Role of CFTR and MRP1 in determining intra-and extra- cellular glutathione in Calu-3 cells
Cystic Fibrosis (CF), the most common fatal genetic disorder, is due to mutations of the cystic fibrosis transmembrane regulator protein (CFTR). Loss of functional CFTR leads to mucus thickening with the consequences of chronic pulmonary infection and inflammation, the most common fatal complication...
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| Format: | Others |
| Language: | en |
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McGill University
2009
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| Online Access: | http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=40733 |