Physical basis of chemical carcinogenesis by N -2-fluorenylacetamide derivatives and analogs-Reference-Cited by-同舟云学术

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Physical basis of chemical carcinogenesis by N -2-fluorenylacetamide derivatives and analogs

Published:1973-08-15 Issue:2 Volume:34 Page:295-298
ISSN:0014-5793
Container-title:FEBS Letters
language:en
Short-container-title:

Author:

Fuchs R.,Daune M.

Publisher

Wiley

Subject

Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1016/0014-5793(73)80815-4/fullpdf

Reference21 articles.

1. Krebsbildung durch Aminofluorene und verwandte Körper

Cited by 50 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Observing Translesion Synthesis of an Aromatic Amine DNA Adduct by a High-fidelity DNA Polymerase;Journal of Biological Chemistry;2004-11

2. 3'-Exonuclease resistance of DNA oligodeoxynucleotides containing O6-[4-oxo-4-(3-pyridyl)butyl]guanine;Nucleic Acids Research;2003-04-01

3. Mechanisms of Frameshift Mutations: Insight from Aromatic Amines;Chemical Research in Toxicology;1997-04-01

4. Solution Conformation of [AF]dG Opposite a -2 Deletion Site in a DNA Duplex: Intercalation of the Covalently Attached Aminofluorene Ring into the Helix with Base Displacement of the C8-Modified syn Guanine and Adjacent Unpaired 3'-Adenine into the Major Groove;Biochemistry;1995-12-01

5. Genetic toxicity of 2-acetylaminofluorene, 2-aminofluorene and some of their metabolites and model metabolites;Mutation Research/Reviews in Genetic Toxicology;1994-10

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