메뉴 건너뛰기




Volumn 450, Issue 1-2, 2000, Pages 107-124

Hydroperoxide-induced DNA damage and mutations

Author keywords

Alkoxyl radicals; Alkyl hydroperoxide; Autooxidation; Fenton reaction; Footprinting of oxidative DNA base damage; Free radical induced DNA damage; Hydrogen peroxide; Hydroxyl radicals; Metal ion induced mutagenesis; Peroxyl radicals

Indexed keywords

CLASTOGEN; DNA BASE; FREE RADICAL; HYDROPEROXIDE; METAL ION; PEROXY RADICAL;

EID: 0034732995     PISSN: 00275107     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0027-5107(00)00019-1     Document Type: Article
Times cited : (124)

References (116)
  • 3
    • 2542609348 scopus 로고    scopus 로고
    • Metal [MLx; M=Fe, Cu, Co, Mn] hydroperoxide-induced activation of dioxygen for the oxygenation of hydrocarbons: Oxygenated Fenton chemistry
    • Sawyer D.T., Sobkowiak A., Matsushita T. Metal [MLx; M=Fe, Cu, Co, Mn] hydroperoxide-induced activation of dioxygen for the oxygenation of hydrocarbons: oxygenated Fenton chemistry. Acc. Chem. Res. 29:1996;409-416.
    • (1996) Acc. Chem. Res. , vol.29 , pp. 409-416
    • Sawyer, D.T.1    Sobkowiak, A.2    Matsushita, T.3
  • 5
    • 0005955494 scopus 로고
    • ESR spin trapping study on the oxidizing species formed in the reaction of the ferrous ion with hydrogen peroxide
    • Yamazaki I., Piette L.H. ESR spin trapping study on the oxidizing species formed in the reaction of the ferrous ion with hydrogen peroxide. J. Am. Chem. Soc. 113:1991;7588-7593.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 7588-7593
    • Yamazaki, I.1    Piette, L.H.2
  • 6
    • 0019881197 scopus 로고
    • Formation of thiobarbituric acid substrates from deoxyribose in the presence of iron salts - The role of superoxide and hydroxyl radicals
    • Halliwell B., Gutteridge J.M.C. Formation of thiobarbituric acid substrates from deoxyribose in the presence of iron salts - the role of superoxide and hydroxyl radicals. FEBS Lett. 128:1981;347-351.
    • (1981) FEBS Lett. , vol.128 , pp. 347-351
    • Halliwell, B.1    Gutteridge, J.M.C.2
  • 7
    • 0023085803 scopus 로고
    • The ability of scavengers to distinguish ·oH production in the iron-catalyzed Haber-Weiss reaction. Comparison of four assays for ·oH
    • Winterbourn C.C. The ability of scavengers to distinguish ·OH production in the iron-catalyzed Haber-Weiss reaction. Comparison of four assays for ·OH. Free Radical Biol. Med. 3:1987;33-39.
    • (1987) Free Radical Biol. Med. , vol.3 , pp. 33-39
    • Winterbourn, C.C.1
  • 8
    • 0022336840 scopus 로고
    • Efficiency of chelated iron compounds as catalysts for the Haber-Weiss reaction
    • Sutton H.C. Efficiency of chelated iron compounds as catalysts for the Haber-Weiss reaction. Free Radical Biol. Med. 1:1985;195-202.
    • (1985) Free Radical Biol. Med. , vol.1 , pp. 195-202
    • Sutton, H.C.1
  • 9
    • 33847804492 scopus 로고
    • Fentons reagent: IV. Structure and reactivity relations in the reactions of hydroxyl radicals and the redox reactions of radicals
    • Walling C., El-Taliawi G.M., Johnson R.A. Fentons reagent: IV. Structure and reactivity relations in the reactions of hydroxyl radicals and the redox reactions of radicals. J. Am. Chem. Soc. 96:1974;133-139.
    • (1974) J. Am. Chem. Soc. , vol.96 , pp. 133-139
    • Walling, C.1    El-Taliawi, G.M.2    Johnson, R.A.3
  • 13
    • 0030728024 scopus 로고    scopus 로고
    • A putative monoxygenase mimic which functions via well-disguised free radical chemistry
    • MacFaul P.A., Ingold K.U., Wayner D.D.D., Que L. Jr. A putative monoxygenase mimic which functions via well-disguised free radical chemistry. J. Am. Chem. Soc. 119:1997;10594-10598.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 10594-10598
    • MacFaul, P.A.1    Ingold, K.U.2    Wayner, D.D.D.3    Que L., Jr.4
  • 14
    • 0025232568 scopus 로고
    • The hydroxylation of the salicylate anion by a Fenton reaction and γ radiolysis: A consideration of the respective mechanisms
    • Maskos Z., Rush J.D., Koppenol W.H. The hydroxylation of the salicylate anion by a Fenton reaction and γ radiolysis: a consideration of the respective mechanisms. Free Radical Biol. Med. 8:1990;153-162.
    • (1990) Free Radical Biol. Med. , vol.8 , pp. 153-162
    • Maskos, Z.1    Rush, J.D.2    Koppenol, W.H.3
  • 16
  • 17
    • 0029053451 scopus 로고
    • Superoxide radical and superoxide dismutases
    • Fridovich I. Superoxide radical and superoxide dismutases. Annu. Rev. Biochem. 64:1995;97-112.
    • (1995) Annu. Rev. Biochem. , vol.64 , pp. 97-112
    • Fridovich, I.1
  • 18
    • 0343066956 scopus 로고
    • The mechanism of the reaction of Mn(III) with hydrogen peroxide
    • Wells C.F., Moys D. The mechanism of the reaction of Mn(III) with hydrogen peroxide. Inorg. Chem. Lett. 4:1968;43-45.
    • (1968) Inorg. Chem. Lett. , vol.4 , pp. 43-45
    • Wells, C.F.1    Moys, D.2
  • 19
    • 37049060970 scopus 로고
    • The reaction of Co(II) with water and hydrogen peroxide
    • Baxendale O.H., Wells C.F. The reaction of Co(II) with water and hydrogen peroxide. Trans. Faraday Soc. 53:1957;800-812.
    • (1957) Trans. Faraday Soc. , vol.53 , pp. 800-812
    • Baxendale, O.H.1    Wells, C.F.2
  • 20
    • 84995103199 scopus 로고
    • Re-evaluation of the spectral and kinetic properties of hydroperoxo and superoxide anion free radicals
    • Bielski B.H.J. Re-evaluation of the spectral and kinetic properties of hydroperoxo and superoxide anion free radicals. Photochem. Photobiol. 28:1978;645-649.
    • (1978) Photochem. Photobiol. , vol.28 , pp. 645-649
    • Bielski, B.H.J.1
  • 22
    • 33947292477 scopus 로고
    • Paramagnetic resonance study of liquids during photolysis: XIII. Uracil and derivatives
    • Dohrmann J.K., Livingston R. Paramagnetic resonance study of liquids during photolysis: XIII. Uracil and derivatives. J. Am. Chem. Soc. 93:1971;5363-5370.
    • (1971) J. Am. Chem. Soc. , vol.93 , pp. 5363-5370
    • Dohrmann, J.K.1    Livingston, R.2
  • 23
    • 0015918851 scopus 로고
    • Trapping of radicals formed in the photochemical reaction between hydrogen peroxide and some pyrimidine bases, nucleosides, nucleotides, and yeast nucleic acids
    • Lagercrantz C. Trapping of radicals formed in the photochemical reaction between hydrogen peroxide and some pyrimidine bases, nucleosides, nucleotides, and yeast nucleic acids. J. Am. Chem. Soc. 95:1973;220-225.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 220-225
    • Lagercrantz, C.1
  • 24
    • 0000419648 scopus 로고
    • Pattern of OH radical addition to uracil and methyl- And carboxyl-substituted uracils. Electron transfer of OH adducts with N,N,NôNô-tetramethyl-p-phenylenediamine and tetranitromethane
    • Fujita S., Steenken S. Pattern of OH radical addition to uracil and methyl- and carboxyl-substituted uracils. Electron transfer of OH adducts with N,N,NôNô-tetramethyl-p-phenylenediamine and tetranitromethane. J. Am. Chem. Soc. 103:1981;2540-2545.
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 2540-2545
    • Fujita, S.1    Steenken, S.2
  • 25
    • 0022483746 scopus 로고
    • A pulse radiolytic study of the interaction of nitroxyls with free-radical adducts of purines: Consequences for radiosensitization
    • O'Neill P., Davies S.E. A pulse radiolytic study of the interaction of nitroxyls with free-radical adducts of purines: consequences for radiosensitization. Int. J. Radiat. Biol. 49:1986;937-950.
    • (1986) Int. J. Radiat. Biol. , vol.49 , pp. 937-950
    • O'Neill, P.1    Davies, S.E.2
  • 26
    • 0001434563 scopus 로고
    • Isolation and characterization of the radiation induced degradation products of 2ô-deoxyguansine in oxygen free aqueous solutions
    • Berger M., Cadet J. Isolation and characterization of the radiation induced degradation products of 2ô-deoxyguansine in oxygen free aqueous solutions. Z. Naturforsch. 40b:1985;1519-1531.
    • (1985) Z. Naturforsch. , vol.40 , pp. 1519-1531
    • Berger, M.1    Cadet, J.2
  • 27
    • 0021921097 scopus 로고
    • Formation of an 8-hydroxyguanine moiety in DNA on gamma irradiation in aqueous solution
    • Dizdaroglu M. Formation of an 8-hydroxyguanine moiety in DNA on gamma irradiation in aqueous solution. Biochemistry. 24:1985;4476.
    • (1985) Biochemistry , vol.24 , pp. 4476
    • Dizdaroglu, M.1
  • 28
    • 33748366270 scopus 로고
    • - And OH adducts
    • - and OH adducts. Chem. Rev. 89:1989;503-520.
    • (1989) Chem. Rev. , vol.89 , pp. 503-520
    • Steenken, S.1
  • 29
    • 0026087716 scopus 로고
    • The possible role of lipid peroxidation in breast cancer risk
    • Boyd N.F., McGuire V. The possible role of lipid peroxidation in breast cancer risk. Free Radical Biol. Med. 10:1991;185-190.
    • (1991) Free Radical Biol. Med. , vol.10 , pp. 185-190
    • Boyd, N.F.1    McGuire, V.2
  • 32
    • 0033535371 scopus 로고    scopus 로고
    • Lipid peroxidation-DNA damage by malondialdehyde
    • Marnett L.J. Lipid peroxidation-DNA damage by malondialdehyde. Mutat. Res. 424:1999;83-95.
    • (1999) Mutat. Res. , vol.424 , pp. 83-95
    • Marnett, L.J.1
  • 33
    • 0025305055 scopus 로고
    • Possible mutagens derived from lipids and lipid precursors
    • Esterbauer H., Eckl P., Ortner A. Possible mutagens derived from lipids and lipid precursors. Mutat. Res. 238:1990;223-233.
    • (1990) Mutat. Res. , vol.238 , pp. 223-233
    • Esterbauer, H.1    Eckl, P.2    Ortner, A.3
  • 35
    • 0027389280 scopus 로고
    • Formation of peroxides in amino acids and proteins exposed to oxygen free radicals
    • Gebicki S., Gebicki J.M. Formation of peroxides in amino acids and proteins exposed to oxygen free radicals. Biochem. J. 289:1993;743-749.
    • (1993) Biochem. J. , vol.289 , pp. 743-749
    • Gebicki, S.1    Gebicki, J.M.2
  • 36
    • 0022559216 scopus 로고
    • Oxy-radicals and related species: Their formation, lifetimes and reactions
    • Pryor W.A. Oxy-radicals and related species: their formation, lifetimes and reactions. Ann. Rev. Physiol. 48:1986;657-667.
    • (1986) Ann. Rev. Physiol. , vol.48 , pp. 657-667
    • Pryor, W.A.1
  • 37
    • 0030980116 scopus 로고    scopus 로고
    • Time-resolved EPR studies on the reaction rates of peroxy radicals of poly(acrylic acid) and of calf-thymus DNA with glutathione. Re-examination of a rate constant for DNA
    • Hildebrand K., Schulte-Frohlinde D. Time-resolved EPR studies on the reaction rates of peroxy radicals of poly(acrylic acid) and of calf-thymus DNA with glutathione. Re-examination of a rate constant for DNA. Int. J. Radiat. Biol. 71:1997;377-385.
    • (1997) Int. J. Radiat. Biol. , vol.71 , pp. 377-385
    • Hildebrand, K.1    Schulte-Frohlinde, D.2
  • 38
    • 0031047884 scopus 로고    scopus 로고
    • Peroxy radical oxidation of thymidine
    • Martini M., Termini J. Peroxy radical oxidation of thymidine. Chem. Res. Toxicol. 10:1997;234-241.
    • (1997) Chem. Res. Toxicol. , vol.10 , pp. 234-241
    • Martini, M.1    Termini, J.2
  • 39
    • 0028959042 scopus 로고
    • Mechanisms of free radical oxidation of unsaturated lipids
    • Porter N.A., Caldwell S.E., Mills K.A. Mechanisms of free radical oxidation of unsaturated lipids. Lipids. 30:1995;277-290.
    • (1995) Lipids , vol.30 , pp. 277-290
    • Porter, N.A.1    Caldwell, S.E.2    Mills, K.A.3
  • 40
    • 0028207325 scopus 로고
    • Free radical-mediated lipid peroxidation in cells: Oxidizability is a function of cell lipid bis-allylic hydrogen content
    • Wagner B.A., Buettner G.R., Burns C.P. Free radical-mediated lipid peroxidation in cells: oxidizability is a function of cell lipid bis-allylic hydrogen content. Biochemistry. 33:1994;4449-4453.
    • (1994) Biochemistry , vol.33 , pp. 4449-4453
    • Wagner, B.A.1    Buettner, G.R.2    Burns, C.P.3
  • 41
    • 0021035001 scopus 로고
    • The generation of hydroxy and alkoxyl radicals from the interaction of ferrous bipyridyl with peroxides
    • Winston G.W., Harvey W., Berl L., Cederbaum A.L. The generation of hydroxy and alkoxyl radicals from the interaction of ferrous bipyridyl with peroxides. Biochem. J. 216:1983;415-421.
    • (1983) Biochem. J. , vol.216 , pp. 415-421
    • Winston, G.W.1    Harvey, W.2    Berl, L.3    Cederbaum, A.L.4
  • 42
    • 0002297720 scopus 로고
    • Self-reactions of alkylperoxy radicals in solution
    • Howard J.A. Self-reactions of alkylperoxy radicals in solution. Am. Chem. Soc. Symp. Ser. 69:1978;413-432.
    • (1978) Am. Chem. Soc. Symp. Ser. , vol.69 , pp. 413-432
    • Howard, J.A.1
  • 43
    • 0007758844 scopus 로고
    • Deuterium isotope effects in the autoxidation of aralkyl hydrocarbons. Mechanism of the interaction of peroxy radicals
    • Russell G.A. Deuterium isotope effects in the autoxidation of aralkyl hydrocarbons. Mechanism of the interaction of peroxy radicals. J. Am. Chem. Soc. 79:1957;3871-3877.
    • (1957) J. Am. Chem. Soc. , vol.79 , pp. 3871-3877
    • Russell, G.A.1
  • 44
    • 0010799718 scopus 로고
    • The self-reaction of sec-alkylperoxyl radicals: A kinetic electron spin resonance study
    • Howard J.A., Bennett J.E. The self-reaction of sec-alkylperoxyl radicals: a kinetic electron spin resonance study. Can. J. Chem. 50:1973;2374-2376.
    • (1973) Can. J. Chem. , vol.50 , pp. 2374-2376
    • Howard, J.A.1    Bennett, J.E.2
  • 45
    • 33847799157 scopus 로고
    • Spectroscopic evidence for the generation of singlet oxygen in self-reaction of sec-peroxyl radicals
    • Nakano M., Takayama K., Shimizu Y., Tsuji Y., Inaba H., Migita T. Spectroscopic evidence for the generation of singlet oxygen in self-reaction of sec-peroxyl radicals. J. Am. Chem. Soc. 98:1976;1974-1975.
    • (1976) J. Am. Chem. Soc. , vol.98 , pp. 1974-1975
    • Nakano, M.1    Takayama, K.2    Shimizu, Y.3    Tsuji, Y.4    Inaba, H.5    Migita, T.6
  • 46
    • 0031697188 scopus 로고    scopus 로고
    • DNA damage by tert-butoxyl radicals generated in the photolysis of a water soluble DNA binding peroxyester acting as a radical source
    • Adam W., Grimm G.N., Saha-Moller C.R., Dall'Acqua F., Miolo G., Vedaldi D. DNA damage by tert-butoxyl radicals generated in the photolysis of a water soluble DNA binding peroxyester acting as a radical source. Chem. Res. Toxicol. 11:1998;1089-1097.
    • (1998) Chem. Res. Toxicol. , vol.11 , pp. 1089-1097
    • Adam, W.1    Grimm, G.N.2    Saha-Moller, C.R.3    Dall'Acqua, F.4    Miolo, G.5    Vedaldi, D.6
  • 47
    • 0024354775 scopus 로고
    • Oxygen radical chemistry of polyunsaturated fatty acids
    • Gardner H.W. Oxygen radical chemistry of polyunsaturated fatty acids. Free Radical Biol. Med. 7:1989;65-86.
    • (1989) Free Radical Biol. Med. , vol.7 , pp. 65-86
    • Gardner, H.W.1
  • 48
    • 0023858329 scopus 로고
    • Detection of peroxyl and alkoxyl radicals produced by reaction of hydroperoxides with heme proteins by electron spin resonance spectroscopy
    • Davies M.J. Detection of peroxyl and alkoxyl radicals produced by reaction of hydroperoxides with heme proteins by electron spin resonance spectroscopy. Biochim. Biophys. Acta. 964:1988;28-35.
    • (1988) Biochim. Biophys. Acta , vol.964 , pp. 28-35
    • Davies, M.J.1
  • 49
    • 0020524329 scopus 로고
    • A direct electron spin resonance and spin-trapping investigation of peroxyl free radical formation by hematin/hydroperoxide systems
    • Kalyanaraman B., Mottley C., Mason R.P. A direct electron spin resonance and spin-trapping investigation of peroxyl free radical formation by hematin/hydroperoxide systems. J. Biol. Chem. 258:1983;3855-3858.
    • (1983) J. Biol. Chem. , vol.258 , pp. 3855-3858
    • Kalyanaraman, B.1    Mottley, C.2    Mason, R.P.3
  • 50
    • 0026546319 scopus 로고
    • Bactericidal activity of alkyl peroxyl radicals generated by heme-iron catalyzed decomposition of organic peroxides
    • Akaike T., Sato K., Ijiri S., Miyamoto Y., Kohno M., Ando M., Maeda H. Bactericidal activity of alkyl peroxyl radicals generated by heme-iron catalyzed decomposition of organic peroxides. Arch. Biochem. Biophys. 294:1992;55-63.
    • (1992) Arch. Biochem. Biophys. , vol.294 , pp. 55-63
    • Akaike, T.1    Sato, K.2    Ijiri, S.3    Miyamoto, Y.4    Kohno, M.5    Ando, M.6    Maeda, H.7
  • 51
    • 0021864205 scopus 로고
    • Hematin-catalyzed epoxidation of 7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene by polyunsaturated fatty acid hydroperoxides
    • Dix T.A., Fontana R., Panthani A., Marnett L.J. Hematin-catalyzed epoxidation of 7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene by polyunsaturated fatty acid hydroperoxides. J. Biol. Chem. 260:1985;5358-5365.
    • (1985) J. Biol. Chem. , vol.260 , pp. 5358-5365
    • Dix, T.A.1    Fontana, R.2    Panthani, A.3    Marnett, L.J.4
  • 52
    • 0028361161 scopus 로고
    • Hydrogen peroxide induces G:C to T:A and G:C to C:G transversion in the supF gene of Escherichia coli
    • Akasaka S., Yamamoto K. Hydrogen peroxide induces G:C to T:A and G:C to C:G transversion in the supF gene of Escherichia coli. Mol. Gen. Genet. 243:1994;500-505.
    • (1994) Mol. Gen. Genet. , vol.243 , pp. 500-505
    • Akasaka, S.1    Yamamoto, K.2
  • 53
    • 0024443522 scopus 로고
    • The spectrum of mutations generated by passage of a hydrogen peroxide damaged shuttle vector plasmid through a mammalian host
    • Moraes E.C., Keyse S.M., Pidoux M., Tyrell R.M. The spectrum of mutations generated by passage of a hydrogen peroxide damaged shuttle vector plasmid through a mammalian host. Nucleic Acids Res. 17:1989;8301-8311.
    • (1989) Nucleic Acids Res. , vol.17 , pp. 8301-8311
    • Moraes, E.C.1    Keyse, S.M.2    Pidoux, M.3    Tyrell, R.M.4
  • 54
    • 0021793987 scopus 로고
    • Superoxide dismutase inhibits the superoxide driven Fenton reaction at two different levels
    • Gutteridge J.M.C. Superoxide dismutase inhibits the superoxide driven Fenton reaction at two different levels. FEBS Lett. 185:1985;19-23.
    • (1985) FEBS Lett. , vol.185 , pp. 19-23
    • Gutteridge, J.M.C.1
  • 55
    • 0026011652 scopus 로고
    • Mutagenic spectrum resulting from DNA damage by oxygen radicals
    • McBride T.J., Preston B.D., Loeb L.A. Mutagenic spectrum resulting from DNA damage by oxygen radicals. Biochemistry. 30:1991;207-213.
    • (1991) Biochemistry , vol.30 , pp. 207-213
    • McBride, T.J.1    Preston, B.D.2    Loeb, L.A.3
  • 57
    • 0025981359 scopus 로고
    • Insertion of specific bases during DNA synthesis past the oxidized base 8-oxodG
    • Shibutani S., Takeshita M., Grollman A.P. Insertion of specific bases during DNA synthesis past the oxidized base 8-oxodG. Nature. 391:1991;431-434.
    • (1991) Nature , vol.391 , pp. 431-434
    • Shibutani, S.1    Takeshita, M.2    Grollman, A.P.3
  • 58
    • 0021102422 scopus 로고
    • Insertion of nucleotides opposite apurinic/apyrimidinic sites in deoxyribonucleic acid during in vitro synthesis: Uniqueness of adenine nucleotides
    • Sagher D., Strauss B. Insertion of nucleotides opposite apurinic/apyrimidinic sites in deoxyribonucleic acid during in vitro synthesis: uniqueness of adenine nucleotides. Biochemistry. 22:1983;4518-4526.
    • (1983) Biochemistry , vol.22 , pp. 4518-4526
    • Sagher, D.1    Strauss, B.2
  • 59
    • 0033555373 scopus 로고    scopus 로고
    • Insertion of dGMP and dAMP during in vitro DNA synthesis opposite an oxidized form of 7,8-dihydro-8-oxoguanine
    • Duarte V., Muller J.G., Burrows C.J. Insertion of dGMP and dAMP during in vitro DNA synthesis opposite an oxidized form of 7,8-dihydro-8-oxoguanine. Nucleic Acids Res. 27:1999;496-502.
    • (1999) Nucleic Acids Res. , vol.27 , pp. 496-502
    • Duarte, V.1    Muller, J.G.2    Burrows, C.J.3
  • 60
    • 0026591033 scopus 로고
    • Endogenous oxidative damage of deoxycytidine in DNA
    • Wagner J.R., Hu C.-C., Ames B.N. Endogenous oxidative damage of deoxycytidine in DNA. Proc. Natl. Acad. Sci. 89:1992;3380-3384.
    • (1992) Proc. Natl. Acad. Sci. , vol.89 , pp. 3380-3384
    • Wagner, J.R.1    Hu, C.-C.2    Ames, B.N.3
  • 61
    • 0027983621 scopus 로고
    • 5-Hydroxypyrimidine deoxynucleoside triphosphates are more efficiently incorporated into DNA by exonuclease free Klenow fragment than 8-oxopurine deoxynucleoside triphosphates
    • Purmal A.A., Kow Y.W., Wallace S.S. 5-Hydroxypyrimidine deoxynucleoside triphosphates are more efficiently incorporated into DNA by exonuclease free Klenow fragment than 8-oxopurine deoxynucleoside triphosphates. Nucleic Acids Res. 22:1994;3930-3935.
    • (1994) Nucleic Acids Res. , vol.22 , pp. 3930-3935
    • Purmal, A.A.1    Kow, Y.W.2    Wallace, S.S.3
  • 62
    • 0028335058 scopus 로고
    • Reverse chemical mutagenesis: Identification of the mutagenic lesions resulting from reactive oxygen species-mediated damage to DNA
    • Feig D.I., Sowers L.C., Loeb L.A. Reverse chemical mutagenesis: identification of the mutagenic lesions resulting from reactive oxygen species-mediated damage to DNA. Proc. Natl. Acad. Sci. 91:1994;6609-6613.
    • (1994) Proc. Natl. Acad. Sci. , vol.91 , pp. 6609-6613
    • Feig, D.I.1    Sowers, L.C.2    Loeb, L.A.3
  • 63
    • 0032584107 scopus 로고    scopus 로고
    • Oxidized, deaminated cytosines are a source of C→T transitions in vivo
    • Kreutzer D.A., Essignman J.M. Oxidized, deaminated cytosines are a source of C→T transitions in vivo. Proc. Natl. Acad. Sci. 95:1998;3578-3582.
    • (1998) Proc. Natl. Acad. Sci. , vol.95 , pp. 3578-3582
    • Kreutzer, D.A.1    Essignman, J.M.2
  • 65
    • 0027153293 scopus 로고
    • Tandem double CC→TT mutations are produced by reactive oxygen species
    • Reid T.M., Loeb L.A. Tandem double CC→TT mutations are produced by reactive oxygen species. Proc. Natl. Acad. Sci. 90:1993;3904-3907.
    • (1993) Proc. Natl. Acad. Sci. , vol.90 , pp. 3904-3907
    • Reid, T.M.1    Loeb, L.A.2
  • 66
    • 0027892519 scopus 로고
    • Nickel induces a signature mutation for oxygen free radical damage
    • Tkeshelashvili L.K., Reid T.M., McBride T.J., Loeb L.A. Nickel induces a signature mutation for oxygen free radical damage. Cancer Res. 53:1993;4172-4174.
    • (1993) Cancer Res. , vol.53 , pp. 4172-4174
    • Tkeshelashvili, L.K.1    Reid, T.M.2    McBride, T.J.3    Loeb, L.A.4
  • 67
    • 0033151503 scopus 로고    scopus 로고
    • Detection of tandem CC→TT mutations induced by oxygen radicals using mutation specific PCR
    • Newcomb T.G., Allen K.J., Tkeshelashvili L., Loeb L.A. Detection of tandem CC→TT mutations induced by oxygen radicals using mutation specific PCR. Mutat. Res. 427:1999;21-30.
    • (1999) Mutat. Res. , vol.427 , pp. 21-30
    • Newcomb, T.G.1    Allen, K.J.2    Tkeshelashvili, L.3    Loeb, L.A.4
  • 69
    • 0017406676 scopus 로고
    • Induction of mutations in bacteriophage T7 by gamma rays: Independence of host repair mechanisms
    • Bleichrodt J.F., Roos A.L., Roos-Verheij W.S. Induction of mutations in bacteriophage T7 by gamma rays: independence of host repair mechanisms. Mutat. Res. 43:1977;313-326.
    • (1977) Mutat. Res. , vol.43 , pp. 313-326
    • Bleichrodt, J.F.1    Roos, A.L.2    Roos-Verheij, W.S.3
  • 71
    • 0000820622 scopus 로고
    • A new Salmonella tester strain (TA102) with AT base pairs at the site of mutation detects oxidative mutants
    • Levin D.E., Hollstein M., Christman M.F., Schwiers E.A., Ames B.N. A new Salmonella tester strain (TA102) with AT base pairs at the site of mutation detects oxidative mutants. Proc. Natl. Acad. Sci. 79:1982;7445-7449.
    • (1982) Proc. Natl. Acad. Sci. , vol.79 , pp. 7445-7449
    • Levin, D.E.1    Hollstein, M.2    Christman, M.F.3    Schwiers, E.A.4    Ames, B.N.5
  • 73
    • 0019118979 scopus 로고
    • Mutagenicity of hydroperoxides of fatty acids and some hydrocarbons
    • Yamaguchi T., Yamashita Y. Mutagenicity of hydroperoxides of fatty acids and some hydrocarbons. Agric. Biol. Chem. 44:1980;959-961.
    • (1980) Agric. Biol. Chem. , vol.44 , pp. 959-961
    • Yamaguchi, T.1    Yamashita, Y.2
  • 74
    • 0002161574 scopus 로고    scopus 로고
    • Specificity of spontaneous and t-butyl hydroperoxide-induced mutations in ΔoxyR strains of Escherichia coli differing with respect to SOS mutagenesis proficiency and to the MutY and MutM functions
    • Urios A., Blanco M. Specificity of spontaneous and t-butyl hydroperoxide-induced mutations in ΔoxyR strains of Escherichia coli differing with respect to SOS mutagenesis proficiency and to the MutY and MutM functions. Mutat. Res. 354:1996;95-101.
    • (1996) Mutat. Res. , vol.354 , pp. 95-101
    • Urios, A.1    Blanco, M.2
  • 75
    • 0032993520 scopus 로고    scopus 로고
    • Mutation spectra of chemical mutagens determined by Lac+ reversion assay with Escherichia coli WP3101P-W3106P tester strains
    • Ohta T., Watanabe-Akanuma M., Tokishita S., Yamagata H. Mutation spectra of chemical mutagens determined by Lac+ reversion assay with Escherichia coli WP3101P-W3106P tester strains. Mutat. Res. 440:1999;59-74.
    • (1999) Mutat. Res. , vol.440 , pp. 59-74
    • Ohta, T.1    Watanabe-Akanuma, M.2    Tokishita, S.3    Yamagata, H.4
  • 76
    • 0028074914 scopus 로고
    • Mutagenesis resulting from DNA damage by lipid peroxidation in the supF gene of Escherichia coli
    • Akasaka S., Yamamoto K. Mutagenesis resulting from DNA damage by lipid peroxidation in the supF gene of Escherichia coli. Mutat. Res. 315:1994;105-112.
    • (1994) Mutat. Res. , vol.315 , pp. 105-112
    • Akasaka, S.1    Yamamoto, K.2
  • 77
    • 0025836793 scopus 로고
    • The vinyl chloride DNA derivative N2,3-ethenoguanine produces G→A transitions in Escherichia coli
    • Cheng K.C., Preston B.D., Cahill D.S., Dosanjh M.K., Singer B., Loeb L.A. The vinyl chloride DNA derivative N2,3-ethenoguanine produces G→A transitions in Escherichia coli. Proc. Natl. Acad. Sci. 88:1991;9974-9978.
    • (1991) Proc. Natl. Acad. Sci. , vol.88 , pp. 9974-9978
    • Cheng, K.C.1    Preston, B.D.2    Cahill, D.S.3    Dosanjh, M.K.4    Singer, B.5    Loeb, L.A.6
  • 78
    • 0030794076 scopus 로고    scopus 로고
    • Mutational specificity of glyoxal, a product of DNA oxidation, in the lacI gene of wild type Escherichia coli W3110
    • Murata-Kamiya N., Kamiya H., Kaji H., Kasai H. Mutational specificity of glyoxal, a product of DNA oxidation, in the lacI gene of wild type Escherichia coli W3110. Mutat. Res. 377:1997;255-262.
    • (1997) Mutat. Res. , vol.377 , pp. 255-262
    • Murata-Kamiya, N.1    Kamiya, H.2    Kaji, H.3    Kasai, H.4
  • 79
    • 0030744202 scopus 로고    scopus 로고
    • Mutagenicity in Escherichia coli of the major DNA adduct derived from the endogenous mutagen malondialdehyde
    • Fink S.P., Reddy G.R., Marnett L.J. Mutagenicity in Escherichia coli of the major DNA adduct derived from the endogenous mutagen malondialdehyde. Proc. Natl. Acad. Sci. 94:1997;8652-8657.
    • (1997) Proc. Natl. Acad. Sci. , vol.94 , pp. 8652-8657
    • Fink, S.P.1    Reddy, G.R.2    Marnett, L.J.3
  • 80
    • 0021099440 scopus 로고
    • Depurination induced infidelity of deoxyribonucleic acid synthesis with purified deoxyribonucleic acid replication proteins in vitro
    • Kunkel T.A., Loeb L.A. Depurination induced infidelity of deoxyribonucleic acid synthesis with purified deoxyribonucleic acid replication proteins in vitro. Biochemistry. 22:1983;2378-2384.
    • (1983) Biochemistry , vol.22 , pp. 2378-2384
    • Kunkel, T.A.1    Loeb, L.A.2
  • 81
    • 0026592966 scopus 로고
    • 8-Hydroxyguanine, an abundant form of oxidative DNA damage, causes G→T and A→C transversions
    • Cheng K.C., Cahill D.S., Kasai H., Nishimura S., Loeb L.A. 8-Hydroxyguanine, an abundant form of oxidative DNA damage, causes G→T and A→C transversions. J. Biol. Chem. 267:1992;166-172.
    • (1992) J. Biol. Chem. , vol.267 , pp. 166-172
    • Cheng, K.C.1    Cahill, D.S.2    Kasai, H.3    Nishimura, S.4    Loeb, L.A.5
  • 82
    • 0021434278 scopus 로고
    • Oxidation of lipids: V. Oxidation of methyl linoleate in aqueous dispersion
    • Yamamoto Y., Haga S., Niki E., Kamiya Y. Oxidation of lipids: V. Oxidation of methyl linoleate in aqueous dispersion. Bull. Chem. Soc. Jpn. 57:1984;1260-1264.
    • (1984) Bull. Chem. Soc. Jpn. , vol.57 , pp. 1260-1264
    • Yamamoto, Y.1    Haga, S.2    Niki, E.3    Kamiya, Y.4
  • 83
    • 33845470074 scopus 로고
    • Autoxidation of micelles and model membranes. Quantitative kinetic measurements can be made using either water soluble or lipid soluble initiators with water soluble or lipid soluble chain-breaking antioxidants
    • Barclay L.R.C., Locke S.J., MacNeil J.M., VanKessel J. Autoxidation of micelles and model membranes. Quantitative kinetic measurements can be made using either water soluble or lipid soluble initiators with water soluble or lipid soluble chain-breaking antioxidants. J. Am. Chem. Soc. 106:1984;2479-2481.
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 2479-2481
    • Barclay, L.R.C.1    Locke, S.J.2    MacNeil, J.M.3    Vankessel, J.4
  • 84
    • 0025082043 scopus 로고
    • Free radical initiators as sources of water- Or lipid-soluble peroxyl radicals
    • Niki E. Free radical initiators as sources of water- or lipid-soluble peroxyl radicals. Methods Enzymol. 186:1990;100-108.
    • (1990) Methods Enzymol. , vol.186 , pp. 100-108
    • Niki, E.1
  • 85
    • 0032510701 scopus 로고    scopus 로고
    • Mutagenesis by peroxy radical is dominated by transversions at deoxyguanosine: Evidence for a lack of involvement of 8-oxodG and/or abasic site formation
    • Valentine M.R., Rodriguez H., Termini J. Mutagenesis by peroxy radical is dominated by transversions at deoxyguanosine: evidence for a lack of involvement of 8-oxodG and/or abasic site formation. Biochemistry. 37:1998;7030-7038.
    • (1998) Biochemistry , vol.37 , pp. 7030-7038
    • Valentine, M.R.1    Rodriguez, H.2    Termini, J.3
  • 86
    • 0032913246 scopus 로고    scopus 로고
    • Mutations at GC base pairs predominate after replication of peroxyl radical-damaged pSP189 plasmid in human cells
    • Burcham P.C., Harkin L.A. Mutations at GC base pairs predominate after replication of peroxyl radical-damaged pSP189 plasmid in human cells. Mutagenesis. 14:1999;135-140.
    • (1999) Mutagenesis , vol.14 , pp. 135-140
    • Burcham, P.C.1    Harkin, L.A.2
  • 87
    • 0026577281 scopus 로고
    • Lipid peroxidation products mediate the formation of 8-hydroxydeoxyguanosine in DNA
    • Park J.-W., Floyd R.A. Lipid peroxidation products mediate the formation of 8-hydroxydeoxyguanosine in DNA. Free Radical Biol. Med. 112:1992;245-250.
    • (1992) Free Radical Biol. Med. , vol.112 , pp. 245-250
    • Park, J.-W.1    Floyd, R.A.2
  • 88
    • 0024571329 scopus 로고
    • Site-specific oxidative DNA damage at polyguanosine produced by copper plus hydrogen peroxide
    • Sagripanti J.-L., Kraemer K.H. Site-specific oxidative DNA damage at polyguanosine produced by copper plus hydrogen peroxide. J. Biol. Chem. 264:1989;1729-1734.
    • (1989) J. Biol. Chem. , vol.264 , pp. 1729-1734
    • Sagripanti, J.-L.1    Kraemer, K.H.2
  • 89
    • 29544444893 scopus 로고
    • Photoinduced DNA cleavage via electron transfer: Demonstration that guanine residues located 5ô to guanine are the most electron donating sites
    • Saito I., Takayama M., Sugiyama H., Nakatani N., Tsuchida A., Yamamoto M. Photoinduced DNA cleavage via electron transfer: demonstration that guanine residues located 5ô to guanine are the most electron donating sites. J. Biol. Chem. Soc. 117:1995;6406-6407.
    • (1995) J. Biol. Chem. Soc. , vol.117 , pp. 6406-6407
    • Saito, I.1    Takayama, M.2    Sugiyama, H.3    Nakatani, N.4    Tsuchida, A.5    Yamamoto, M.6
  • 90
    • 0024458564 scopus 로고
    • Hydroxyl free radical is not the main active species in site specific DNA damage induced by copper(II) ion and hydrogen peroxide
    • Yamamoto K., Kawanishi S. Hydroxyl free radical is not the main active species in site specific DNA damage induced by copper(II) ion and hydrogen peroxide. J. Biol. Chem. 264:1989;15435-15440.
    • (1989) J. Biol. Chem. , vol.264 , pp. 15435-15440
    • Yamamoto, K.1    Kawanishi, S.2
  • 91
    • 0029128743 scopus 로고
    • Mapping of copper/hydrogen peroxide induced DNA damage at nucleotide resolution in human genomic DNA by ligation mediated polymerase chain reaction
    • Rodriguez H., Drouin R., Holmquist G.P., O'Connor T.R., Boiteux S., Laval J., Doroshow J.H., Akman S.A. Mapping of copper/hydrogen peroxide induced DNA damage at nucleotide resolution in human genomic DNA by ligation mediated polymerase chain reaction. J. Biol. Chem. 270:1995;17633-17640.
    • (1995) J. Biol. Chem. , vol.270 , pp. 17633-17640
    • Rodriguez, H.1    Drouin, R.2    Holmquist, G.P.3    O'Connor, T.R.4    Boiteux, S.5    Laval, J.6    Doroshow, J.H.7    Akman, S.A.8
  • 92
    • 0024161399 scopus 로고
    • AP endonucleases and DNA glycosylases that recognized oxidative DNA damage
    • Wallace S.S. AP endonucleases and DNA glycosylases that recognized oxidative DNA damage. Environ. Mol. Mutagen. 12:1988;431-477.
    • (1988) Environ. Mol. Mutagen. , vol.12 , pp. 431-477
    • Wallace, S.S.1
  • 93
    • 0030979263 scopus 로고    scopus 로고
    • DNA glycosylases
    • Cunningham R.P. DNA glycosylases. Mutat. Res. 383:1997;189-196.
    • (1997) Mutat. Res. , vol.383 , pp. 189-196
    • Cunningham, R.P.1
  • 94
    • 0030976277 scopus 로고    scopus 로고
    • Metal ion-dependent hydrogen peroxide induced DNA damage is more sequence specific than metal specific
    • Rodriguez H., Holmquist G.P., D'Agostino R. Jr., Keller J., Akman S.A. Metal ion-dependent hydrogen peroxide induced DNA damage is more sequence specific than metal specific. Cancer Res. 57:1997;2394-2403.
    • (1997) Cancer Res. , vol.57 , pp. 2394-2403
    • Rodriguez, H.1    Holmquist, G.P.2    D'Agostino R., Jr.3    Keller, J.4    Akman, S.A.5
  • 95
    • 0023841337 scopus 로고
    • Harms-Ringdahl interaction of lipid peroxidation products with DNA, a review
    • Vaca C.E., Wilhelm J. Harms-Ringdahl interaction of lipid peroxidation products with DNA, a review. Mutat. Res. 195:1988;137-149.
    • (1988) Mutat. Res. , vol.195 , pp. 137-149
    • Vaca, C.E.1    Wilhelm, J.2
  • 96
    • 0028175960 scopus 로고
    • Generation of alpha hydroxyaldehydic compounds in the course of lipid peroxidation
    • Loidl-Stahlhofen A., Hannemann K., Spiteller G. Generation of alpha hydroxyaldehydic compounds in the course of lipid peroxidation. Biochim. Biophys. Acta. 1213:1994;140-148.
    • (1994) Biochim. Biophys. Acta , vol.1213 , pp. 140-148
    • Loidl-Stahlhofen, A.1    Hannemann, K.2    Spiteller, G.3
  • 98
    • 0028107094 scopus 로고
    • Reinvestigation of lipid peroxidation of linolenic acid
    • Mlakar A., Spiteller G. Reinvestigation of lipid peroxidation of linolenic acid. Biochim. Biophys. Acta. 1214:1994;209-220.
    • (1994) Biochim. Biophys. Acta , vol.1214 , pp. 209-220
    • Mlakar, A.1    Spiteller, G.2
  • 100
    • 0023905646 scopus 로고
    • Toxic DNA damage by hydrogen peroxide through the Fenton reaction in vivo and in vitro
    • Imlay J.A., Chin S.M., Linn S. Toxic DNA damage by hydrogen peroxide through the Fenton reaction in vivo and in vitro. Science. 240:1988;640-642.
    • (1988) Science , vol.240 , pp. 640-642
    • Imlay, J.A.1    Chin, S.M.2    Linn, S.3
  • 101
    • 0023240996 scopus 로고
    • Radiation and hydrogen peroxide induced free radical damage to DNA
    • Ward J.F., Evans J.W., Limoli C.I., Calabro-Jones P.M. Radiation and hydrogen peroxide induced free radical damage to DNA. Br. J. Cancer. 55(Suppl. VIII):1987;105-112.
    • (1987) Br. J. Cancer , vol.55 , Issue.SUPPL. VIII , pp. 105-112
    • Ward, J.F.1    Evans, J.W.2    Limoli, C.I.3    Calabro-Jones, P.M.4
  • 102
    • 0021360269 scopus 로고
    • In vivo formation of single-strand breaks in DNA by hydrogen peroxide is mediated by the Haber-Weiss reaction
    • Filho A.C.M., Meneghini R. In vivo formation of single-strand breaks in DNA by hydrogen peroxide is mediated by the Haber-Weiss reaction. Biochim. Biophys. Acta. 781:1984;56-63.
    • (1984) Biochim. Biophys. Acta , vol.781 , pp. 56-63
    • Filho, A.C.M.1    Meneghini, R.2
  • 103
    • 0024419843 scopus 로고
    • Hydrogen peroxide insult in cultured mammalian cells: Relationships between DNA single strand breakage, poly(ADP-ribose) metabolism and cell killing
    • Cantoni O., Cattabeni F., Stocchi V., Meyn R.I., Cerutti P., Murray D. Hydrogen peroxide insult in cultured mammalian cells: relationships between DNA single strand breakage, poly(ADP-ribose) metabolism and cell killing. Biochim. Biophys. Acta. 1010:1989;1-7.
    • (1989) Biochim. Biophys. Acta , vol.1010 , pp. 1-7
    • Cantoni, O.1    Cattabeni, F.2    Stocchi, V.3    Meyn, R.I.4    Cerutti, P.5    Murray, D.6
  • 104
    • 0026344421 scopus 로고
    • Elaboration of cellular DNA breaks by hydroperoxides
    • Baker M.A., He S. Elaboration of cellular DNA breaks by hydroperoxides. Free Radical Biol. Med. 11:1991;563-572.
    • (1991) Free Radical Biol. Med. , vol.11 , pp. 563-572
    • Baker, M.A.1    He, S.2
  • 105
    • 0024516338 scopus 로고
    • Cell killing and DNA damage in Chinese hamster V79 cells treated with hydrogen peroxide
    • Prise K.M., Davies S., Michael B.D. Cell killing and DNA damage in Chinese hamster V79 cells treated with hydrogen peroxide. Int. J. Radiat. Biol. 55:1989;583-592.
    • (1989) Int. J. Radiat. Biol. , vol.55 , pp. 583-592
    • Prise, K.M.1    Davies, S.2    Michael, B.D.3
  • 106
    • 0030034478 scopus 로고    scopus 로고
    • Factors affecting DNA damage caused by lipid hydroperoxides and aldehydes
    • Yang M.-H., Schaich K.M. Factors affecting DNA damage caused by lipid hydroperoxides and aldehydes. Free Radical Biol. Med. 20:1996;225-236.
    • (1996) Free Radical Biol. Med. , vol.20 , pp. 225-236
    • Yang, M.-H.1    Schaich, K.M.2
  • 107
    • 0023157655 scopus 로고
    • Clastogenic action of hydroperoxy-5,8,11,13-icosatetraenoic acids on the mouse embryo fibroblasts C3H/10T1/2
    • Ochi T., Cerutti P.A. Clastogenic action of hydroperoxy-5,8,11,13-icosatetraenoic acids on the mouse embryo fibroblasts C3H/10T1/2. Proc. Natl. Acad. Sci. 84:1987;990-994.
    • (1987) Proc. Natl. Acad. Sci. , vol.84 , pp. 990-994
    • Ochi, T.1    Cerutti, P.A.2
  • 108
    • 3042877493 scopus 로고    scopus 로고
    • Lipid peroxidation product-mediated DNA damage and mutagenicity
    • Koh Y.-H., Yoon S.J., Park J.W. Lipid peroxidation product-mediated DNA damage and mutagenicity. J. Biochem. Mol. Biol. 30:1997;188-193.
    • (1997) J. Biochem. Mol. Biol. , vol.30 , pp. 188-193
    • Koh, Y.-H.1    Yoon, S.J.2    Park, J.W.3
  • 109
    • 0022645020 scopus 로고
    • Hydroxyl radical-induced strand break formation of poly(U) in the presence of oxygen: Comparison of the rates as determined by conductivity, e.s.r. and rapid-mix experiments with a thio
    • Bothe E., Behrens G., Böhm E., Sethuram B., Schulte-Frohlinde D. Hydroxyl radical-induced strand break formation of poly(U) in the presence of oxygen: comparison of the rates as determined by conductivity, e.s.r. and rapid-mix experiments with a thio. Int. J. Radiat. Biol. 49:1986;57-66.
    • (1986) Int. J. Radiat. Biol. , vol.49 , pp. 57-66
    • Bothe, E.1    Behrens, G.2    Böhm, E.3    Sethuram, B.4    Schulte-Frohlinde, D.5
  • 110
    • 0025360798 scopus 로고
    • The kinetics of radiation-induced strand breakage in polynucleotides in the presence of oxygen: A time-resolved light-scattering study
    • Jones G.D.D., O'Neill P. The kinetics of radiation-induced strand breakage in polynucleotides in the presence of oxygen: a time-resolved light-scattering study. Int. J. Radiat. Biol. 57:1990;1123-1139.
    • (1990) Int. J. Radiat. Biol. , vol.57 , pp. 1123-1139
    • Jones, G.D.D.1    O'Neill, P.2
  • 112
    • 33748719327 scopus 로고
    • Mechanisms of bleomycin-induced DNA degradation
    • Stubbe J., Kozarich J.W. Mechanisms of bleomycin-induced DNA degradation. Chem. Rev. 87:1987;1107-1136.
    • (1987) Chem. Rev. , vol.87 , pp. 1107-1136
    • Stubbe, J.1    Kozarich, J.W.2
  • 113
    • 0028857739 scopus 로고
    • Oxidative DNA damage by t-butyl hydroperoxide causes DNA strand breaks which is not linked to cell lysis. A mechanistic study in freshly isolated rat hepatocytes
    • Latour I., Demoulin J.B., Buc-Calderon P. Oxidative DNA damage by t-butyl hydroperoxide causes DNA strand breaks which is not linked to cell lysis. A mechanistic study in freshly isolated rat hepatocytes. FEBS Lett. 373:1995;299-302.
    • (1995) FEBS Lett. , vol.373 , pp. 299-302
    • Latour, I.1    Demoulin, J.B.2    Buc-Calderon, P.3
  • 114
    • 0030321158 scopus 로고    scopus 로고
    • The oxidizing agent tertiary butyl hydroperoxide induces disturbances in spindle organization, c-meiosis, and aneuploidy in mouse oocytes
    • Tarin J.J., Vendrell F.J., Ten J., Blanes R., van Blerkom J., Cano A. The oxidizing agent tertiary butyl hydroperoxide induces disturbances in spindle organization, c-meiosis, and aneuploidy in mouse oocytes. Mol. Hum. Reprod. 12:1996;895-901.
    • (1996) Mol. Hum. Reprod. , vol.12 , pp. 895-901
    • Tarin, J.J.1    Vendrell, F.J.2    Ten, J.3    Blanes, R.4    Van Blerkom, J.5    Cano, A.6
  • 115
    • 0021758865 scopus 로고
    • Site-specific cleavage of double-strand DNA by hydroperoxide of linoleic acid
    • Inouye S. Site-specific cleavage of double-strand DNA by hydroperoxide of linoleic acid. FEBS Lett. 172:1984;231-234.
    • (1984) FEBS Lett. , vol.172 , pp. 231-234
    • Inouye, S.1
  • 116
    • 0027318463 scopus 로고
    • Sequence dependent DNA structure. The role of base stacking interactions
    • Hunter C.A. Sequence dependent DNA structure. The role of base stacking interactions. J. Mol. Biol. 230:1993;1025-1054.
    • (1993) J. Mol. Biol. , vol.230 , pp. 1025-1054
    • Hunter, C.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.