Bilinski, T. Oxygen toxicity and microbial evolution. Biosystems 24: 305 — 312; 1991.
McCord, J. М. and Fridovich, I. Superoxide dismutase. An enzymic function for erythrocuprein (hemocuprein). Journal of Вiologiсal Chemistry 244: 6049 — 6055; 1969.
Fridovich, I. Oxygen toxicity: а radical explanation. Jоиrnal of Еxpеrimеntal Biology 201: 1203 — 1209; 1998.
Lebovitz, R. М., Zhang, Н., Vogel, H., Cartwright, J., Dionne, L., Lu, N., Huang, S. and Matzuk М. M. Neurode-generation, myocardial injury and perinatal death in mitochondrial superoxide dismutase-deficient mice. Proceedings of the National Academy of Sciences USA 93: 9782 — 9787; 1996.
Chae, Н. Z., Robison, К., Poole, L. В., Church, G.. Storz, G., Rhee, S. G. Cloning and sequencing of thiol-specific antioxidant from mammalian brain: alkyl hydroperoxide reductase and thiol-specific antioxidant define а large family of antioxidant enzymes. Proceedings of the National Academy of Sciences USA 91: 7017 — 7021; 1994.
McGonigle, S., Dalton, J. Р. аnd Jаmes, Е. R. Peroxidoxins: а new antioxidant family. Рarasitology Today 14: 139 — 145; 1998.
Arrigo, А. P. Gene expression and the thiol redox state. Free Radical Biology and Меdiciпе 27: 936 — 944; 1999.
Marshall, Н. E., Merchant, К. and Stamler, J. S. Nitrosation and oxidation in the regulation of gene expression. FASEB Jоиrпаl 14: 1889 — 1900; 2000.
Groves, J. Т. Peroxynitrite: reactive, invasive and enigmatic. Current Opinion in Chemical Biology 3: 226 — 235; 1999.
Yachie, А., Niida, Y., Wada, Т., Igarashi, N., Каnedа, Н., Toma,Т., Ohta, К., Kasahara, Y. and Koizumi, S. Oxidative stress causes enhanced endothelial cell injury in human home oxygenase-1 deficiency. Jоиrпаl of Сlinical Investigation 103: 129 — 135; 1999.
Cai, L., Satoh, М., Tohyama, С. and Cherian, M. С. Metallothionein in radiation exposure: its induction and protection role. Toxicology 132: 85 — 98 1999.
Foresti, R., Clark, J. Е., Green, С. J. and Motterlini, R. Thiol compounds interact with nitric oxide in regulating heme-oxygenase-1 induction in endothelial cells. Involvement of superoxide and peroxynitrite anions.Jоиrпаl of Biological Chemistry 272: 18411 — 18417; 1997.
Motterlini, R., Foresti, R., Bassi, R., Calabrese, V., Clark, J. Е. and Green, С.J. Endothelial home oxygenase-1 induction by hypoxia: modulation by inducible nitric oxide synthase and S-nitrosothiols. Jоиrnаl of Вiological Chemistry 27 Si 13613 — 13620; 2000.
Orgel, L. E. The origin of life on the earth. Scientific American 271: 76 — 83; 1994.
Atmar, W. On the role of males. Animal Behaviour 41: 195 — 205 1991.
Clark, W. Sex and the Origins of Deаth. Oxford University Press, Oxford, 1998.
Kirkwood, Т. В. L. Evolution of ageing. Nature 270: 301 — 304; 1977.
Kirkwood, T. В. L. and Holliday, R. The evolution of аgеing and longevity. Proceedings of the Royal Society of London В 205: 531 — 546; 1979.
Austad, S, N. Retarded senescence in an insular population of Virginia opossums (Didelphis virgʼmiana). Jоиrnаl of Zoology 229: 695 — 708; 1993.
Rose, М. R. Can human aging be postponed? Scientific Атеriсап 281: 106 — 111; 1999.
Westendorp, R. G. and Kirkwood, Т. В. L. Human longevity at the cost of reproductive success. Nature 396: 743 — 746; 1998.
Partridge L. and Barton N. Н. Optimality, mutation and the evolution of ageing. Nature 362: 305 — 311; 1993.
Haldane, J. В. S. New Paths in Genetics. Harper, London, 1942.
Williams, G. С. Pleiotropy, natural selection and the evolution of senescence. Evolution 11: 398 — 411; 1957.
Shokeir, М. Н. Investigation on Huntington's disease in the Canadian Prairies. II. Fecundity and fitness. Clinical Genetics 7: 349 — 353; 1975.
Walker, D. А., Harper, Р. S., Newcombe, R. G. and Davies, К. Huntington's chorea in South Wales: mutation, fertility, and genetic fitness. Journal of Мedical Genetics 20: 12 — 17; 1983.
Friedman, D. В. and Johnson, Т. Е. А mutation in the age-1 gene in Caenorhabditis elegans lengthens life and reduced hermaphrodite fertility. Genetics 118: 75 — 86; 1988.
Кеnyon, C., Chang, J., Gensch, Е., Rudner, А. and Таbtiang, R. А. С. elegans mutant that lives twice as long as wild type. Nature 366: 404 — 405; 1993.
Morris, J. Z., Tissenbaum, Н. А. and Ruvkun, G. А phosphotidylinositol-3-ОН kinase family member regulating longevity and diapause in Caenorhabditis elegans. Naturе 382: 536 — 539; 1996.
Kimura, К. D., Tissenbaum, Н. А. and Ruvken G. daf-2, an insulin-receptor-like gene that regulates longevity and diapause in Caenorhabditis elegans. Science 277: 942 — 946; 1997.
Ogg, S., Paradis, S., Gottlieb, S., Patterson, G. I., Lee, L., Tissenbaum, Н. А. and Ruvkun, G. The fork head transcription factor DAF-16 transduces insulin-like metabolic and longevity signals in С. elegans. Nature 389: 994 — 999; 1997.
Tissenbaum, Н. А. and Ruvkun, G. An insulin-like signalling pathway affects both longevity and reproduction in Caenorhabditis elegans. Genetics 148: 703 — 717; 1998.
Clancy, D., Gems, D., Harshman, L. G., Oldham, S., Stocker, Н., Hafen, Е., Leevers, S. J. and Partridge, L. Extension of lifespan by loss of CHICO, а Drosophila insulin receptor substrate protein. Science 292: 104 — 106; 2001.