Joshua Brooks, Ph.D.
Affiliations: | Pharmacology | University of California, San Diego, La Jolla, CA |
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| Musiek ES, Brooks JD, Joo M, et al. (2019) Correction: Electrophilic cyclopentenone neuroprostanes are anti-inflammatory mediators formed from the peroxidation of the ω -3 polyunsaturated fatty acid docosahexaenoic acid. The Journal of Biological Chemistry. 294: 6657 |
| Brooks JD, Musiek ES, Koestner TR, et al. (2011) The fatty acid oxidation product 15-A3t-isoprostane is a potent inhibitor of NFκB transcription and macrophage transformation. Journal of Neurochemistry. 119: 604-16 |
| Lwin S, Brooks J, Jacobson R, et al. (2011) Isoprostane levels are altered in rheumatoid arthritis and suppress NFκB activity to inhibit osteoclast formation Bone. 48: S136 |
| Kleman AM, Brown JE, Zeiger SL, et al. (2010) p66(shc)'s role as an essential mitophagic molecule in controlling neuronal redox and energetic tone. Autophagy. 6: 948-9 |
| Brown JE, Zeiger SL, Hettinger JC, et al. (2010) Essential role of the redox-sensitive kinase p66shc in determining energetic and oxidative status and cell fate in neuronal preconditioning. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 5242-52 |
| Musiek ES, Brooks JD, Joo M, et al. (2008) Electrophilic cyclopentenone neuroprostanes are anti-inflammatory mediators formed from the peroxidation of the omega-3 polyunsaturated fatty acid docosahexaenoic acid. The Journal of Biological Chemistry. 283: 19927-35 |
| Brooks JD, Milne GL, Yin H, et al. (2008) Formation of highly reactive cyclopentenone isoprostane compounds (A3/J3-isoprostanes) in vivo from eicosapentaenoic acid. The Journal of Biological Chemistry. 283: 12043-55 |
| Dostalek M, Brooks JD, Hardy KD, et al. (2007) In vivo oxidative damage in rats is associated with barbiturate response but not other cytochrome P450 inducers. Molecular Pharmacology. 72: 1419-24 |