Please use this identifier to cite or link to this item:
https://doi.org/10.1016/j.tibs.2006.07.005
DC Field | Value | |
---|---|---|
dc.title | Phagocyte-derived reactive species: salvation or suicide? | |
dc.contributor.author | Halliwell, B. | |
dc.date.accessioned | 2011-11-29T05:59:09Z | |
dc.date.available | 2011-11-29T05:59:09Z | |
dc.date.issued | 2006 | |
dc.identifier.citation | Halliwell, B. (2006). Phagocyte-derived reactive species: salvation or suicide?. Trends in Biochemical Sciences 31 (9) : 509-515. ScholarBank@NUS Repository. https://doi.org/10.1016/j.tibs.2006.07.005 | |
dc.identifier.issn | 09680004 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/28763 | |
dc.description.abstract | Activated phagocytes produce 'reactive oxygen, halogen and nitrogen species' that help to kill some types of microorganism. How these species destroy microorganisms remains, however, an enigma: both direct oxidative damage and indirect damage (whereby reactive species promote the actions of other antibacterial agents) are involved, and no single mechanism is likely to account for the killing of all microorganisms. Phagocyte-derived reactive species are known to injure human tissues and to contribute to inflammation. Recently, however, we have learned that they can also be anti-inflammatory by modulating the immune response. These data have implications for the proposed use of antioxidants to treat inflammation. © 2006 Elsevier Ltd. All rights reserved. | |
dc.description.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.tibs.2006.07.005 | |
dc.source | Scopus | |
dc.type | Review | |
dc.contributor.department | BIOCHEMISTRY | |
dc.description.doi | 10.1016/j.tibs.2006.07.005 | |
dc.description.sourcetitle | Trends in Biochemical Sciences | |
dc.description.volume | 31 | |
dc.description.issue | 9 | |
dc.description.page | 509-515 | |
dc.description.coden | TBSCD | |
dc.identifier.isiut | 000240789600006 | |
Appears in Collections: | Staff Publications |
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