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Cited by 292

The DOI matches its Crossref record; 221 of the 221 references it cites were found in a registry or an index.

TGF‐β as a driver of fibrosis: physiological roles and therapeutic opportunities

Budi, Erine H, Schaub, Johanna R, Decaris, Martin, Turner, Scott, Derynck, Rik·2021·The Journal of Pathology

Abstract

Many chronic diseases are marked by fibrosis, which is defined by an abundance of activated fibroblasts and excessive deposition of extracellular matrix, resulting in loss of normal function of the affected organs. The initiation and progression of fibrosis are elaborated by pro‐fibrotic cytokines, the most critical of which is transforming growth factor‐β1 (TGF‐β1). This review focuses on the fibrogenic roles of increased TGF‐β activities and underlying signaling mechanisms in the activated fibroblast population and other cell types that contribute to progression of fibrosis. Insight into these roles and mechanisms of TGF‐β as a universal driver of fibrosis has stimulated the development of therapeutic interventions to attenuate fibrosis progression, based on interference with TGF‐β signaling. Their promise in preclinical and clinical settings will be discussed. © 2021 The Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

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Crossref · 10.1002/path.5680

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Metadata

Authors
Budi, E. H., Schaub, J. R., Decaris, M., Turner, S., & Derynck, R.
Venue
The Journal of Pathology
Publisher
Wiley
Published
2021-05-19
Volume
254
Issue
4
Pages
358-373
ISSN
  • 0022-3417 (ISSN-L)
  • 1096-9896
OpenAlex
W3149662796
Cited by
292
References
221
FWCI
10.87
Type
journal article
Language
en
Open access
closed

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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.