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. 1987 Jun;8:5–10.

Free radicals and tissue injury: fact and fiction.

T F Slater 1
PMCID: PMC2149453  PMID: 3307873

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Albano E., Lott K. A., Slater T. F., Stier A., Symons M. C., Tomasi A. Spin-trapping studies on the free-radical products formed by metabolic activation of carbon tetrachloride in rat liver microsomal fractions isolated hepatocytes and in vivo in the rat. Biochem J. 1982 May 15;204(2):593–603. doi: 10.1042/bj2040593. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Benedetti A., Comporti M., Esterbauer H. Identification of 4-hydroxynonenal as a cytotoxic product originating from the peroxidation of liver microsomal lipids. Biochim Biophys Acta. 1980 Nov 7;620(2):281–296. doi: 10.1016/0005-2760(80)90209-x. [DOI] [PubMed] [Google Scholar]
  3. Benedetto C., Bocci A., Dianzani M. U., Ghiringhello B., Slater T. F., Tomasi A., Vannini V. Electron spin resonance studies on normal human uterus and cervix and on benign and malignant uterine tumors. Cancer Res. 1981 Jul;41(7):2936–2942. [PubMed] [Google Scholar]
  4. Capdevila J., Chacos N., Falck J. R., Manna S., Negro-Vilar A., Ojeda S. R. Novel hypothalamic arachidonate products stimulate somatostatin release from the median eminence. Endocrinology. 1983 Jul;113(1):421–423. doi: 10.1210/endo-113-1-421. [DOI] [PubMed] [Google Scholar]
  5. Cheeseman K. H., Collins M., Maddix S., Milia A., Proudfoot K., Slater T. F., Burton G. W., Webb A., Ingold K. U. Lipid peroxidation in regenerating rat liver. FEBS Lett. 1986 Dec 15;209(2):191–196. doi: 10.1016/0014-5793(86)81109-7. [DOI] [PubMed] [Google Scholar]
  6. Cheeseman K. H., Collins M., Proudfoot K., Slater T. F., Burton G. W., Webb A. C., Ingold K. U. Studies on lipid peroxidation in normal and tumour tissues. The Novikoff rat liver tumour. Biochem J. 1986 Apr 15;235(2):507–514. doi: 10.1042/bj2350507. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Connor H. D., Thurman R. G., Galizi M. D., Mason R. P. The formation of a novel free radical metabolite from CCl4 in the perfused rat liver and in vivo. J Biol Chem. 1986 Apr 5;261(10):4542–4548. [PubMed] [Google Scholar]
  8. Hiller K. O., Hodd P. L., Willson R. L. Antiinflammatory drugs: protection of a bacterial virus as an in vitro biological measure of free radical activity. Chem Biol Interact. 1983 Dec;47(3):293–305. doi: 10.1016/0009-2797(83)90165-5. [DOI] [PubMed] [Google Scholar]
  9. Hopkins H. A., Campbell H. A., Barbiroli B., Potter V. R. Thymidine kinase and deoxyribonucleic acid metabolism in growing and regenerating livers from rats on controlled feeding schedules. Biochem J. 1973 Dec;136(4):955–966. doi: 10.1042/bj1360955. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Ingall A., Lott K. A., Slater T. F. Metabolic activation of carbon tetrachloride to a free-radical product: studies using a spin trap. Biochem Soc Trans. 1978;6(5):962–964. doi: 10.1042/bst0060962. [DOI] [PubMed] [Google Scholar]
  11. Lai E. K., McCay P. B., Noguchi T., Fong K. L. In vivo spin-trapping of trichloromethyl radicals formed from CCl4. Biochem Pharmacol. 1979 Jul 15;28(14):2231–2235. doi: 10.1016/0006-2952(79)90212-0. [DOI] [PubMed] [Google Scholar]
  12. Mönig J., Bahnemann D., Asmus K. D. One electron reduction of CCl4 in oxygenated aqueous solutions: a CCl3O2-free radical mediated formation of Cl- and CO2. Chem Biol Interact. 1983 Oct 15;47(1):15–27. doi: 10.1016/0009-2797(83)90144-8. [DOI] [PubMed] [Google Scholar]
  13. Nöhammer G., Bajardi F., Benedetto C., Schauenstein E., Slater T. F. Quantitative cytospectrophotometric studies on protein thiols and reactive protein disulphides in samples of normal human uterine cervix and on samples obtained from patients with dysplasia or carcinoma-in-situ. Br J Cancer. 1986 Feb;53(2):217–222. doi: 10.1038/bjc.1986.38. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Packer J. E., Slater T. F., Willson R. L. Reactions of the carbon tetrachloride-related peroxy free radical (CC13O.2) with amino acids: pulse radiolysis evidence. Life Sci. 1978 Dec 25;23(26):2617–2620. doi: 10.1016/0024-3205(78)90378-8. [DOI] [PubMed] [Google Scholar]
  15. Poyer J. L., Floyd R. A., McCay P. B., Janzen E. G., Davis E. R. Spin-trapping of the trichloromethyl radical produced during enzymic NADPH oxidation in the presence of carbon tetrachloride or bromotrichloromethane. Biochim Biophys Acta. 1978 Mar 20;539(3):402–409. doi: 10.1016/0304-4165(78)90044-2. [DOI] [PubMed] [Google Scholar]
  16. Slater T. F., Cheeseman K. H., Ingold K. U. Carbon tetrachloride toxicity as a model for studying free-radical mediated liver injury. Philos Trans R Soc Lond B Biol Sci. 1985 Dec 17;311(1152):633–645. doi: 10.1098/rstb.1985.0169. [DOI] [PubMed] [Google Scholar]
  17. Slater T. F. Free-radical mechanisms in tissue injury. Biochem J. 1984 Aug 15;222(1):1–15. doi: 10.1042/bj2220001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Slater T. F., Sawyer B. C. The stimulatory effects of carbon tetrachloride on peroxidative reactions in rat liver fractions in vitro. Inhibitory effects of free-radical scavengers and other agents. Biochem J. 1971 Aug;123(5):823–828. doi: 10.1042/bj1230823. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Williams R. J. The necessary and the desirable production of radicals in biology. Philos Trans R Soc Lond B Biol Sci. 1985 Dec 17;311(1152):593–603. doi: 10.1098/rstb.1985.0166. [DOI] [PubMed] [Google Scholar]

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