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Cited by 450

The DOI matches its Crossref record; 134 of the 134 references it cites were found in a registry or an index.

Micronuclei in genotoxicity assessment: from genetics to epigenetics and beyond

Open access
Luzhna, Lidiya, Kathiria, Palak, Kovalchuk, Olga·2013·Frontiers in Genetics

Abstract

Micronuclei (MN) are extra-nuclear bodies that contain damaged chromosome fragments and/or whole chromosomes that were not incorporated into the nucleus after cell division. MN can be induced by defects in the cell repair machinery and accumulation of DNA damages and chromosomal aberrations. A variety of genotoxic agents may induce MN formation leading to cell death, genomic instability, or cancer development. In this review, the genetic and epigenetic mechanisms of MN formation after various clastogenic and aneugenic effects on cell division and cell cycle are described. The knowledge accumulated in literature on cytotoxicity of various genotoxins is precisely reflected and individual sensitivity to MN formation due to single gene polymorphisms is discussed. The importance of rapid MN scoring with respect to the cytokinesis-block micronucleus assay is also evaluated.

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Metadata

Authors
Luzhna, L., Kathiria, P., & Kovalchuk, O.
Venue
Frontiers in Genetics
Published
2013
Volume
4
Pages
131-131
ISSN
1664-8021 (ISSN-L)
OpenAlex
W2103013707
Cited by
450
References
134
FWCI
3.93
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Micronuclei in genotoxicity assessment: from genetics to epigenetics and beyond. https://app.cochat.ai/papers/10.3389/fgene.2013.00131
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Luzhna, L., Kathiria, P., & Kovalchuk, O. (2013). Micronuclei in genotoxicity assessment: from genetics to epigenetics and beyond. Frontiers in Genetics. https://doi.org/10.3389/fgene.2013.00131

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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.