Spatiotemporal regulation of anti-remodelling signalling pathways in primary human lung fibroblasts
Idiopathic pulmonary fibrosis (IPF) is a devastating chronic lung disease caused by a dysregulated wound healing process that results in fibrosis and scarring of lung tissue rather than repair. Current approved IPF therapeutics target multiple known fibrotic mediators and pathways, however this mult...
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| Format: | Thesis (University of Nottingham only) |
| Language: | English |
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2020
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| Online Access: | https://eprints.nottingham.ac.uk/59568/ |