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Cited by 827

The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

Expression of Cellular Oncogenes in Human Malignancies

Slamon, Dennis J., deKernion, Jean B., Verma, Inder M., Cline, Martin J.·1984·Science

Abstract

Cellular oncogenes have been implicated in the induction of malignant transformation in some model systems in vitro and may be related to malignancies in vivo in some vertebrate species. This article describes a study of the expression of 15 cellular oncogenes in fresh human tumors from 54 patients, representing 20 different tumor types. More than one cellular oncogene was transcriptionally active in all of the tumors examined. In 14 patients it was possible to study normal and malignant tissue from the same organ. In many of these patients, the transcriptional activity of certain oncogenes was greater in the malignant than the normal tissue. The cellular fes (feline sarcoma) oncogene, not previously known to be transcribed in mammalian tissue, was found to be active in lung and hematopoietic malignancies.

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Crossref · 10.1126/science.6538699

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Metadata

Authors
Slamon, D. J., deKernion, J. B., Verma, I. M., & Cline, M. J.
Venue
Science
Published
1984-04-20
Volume
224
Issue
4646
Pages
256-262
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2063837791
Cited by
827
References
3
FWCI
60.02
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Expression of Cellular Oncogenes in Human Malignancies. https://app.cochat.ai/papers/10.1126/science.6538699
The paper
Slamon, D. J., deKernion, J. B., Verma, I. M., & Cline, M. J. (1984). Expression of Cellular Oncogenes in Human Malignancies. Science. https://doi.org/10.1126/science.6538699

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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.