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The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

Translational Control of p27 Kip1 Accumulation During the Cell Cycle

Hengst, Ludger, Reed, Steven I.·1996·Science

Abstract

Cell cycle phase transitions in eukaryotic cells are driven by regulation of the activity of protein kinases known as cyclin-dependent kinases (Cdks). A broad spectrum Cdk-inhibitory activity associated with a 28-kilodalton protein (p28 Ick1 ) was induced in cells treated with the drug lovastatin or upon density-mediated growth arrest and was periodic in the cell cycle, with peak activity in G 1 . The p28 Ick1 protein was shown to be identical to p27 Kip1 , and the periodic or induced inhibitory activity resulted from a periodic accumulation of the protein. Variations in the amount of p27 protein occurred, whereas the abundance of the p27 messenger RNA remained unchanged. In every instance investigated, the posttranscriptional alteration of p27 protein levels was achieved in part by a mechanism of translational control, although in density-arrested fibroblasts and thymidine-arrested HeLa cells the half-life of the protein was also changed.

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Crossref · 10.1126/science.271.5257.1861

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Metadata

Authors
Hengst, L., & Reed, S. I.
Venue
Science
Published
1996-03-29
Volume
271
Issue
5257
Pages
1861-1864
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W1980123375
Cited by
846
References
3
FWCI
33.78
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Translational Control of p27 Kip1 Accumulation During the Cell Cycle. https://app.cochat.ai/papers/10.1126/science.271.5257.1861
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Hengst, L., & Reed, S. I. (1996). Translational Control of p27 Kip1 Accumulation During the Cell Cycle. Science. https://doi.org/10.1126/science.271.5257.1861

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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.