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Cited by 294

The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.

Re‐programming of translation following cell stress allows IRES‐mediated translation to predominate

Spriggs, Keith A., Stoneley, Mark, Bushell, Martin, Willis, Anne E.·2008·Biology of the Cell

Abstract

There is now an overwhelming body of evidence to suggest that internal ribosome entry is required to maintain the expression of specific proteins during patho‐physiological situations when cap‐dependent translation is compromised, for example, following heat shock or during mitosis, hypoxia, differentiation and apoptosis. Translational profiling has been used by several groups to assess the extent to which alternative mechanisms of translation initiation selectively recruit mRNAs to polysomes during cell stress. The data from these studies have shown that under each condition 3–5% of coding mRNAs remain associated with the polysomes. Importantly, the genes identified in each of these studies do not show a significant amount of overlap, suggesting that 10–15% of all mRNAs have the capability for their initiation to occur via alternative mechanism(s).

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Crossref · 10.1042/bc20070098

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Metadata

Authors
Spriggs, K. A., Stoneley, M., Bushell, M., & Willis, A. E.
Venue
Biology of the Cell
Publisher
Wiley
Published
2008-01
Volume
100
Issue
1
Pages
27-38
ISSN
  • 0248-4900 (ISSN-L)
  • 1768-322X
OpenAlex
W1964221844
Cited by
294
References
7
FWCI
5.87
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Re‐programming of translation following cell stress allows IRES‐mediated translation to predominate. https://app.cochat.ai/papers/10.1042/bc20070098
The paper
Spriggs, K. A., Stoneley, M., Bushell, M., & Willis, A. E. (2008). Re‐programming of translation following cell stress allows IRES‐mediated translation to predominate. Biology of the Cell. https://doi.org/10.1042/bc20070098

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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.