489 related articles for article (PubMed ID: 9671708)
1. 3,N4-ethenocytosine, a highly mutagenic adduct, is a primary substrate for Escherichia coli double-stranded uracil-DNA glycosylase and human mismatch-specific thymine-DNA glycosylase.
Saparbaev M; Laval J
Proc Natl Acad Sci U S A; 1998 Jul; 95(15):8508-13. PubMed ID: 9671708
[TBL] [Abstract][Full Text] [Related]
2. Enzymology of the repair of etheno adducts in mammalian cells and in Escherichia coli.
Saparbaev M; Laval J
IARC Sci Publ; 1999; (150):249-61. PubMed ID: 10626225
[TBL] [Abstract][Full Text] [Related]
3. Novel activity of Escherichia coli mismatch uracil-DNA glycosylase (Mug) excising 8-(hydroxymethyl)-3,N4-ethenocytosine, a potential product resulting from glycidaldehyde reaction.
Hang B; Downing G; Guliaev AB; Singer B
Biochemistry; 2002 Feb; 41(7):2158-65. PubMed ID: 11841206
[TBL] [Abstract][Full Text] [Related]
4. Chloroethylnitrosourea-derived ethano cytosine and adenine adducts are substrates for Escherichia coli glycosylases excising analogous etheno adducts.
Guliaev AB; Singer B; Hang B
DNA Repair (Amst); 2004 Oct; 3(10):1311-21. PubMed ID: 15336626
[TBL] [Abstract][Full Text] [Related]
5. Hijacking of the human alkyl-N-purine-DNA glycosylase by 3,N4-ethenocytosine, a lipid peroxidation-induced DNA adduct.
Gros L; Maksimenko AV; Privezentzev CV; Laval J; Saparbaev MK
J Biol Chem; 2004 Apr; 279(17):17723-30. PubMed ID: 14761949
[TBL] [Abstract][Full Text] [Related]
6. A new class of uracil-DNA glycosylases related to human thymine-DNA glycosylase.
Gallinari P; Jiricny J
Nature; 1996 Oct; 383(6602):735-8. PubMed ID: 8878487
[TBL] [Abstract][Full Text] [Related]
7. The role of the Escherichia coli mug protein in the removal of uracil and 3,N(4)-ethenocytosine from DNA.
Lutsenko E; Bhagwat AS
J Biol Chem; 1999 Oct; 274(43):31034-8. PubMed ID: 10521502
[TBL] [Abstract][Full Text] [Related]
8. A 55-kDa protein isolated from human cells shows DNA glycosylase activity toward 3,N4-ethenocytosine and the G/T mismatch.
Hang B; Medina M; Fraenkel-Conrat H; Singer B
Proc Natl Acad Sci U S A; 1998 Nov; 95(23):13561-6. PubMed ID: 9811839
[TBL] [Abstract][Full Text] [Related]
9. 1,N(2)-ethenoguanine, a mutagenic DNA adduct, is a primary substrate of Escherichia coli mismatch-specific uracil-DNA glycosylase and human alkylpurine-DNA-N-glycosylase.
Saparbaev M; Langouët S; Privezentzev CV; Guengerich FP; Cai H; Elder RH; Laval J
J Biol Chem; 2002 Jul; 277(30):26987-93. PubMed ID: 12016206
[TBL] [Abstract][Full Text] [Related]
10. Crystal structure of a G:T/U mismatch-specific DNA glycosylase: mismatch recognition by complementary-strand interactions.
Barrett TE; Savva R; Panayotou G; Barlow T; Brown T; Jiricny J; Pearl LH
Cell; 1998 Jan; 92(1):117-29. PubMed ID: 9489705
[TBL] [Abstract][Full Text] [Related]
11. Escherichia coli, Saccharomyces cerevisiae, rat and human 3-methyladenine DNA glycosylases repair 1,N6-ethenoadenine when present in DNA.
Saparbaev M; Kleibl K; Laval J
Nucleic Acids Res; 1995 Sep; 23(18):3750-5. PubMed ID: 7479006
[TBL] [Abstract][Full Text] [Related]
12. Mammalian enzymatic repair of etheno and para-benzoquinone exocyclic adducts derived from the carcinogens vinyl chloride and benzene.
Singer B; Hang B
IARC Sci Publ; 1999; (150):233-47. PubMed ID: 10626224
[TBL] [Abstract][Full Text] [Related]
13. The HAP1 protein stimulates the turnover of human mismatch-specific thymine-DNA-glycosylase to process 3,N(4)-ethenocytosine residues.
Privezentzev CV; Saparbaev M; Laval J
Mutat Res; 2001 Sep; 480-481():277-84. PubMed ID: 11506820
[TBL] [Abstract][Full Text] [Related]
14. New substrates for old enzymes. 5-Hydroxy-2'-deoxycytidine and 5-hydroxy-2'-deoxyuridine are substrates for Escherichia coli endonuclease III and formamidopyrimidine DNA N-glycosylase, while 5-hydroxy-2'-deoxyuridine is a substrate for uracil DNA N-glycosylase.
Hatahet Z; Kow YW; Purmal AA; Cunningham RP; Wallace SS
J Biol Chem; 1994 Jul; 269(29):18814-20. PubMed ID: 8034633
[TBL] [Abstract][Full Text] [Related]
15. Highly mutagenic exocyclic DNA adducts are substrates for the human nucleotide incision repair pathway.
Prorok P; Saint-Pierre C; Gasparutto D; Fedorova OS; Ishchenko AA; Leh H; Buckle M; Tudek B; Saparbaev M
PLoS One; 2012; 7(12):e51776. PubMed ID: 23251620
[TBL] [Abstract][Full Text] [Related]
16. Human DNA glycosylase enzyme TDG repairs thymine mispaired with exocyclic etheno-DNA adducts.
Goto M; Shinmura K; Matsushima Y; Ishino K; Yamada H; Totsuka Y; Matsuda T; Nakagama H; Sugimura H
Free Radic Biol Med; 2014 Nov; 76():136-46. PubMed ID: 25151120
[TBL] [Abstract][Full Text] [Related]
17. Mismatch uracil glycosylase from Escherichia coli: a general mismatch or a specific DNA glycosylase?
O'Neill RJ; Vorob'eva OV; Shahbakhti H; Zmuda E; Bhagwat AS; Baldwin GS
J Biol Chem; 2003 Jun; 278(23):20526-32. PubMed ID: 12668677
[TBL] [Abstract][Full Text] [Related]
18. Influence of local duplex stability and N6-methyladenine on uracil recognition by mismatch-specific uracil-DNA glycosylase (Mug).
Valinluck V; Liu P; Burdzy A; Ryu J; Sowers LC
Chem Res Toxicol; 2002 Dec; 15(12):1595-601. PubMed ID: 12482242
[TBL] [Abstract][Full Text] [Related]
19. Role of mismatch-specific uracil-DNA glycosylase in repair of 3,N4-ethenocytosine in vivo.
Jurado J; Maciejewska A; Krwawicz J; Laval J; Saparbaev MK
DNA Repair (Amst); 2004 Dec; 3(12):1579-90. PubMed ID: 15474419
[TBL] [Abstract][Full Text] [Related]
20. Targeted deletion of alkylpurine-DNA-N-glycosylase in mice eliminates repair of 1,N6-ethenoadenine and hypoxanthine but not of 3,N4-ethenocytosine or 8-oxoguanine.
Hang B; Singer B; Margison GP; Elder RH
Proc Natl Acad Sci U S A; 1997 Nov; 94(24):12869-74. PubMed ID: 9371767
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
