Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 631

The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.

Stress granules and cell signaling: more than just a passing phase?

Open access
Kedersha, Nancy, Ivanov, Pavel, Anderson, Paul·2013·Trends in Biochemical Sciences

Abstract

Stress granules (SGs) contain translationally-stalled mRNAs, associated preinitiation factors and specific RNA-binding proteins. In addition, many signaling proteins are recruited to SGs and/or influence their assembly, which is transient, lasting only until the cells adapt to stress or die. Beyond their role as mRNA triage centers, we posit that SGs constitute RNA-centric signaling hubs analogous to classical multiprotein signaling domains such as transmembrane receptor complexes. As signaling centers, SG formation communicates a “state of emergency”, and their transient existence alters multiple signaling pathways by intercepting and sequestering signaling components. SG assembly and downstream signaling functions may require a cytosolic phase transition facilitated by intrinsically disordered, aggregation-prone protein regions shared by RNA-binding and signaling proteins.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1016/j.tibs.2013.07.004

Cites

9 of 9 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 9 references

Cited by

See all 631

Metadata

Authors
Kedersha, N., Ivanov, P., & Anderson, P.
Venue
Trends in Biochemical Sciences
Publisher
Elsevier BV
Published
2013-10
Volume
38
Issue
10
Pages
494-506
ISSN
0968-0004 (ISSN-L)
OpenAlex
W2007400675
Cited by
631
References
9
FWCI
3.02
Type
journal article
Language
en
Open access
green

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: Stress granules and cell signaling: more than just a passing phase? https://app.cochat.ai/papers/10.1016/j.tibs.2013.07.004
The paper
Kedersha, N., Ivanov, P., & Anderson, P. (2013). Stress granules and cell signaling: more than just a passing phase? Trends in Biochemical Sciences. https://doi.org/10.1016/j.tibs.2013.07.004

Data sources

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.