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Cited by 263

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

14-3-3 proteins as signaling integration points for cell cycle control and apoptosis

Open access
Gardino, Alexandra K., Yaffe, Michael B.·2011·Seminars in Cell & Developmental Biology

Abstract

14-3-3 proteins play critical roles in the regulation of cell fate through phospho-dependent binding to a large number of intracellular proteins that are targeted by various classes of protein kinases. 14-3-3 proteins play particularly important roles in coordinating progression of cells through the cell cycle, regulating their response to DNA damage, and influencing life-death decisions following internal injury or external cytokine-mediated cues. This review focuses on 14-3-3-dependent pathways that control cell cycle arrest and recovery, and the influence of 14-3-3 on the apoptotic machinery at multiple levels of regulation. Recognition of 14-3-3 proteins as signaling integrators that connect protein kinase signaling pathways to resulting cellular phenotypes, and their exquisite control through feedforward and feedback loops, identifies new drug targets for human disease, and highlights the emerging importance of using systems-based approaches to understand signal transduction events at the network biology level.

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Crossref · 10.1016/j.semcdb.2011.09.008

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Metadata

Authors
Gardino, A. K., & Yaffe, M. B.
Venue
Seminars in Cell & Developmental Biology
Publisher
Elsevier BV
Published
2011-09
Volume
22
Issue
7
Pages
688-695
ISSN
1084-9521 (ISSN-L)
OpenAlex
W2041031771
Cited by
263
References
9
FWCI
8.58
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: 14-3-3 proteins as signaling integration points for cell cycle control and apoptosis. https://app.cochat.ai/papers/10.1016/j.semcdb.2011.09.008
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Gardino, A. K., & Yaffe, M. B. (2011). 14-3-3 proteins as signaling integration points for cell cycle control and apoptosis. Seminars in Cell & Developmental Biology. https://doi.org/10.1016/j.semcdb.2011.09.008

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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.