Corrective effects on airway epithelial function by human amniotic epithelial cells (HAEC) when treating cystic fibrosis

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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...

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Main Authors:	Kicic, Anthony, Ling, K., Martinovich, K., Garratt, L., Looi, K., Kicic-Starcevich, E., Iosifidis, T., Sutanto, E., Tarran, R., Cmielewski, P., Donnelley, M., Parsons, D., Stick, S., Moodley, Y.
Format:	Conference Paper
Published:	2015
Online Access:	http://hdl.handle.net/20.500.11937/57199

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