|1.||Sanada, Hisakazu: 1 article (03/2010)|
|2.||Hayashi, Hiroyuki: 1 article (03/2010)|
|3.||Inoue, Tomoki: 1 article (03/2010)|
|4.||Toyoda-Hokaiwado, Naomi: 1 article (03/2010)|
|5.||Takamune, Makiko: 1 article (03/2010)|
|6.||Kawamura, Yuji: 1 article (03/2010)|
|7.||Kurata, Yasushi: 1 article (03/2010)|
|8.||Nohmi, Takehiko: 1 article (03/2010)|
|9.||Nishikawa, Akiyoshi: 1 article (03/2010)|
|10.||Umemura, Takashi: 1 article (03/2010)|
04/06/1996 - "In this study, we have assessed the extent of DNA damage in rats treated with a carcinogenic toluenediamine isomer, 2,4-toluenediamine (2,4-TDA), under conditions that result in tumor induction, and in rats implanted with Microthane polyesterurethane foam. "
03/01/2010 - "Although both compounds are genotoxic in the Ames/Salmonella assay, only 2,4-DAT induces tumors in rat livers. "
07/01/1991 - "In the most dramatic case, the powerful tumor promoter PMA was completely masked by 2,4-diaminotoluene. "
10/01/1995 - "However, the differences in the results of chronic rodent carcinogen bioassays using these two compounds are significant, in that 2,4-DAT is a potent hepatocarcinogen, whereas 2,6-DAT does not produce an increased incidence of tumors in rats or mice at similar doses. "
03/01/1991 - "2,4-DAT is a potent hepatocarcinogen whereas 2,6-DAT failed to produce an increased incidence of tumors in any tissue even when administered at a dose higher than that of 2,4-DAT. "
02/01/1984 - "Locus specificity of mutagenicity of 2,4-diaminotoluene in both L5178Y mouse lymphoma and AT3-2 Chinese hamster ovary cells."
02/01/1984 - "2,4-Diaminotoluene, a hepatocarcinogenic aromatic amine, was tested for mutagenic potential at both the autosomal tk locus and the sex-linked hgprt locus of both L5178Y 3.7.2C mouse lymphoma cells and Chinese hamster ovary (CHO) AT3-2 cells. "
|3.||Hepatocellular Carcinoma (Hepatoma)
|2.||Aflatoxin B1 (Aflatoxin B)
|5.||Hypoxanthine Phosphoribosyltransferase (Hypoxanthine Guanine Phosphoribosyltransferase)