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Cited by 167

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Fas-activated serine/threonine kinase (FAST) phosphorylates TIA-1 during Fas-mediated apoptosis.

Open access
Tian, Q, Taupin, J, Elledge, S, Robertson, M, Anderson, P·1995·The Journal of experimental medicine

Abstract

We have identified a serine/threonine kinase that is rapidly activated during Fas-mediated apoptosis. Fas-activated serine/threonine kinase (FAST) is phosphorylated on serine and threonine residues in Jurkat cells. In response to Fas ligation, it is rapidly dephosphorylated and concomitantly activated to phosphorylate TIA-1, a nuclear RNA-binding protein that has been implicated as an effector of apoptosis. Phosphorylation of TIA-1 precedes the onset of DNA fragmentation, suggesting a role in signaling downstream events in the apoptotic program. Our results introduce Fast and TIA-1 as components of a molecular cascade involved in signaling Fas-mediated apoptosis.

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Crossref · 10.1084/jem.182.3.865

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Metadata

Authors
Tian, Q., Taupin, J., Elledge, S., Robertson, M., & Anderson, P.
Venue
The Journal of experimental medicine
Published
1995-09-01
Volume
182
Issue
3
Pages
865-874
ISSN
  • 0022-1007 (ISSN-L)
  • 1540-9538
OpenAlex
W2145038749
Cited by
167
References
1
FWCI
3.79
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Fas-activated serine/threonine kinase (FAST) phosphorylates TIA-1 during Fas-mediated apoptosis. https://app.cochat.ai/papers/10.1084/jem.182.3.865
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Tian, Q., Taupin, J., Elledge, S., Robertson, M., & Anderson, P. (1995). Fas-activated serine/threonine kinase (FAST) phosphorylates TIA-1 during Fas-mediated apoptosis. The Journal of experimental medicine. https://doi.org/10.1084/jem.182.3.865

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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.