Abstract
The mechanisms underlying secondary cell death after traumatic brain injury (TBI) are poorly understood. Animal models of TBI recapitulate many clinical and pathologic aspects of human head injury, and the development of genetically engineered animals has offered the opportunity to investigate the specific molecular and cellular mechanisms associated with cell dysfunction and death after TBI, allowing for the evaluation of specific cause-effect relations and mechanistic hypotheses. This article represents a compendium of the current literature using genetically engineered mice in studies designed to better understand the posttraumatic inflammatory response, the mechanisms underlying DNA damage, repair, and cell death, and the link between TBI and neurodegenerative diseases.
| Original language | English |
|---|---|
| Pages (from-to) | 1241-1258 |
| Number of pages | 18 |
| Journal | Journal of Cerebral Blood Flow and Metabolism |
| Volume | 21 |
| Issue number | 11 |
| DOIs | |
| State | Published - 2001 |
Funding
| Funders | Funder number |
|---|---|
| National Institute of Neurological Disorders and Stroke | P50NS008803 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Cell death
- Head injury
- Inflammation
- Neurodegeneration
- Pathophysiology
- Secondary brain damage
- Transgenic mice
ASJC Scopus subject areas
- Neurology
- Clinical Neurology
- Cardiology and Cardiovascular Medicine
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