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- W1963673812 abstract "Engagement of the cell death surface receptor Fas by Fas ligand (FasL) results in apoptotic cell death, mediated by caspase activation. Cell death mediated via Fas/FasL interaction is important for homeostasis of cells in the immune system and for maintaining immune-privileged sites in the body. Killing via the Fas/FasL pathway also constitutes an important pathway of killing for cytotoxic T cells. Fas ligand is induced in activated T cells, resulting in activation-induced cell death by the Fas/FasL pathway. Recently it has been shown that the Fas receptor can also be up-regulated following a lesion to the cell, particularly that induced by DNA-damaging agents. This can then result in killing of the cell by a Fas/FasL-dependent pathway. Up-regulation of Fas receptor following DNA damage appears to be p53 dependent." @default.
- W1963673812 created "2016-06-24" @default.
- W1963673812 creator A5022725690 @default.
- W1963673812 creator A5043391366 @default.
- W1963673812 date "1999-08-01" @default.
- W1963673812 modified "2023-10-13" @default.
- W1963673812 title "Cell death induced by the Fas/Fas ligand pathway and its role in pathology" @default.
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- W1963673812 doi "https://doi.org/10.1046/j.1440-1711.1999.00837.x" @default.
- W1963673812 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/10457197" @default.
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