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Cited by 912

The DOI matches its Crossref record; 175 of the 175 references it cites were found in a registry or an index.

Astrocytes and Brain Injury

Chen, Yongmei, Swanson, Raymond A.·2003·Journal of Cerebral Blood Flow & Metabolism

Abstract

Astrocytes are the most numerous cell type in the central nervous system. They provide structural, trophic, and metabolic support to neurons and modulate synaptic activity. Accordingly, impairment in these astrocyte functions during brain ischemia and other insults can critically influence neuron survival. Astrocyte functions that are known to influence neuronal survival include glutamate uptake, glutamate release, free radical scavenging, water transport, and the production of cytokines and nitric oxide. Long-term recovery after brain injury, through neurite outgrowth, synaptic plasticity, or neuron regeneration, is influenced by astrocyte surface molecule expression and trophic factor release. In addition, the death or survival of astrocytes themselves may affect the ultimate clinical outcome and rehabilitation through effects on neurogenesis and synaptic reorganization.

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Crossref · 10.1097/00004647-200302000-00001

Cites

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Metadata

Authors
Chen, Y., & Swanson, R. A.
Venue
Journal of Cerebral Blood Flow & Metabolism
Published
2003-02
Volume
23
Issue
2
Pages
137-149
ISSN
0271-678X (ISSN-L)
OpenAlex
W1983836947
Cited by
912
References
175
FWCI
35.00
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Astrocytes and Brain Injury. https://app.cochat.ai/papers/10.1097/00004647-200302000-00001
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Chen, Y., & Swanson, R. A. (2003). Astrocytes and Brain Injury. Journal of Cerebral Blood Flow & Metabolism. https://doi.org/10.1097/00004647-200302000-00001

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.