BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

223 related articles for article (PubMed ID: 18847226)

  • 1. The stereochemistry of trans-4-hydroxynonenal-derived exocyclic 1,N2-2'-deoxyguanosine adducts modulates formation of interstrand cross-links in the 5'-CpG-3' sequence.
    Huang H; Wang H; Qi N; Lloyd RS; Rizzo CJ; Stone MP
    Biochemistry; 2008 Nov; 47(44):11457-72. PubMed ID: 18847226
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rearrangement of the (6S,8R,11S) and (6R,8S,11R) exocyclic 1,N2-deoxyguanosine adducts of trans-4-hydroxynonenal to N2-deoxyguanosine cyclic hemiacetal adducts when placed complementary to cytosine in duplex DNA.
    Huang H; Wang H; Qi N; Kozekova A; Rizzo CJ; Stone MP
    J Am Chem Soc; 2008 Aug; 130(33):10898-906. PubMed ID: 18661996
    [TBL] [Abstract][Full Text] [Related]  

  • 3. DNA cross-link induced by trans-4-hydroxynonenal.
    Huang H; Kozekov ID; Kozekova A; Wang H; Lloyd RS; Rizzo CJ; Stone MP
    Environ Mol Mutagen; 2010 Jul; 51(6):625-34. PubMed ID: 20577992
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Formation of a N2-dG:N2-dG carbinolamine DNA cross-link by the trans-4-hydroxynonenal-derived (6S,8R,11S) 1,N2-dG adduct.
    Huang H; Wang H; Kozekova A; Rizzo CJ; Stone MP
    J Am Chem Soc; 2011 Oct; 133(40):16101-10. PubMed ID: 21916419
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Conformational interconversion of the trans-4-hydroxynonenal-derived (6S,8R,11S) 1,N(2)-deoxyguanosine adduct when mismatched with deoxyadenosine in DNA.
    Huang H; Wang H; Lloyd RS; Rizzo CJ; Stone MP
    Chem Res Toxicol; 2009 Jan; 22(1):187-200. PubMed ID: 19053179
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Site-specific mutagenicity of stereochemically defined 1,N2-deoxyguanosine adducts of trans-4-hydroxynonenal in mammalian cells.
    Fernandes PH; Wang H; Rizzo CJ; Lloyd RS
    Environ Mol Mutagen; 2003; 42(2):68-74. PubMed ID: 12929118
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Orientation of the crotonaldehyde-derived N2-[3-Oxo-1(S)-methyl-propyl]-dG DNA adduct hinders interstrand cross-link formation in the 5'-CpG-3' sequence.
    Cho YJ; Wang H; Kozekov ID; Kozekova A; Kurtz AJ; Jacob J; Voehler M; Smith J; Harris TM; Rizzo CJ; Lloyd RS; Stone MP
    Chem Res Toxicol; 2006 Aug; 19(8):1019-29. PubMed ID: 16918240
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Stereospecific formation of the (R)-gamma-hydroxytrimethylene interstrand N2-dG:N2-dG cross-link arising from the gamma-OH-1,N2-propano-2'-deoxyguanosine adduct in the 5'-CpG-3' DNA sequence.
    Huang H; Kim HY; Kozekov ID; Cho YJ; Wang H; Kozekova A; Harris TM; Rizzo CJ; Stone MP
    J Am Chem Soc; 2009 Jun; 131(24):8416-24. PubMed ID: 19530727
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Stereospecific formation of interstrand carbinolamine DNA cross-links by crotonaldehyde- and acetaldehyde-derived alpha-CH3-gamma-OH-1,N2-propano-2'-deoxyguanosine adducts in the 5'-CpG-3' sequence.
    Cho YJ; Wang H; Kozekov ID; Kurtz AJ; Jacob J; Voehler M; Smith J; Harris TM; Lloyd RS; Rizzo CJ; Stone MP
    Chem Res Toxicol; 2006 Feb; 19(2):195-208. PubMed ID: 16485895
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Replication bypass of the trans-4-Hydroxynonenal-derived (6S,8R,11S)-1,N(2)-deoxyguanosine DNA adduct by the sulfolobus solfataricus DNA polymerase IV.
    Banerjee S; Christov PP; Kozekova A; Rizzo CJ; Egli M; Stone MP
    Chem Res Toxicol; 2012 Feb; 25(2):422-35. PubMed ID: 22313351
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Stereochemistry modulates the stability of reduced interstrand cross-links arising from R- and S-alpha-CH3-gamma-OH-1,N2-propano-2'-deoxyguanosine in the 5'-CpG-3' DNA sequence.
    Cho YJ; Kozekov ID; Harris TM; Rizzo CJ; Stone MP
    Biochemistry; 2007 Mar; 46(10):2608-21. PubMed ID: 17305317
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Chemistry and biology of DNA containing 1,N(2)-deoxyguanosine adducts of the alpha,beta-unsaturated aldehydes acrolein, crotonaldehyde, and 4-hydroxynonenal.
    Minko IG; Kozekov ID; Harris TM; Rizzo CJ; Lloyd RS; Stone MP
    Chem Res Toxicol; 2009 May; 22(5):759-78. PubMed ID: 19397281
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Spectroscopic characterization of interstrand carbinolamine cross-links formed in the 5'-CpG-3' sequence by the acrolein-derived gamma-OH-1,N2-propano-2'-deoxyguanosine DNA adduct.
    Cho YJ; Kim HY; Huang H; Slutsky A; Minko IG; Wang H; Nechev LV; Kozekov ID; Kozekova A; Tamura P; Jacob J; Voehler M; Harris TM; Lloyd RS; Rizzo CJ; Stone MP
    J Am Chem Soc; 2005 Dec; 127(50):17686-96. PubMed ID: 16351098
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Interstrand DNA cross-links induced by alpha,beta-unsaturated aldehydes derived from lipid peroxidation and environmental sources.
    Stone MP; Cho YJ; Huang H; Kim HY; Kozekov ID; Kozekova A; Wang H; Minko IG; Lloyd RS; Harris TM; Rizzo CJ
    Acc Chem Res; 2008 Jul; 41(7):793-804. PubMed ID: 18500830
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Site-specific synthesis and reactivity of oligonucleotides containing stereochemically defined 1,N2-deoxyguanosine adducts of the lipid peroxidation product trans-4-hydroxynonenal.
    Wang H; Kozekov ID; Harris TM; Rizzo CJ
    J Am Chem Soc; 2003 May; 125(19):5687-700. PubMed ID: 12733907
    [TBL] [Abstract][Full Text] [Related]  

  • 16. DNA sequence modulates the conformation of the food mutagen 2-amino-3-methylimidazo[4,5-f]quinoline in the recognition sequence of the NarI restriction enzyme.
    Wang F; Elmquist CE; Stover JS; Rizzo CJ; Stone MP
    Biochemistry; 2007 Jul; 46(29):8498-516. PubMed ID: 17602664
    [TBL] [Abstract][Full Text] [Related]  

  • 17. γ-Hydroxy-1,N2-propano-2'-deoxyguanosine DNA adduct conjugates the N-terminal amine of the KWKK peptide via a carbinolamine linkage.
    Huang H; Wang H; Voehler MW; Kozekova A; Rizzo CJ; McCullough AK; Lloyd RS; Stone MP
    Chem Res Toxicol; 2011 Jul; 24(7):1123-33. PubMed ID: 21561113
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The exocyclic 1,N2-deoxyguanosine pyrimidopurinone M1G is a chemically stable DNA adduct when placed opposite a two-base deletion in the (CpG)3 frameshift hotspot of the Salmonella typhimurium hisD3052 gene.
    Schnetz-Boutaud NC; Saleh S; Marnett LJ; Stone MP
    Biochemistry; 2001 Dec; 40(51):15638-49. PubMed ID: 11747439
    [TBL] [Abstract][Full Text] [Related]  

  • 19. DNA interchain cross-links formed by acrolein and crotonaldehyde.
    Kozekov ID; Nechev LV; Moseley MS; Harris CM; Rizzo CJ; Stone MP; Harris TM
    J Am Chem Soc; 2003 Jan; 125(1):50-61. PubMed ID: 12515506
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Solution conformation of the (-)-trans-anti-[BP]dG adduct opposite a deletion site in a DNA duplex: intercalation of the covalently attached benzo[a]pyrene into the helix with base displacement of the modified deoxyguanosine into the minor groove.
    Feng B; Gorin A; Kolbanovskiy A; Hingerty BE; Geacintov NE; Broyde S; Patel DJ
    Biochemistry; 1997 Nov; 36(45):13780-90. PubMed ID: 9374854
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.