A translational preclinical model of interstitial pulmonary fibrosis and pulmonary hypertension: mechanistic pathways driving disease pathophysiology

Author:

Jarman Elizabeth R.1,Khambata Valerie S.1,Li Yun Ye1,Cheung Kenneth1,Thomas Matthew1,Duggan Nicholas1,Jarai Gabor1

Affiliation:

1. Respiratory Disease Area; Novartis Institutes for BioMedical Research; Horsham West Sussex UK

Funder

Novartis Institutes for Biomedical Research

Publisher

Wiley

Subject

Physiology (medical),Physiology

Reference61 articles.

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2. Activated MCTC mast cells infiltrate diseased lung areas in cystic fibrosis and idiopathic pulmonary fibrosis;Andersson;Respir. Res.,2011

3. Fibrocytes are a potential source of lung fibroblasts in idiopathic pulmonary fibrosis;Andersson-Sjoland;Int. J. Biochem. Cell Biol.,2008

4. Role of repeated lung injury and genetic background in bleomycin-induced fibrosis;Chung;Am. J. Respir. Cell Mol. Biol.,2003

5. Therapies for bleomycin induced lung fibrosis through regulation of transforming growth factor-beta 1 induced collagen gene expression;Cutroneo;J. Cell. Physiol.,2007

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