Mutagenic properties of dimethylaniline isomers in mice as evaluated by comet, micronucleus and transgenic mutation assays

about

Mutagenic properties of dimethylaniline isomers in mice as evaluated by comet, micronucleus and transgenic mutation assays

Item

http://www.wikidata.org/entity/Q56515976

description

scientific article published on 22 August 2018

@en

wetenschappelijk artikel

@nl

наукова стаття, опублікована у 2018

@uk

name

Mutagenic properties of dimeth ...... and transgenic mutation assays

@en

Mutagenic properties of dimeth ...... and transgenic mutation assays

@nl

type

Item

label

Mutagenic properties of dimeth ...... and transgenic mutation assays

@en

Mutagenic properties of dimeth ...... and transgenic mutation assays

@nl

prefLabel

Mutagenic properties of dimeth ...... and transgenic mutation assays

@en

Mutagenic properties of dimeth ...... and transgenic mutation assays

@nl

P1476

Mutagenic properties of dimeth ...... and transgenic mutation assays

@en

P2093

Akihiko Hirose

http://www.w3.org/2001/XMLSchema#string

Arihiro Kohara

http://www.w3.org/2001/XMLSchema#string

Makoto Hayashi

http://www.w3.org/2001/XMLSchema#string

Mariko Matsumoto

http://www.w3.org/2001/XMLSchema#string

Masamitsu Honma

http://www.w3.org/2001/XMLSchema#string

P2860

Tumor-promoting activity of 2,6-dimethylaniline in a two-stage nasal carcinogenesis model in N-bis(2-hydroxypropyl)nitrosamine-treated rats

Assessment of aniline derivatives-induced DNA damage in the liver cells of B6C3F1 mice using the alkaline single cell gel electrophoresis ('comet') assay.

Elevated 4-aminobiphenyl and 2,6-dimethylaniline hemoglobin adducts and increased risk of bladder cancer among lifelong nonsmokers--The Shanghai Bladder Cancer Study

Acute toxicity and skin corrosion data for some organic and inorganic compounds and aqueous solutions.

Genotoxicity of 2,6- and 3,5-dimethylaniline in cultured mammalian cells: the role of reactive oxygen species.

Testing of twenty-one environmental aromatic amines or derivatives for long-term toxicity or carcinogenicity.

Identification of adducts formed by reaction of N-acetoxy-3,5-dimethylaniline with DNA.

Sequential observation of 2,6-dimethylaniline-induced nasal lesions in a rat two-stage nasal carcinogenesis model after initiation with N-bis(2-hydroxypropyl) nitrosamine.

Synthesis, characterization, and comparative 32P-postlabeling efficiencies of 2,6-dimethylaniline-DNA adducts.

Immunohistochemical and ultrastructural studies of 2,6-dimethylaniline-induced nasal proliferative lesions in a rat two-stage nasal carcinogenesis model initiated with N-bis(2-hydroxypropyl)nitrosamine.

P2888

s41021-018-0106-3

P304

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1186/S41021-018-0106-3

http://www.w3.org/2001/XMLSchema#string

P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Takayoshi Suzuki

P577

2018-08-22T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P6179

1105995265

http://www.w3.org/2001/XMLSchema#string

P698

30151062

http://www.w3.org/2001/XMLSchema#string

P932

6103965

http://www.w3.org/2001/XMLSchema#string