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Cited by 379

The DOI matches its Crossref record; 85 of the 85 references it cites were found in a registry or an index.

Idiopathic pulmonary fibrosis: an epithelial/fibroblastic cross-talk disorder

Open access
Selman, Moisés, Pardo, Annie·2001·Respiratory Research

Abstract

Idiopathic pulmonary fibrosis is a chronic and usually progressive lung disorder of unknown etiology. A growing body of evidence suggests that, in contrast to other interstitial lung diseases, IPF is a distinct entity in which inflammation is a secondary and non-relevant pathogenic partner. Evidence includes the presence of similar mild/moderate inflammation either in early or late disease, and the lack of response to potent anti-inflammatory therapy. Additionally, it is clear from experimental models and some human diseases that it is possible to have fibrosis without inflammation. An evolving hypothesis proposes that IPF may result from epithelial micro-injuries and abnormal wound healing.

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Crossref · 10.1186/rr175

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Metadata

Authors
Selman, M., & Pardo, A.
Venue
Respiratory Research
Published
2001-10-11
Volume
3
Issue
1
Pages
3-3
ISSN
  • 1465-9921 (ISSN-L)
  • 1465-993X
OpenAlex
W1585502126
Cited by
379
References
85
FWCI
7.72
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Idiopathic pulmonary fibrosis: an epithelial/fibroblastic cross-talk disorder. https://app.cochat.ai/papers/10.1186/rr175
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Selman, M., & Pardo, A. (2001). Idiopathic pulmonary fibrosis: an epithelial/fibroblastic cross-talk disorder. Respiratory Research. https://doi.org/10.1186/rr175

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.