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Cited by 196

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Nucleocytoplasmic protein traffic and its significance to cell function

Open access
Yoneda, Yoshihiro·2000·Genes to Cells

Abstract

In eukaryotic cells, cell functions are maintained in an orderly manner through the continuous traffic of various proteins between the cell nucleus and the cytoplasm. The nuclear import and export of proteins occurs through nuclear pore complexes and typically requires specific signals: the nuclear localization signal and nuclear export signal, respectively. The transport pathways have been found to be highly divergent, but are known to be largely mediated by importin β‐like transport receptor family molecules. These receptor molecules bind to and carry their cargoes directly or via adapter molecules. A small GTPase Ran ensures the directionality of nuclear transport by regulating the interaction between the receptors and their cargoes through its GTP/GDP cycle. Moreover, it has been recently elucidated how the transport system is involved in various functions of cell physiology, such as cell cycle control.

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Crossref · 10.1046/j.1365-2443.2000.00366.x

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Metadata

Authors
Yoneda, Y.
Venue
Genes to Cells
Publisher
Wiley
Published
2000-10
Volume
5
Issue
10
Pages
777-787
ISSN
  • 1356-9597 (ISSN-L)
  • 1365-2443
OpenAlex
W1994511343
Cited by
196
References
1
FWCI
4.62
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Nucleocytoplasmic protein traffic and its significance to cell function. https://app.cochat.ai/papers/10.1046/j.1365-2443.2000.00366.x
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Yoneda, Y. (2000). Nucleocytoplasmic protein traffic and its significance to cell function. Genes to Cells. https://doi.org/10.1046/j.1365-2443.2000.00366.x

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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.