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Cited by 380

The DOI matches its Crossref record; 98 of the 98 references it cites were found in a registry or an index.

Hormetic mechanisms

Calabrese, Edward J.·2013·Critical Reviews in Toxicology

Abstract

This article provides the first extensive documentation of mechanisms of hormetic dose/concentration responses. The mechanisms selected were principally those mediated via receptor and/or cell signaling pathways. Mechanisms are reported for greater than 100 agents affecting nearly 400 dose/concentration responses from a wide range of chemical classes, affecting a broad range of cell types and endpoints. Regardless of the model (i.e. in vitro or in vivo), inducing agent, endpoint, or receptor/cell signaling pathway mediated mechanism, the quantitative features of the hormetic dose/concentration responses are similar, suggesting that the magnitude of the response is a measure of biological plasticity, within a broad range of biological contexts. These findings represent an important advance in the understanding of the hormetic dose/concentration response, its generalizability and potential biomedical applications, including drug discovery/efficacy assessment and the risk assessment process.

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Metadata

Authors
Calabrese, E. J.
Venue
Critical Reviews in Toxicology
Published
2013-07-23
Volume
43
Issue
7
Pages
580-606
ISSN
  • 0045-6446 (ISSN-L)
  • 1040-8444
  • 1547-6898
OpenAlex
W4233403863
Cited by
380
References
98
FWCI
21.15
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Hormetic mechanisms. https://app.cochat.ai/papers/10.3109/10408444.2013.808172
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Calabrese, E. J. (2013). Hormetic mechanisms. Critical Reviews in Toxicology. https://doi.org/10.3109/10408444.2013.808172

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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.