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Cited by 459

The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.

mRNP granules: Assembly, function, and connections with disease

Open access
Buchan, J Ross·2014·RNA Biology

Abstract

Messenger ribonucleoprotein (mRNP) granules are dynamic, self-assembling structures that harbor non-translating mRNAs bound by various proteins that regulate mRNA translation, localization, and turnover. Their importance in gene expression regulation is far reaching, ranging from precise spatial-temporal control of mRNAs that drive developmental programs in oocytes and embryos, to similarly exquisite control of mRNAs in neurons that underpin synaptic plasticity, and thus, memory formation. Analysis of mRNP granules in their various contexts has revealed common themes of assembly, disassembly, and modes of mRNA regulation, yet new studies continue to reveal unexpected and important findings, such as links between aberrant mRNP granule assembly and neurodegenerative disease. Continued study of these enigmatic structures thus promises fascinating new insights into cellular function, and may also suggest novel therapeutic strategies in various disease states.

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Metadata

Authors
Buchan, J. R.
Venue
RNA Biology
Published
2014-08-03
Volume
11
Issue
8
Pages
1019-1030
ISSN
  • 1547-6286 (ISSN-L)
  • 1555-8584
OpenAlex
W2073910361
Cited by
459
References
5
FWCI
14.11
Type
journal article
Language
en
Status
Retracted
Open access
hybrid

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CoChat. (2026). Citation check: mRNP granules: Assembly, function, and connections with disease. https://app.cochat.ai/papers/10.4161/15476286.2014.972208
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Buchan, J. R. (2014). mRNP granules: Assembly, function, and connections with disease. RNA Biology. https://doi.org/10.4161/15476286.2014.972208

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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.