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Cited by 1,071

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

PKB/Akt

Lawlor, Margaret A., Alessi, Dario R.·2001·Journal of Cell Science

Abstract

The serine/threonine protein kinase PKB (also known as Akt) is thought to be a key mediator of signal transduction processes. The identification of PKB substrates and the role PKB phosphorylation plays in regulating these molecules have been a major focus of research in recent years. A recently developed motif-profile scoring algorithm that can be used to scan the genome for potential PKB substrates is therefore a useful tool, although additional considerations, such as the evolutionary conservation of the phosphorylation site, must also be taken into account. Recent evidence indicates that PKB plays a key role in cancer progression by stimulating cell proliferation and inhibiting apoptosis and is also probably a key mediator of insulin signalling. These findings indicate that PKB is likely to be a hot drug target for the treatment of cancer, diabetes and stroke. There are, however, a number of pitfalls of methodologies currently employed to study PKB function, and therefore caution should be used in interpretation of such experiments.

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Metadata

Authors
Lawlor, M. A., & Alessi, D. R.
Venue
Journal of Cell Science
Published
2001-08-15
Volume
114
Issue
16
Pages
2903-2910
ISSN
  • 0021-9533 (ISSN-L)
  • 1477-9137
OpenAlex
W1908445283
Cited by
1,071
References
5
FWCI
23.34
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: PKB/Akt. https://app.cochat.ai/papers/10.1242/jcs.114.16.2903
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Lawlor, M. A., & Alessi, D. R. (2001). PKB/Akt. Journal of Cell Science. https://doi.org/10.1242/jcs.114.16.2903

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.