrosis (CF) is a chronic disease caused by mutations in the CF transmembrane conductance regulator (CFTR) gene, which encodes for a channel expressed at the apical surface of epithelial tissues. Defective chloride and bicarbonate secretion, arising from CFTR mutations, cause a multi-organ d...
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| I publikationen: | Front Pharmacol |
|---|---|
| Huvudupphovsmän: | , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Frontiers Media S.A.
2018
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6212516/ https://ncbi.nlm.nih.gov/pubmed/30416443 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphar.2018.01176 |
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