Corrective effects on airway epithelial function by human amniotic epithelial cells (HAEC) when treating cystic fibrosis
Background: Cystic fibrosis (CF) remains the most common life-shortening genetic disease affecting children. The defective protein product of the affected gene, cystic fibrosis transmembrane conductance regulator (CFTR), blocks Cl - and water absorption into the airway epithelium resulting in a r...
| Main Authors: | , , , , , , , , , , , , , |
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| Format: | Conference Paper |
| Published: |
2015
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| Online Access: | http://hdl.handle.net/20.500.11937/57199 |