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The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.

The ErbB signaling network in embryogenesis and oncogenesis: signal diversification through combinatorial ligand‐receptor interactions

Open access
Alroy, Iris, Yarden, Yosef·1997·FEBS Letters

Abstract

Ligand‐induced activation of receptor tyrosine kinases (RTK) results in the initiation of diverse cellular pathways, including proliferation, differentiation and cell migration. The ErbB family of RTKs represents a model for signal diversification through the formation of homo‐ and heterodimeric receptor complexes. Each dimeric receptor complex will initiate a distinct signaling pathway by recruiting a different set of Src homology 2‐ (SH2‐) containing effector proteins. Further complexity is added due to the existence of an oncogenic receptor that enhances and stabilizes dimerization but has no ligand (ErbB‐2), and a receptor that can recruit novel SH‐2‐containing proteins, but is itself devoid of kinase activity (ErbB‐3). The resulting signaling network has important implications for embryonic development and malignant transformation.

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Metadata

Authors
Alroy, I., & Yarden, Y.
Venue
FEBS Letters
Publisher
Wiley
Published
1997-06-23
Volume
410
Issue
1
Pages
83-86
ISSN
  • 0014-5793 (ISSN-L)
  • 1873-3468
OpenAlex
W2058586542
Cited by
714
References
4
FWCI
16.90
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: The ErbB signaling network in embryogenesis and oncogenesis: signal diversification through combinatorial ligand‐receptor interactions. https://app.cochat.ai/papers/10.1016/s0014-5793(97)00412-2
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Alroy, I., & Yarden, Y. (1997). The ErbB signaling network in embryogenesis and oncogenesis: signal diversification through combinatorial ligand‐receptor interactions. FEBS Letters. https://doi.org/10.1016/s0014-5793(97)00412-2

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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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