-
1
-
-
2442605692
-
MCLA-dependent chemiluminescence suggests that singlet oxygen plays a pivotal role in myeloperoxidase-catalysed bactericidal action in neutrophil phagosomes
-
Arisawa F., Tatsuzawa H., Kambayashi Y., Kuwano H., Fujimori K., Nakano M. MCLA-dependent chemiluminescence suggests that singlet oxygen plays a pivotal role in myeloperoxidase-catalysed bactericidal action in neutrophil phagosomes. Luminescence 2003, 18:229-238.
-
(2003)
Luminescence
, vol.18
, pp. 229-238
-
-
Arisawa, F.1
Tatsuzawa, H.2
Kambayashi, Y.3
Kuwano, H.4
Fujimori, K.5
Nakano, M.6
-
2
-
-
34248525587
-
Direct detection of singlet oxygen generated by UVA irradiation in human cells and skin
-
Baier J., Maisch T., Maier M., Landthaler M., Baumler W. Direct detection of singlet oxygen generated by UVA irradiation in human cells and skin. J. Invest. Dermatol. 2007, 127:1498-1506.
-
(2007)
J. Invest. Dermatol.
, vol.127
, pp. 1498-1506
-
-
Baier, J.1
Maisch, T.2
Maier, M.3
Landthaler, M.4
Baumler, W.5
-
3
-
-
0024660607
-
Singlet oxygen induces frank strand breaks as well as alkali- and piperidine-labile sites in supercoiled plasmid DNA
-
Blazek E.R., Peak J.G., Peak M.J. Singlet oxygen induces frank strand breaks as well as alkali- and piperidine-labile sites in supercoiled plasmid DNA. Photochem. Photobiol. 1989, 49:607-613.
-
(1989)
Photochem. Photobiol.
, vol.49
, pp. 607-613
-
-
Blazek, E.R.1
Peak, J.G.2
Peak, M.J.3
-
4
-
-
33846846509
-
The substrate specificity of mutY for hyperoxidized guanine lesions in vivo
-
Delaney S., Neeley W.L., Delaney J.C., Essigmann J.M. The substrate specificity of mutY for hyperoxidized guanine lesions in vivo. Biochemistry 2007, 46:1448-1455.
-
(2007)
Biochemistry
, vol.46
, pp. 1448-1455
-
-
Delaney, S.1
Neeley, W.L.2
Delaney, J.C.3
Essigmann, J.M.4
-
5
-
-
0028802733
-
Protection of plasmid pBR322 DNA by flavonoids against single-strand breaks induced by singlet molecular oxygen
-
Devasagayam T.P.A., Subramanian M., Singh B.B., Ramanathan R., Das N.P. Protection of plasmid pBR322 DNA by flavonoids against single-strand breaks induced by singlet molecular oxygen. J. Photochem. Photobiol. B 1995, 30:97-103.
-
(1995)
J. Photochem. Photobiol. B
, vol.30
, pp. 97-103
-
-
Devasagayam, T.P.A.1
Subramanian, M.2
Singh, B.B.3
Ramanathan, R.4
Das, N.P.5
-
6
-
-
0000978276
-
Quantification of singlet oxygen generated by thermolysis of 3,3'-(1,4-naphthylidene)dipropionate. Monomol and dimol photoemission and the effects of 1,4-diazabicyclo[2.2.2]octane
-
Di Mascio P., Sies H. Quantification of singlet oxygen generated by thermolysis of 3,3'-(1,4-naphthylidene)dipropionate. Monomol and dimol photoemission and the effects of 1,4-diazabicyclo[2.2.2]octane. J. Am. Chem. Soc. 1989, 111:2909-2915.
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 2909-2915
-
-
Di Mascio, P.1
Sies, H.2
-
7
-
-
0025397754
-
Singlet molecular oxygen induced mutagenicity in a mammalian SV40-based shuttle vector
-
Di Mascio P., Menck C.F., Nigro R.G., Sarasin A., Sies H. Singlet molecular oxygen induced mutagenicity in a mammalian SV40-based shuttle vector. Photochem. Photobiol. 1990, 51:293-298.
-
(1990)
Photochem. Photobiol.
, vol.51
, pp. 293-298
-
-
Di Mascio, P.1
Menck, C.F.2
Nigro, R.G.3
Sarasin, A.4
Sies, H.5
-
8
-
-
0034177417
-
In vitro DNA synthesis opposite oxazolone and repair of this DNA damage using modified oligonucleotides
-
Duarte V., Gasparutto D., Jaquinod M., Cadet J.-L. In vitro DNA synthesis opposite oxazolone and repair of this DNA damage using modified oligonucleotides. Nucleic Acids Res. 2000, 28:1555-1563.
-
(2000)
Nucleic Acids Res.
, vol.28
, pp. 1555-1563
-
-
Duarte, V.1
Gasparutto, D.2
Jaquinod, M.3
Cadet, J.-L.4
-
9
-
-
0034723011
-
Oxaluric acid as the major product of singlet oxygen-mediated oxidation of 8-oxo-7,8-dihydroguanine in DNA
-
Duarte V., Gasparutto D., Yamaguchi L.F., Ravanat J.-L., Martinez G.R., Medeiros M.H.G., Di Mascio P., Cadet J. Oxaluric acid as the major product of singlet oxygen-mediated oxidation of 8-oxo-7,8-dihydroguanine in DNA. J. Am. Chem. Soc. 2000, 122:12622-12628.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 12622-12628
-
-
Duarte, V.1
Gasparutto, D.2
Yamaguchi, L.F.3
Ravanat, J.-L.4
Martinez, G.R.5
Medeiros, M.H.G.6
Di Mascio, P.7
Cadet, J.8
-
10
-
-
0035157221
-
Repair and mutagenic potential of oxaluric acid, a major product of singlet oxygen-mediated oxidation of 8-oxo-7,8-dihydroguanine
-
Duarte V., Gasparutto D., Jaquinod M., Ravanat J.-L., Cadet J. Repair and mutagenic potential of oxaluric acid, a major product of singlet oxygen-mediated oxidation of 8-oxo-7,8-dihydroguanine. Chem. Res. Toxicol. 2001, 14:46-53.
-
(2001)
Chem. Res. Toxicol.
, vol.14
, pp. 46-53
-
-
Duarte, V.1
Gasparutto, D.2
Jaquinod, M.3
Ravanat, J.-L.4
Cadet, J.5
-
11
-
-
0036849077
-
The biochemistry and medical significance of the flavonoids
-
Havsteen B.H. The biochemistry and medical significance of the flavonoids. Pharmacol. Ther. 2002, 96:67-202.
-
(2002)
Pharmacol. Ther.
, vol.96
, pp. 67-202
-
-
Havsteen, B.H.1
-
12
-
-
0035339684
-
Repair of hydantoins, one electron oxidation product of 8-oxoguanine, by DNA glycosylases of Escherichia coli
-
Hazra T.K., Muller J.G., Manuel R.C., Burrows C.J., Lloyd R.S., Miltra S. Repair of hydantoins, one electron oxidation product of 8-oxoguanine, by DNA glycosylases of Escherichia coli. Nucleic Acids Res. 2001, 29:1967-1974.
-
(2001)
Nucleic Acids Res.
, vol.29
, pp. 1967-1974
-
-
Hazra, T.K.1
Muller, J.G.2
Manuel, R.C.3
Burrows, C.J.4
Lloyd, R.S.5
Miltra, S.6
-
13
-
-
0041571565
-
The hydantoin lesions formed from oxidation of 7,8-dihydro-8-oxoguanine are potent sources of replication errors in vivo
-
Henderson P.T., Delaney J.C., Muller J.G., Neeley W.L., Tannenbaum S.R., Burrows C.J., Essigmann J.M. The hydantoin lesions formed from oxidation of 7,8-dihydro-8-oxoguanine are potent sources of replication errors in vivo. Biochemistry 2003, 42:9257-9262.
-
(2003)
Biochemistry
, vol.42
, pp. 9257-9262
-
-
Henderson, P.T.1
Delaney, J.C.2
Muller, J.G.3
Neeley, W.L.4
Tannenbaum, S.R.5
Burrows, C.J.6
Essigmann, J.M.7
-
14
-
-
34548179685
-
Flavonoids as protectors against doxorubicin cardiotoxicity: role of iron chelation, antioxidant activity and inhibition of carbonyl reductase
-
Kaiserová H., Simunek T., van der Vijgh W.J., Bast A., Kvasničková E. Flavonoids as protectors against doxorubicin cardiotoxicity: role of iron chelation, antioxidant activity and inhibition of carbonyl reductase. Biochim. Biophys. Acta 2007, 1772:1065-1074.
-
(2007)
Biochim. Biophys. Acta
, vol.1772
, pp. 1065-1074
-
-
Kaiserová, H.1
Simunek, T.2
van der Vijgh, W.J.3
Bast, A.4
Kvasničková, E.5
-
15
-
-
0037168491
-
In vitro nucleotide misinsertion opposite the oxidized guanosine lesions spiroiminodihydantoin and guanidinohydantoin and DNA synthesis past the lesions using Escherichia coli DNA polymerase I (Klenow fragment)
-
Kornyushyna O., Berges A.M., Muller J.G., Burrows C.J. In vitro nucleotide misinsertion opposite the oxidized guanosine lesions spiroiminodihydantoin and guanidinohydantoin and DNA synthesis past the lesions using Escherichia coli DNA polymerase I (Klenow fragment). Biochemistry 2002, 41:15304-15314.
-
(2002)
Biochemistry
, vol.41
, pp. 15304-15314
-
-
Kornyushyna, O.1
Berges, A.M.2
Muller, J.G.3
Burrows, C.J.4
-
16
-
-
34548085699
-
Unusual structural features of hydantoin lesions translate into efficient recognition by Escherichia coli Fpg
-
Krishnamurthy N., Muller J.G., Burrows C.J., David S.S. Unusual structural features of hydantoin lesions translate into efficient recognition by Escherichia coli Fpg. Biochemistry 2007, 46:9355-9365.
-
(2007)
Biochemistry
, vol.46
, pp. 9355-9365
-
-
Krishnamurthy, N.1
Muller, J.G.2
Burrows, C.J.3
David, S.S.4
-
17
-
-
46849104669
-
Superior removal of hydantoin lesions relative to other oxidized bases by the human DNA glycosylase hNEIL1
-
Krishnamurthy N., Zhao X., Burrows C.J., David S.S. Superior removal of hydantoin lesions relative to other oxidized bases by the human DNA glycosylase hNEIL1. Biochemistry 2008, 47:7137-7146.
-
(2008)
Biochemistry
, vol.47
, pp. 7137-7146
-
-
Krishnamurthy, N.1
Zhao, X.2
Burrows, C.J.3
David, S.S.4
-
18
-
-
0034610403
-
Removal of hydantoin products of 8-oxoguanine oxidation by the Escherichia coli DNA repair enzyme, Fpg
-
Leipold M.D., Muller J.G., Burrows C.J., David S.S. Removal of hydantoin products of 8-oxoguanine oxidation by the Escherichia coli DNA repair enzyme, Fpg. Biochemistry 2000, 39:14984-14992.
-
(2000)
Biochemistry
, vol.39
, pp. 14984-14992
-
-
Leipold, M.D.1
Muller, J.G.2
Burrows, C.J.3
David, S.S.4
-
19
-
-
0034684183
-
Synthesis of a naphthalene endoperoxide as a source of 18O-labeled singlet oxygen for mechanistic
-
Martinez G.R., Ravanat J.-L., Medeiros M.H.G., Cadet J., Di Mascio P.J. Synthesis of a naphthalene endoperoxide as a source of 18O-labeled singlet oxygen for mechanistic. J. Am. Chem. Soc. 2000, 122:10212-10213.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 10212-10213
-
-
Martinez, G.R.1
Ravanat, J.-L.2
Medeiros, M.H.G.3
Cadet, J.4
Di Mascio, P.J.5
-
20
-
-
0036012746
-
[18O]-labeled singlet oxygen as a tool for mechanistic studies of 8-oxo-7,8-dihydroguanine oxidative damage: detection of spiroiminodihydantoin, imidazolone and oxazolone derivatives
-
Martinez G.R., Ravanat J.-L., Medeiros M.H.G., Cadet J., Di Mascio P. [18O]-labeled singlet oxygen as a tool for mechanistic studies of 8-oxo-7,8-dihydroguanine oxidative damage: detection of spiroiminodihydantoin, imidazolone and oxazolone derivatives. Biol. Chem. 2002, 383:607-617.
-
(2002)
Biol. Chem.
, vol.383
, pp. 607-617
-
-
Martinez, G.R.1
Ravanat, J.-L.2
Medeiros, M.H.G.3
Cadet, J.4
Di Mascio, P.5
-
21
-
-
10744231806
-
Oxidative and alkylating damage in DNA
-
Martinez G.R., Miyamoto S., Loureiro A.P., Marques S.A., Yamaguchi L.F., Onuki J., Almeida E.A., Garcia C.C., Barbosa L.F., Medeiros M.H.G., Di Mascio P. Oxidative and alkylating damage in DNA. Mutat. Res. 2003, 544:115-127.
-
(2003)
Mutat. Res.
, vol.544
, pp. 115-127
-
-
Martinez, G.R.1
Miyamoto, S.2
Loureiro, A.P.3
Marques, S.A.4
Yamaguchi, L.F.5
Onuki, J.6
Almeida, E.A.7
Garcia, C.C.8
Barbosa, L.F.9
Medeiros, M.H.G.10
Di Mascio, P.11
-
22
-
-
35649011915
-
Spiroiminodihydantoin nucleoside formation from 2'-deoxyguanosine oxidation by 18O-labeled singlet molecular oxygen in aqueous solution
-
Martinez G.R., Ravanat J.-L., Cadet J., Medeiros M.H.G., Di Mascio P. Spiroiminodihydantoin nucleoside formation from 2'-deoxyguanosine oxidation by 18O-labeled singlet molecular oxygen in aqueous solution. J. Mass Spectrom. 2007, 42:1326-1332.
-
(2007)
J. Mass Spectrom.
, vol.42
, pp. 1326-1332
-
-
Martinez, G.R.1
Ravanat, J.-L.2
Cadet, J.3
Medeiros, M.H.G.4
Di Mascio, P.5
-
23
-
-
36849037908
-
Flavonoid effects on DNA oxidation at low concentrations relevant to physiological levels
-
Min K., Ebeler S.E. Flavonoid effects on DNA oxidation at low concentrations relevant to physiological levels. Food Chem. Toxicol. 2008, 46:96-104.
-
(2008)
Food Chem. Toxicol.
, vol.46
, pp. 96-104
-
-
Min, K.1
Ebeler, S.E.2
-
24
-
-
0038288716
-
Singlet molecular oxygen generated from lipid hydroperoxides by the Russell mechanism: studies using 18O-labeled linoleic acid hydroperoxide and monomol light emission measurements
-
Miyamoto S., Martinez G.R., Medeiros M.H.G., Di Mascio P. Singlet molecular oxygen generated from lipid hydroperoxides by the Russell mechanism: studies using 18O-labeled linoleic acid hydroperoxide and monomol light emission measurements. J. Am. Chem. Soc. 2003, 125:6172-6179.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 6172-6179
-
-
Miyamoto, S.1
Martinez, G.R.2
Medeiros, M.H.G.3
Di Mascio, P.4
-
25
-
-
23744469411
-
Kinetic study of the quenching reaction of singlet oxygen by tea catechins in ethanol solution
-
Mukai K., Nagai S., Ohara K. Kinetic study of the quenching reaction of singlet oxygen by tea catechins in ethanol solution. Free Radical Biol. Med. 2005, 39:752-761.
-
(2005)
Free Radical Biol. Med.
, vol.39
, pp. 752-761
-
-
Mukai, K.1
Nagai, S.2
Ohara, K.3
-
26
-
-
15544387089
-
Kinetic study of the quenching reaction of singlet oxygen by flavonoids in ethanol solution
-
Nagai S., Ohara K., Mukai K. Kinetic study of the quenching reaction of singlet oxygen by flavonoids in ethanol solution. J. Phys. Chem. B 2005, 109:4234-4240.
-
(2005)
J. Phys. Chem. B
, vol.109
, pp. 4234-4240
-
-
Nagai, S.1
Ohara, K.2
Mukai, K.3
-
27
-
-
0030266005
-
Water-soluble naphthalene derivatives as singlet oxygen (1O2,1Δg) carriers for biological media
-
Pierlot C., Hajjam S., Barthélémy C., Aubry J.-M. Water-soluble naphthalene derivatives as singlet oxygen (1O2,1Δg) carriers for biological media. J. Photochem. Photobiol. B 1996, 36:31-39.
-
(1996)
J. Photochem. Photobiol. B
, vol.36
, pp. 31-39
-
-
Pierlot, C.1
Hajjam, S.2
Barthélémy, C.3
Aubry, J.-M.4
-
28
-
-
0031005141
-
Determination of the quenching rate constants of singlet oxygen by derivatized nucleosides in nonaqueous solution
-
Prat F., Houk K.N., Foote C.S. Determination of the quenching rate constants of singlet oxygen by derivatized nucleosides in nonaqueous solution. J. Am. Chem. Soc. 1997, 119:5051-5052.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 5051-5052
-
-
Prat, F.1
Houk, K.N.2
Foote, C.S.3
-
29
-
-
0028927763
-
Reaction of singlet oxygen with 2'-deoxyguanosine and DNA. Isolation and characterization of the main oxidation products
-
Ravanat J.-L., Cadet J. Reaction of singlet oxygen with 2'-deoxyguanosine and DNA. Isolation and characterization of the main oxidation products. Chem. Res. Toxicol. 1995, 8:379-388.
-
(1995)
Chem. Res. Toxicol.
, vol.8
, pp. 379-388
-
-
Ravanat, J.-L.1
Cadet, J.2
-
30
-
-
0001014503
-
Phthalocyanine and naphthalocyanine photosensitized oxidation of 2'-deoxyguanosine: distinct type I and type II products
-
Ravanat J.-L., Berger M., Benard F., Langlois R., Ouellet R., van Lier J.E., Cadet J. Phthalocyanine and naphthalocyanine photosensitized oxidation of 2'-deoxyguanosine: distinct type I and type II products. Photochem. Photobiol. 1992, 55:809-814.
-
(1992)
Photochem. Photobiol.
, vol.55
, pp. 809-814
-
-
Ravanat, J.-L.1
Berger, M.2
Benard, F.3
Langlois, R.4
Ouellet, R.5
van Lier, J.E.6
Cadet, J.7
-
31
-
-
0035691928
-
Damage to isolated DNA mediated by singlet oxygen
-
Ravanat J.-L., Saint-Pierre C., Di Mascio P., Martinez G.R., Medeiros M.H.G., Cadet J. Damage to isolated DNA mediated by singlet oxygen. Helv. Chim. Acta 2001, 84:3702-3709.
-
(2001)
Helv. Chim. Acta
, vol.84
, pp. 3702-3709
-
-
Ravanat, J.-L.1
Saint-Pierre, C.2
Di Mascio, P.3
Martinez, G.R.4
Medeiros, M.H.G.5
Cadet, J.6
-
32
-
-
34248356804
-
Efficient and erroneous incorporation of oxidized DNA precursors by human DNA polymerase η
-
Shimizu M., Gruz P., Kamiya H., Masutani C., Xu Y., Usui Y., Sugiyama H., Harashima H., Hanaoka F., Nohmi T. Efficient and erroneous incorporation of oxidized DNA precursors by human DNA polymerase η. Biochemistry 2007, 46:5515-5522.
-
(2007)
Biochemistry
, vol.46
, pp. 5515-5522
-
-
Shimizu, M.1
Gruz, P.2
Kamiya, H.3
Masutani, C.4
Xu, Y.5
Usui, Y.6
Sugiyama, H.7
Harashima, H.8
Hanaoka, F.9
Nohmi, T.10
-
33
-
-
42949175751
-
Base excision repair system suppresses mutagenesis caused by 8-hydroxy-dGTP in Escherichia coli
-
Suzuki T., Yamamoto K., Harashima H., Kamiya H. Base excision repair system suppresses mutagenesis caused by 8-hydroxy-dGTP in Escherichia coli. Nucleic Acids Symp. Ser. 2007, 51:51-52.
-
(2007)
Nucleic Acids Symp. Ser.
, vol.51
, pp. 51-52
-
-
Suzuki, T.1
Yamamoto, K.2
Harashima, H.3
Kamiya, H.4
-
34
-
-
0027177780
-
Antioxidant activity of flavonoids: efficiency of singlet oxygen quenching
-
Tournaire C., Croux S., Maurette M.T., Beck I., Hocquaux M., Braun M., Oliveros E. Antioxidant activity of flavonoids: efficiency of singlet oxygen quenching. J. Photochem. Photobiol. B 1993, 19:205-215.
-
(1993)
J. Photochem. Photobiol. B
, vol.19
, pp. 205-215
-
-
Tournaire, C.1
Croux, S.2
Maurette, M.T.3
Beck, I.4
Hocquaux, M.5
Braun, M.6
Oliveros, E.7
-
36
-
-
0033186064
-
Lycopene entrapped in human albumin protects 2'-deoxyguanosine against singlet oxygen damage
-
Yamaguchi L.F., Martinez G.R., Catalani L.H., Medeiros M.H.G., Di Mascio P. Lycopene entrapped in human albumin protects 2'-deoxyguanosine against singlet oxygen damage. Arch. Latinoam. Nutr. 1999, 49:12S-20S.
-
(1999)
Arch. Latinoam. Nutr.
, vol.49
-
-
Yamaguchi, L.F.1
Martinez, G.R.2
Catalani, L.H.3
Medeiros, M.H.G.4
Di Mascio, P.5
-
37
-
-
24344474364
-
Biflavonoids from Brazilian pine Araucaria angustifolia as potentials protective agents against DNA damage and lipoperoxidation
-
Yamaguchi L.F., Vassao D.G., Kato M.J., Di Mascio P. Biflavonoids from Brazilian pine Araucaria angustifolia as potentials protective agents against DNA damage and lipoperoxidation. Phytochemistry 2005, 66:2238-2247.
-
(2005)
Phytochemistry
, vol.66
, pp. 2238-2247
-
-
Yamaguchi, L.F.1
Vassao, D.G.2
Kato, M.J.3
Di Mascio, P.4
|