Schneider M, Thoß G, Hübner-Parajsz C, Kientsch-Engel R, Stahl P, Pischetsrieder M (2004)
Publication Type: Journal article
Publication year: 2004
Publisher: American Chemical Society
Book Volume: 17
Pages Range: 1385-1390
URI: http://pubs.acs.org/cgi-bin/download.pl?tx049929d/Z5Pv
DOI: 10.1021/tx049929d
Sugars and sugar degradation products react in vivo readily with proteins (glycation) resulting in the formation of a heterogeneous group of reaction products, which are called advanced glycation end products (AGEs). AGEs notably change the structure and function of proteins so that extended protein-AGE formation is linked to complications such as nephropathy, atherosclerosis, and cataract. DNA can be glycated in vitro in a similar way as proteins, and the two diastereomers of N2-carboxyethyl-2′-deoxyguanosine (CEdG
APA:
Schneider, M., Thoß, G., Hübner-Parajsz, C., Kientsch-Engel, R., Stahl, P., & Pischetsrieder, M. (2004). Determination of Glycated Nucleobases in Human Urine by a New Monoclonal Antibody Specific for N²-Carboxyethyl-2'-deoxyguanosine. Chemical Research in Toxicology, 17, 1385-1390. https://doi.org/10.1021/tx049929d
MLA:
Schneider, Marc, et al. "Determination of Glycated Nucleobases in Human Urine by a New Monoclonal Antibody Specific for N²-Carboxyethyl-2'-deoxyguanosine." Chemical Research in Toxicology 17 (2004): 1385-1390.
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