Dara A. Reeves, Ph.D.
Affiliations: | 2010 | Chemistry | New York University, New York, NY, United States |
Area:
Biochemistry, Molecular Biology, General ChemistryGoogle:
"Dara Reeves"Mean distance: 4976.62
Parents
Sign in to add mentor| Nicholas E. Geacintov | grad student | 2010 | NYU | |
| (Impact of DNA Conformation and Base Sequence Context on Efficiencies of Nucleotide Excision Repair of Bulky DNA Adducts.) | ||||
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Publications
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| Krzeminski J, Kropachev K, Reeves D, et al. (2013) Adenine-DNA adduct derived from the nitroreduction of 6-nitrochrysene is more resistant to nucleotide excision repair than guanine-DNA adducts. Chemical Research in Toxicology. 26: 1746-54 |
| Reeves DA, Mu H, Kropachev K, et al. (2011) Resistance of bulky DNA lesions to nucleotide excision repair can result from extensive aromatic lesion-base stacking interactions. Nucleic Acids Research. 39: 8752-64 |
| Liu Y, Reeves D, Kropachev K, et al. (2011) Probing for DNA damage with β-hairpins: similarities in incision efficiencies of bulky DNA adducts by prokaryotic and human nucleotide excision repair systems in vitro. Dna Repair. 10: 684-96 |
| Krzeminski J, Kropachev K, Kolbanovskiy M, et al. (2011) Inefficient nucleotide excision repair in human cell extracts of the N-(deoxyguanosin-8-yl)-6-aminochrysene and 5-(deoxyguanosin-N(2)-yl)-6-aminochrysene adducts derived from 6-nitrochrysene. Chemical Research in Toxicology. 24: 65-72 |
| Krzeminski J, Kropachev K, Reeves D, et al. (2010) Abstract 3945: Inefficient nucleotide excision repair of the N-(dG-8-yl)-6-AC adduct derived from 6-nitrochrysene, an environmental mammary carcinogen, in human cell extracts Cancer Research. 70: 3945-3945 |