[247] Osthus I.B., Sgura A., Berardinelli F., Alsnes I.V., Bronstad E., Rehn T., Stobakk P.K., Hatle H., Wisloff U., Nauman J. (2012) Telomere length and long-term endurance exercise: does exercise training affect biological age? A pilot study. PLoS.One. 7, 12, e52769.

[248] Ott M., Gogvadze V., Orrenius S., Zhivotovsky B. (2007) Mitochondria, oxidative stress and cell death. Apoptosis 12, 5, 913-22.

[249] Ozdemir M., Temizdemir H. (2010) Age- and gender-related tear function changes in normal population. Eye 24, 1, 79–83.

[250] Paglialunga S., van Bree B., Bosma M., Valdecantos M.P., Amengual-Cladera E., Jorgensen J.A., van Beurden D., den Hartog G.J., Ouwens D.M., Briede J.J., Schrauwen P., Hoeks J. (2012) Targeting of mitochondrial reactive oxygen species production does not avert lipid-induced insulin resistance in muscle tissue from mice. Diabetologia 10.1007/s00125-012-2626-x, (accepted).

[251] Palm W., de Lange T. (2008) How shelterin protects mammalian telomeres. Annu.Rev.Genet. 42:301-34. doi: 10.1146/annurev.genet.41.110306.130350., 301–334.

[252] Palmer A.K., Street A.E., Roe F.J.C., Worden A.N., Vanabbe N.J. (1979) Safety evaluation of toothpaste containing chloroform. 2. Long-term studies in rats. JEnvir Pathol Toxicol 2, 3, 821–833.

[253] Pamplona R., Portero-Otin M., Riba D., Ruiz C., Prat J., Bellmunt M.J., Barja G. (1998) Mitochondrial membrane peroxidizability index is inversely related to maximum life span in mammals. J Lipid Res 39, 10, 1989-94.

[254] Paradies G., Petrosillo G., Paradies V., Ruggiero F.M. (2010) Oxidative stress, mitochondrial bioenergetics, and cardiolipin in aging. Free Radic Biol Med 48, 10, 1286-95.

[255] Park S.K., Kim K., Page G.P., Allison D.B., Weindruch R., Prolla T.A.(2009) Gene expression profiling of aging in multiple mouse strains: identification of aging biomarkers and impact of dietary antioxidants. Aging Cell 8, 4, 484-95.

[256] Parrinello S., Samper E., Krtolica A., Goldstein J., Melov S., Campisi J. (2003) Oxygen sensitivity severely limits the replicative lifespan of murine fibroblasts. Nat.Cell Biol. 5, 8, 741–747.

[257] Patten D.A., Lafleur V.N., Robitaille G.A., Chan D.A., Giaccia A.J., Richard D.E. (2010) Hypoxia-inducible factor-1 activation in nonhypoxic conditions: the essential role of mitochondrial-derived reactive oxygen species. Mol Biol Cell 21, 18, 3247-57.

[258] Penninx B.W., van Tilburg T., Kriegsman D.M., Deeg D.J., Boeke A.J., van Eijk J.T. (1997) Effects of social support and personal coping resources on mortality in older age: the longitudinal aging study. Am J Epidemiol 146, 6, 510-9.

[259] Pepper J.W., Shelton D.E., Rashidi A., Durand P.M. (2013) Are internal, death-promoting mechanisms ever adaptive? J Phylogen Evolution Biol 1, 3, 1000113.

[260] Petrosillo G., Matera M., Casanova G., Ruggiero F.M., Paradies G. (2008) Mitochondrial dysfunction in rat brain with aging. Involvement of complex I, reactive oxygen species and cardiolipin. Neurochem Int 53, 5, 126-31.

[261] Piddock L.J., Walters R.N. (1992) Bactericidal activities of five quinolones for Escherichia coli strains with mutations in genes encoding the SOS response or cell division. Antimicrob.Agents Chemother. 36, 4, 819–825.

[262] Pierpaoli W., Bulian D. (2005) The pineal aging and death program: life prolongation in pre-aging pinealectomized mice. Ann N Y Acad Sci 1057, 133-44.

[263] Plotnikov E.Y., Chupyrkina A.A., Jankauskas S.S., Pevzner I.B., Silachev D.N., Skulachev V.P., Zorov D.B. (2011) Mechanisms of nephroprotective effect of mitochondria-targeted antioxidants under rhabdomyolysis and ischemia/reperfusion. Biochim Biophys Acta 1812, 1, 77–86.

[264] Plotnikov E.Y., Kazachenko A.V., Vyssokikh M.Y., Vasileva A.K., Tcvirkun D.V., Isaev N.K., Kirpatovsky V.I., Zorov D.B. (2007) The role of mitochondria in oxidative and nitrosative stress during ischemia/reperfusion in the rat kidney. Kidney Int 72, 12, 1493-502.

[265] Plotnikov E.Y., Morosanova M.A., Pevzner I.B., Zorova L.D., Manskikh V.N., Pulkova N.V., Galkina S.I., Skulachev V.P., Zorov D.B. (2013) Protective effect of mitochondria-targeted antioxidants in an acute bacterial infection. PNAS doi/10.1073/pnas.1307096110

[266] Pozniakovsky A.I., Knorre D.A., Markova O.V., Hyman A.A., Skulachev V.P., Severin F.F. (2005) Role of mitochondria in the pheromone- and amiodarone-induced programmed death of yeast. J Cell Biol 168, 2, 257–269.

[267] Prowse K.R., Greider C.W. (1995) Developmental and tissue-specific regulation of mouse telomerase and telomere length. Proc.Natl.Acad.Sci.U.S.A. 92, 11, 4818–4822.

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