References
- Kon S. H. Biological autoxidation. I. Decontrolled iron: an ultimate carcinogen and toxicant: an hypothesis. Medical Hypotheses 1978; 4: 445–471
- Reinke L. A., Rau J. M., McCay P. B. Characteristics of an oxidant formed during iron (II) autoxidation. Free Radical Biology & Medicine 1994; 16: 485–492
- Burkitt M. J. ESR spin trapping studies into the nature of the oxidizing species formed in the Fenton reaction: pitfalls associated with the use of 5,5–dimethyl-1–pyrroline-N-oxide in the detection of the hydroxyl radical. Free Radical Research Communications 1993; 18: 43–57
- Tadolini B. The influence of adenine-nucleotides and phosphate on Fe2+ oxidation. Free Radical Research Communications 1989; 5: 237–243
- Rush J. D., Maskos Z., Koppenol W. H. Reaction of iron(II) nucleotide complexes with hydrogen peroxide. FEBS Letters 1990; 261: 121–123
- Biaglow J. E., Held K. D., Manevich Y., Tuttle S., Kachur A., Uckun F. Role of guanosine triphosphate in ferric ion-linked Fenton chemistry. Radiation Research 1996; 145: 554–562
- Biaglow J. E., Kachur A. V., Manevich Y. The detection and quantization of hydroxyl radicals produced by the reaction of oxygen with polyphosphate complexes of ferrous ion. 1996, Submitted to Radiation Research
- Peterson D. A., Gerard J. M. Enhanced electron transfer by GTP: cross-membrane electron signaling by G-proteins?. Free Radical Biology and Medicine 1991; 11: 187–190
- Winterbourn C. C., Sutton H. C. Iron and xan-thine catalyze formation of an oxidant species distinguishable from OH.: comparison with Haber-Weiss reaction. Archives of Biochemistry and Biophysics, 244: 27–34, [10] A. K. Collins, G. M. Makrigiorgos and G. K. Svensson (1994). Coumarin chemical dosimeter for radiation therapy, Medical Physics 1986; 21: 1741–1747
- Weaver J., Pollack S. Low-M, iron isolated from guinea pig reticulocytes as AMP-Fe and ATP-Fe complexes. Biochemical Journal 1989; 261: 787–792
- Emerit I., Oganesian N., Sarkisian T. Clastogenic factors in the plasma of Chernobyl accident recovery workers: anticlastogenic effect of Ginkgo biloba extract. Radiation Research 1995; 144: 198–205
- von Sonntag S. The chemical basis of radiation biology. Taylor & Fransis, Philadelphia 1987
- Lange's handbook of chemistry, thirteen edition. J. A. Dean, NY 1985
- Gutteridge J. M. Ferrous-salt-promoted damage to deoxyribose and benzoate. The increased effectiveness of hydroxyl-radical scavengers in the presence of EDTA. Biochemical Journal 1987; 243: 709–714
- Breen A. P., Murphy J. A. Reaction of oxyl radicals with DNA. Free Radical Biology and Medicine 1995; 18: 1033–1077
- Aruoma O. I., Chaudhary S. S., Grootveld M., Halliwell B. Binding of iron(II) ions to the pentose sugar 2–deoxyribose. Journal of lnorganic Biochemistry 1989; 35: 149–155
- de Silva D. M., Aust S. D. Ferritin and cerulo-plasmin in oxidative damage: review and recent findings. Canadian Journal Physiology and Pharmacology 1993; 71: 715–720
- Vile G. F., Winterbourn C. C. Microsomal reduction of low-molecular weight Fe3+ chelates and ferritin: enhancement by adriamycin, paraquat, menadione and antraquinone 2–sulfonate and inhibition by oxygen. Archives of Biochemistry and Biophysics 1988; 267: 606–613
- Monteiro H. P., Vile G. F., Winterbourn C. C. An iron chelator is not required for reductive iron release from ferritin by radical generating system. Free Radical Research Communications 1989; 7: 33–35
- Stohs S. J., Bagchi D. Oxidative mechanism in the toxicity of metal ions. Free Radical Biology and Medicine 1995; 18: 321–336
- Herbert V., Shaw S., Jayatilleke E., Stopler-Kasdan T. Most free-radical injury is iron-related: it is promoted by iron, hemin, holoferritin and vitamin C, and inhibited by desferoxamine and apoferritin. Stem Cells 1994; 12: 289–303
- Minotti G., Aust S. D. Redox cycling of iron and lipid peroxydation. Lipids 1992; 27: 219–26