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Cited by 521

The DOI matches its Crossref record; 268 of the 268 references it cites were found in a registry or an index.

X Chromosome Dosage Compensation: How Mammals Keep the Balance

Payer, Bernhard, Lee, Jeannie T.·2008·Annual Review of Genetics

Abstract

The development of genetic sex determination and cytologically distinct sex chromosomes leads to the potential problem of gene dosage imbalances between autosomes and sex chromosomes and also between males and females. To circumvent these imbalances, mammals have developed an elaborate system of dosage compensation that includes both upregulation and repression of the X chromosome. Recent advances have provided insights into the evolutionary history of how both the imprinted and random forms of X chromosome inactivation have come about. Furthermore, our understanding of the epigenetic switch at the X-inactivation center and the molecular aspects of chromosome-wide silencing has greatly improved recently. Here, we review various facets of the ever-expanding field of mammalian dosage compensation and discuss its evolutionary, developmental, and mechanistic components.

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Crossref · 10.1146/annurev.genet.42.110807.091711

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Metadata

Authors
Payer, B., & Lee, J. T.
Venue
Annual Review of Genetics
Published
2008-12-01
Volume
42
Issue
1
Pages
733-772
ISSN
  • 0066-4197 (ISSN-L)
  • 1545-2948
OpenAlex
W2101378716
Cited by
521
References
268
FWCI
4.05
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: X Chromosome Dosage Compensation: How Mammals Keep the Balance. https://app.cochat.ai/papers/10.1146/annurev.genet.42.110807.091711
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Payer, B., & Lee, J. T. (2008). X Chromosome Dosage Compensation: How Mammals Keep the Balance. Annual Review of Genetics. https://doi.org/10.1146/annurev.genet.42.110807.091711

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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.