The DOI matches its Crossref record; 18 of the 18 references it cites were found in a registry or an index.
Pathogenesis of Idiopathic Pulmonary Fibrosis
Open accessAbstract
Idiopathic pulmonary fibrosis (IPF) is a fibrosing interstitial lung disease associated with aging that is characterized by the histopathological pattern of usual interstitial pneumonia. Although an understanding of the pathogenesis of IPF is incomplete, recent advances delineating specific clinical and pathologic features of IPF have led to better definition of the molecular pathways that are pathologically activated in the disease. In this review we highlight several of these advances, with a focus on genetic predisposition to IPF and how genetic changes, which occur primarily in epithelial cells, lead to activation of profibrotic pathways in epithelial cells. We then discuss the pathologic changes within IPF fibroblasts and the extracellular matrix, and we conclude with a summary of how these profibrotic pathways may be interrelated.
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Cites
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“mutation and a frameshift V747fs mutation in the probands of the two kindreds (34).”
Short telomeres are a risk factor for idiopathic pulmonary fibrosis
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Metadata
- Authors
- Wolters, P. J., Collard, H. R., & Jones, K. D.
- Venue
- Annual Review of Pathology: Mechanisms of Disease
- Publisher
- Annual Reviews
- Published
- 2014-01-24
- Volume
- 9
- Issue
- 1
- Pages
- 157-179
- ISSN
- 1553-4006 (ISSN-L)
- 1553-4014
- OpenAlex
- W2101960743
- Cited by
- 862
- References
- 18
- FWCI
- 6.16
- Type
- journal article
- Language
- en
- Open access
- bronze
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