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Cited by 605

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Cytokine Receptors and Signal Transduction

Miyajima, Atsushi, Kitamura, Toshio, Harada, Nobuyuki, Yokota, Takashi, Arai, Ken-ichi·1992·Annual Review of Immunology

Abstract

Cytokinesp lay a vital role in coordinating immune and inflammatory responses. Unlike growth factor receptors with a tyrosine kinase, cytokine receptors have no intrinsic tyrosine kinase activity. Based on their structure, cytokinere ceptors are classified into several groups. High affinity receptors for IL-2, IL-3, IL-5, IL-6, and GM-CSF are composed of at least two distinct subunits, α and β. The α subunits are primary cytokine binding proteins, and the β subunits are required for formation of high affinity binding sites as well as for signal transduction. The GM-CSF, IL-3, and IL-5 receptors appear to share the same β subunit in human, and therefore cross-talk among these cytokines may occur at the receptor level. High affinity receptors presumably are linked to various signal transduction pathways that lead to different cytokine functions. Differential expression of the cytokine receptors as well as reorganization of intracellular signalling pathways are critical for development of hemopoietic cells.

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Crossref · 10.1146/annurev.iy.10.040192.001455

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Metadata

Authors
Miyajima, A., Kitamura, T., Harada, N., Yokota, T., & Arai, K.-I.
Venue
Annual Review of Immunology
Published
1992-04
Volume
10
Issue
1
Pages
295-331
ISSN
  • 0732-0582 (ISSN-L)
  • 1545-3278
OpenAlex
W2139613570
Cited by
605
References
2
FWCI
38.56
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Cytokine Receptors and Signal Transduction. https://app.cochat.ai/papers/10.1146/annurev.iy.10.040192.001455
The paper
Miyajima, A., Kitamura, T., Harada, N., Yokota, T., & Arai, K.-I. (1992). Cytokine Receptors and Signal Transduction. Annual Review of Immunology. https://doi.org/10.1146/annurev.iy.10.040192.001455

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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.