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Cited by 431

The DOI matches its Crossref record; 15 of the 15 references it cites were found in a registry or an index.

COX-2-Derived Prostacyclin Confers Atheroprotection on Female Mice

Egan, Karine M., Lawson, John A., Fries, Susanne, Koller, Beverley, Rader, Daniel J., Smyth, Emer M., FitzGerald, Garret A.·2004·Science

Abstract

Female gender affords relative protection from cardiovascular disease until the menopause. We report that estrogen acts on estrogen receptor subtype alpha to up-regulate the production of atheroprotective prostacyclin, PGI 2 , by activation of cyclooxygenase 2 (COX-2). This mechanism restrained both oxidant stress and platelet activation that contribute to atherogenesis in female mice. Deletion of the PGI 2 receptor removed the atheroprotective effect of estrogen in ovariectomized female mice. This suggests that chronic treatment of patients with selective inhibitors of COX-2 could undermine protection from cardiovascular disease in premenopausal females.

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Crossref · 10.1126/science.1103333

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Metadata

Authors
Egan, K. M., Lawson, J. A., Fries, S., Koller, B., Rader, D. J., Smyth, E. M., & FitzGerald, G. A.
Venue
Science
Published
2004-12-10
Volume
306
Issue
5703
Pages
1954-1957
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2055691692
Cited by
431
References
15
FWCI
24.05
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: COX-2-Derived Prostacyclin Confers Atheroprotection on Female Mice. https://app.cochat.ai/papers/10.1126/science.1103333
The paper
Egan, K. M., Lawson, J. A., Fries, S., Koller, B., Rader, D. J., Smyth, E. M., & FitzGerald, G. A. (2004). COX-2-Derived Prostacyclin Confers Atheroprotection on Female Mice. Science. https://doi.org/10.1126/science.1103333

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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.