Spatiotemporal regulation of anti-remodelling signalling pathways in primary human lung fibroblasts

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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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Bibliographic Details
Main Author:	Roberts, Maxine
Format:	Thesis (University of Nottingham only)
Language:	English
Published:	2020
Subjects:	cAMP elevating agents; Novel therapeutic agents; Lung fibroblasts; Idiopathic pulmonary fibrosis
Online Access:	https://eprints.nottingham.ac.uk/59568/

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