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2-acetylaminofluorene and Chromosomal Translocation

2-acetylaminofluorene has been researched along with Chromosomal Translocation in 1 studies

2-Acetylaminofluorene: A hepatic carcinogen whose mechanism of activation involves N-hydroxylation to the aryl hydroxamic acid followed by enzymatic sulfonation to sulfoxyfluorenylacetamide. It is used to study the carcinogenicity and mutagenicity of aromatic amines.

Research Excerpts

ExcerptRelevanceReference
"Nineteen rearanged chromosomes were in hepatoma 8994, whereas only 8-10 markers could be found in the 80 +/- 3 chromosome complement of hepatoma 7316A."1.26Chromosome banding patterns and breakpoints of three transplantable hepatomas induced in rats by aromatic amines. ( Kovi, E; Kovi, J; Morris, HP; Rao, MS, 1978)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Kovi, J1
Kovi, E1
Morris, HP1
Rao, MS1

Other Studies

1 other study available for 2-acetylaminofluorene and Chromosomal Translocation

ArticleYear
Chromosome banding patterns and breakpoints of three transplantable hepatomas induced in rats by aromatic amines.
    Journal of the National Cancer Institute, 1978, Volume: 61, Issue:2

    Topics: 2-Acetylaminofluorene; Amines; Aminobiphenyl Compounds; Aniline Compounds; Animals; Carcinoma, Hepat

1978