References 1. Praticò D, Rokach J, Lawson J, FitzGerald GA. F2-isoprostanes as indices of lipid peroxidation in inflammatory diseases. Chem Phys Lipids. 2004 Mar;128(1-2):165-71.
2. Frederick A. Villamena. Reactive Species Detection in Biology: From Fluorescence to Electron Paramagnetic Resonance Spectroscopy. Elsevier. 2016.
3. Imbusch R, Mueller MJ. Formation of isoprostane F(2)-like compounds (phytoprostanes F(1)) from alpha-linolenic acid in plants. Free Radic Biol Med. 2000 Mar 1;28(5):720-6.
4. Gao L, Yin H, Milne GL, Porter NA, Morrow JD. Formation of F-ring isoprostane-like compounds (F3-isoprostanes) in vivo from eicosapentaenoic acid. J Biol Chem. 2006 May 19;281(20):14092-9. Epub 2006 Mar 28.
5. Roberts LJ 2nd1, Montine TJ, Markesbery WR, Tapper AR, Hardy P, Chemtob S, Dettbarn WD, Morrow JD. Formation of isoprostane-like compounds (neuroprostanes) in vivo from docosahexaenoic acid. J Biol Chem. 1998 May 29;273(22):13605-12.
6. Roberts LJ 2nd and Morrow JD. Products of the isoprostane pathway: unique bioactive compounds and markers of lipid peroxidation. Cell Mol Life Sci 59: 808–820, 2002.
7. Roberts, L.J., Morrow, J.D., 2000. Measurement of F(2)-isoprostanes as an index of oxidative stress in vivo. Free Radic Biol Med 28, 505-513.
8. Luo J, Mills K, le Cessie S, Noordam R, van Heemst D, Ageing, Age-related Diseases and Oxidative Stress: What to Do Next?, Ageing Research Reviews (2019).
9. Galano, J.-M., Lee, J. C.-Y., Gladine, C., Comte, B., Le Guennec, J.-Y., Oger, C., & Durand, T. (2015). Non-enzymatic cyclic oxygenated metabolites of adrenic, docosahexaenoic, eicosapentaenoic and α-linolenic acids; bioactivities and potential use as biomarkers. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids, 1851(4), 446–455.