Formation of Deoxyguanosine Cross-Links from Calf Thymus DNA Treated with Acrolein and 4-Hydroxy-2-nonenal-Reference-Cited by-同舟云学术

Formation of Deoxyguanosine Cross-Links from Calf Thymus DNA Treated with Acrolein and 4-Hydroxy-2-nonenal

Published:2010-10-22 Issue:11 Volume:23 Page:1701-1713
ISSN:0893-228X
Container-title:Chemical Research in Toxicology
language:en
Short-container-title:Chem. Res. Toxicol.

Author:

Kozekov Ivan D.¹,Turesky Robert J.¹,Alas Guillermo R.¹,Harris Constance M.¹,Harris Thomas M.¹,Rizzo Carmelo J.¹

Affiliation:

1. Departments of Chemistry and Biochemistry and Center in Molecular Toxicology, Vanderbilt University, Nashville, Tennessee 37235-1822, United States, and Division of Environmental Health Sciences, Wadsworth Center, New York State Department of Health, Albany, New York 12201, United States

Publisher

American Chemical Society (ACS)

Subject

Toxicology,General Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/tx100179g

Reference60 articles.

1. Chemistry and biochemistry of 4-hydroxynonenal, malonaldehyde and related aldehydes

2. Acrolein: Sources, metabolism, and biomolecular interactions relevant to human health and disease

3. Cytotoxicity and genotoxicity of lipid-oxidation products

4. Lipid peroxidation: Physiological levels and dual biological effects

5. Chemistry and Biology of DNA Containing 1,N2-Deoxyguanosine Adducts of the α,β-Unsaturated Aldehydes Acrolein, Crotonaldehyde, and 4-Hydroxynonenal

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