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Cited by 557

The DOI matches its Crossref record; 87 of the 87 references it cites were found in a registry or an index.

IRE1: ER stress sensor and cell fate executor

Open access
Chen, Yani, Brandizzi, Federica·2013·Trends in Cell Biology

Abstract

Cells operate a signaling network termed unfolded protein response (UPR) to monitor protein-folding capacity in the endoplasmic reticulum (ER). IRE1 is an ER transmembrane sensor that activates UPR to maintain ER and cellular function. While mammalian IRE1 promotes cell survive, it can initiate apoptosis via decay of anti-apoptotic microRNAs. Convergent and divergent IRE1 characteristics between plants and animals underscore its significance in cellular homeostasis. This review provides an updated scenario of IRE1 signaling model, discusses emerging IRE1 sensing mechanisms, compares IRE1 features among species, and outlines exciting future directions in UPR research.

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Crossref · 10.1016/j.tcb.2013.06.005

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Metadata

Authors
Chen, Y., & Brandizzi, F.
Venue
Trends in Cell Biology
Publisher
Elsevier BV
Published
2013-11
Volume
23
Issue
11
Pages
547-555
ISSN
0962-8924 (ISSN-L)
OpenAlex
W1973400283
Cited by
557
References
87
FWCI
3.35
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: IRE1: ER stress sensor and cell fate executor. https://app.cochat.ai/papers/10.1016/j.tcb.2013.06.005
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Chen, Y., & Brandizzi, F. (2013). IRE1: ER stress sensor and cell fate executor. Trends in Cell Biology. https://doi.org/10.1016/j.tcb.2013.06.005

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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.