HT29 cells endogenously express the cystic fibrosis transmembrane conductance regulator (CFTR) and have been used previously as a model to examine cellular regulation of CFTR expression and chloride secretory function. Homologous recombination has been used to specifically disrupt CFTR transcription
β¦ LIBER β¦
CFTR and lysozyme secretion in human airway epithelial cells
β Scribed by M. Duszyk
- Publisher
- Springer
- Year
- 2001
- Tongue
- English
- Weight
- 209 KB
- Volume
- 443
- Category
- Article
- ISSN
- 0031-6768
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