-
1
-
-
0023710238
-
Effect of DNA conformation on the hydroxyl radical-induced formation of 5′,8-cyclopurine-2′-deoxyribonucleoside residues in DNA
-
M.-L. Dirksen W. F. Brakely E. Holwitt M. Dizdaroglu Effect of DNA conformation on the hydroxyl radical-induced formation of 5′,8-cyclopurine-2′-deoxyribonucleoside residues in DNA Int. J. Radiat. Biol. 1988 54 195-204.
-
(1988)
Int. J. Radiat. Biol.
, vol.54
, pp. 195-204
-
-
Dirksen, M.-L.1
Brakely, W.F.2
Holwitt, E.3
Dizdaroglu, M.4
-
2
-
-
0035313578
-
Identification and quantification of 5′,8-cyclo-2′-deoxyadenosine in DNA by liquid chromatography/mass spectrometry
-
M. Dizdaroglu P. Jaruga H. Rodriguez Identification and quantification of 5′,8-cyclo-2′-deoxyadenosine in DNA by liquid chromatography/mass spectrometry Free Radical Biol. Med. 2001 30 774-784.
-
(2001)
Free Radical Biol. Med.
, vol.30
, pp. 774-784
-
-
Dizdaroglu, M.1
Jaruga, P.2
Rodriguez, H.3
-
3
-
-
0037133531
-
Mass spectrometric assays for the tandem lesion 5′,8-cyclo-2′-deoxyguanosine in mammalian DNA
-
P. Jaruga M. Birincioglu H. Rodriguez M. Dizdaroglu Mass spectrometric assays for the tandem lesion 5′,8-cyclo-2′-deoxyguanosine in mammalian DNA Biochemistry 2002 41 3703-3711.
-
(2002)
Biochemistry
, vol.41
, pp. 3703-3711
-
-
Jaruga, P.1
Birincioglu, M.2
Rodriguez, H.3
Dizdaroglu, M.4
-
4
-
-
0141757434
-
DNA base damage by the antitumor agent 3-amino-1,2,4-benzotriazine 1,4-dioxide (Tirapazamine)
-
M. Birincioglu P. Jaruga G. Chowdhury H. Rodriguez M. Dizdaroglu K. S. Gates DNA base damage by the antitumor agent 3-amino-1,2,4-benzotriazine 1,4-dioxide (tirapazamine) J. Am. Chem. Soc. 2003 125 11607-11615.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 11607-11615
-
-
Birincioglu, M.1
Jaruga, P.2
Chowdhury, G.3
Rodriguez, H.4
Dizdaroglu, M.5
Gates, K.S.6
-
5
-
-
0037414324
-
Model studies of DNA C5′ radicals. Selective generation and reactivity of 2′-deoxyadenosin-5′-yl radical
-
C. Chatgilialoglu M. Guerra Q. C. Mulazzani Model studies of DNA C5′ radicals. Selective generation and reactivity of 2′-deoxyadenosin-5′-yl radical J. Am. Chem. Soc. 2003 125 3839-3848.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 3839-3848
-
-
Chatgilialoglu, C.1
Guerra, M.2
Mulazzani, Q.C.3
-
7
-
-
0000964269
-
Site-specific introduction of (5′S)-5′,8-cyclo-2′-deoxyadenosine into oligodeoxyribonucleotides
-
A. Romieu D. Gasparutto D. Molko J. Cadet Site-specific introduction of (5′S)-5′,8-cyclo-2′-deoxyadenosine into oligodeoxyribonucleotides J. Org. Chem. 1998 63 5245-5249.
-
(1998)
J. Org. Chem.
, vol.63
, pp. 5245-5249
-
-
Romieu, A.1
Gasparutto, D.2
Molko, D.3
Cadet, J.4
-
8
-
-
0032782017
-
Synthesis and characterization of oligonucleotides containing 5′,8-cyclopurine 2′-deoxyribonucleosides: (5′R)-5′,8-cyclo-2′-deoxyadenosine, (5′S)-5′,8-cyclo-2′-deoxyguanosine, and (5′R)-5′,8-cyclo-2′-deoxyguanosine
-
A. Romieu D. Gasparutto J. Cadet Synthesis and characterization of oligonucleotides containing 5′,8-cyclopurine 2′-deoxyribonucleosides: (5′R)-5′,8-cyclo-2′-deoxyadenosine, (5′S)-5′,8-cyclo-2′-deoxyguanosine, and (5′R)-5′,8-cyclo-2′-deoxyguanosine Chem. Res. Toxicol. 1999 12 412-421.
-
(1999)
Chem. Res. Toxicol.
, vol.12
, pp. 412-421
-
-
Romieu, A.1
Gasparutto, D.2
Cadet, J.3
-
9
-
-
0034636004
-
Removal of oxygen free-radical-induced 5′,8-purine cyclodeoxynucleosides from DNA by the nucleotide excision-repair pathway in human cells
-
I. Kuraoka C. Bender A. Romieu J. Cadet R. D. Wood T. Lindahl Removal of oxygen free-radical-induced 5′,8-purine cyclodeoxynucleosides from DNA by the nucleotide excision-repair pathway in human cells Proc. Natl. Acad. Sci. USA 2000 97 3832-3837.
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 3832-3837
-
-
Kuraoka, I.1
Bender, C.2
Romieu, A.3
Cadet, J.4
Wood, R.D.5
Lindahl, T.6
-
10
-
-
0035966003
-
Oxygen free radical damage to DNA: Translesion synthesis by human DNA polymerase η and resistance to exonuclease action at cyclopurine deoxynucleoside residues
-
I. Kuraoka P. Robins C. Masutani F. Hanaoka D. Gasparutto J. Cadet R. D. Wood T. Lindahl Oxygen free radical damage to DNA: translesion synthesis by human DNA polymerase η and resistance to exonuclease action at cyclopurine deoxynucleoside residues J. Biol. Chem. 2001 276 49283-49288.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 49283-49288
-
-
Kuraoka, I.1
Robins, P.2
Masutani, C.3
Hanaoka, F.4
Gasparutto, D.5
Cadet, J.6
Wood, R.D.7
Lindahl, T.8
-
11
-
-
0034698033
-
The oxidative DNA lesion 5′,8-(S)-cyclo-2′-deoxyadenosine is repaired by the nucleotide excision repair pathway and blocks gene expression in mammalian cells
-
P. J. Brooks D. S. Wise D. A. Berry J. V. Kosmoski M. J. Smerdon R. L. Somers H. Mackie A. Y. Spoonde E. J. Ackerman K. Coleman R. E. Tarone J. H. Robbins The oxidative DNA lesion 5′,8-(S)-cyclo-2′-deoxyadenosine is repaired by the nucleotide excision repair pathway and blocks gene expression in mammalian cells J. Biol. Chem. 2000 275 22355-22362.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 22355-22362
-
-
Brooks, P.J.1
Wise, D.S.2
Berry, D.A.3
Kosmoski, J.V.4
Smerdon, M.J.5
Somers, R.L.6
Mackie, H.7
Spoonde, A.Y.8
Ackerman, E.J.9
Coleman, K.10
Tarone, R.E.11
Robbins, J.H.12
-
12
-
-
0035929666
-
32P-postlabeling assay for the oxidative DNA lesion 5′,8-cyclo-2′-deoxyadenosine in mammalian tissues. Evidence that four type II I-compounds are dinucleotides containing the lesion in the 3′ nucleotide
-
32P-postlabeling assay for the oxidative DNA lesion 5′,8-cyclo-2′-deoxyadenosine in mammalian tissues. Evidence that four type II I-compounds are dinucleotides containing the lesion in the 3′ nucleotide J. Biol. Chem. 2001 276 36051-36057.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 36051-36057
-
-
Randerath, K.1
Zhou, G.D.2
Somers, R.L.3
Robbins, J.H.4
Brooks, P.J.5
-
13
-
-
85034351041
-
-
It was reported in a note as unpublished results that photolysis at 254 nm of a de-aerated aqueous solution of 2 afforded (5′S)- and (5′R)-isomers of 1 in 2 and 12% yields, respectively (ref. 3)
-
It was reported in a note as unpublished results that photolysis at 254 nm of a de-aerated aqueous solution of 2 afforded (5′S)- and (5′R)-isomers of 1 in 2 and 12% yields, respectively (ref. 3).
-
-
-
-
14
-
-
1642376596
-
Selective generation and reactivity of 5′-adenosinyl and 2′-adenosinyl radicals
-
For the ribo analogues, see
-
For the ribo analogues, see: C. Chatgilialoglu M. Duca C. Ferreri M. Guerra M. Ioele Q. G. Mulazzani H. Strittmatter B. Giese Selective generation and reactivity of 5′-adenosinyl and 2′-adenosinyl radicals Chem. Eur. J. 2004 10 1249-1255.
-
(2004)
Chem. Eur. J.
, vol.10
, pp. 1249-1255
-
-
Chatgilialoglu, C.1
Duca, M.2
Ferreri, C.3
Guerra, M.4
Ioele, M.5
Mulazzani, Q.G.6
Strittmatter, H.7
Giese, B.8
-
16
-
-
37049081504
-
Pulse radiolysis of aryl bromides in aqueous solutions: Some properties of aryl and arylperoxyl radicals
-
X. Fang R. Mertens C. von Sonntag Pulse radiolysis of aryl bromides in aqueous solutions: Some properties of aryl and arylperoxyl radicals J. Chem. Soc., Perkin Trans. 2 1995 1033-1036.
-
(1995)
J. Chem. Soc., Perkin Trans. 2
, pp. 1033-1036
-
-
Fang, X.1
Mertens, R.2
von Sonntag, C.3
-
17
-
-
84872846883
-
Reduction potentials of one-electron couples involving free radicals in aqueous solution
-
P. Wardman Reduction potentials of one-electron couples involving free radicals in aqueous solution J. Phys. Chem. Ref. Data 1989 18 1637-1755.
-
(1989)
J. Phys. Chem. Ref. Data
, vol.18
, pp. 1637-1755
-
-
Wardman, P.1
|