Toxicogenomics discrimination of potential hepatocarcinogenicity of non-genotoxic compounds in rat liver (Q44776072)

6 December 2017

title

Toxicogenomics discrimination of potential hepatocarcinogenicity of non-genotoxic compounds in rat liver (English)

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6 December 2017

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Fumihiro Yamada

1

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6 December 2017

Kayo Sumida

2

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6 December 2017

Takeki Uehara

3

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6 December 2017

Yuji Morikawa

4

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6 December 2017

Hiroshi Yamada

5

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6 December 2017

Tetsuro Urushidani

6

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6 December 2017

Yasuo Ohno

7

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6 December 2017

language of work or name

English

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publication date

13 July 2012

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Journal of Applied Toxicology

6 December 2017

published in

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6 December 2017

volume

33

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6 December 2017

issue

11

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6 December 2017

page(s)

1284-1293

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Hepatic microsomal enzyme induction, beta-oxidation, and cell proliferation following administration of clofibrate, gemfibrozil, or bezafibrate in the CD rat.

6 December 2017

cites work

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Heparin/heparan sulfate interacting protein plays a role in apoptosis induced by anticancer drugs

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Profiling protein markers associated with lymph node metastasis in prostate cancer by DIGE-based proteomics analysis.

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Effect of the difference in vehicles on gene expression in the rat liver--analysis of the control data in the Toxicogenomics Project Database

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ALKBH3, a human AlkB homologue, contributes to cell survival in human non-small-cell lung cancer

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A toxicogenomics approach for early assessment of potential non-genotoxic hepatocarcinogenicity of chemicals in rats

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Gene expression profiling of methapyrilene-induced hepatotoxicity in rat.

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Species-specific differences in coumarin-induced hepatotoxicity as an example toxicogenomics-based approach to assessing risk of toxicity to humans

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Proteomic profiling of proteins decreased in hepatocellular carcinoma from patients infected with hepatitis C virus

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Acyl-CoA synthetase mRNA expression is controlled by fibric-acid derivatives, feeding and liver proliferation

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21 January 2018

Identifiers

DOI

10.1002/JAT.2790

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6 December 2017

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