Refining in-vivo models of pulmonary fibrosis
Idiopathic pulmonary fibrosis (IPF) is a progressive disease with limited treatment options. IPF is characterized by excessive collagen deposition within the lung resulting in loss of lung function and a survival rate worse than most cancers. There is an urgent need to develop and better characteris...
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| Format: | Thesis (University of Nottingham only) |
| Language: | English |
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2018
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| Online Access: | https://eprints.nottingham.ac.uk/55561/ |