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Cited by 381

The DOI matches its Crossref record; 90 of the 90 references it cites were found in a registry or an index.

Heterogeneity of epidermal growth factor receptor signalling networks in glioblastoma

Open access
Furnari, Frank B., Cloughesy, Timothy F., Cavenee, Webster K., Mischel, Paul S.·2015·Nature Reviews Cancer

Abstract

As tumours evolve, the daughter cells of the initiating cell often become molecularly heterogeneous and develop different functional properties and therapeutic vulnerabilities. In glioblastoma (GBM), a lethal form of brain cancer, the heterogeneous expression of the epidermal growth factor receptor (EGFR) poses a substantial challenge for the effective use of EGFR-targeted therapies. Understanding the mechanisms that cause EGFR heterogeneity in GBM should provide better insights into how they, and possibly other amplified receptor tyrosine kinases, affect cellular signalling, metabolism and drug resistance.

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Crossref · 10.1038/nrc3918

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90 of 90 references verified0 citation errors · 0 not checkable

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Metadata

Authors
Furnari, F. B., Cloughesy, T. F., Cavenee, W. K., & Mischel, P. S.
Venue
Nature Reviews Cancer
Published
2015-04-09
Volume
15
Issue
5
Pages
302-310
ISSN
  • 1474-175X (ISSN-L)
  • 1474-1768
OpenAlex
W2034015235
Cited by
381
References
90
FWCI
7.34
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Heterogeneity of epidermal growth factor receptor signalling networks in glioblastoma. https://app.cochat.ai/papers/10.1038/nrc3918
The paper
Furnari, F. B., Cloughesy, T. F., Cavenee, W. K., & Mischel, P. S. (2015). Heterogeneity of epidermal growth factor receptor signalling networks in glioblastoma. Nature Reviews Cancer. https://doi.org/10.1038/nrc3918

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.