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Cited by 458

The DOI matches its Crossref record; 220 of the 220 references it cites were found in a registry or an index.

Ras oncogenes and their downstream targets

Open access
Rajalingam, Krishnaraj, Schreck, Ralf, Rapp, Ulf R., Albert, Štefan·2007·Biochimica et Biophysica Acta (BBA) - Molecular Cell Research

Abstract

RAS proteins are small GTPases, which serve as master regulators of a myriad of signaling cascades involved in highly diverse cellular processes. RAS oncogenes have been originally discovered as retroviral oncogenes, and ever since constitutively activating RAS mutations have been identified in human tumors, they are in the focus of intense research. In this review, we summarize the biochemical properties of RAS proteins, trace down the evolution of RAS signaling and present an overview of the spatio-temporal activation of major RAS isoforms. We further discuss RAS effector pathways, their role in normal and transformed cell physiology and summarize ongoing attempts to interfere with aberrant RAS signaling. Finally, we comment on the role of micro RNAs in modulating RAS expression, contribution of RAS to stem cell function and on high-throughput analyses of RAS signaling networks.

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Crossref · 10.1016/j.bbamcr.2007.01.012

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Metadata

Authors
Rajalingam, K., Schreck, R., Rapp, U. R., & Albert, Š.
Venue
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
Publisher
Elsevier BV
Published
2007-08
Volume
1773
Issue
8
Pages
1177-1195
ISSN
0167-4889 (ISSN-L)
OpenAlex
W2138498601
Cited by
458
References
220
FWCI
7.78
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Ras oncogenes and their downstream targets. https://app.cochat.ai/papers/10.1016/j.bbamcr.2007.01.012
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Rajalingam, K., Schreck, R., Rapp, U. R., & Albert, Š. (2007). Ras oncogenes and their downstream targets. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. https://doi.org/10.1016/j.bbamcr.2007.01.012

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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