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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| Main Authors: | , , |
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| Format: | Book |
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Frontiers Media S.A.,
2018-10-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |