T. Zaliznyak

NMR Characterization of a DNA Duplex Containing the Major Acrolein-derived Deoxyguanosine Adduct γ-OH-1,-N 2-Propano-2′-deoxyguanosine*

F. Johnson, C. R. de los Santos, T. Zaliznyak, 2001, The Journal of Biological Chemistry.

Solution structure of DNA containing α-OH-PdG: the mutagenic adduct produced by acrolein

F. Johnson, S. Attaluri, C. R. de los Santos, 2009, Nucleic acids research.

Structure and stability of DNA containing an aristolactam II-dA lesion: implications for the NER recognition of bulky adducts

F. Johnson, M. Lukin, C. R. de los Santos, 2011, Nucleic acids research.

Incorporation of 3-Aminobenzanthrone into 2′-Deoxyoligonucleotides and Its Impact on Duplex Stability

F. Johnson, M. Lukin, C. R. de los Santos, 2011, Journal of nucleic acids.

Structure and stability of duplex DNA containing the 3-(deoxyguanosin-N2-yl)-2-acetylaminofluorene (dG(N2)-AAF) lesion: a bulky adduct that persists in cellular DNA.

F. Johnson, R. Bonala, C. R. de los Santos, 2006, Chemical research in toxicology.

NMR structure of duplex DNA containing the alpha-OH-PdG.dA base pair: a mutagenic intermediate of acrolein.

F. Johnson, M. Lukin, C. R. de los Santos, 2012, Biopolymers.

Structure of DNA Containing an Aristolactam II-dA Lesion.

F. Johnson, M. Lukin, C. Santos, 2011 .