Michael Stone
Faculty Member
Last active: 1/20/2015

  1. The cis-(5R,6S)-thymine glycol lesion occupies the wobble position when mismatched with deoxyguanosine in DNA. Brown KL, Basu AK, Stone MP (2009) Biochemistry 48(41): 9722-33
    › Primary publication · 19772348 (PubMed) · PMC2761728 (PubMed Central)
  2. Structural perturbations induced by the alpha-anomer of the aflatoxin B(1) formamidopyrimidine adduct in duplex and single-strand DNA. Brown KL, Voehler MW, Magee SM, Harris CM, Harris TM, Stone MP (2009) J Am Chem Soc 131(44): 16096-107
    › Primary publication · 19831353 (PubMed) · PMC2773149 (PubMed Central)
  3. 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 (2009) J Am Chem Soc 131(24): 8416-24
    › Primary publication · 19530727 (PubMed) · PMC2753404 (PubMed Central)
  4. Modulation of the structure, catalytic activity, and fidelity of African swine fever virus DNA polymerase X by a reversible disulfide switch. Voehler MW, Eoff RL, McDonald WH, Guengerich FP, Stone MP (2009) J Biol Chem 284(27): 18434-44
    › Primary publication · 19419958 (PubMed) · PMC2709365 (PubMed Central)
  5. Inherent stereospecificity in the reaction of aflatoxin B(1) 8,9-epoxide with deoxyguanosine and efficiency of DNA catalysis. Brown KL, Bren U, Stone MP, Guengerich FP (2009) Chem Res Toxicol 22(5): 913-7
    › Primary publication · 19301826 (PubMed) · PMC3141577 (PubMed Central)
  6. Differential base stacking interactions induced by trimethylene interstrand DNA cross-links in the 5'-CpG-3' and 5'-GpC-3' sequence contexts. Huang H, Dooley PA, Harris CM, Harris TM, Stone MP (2009) Chem Res Toxicol 22(11): 1810-6
    › Primary publication · 19916525 (PubMed) · PMC2778138 (PubMed Central)
  7. 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 (2009) Chem Res Toxicol 22(1): 187-200
    › Primary publication · 19053179 (PubMed) · PMC2645987 (PubMed Central)
  8. 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 (2009) Chem Res Toxicol 22(5): 759-78
    › Primary publication · 19397281 (PubMed) · PMC2685875 (PubMed Central)
  9. 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 (2008) Biochemistry 47(44): 11457-72
    › Primary publication · 18847226 (PubMed) · PMC2646759 (PubMed Central)
  10. The modulation of topoisomerase I-mediated DNA cleavage and the induction of DNA-topoisomerase I crosslinks by crotonaldehyde-derived DNA adducts. Dexheimer TS, Kozekova A, Rizzo CJ, Stone MP, Pommier Y (2008) Nucleic Acids Res 36(12): 4128-36
    › Primary publication · 18550580 (PubMed) · PMC2475617 (PubMed Central)