Existence of a Threshold for the Genotoxic Carcinogens : Evidence from Mechanism-based Carcinogenicity Studies
スポンサーリンク
概要
著者
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WANIBUCHI Hideki
Department of Pathology, Osaka City University Medical School
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WEI Min
Department of Pathology, Osaka City University Medical School
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Fukushima S
Japan Bioassay Research Center Japan Industrial Safety And Health Association
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Wanibuchi Hideki
Department Of Pathology Osaka City University Medical School
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Wanibuchi Hideki
大阪府立成人病センター 分子生物学
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Wanibuchi Hideki
大阪市立大学 核医
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Wanibuchi Hideki
Dept. Pathology Osaka City University Medical School
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Wei Min
Department Of Pathology Osaka City University Medical School
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Fukushima Shoji
Japan Bioassay Research Center, Japan Industrial Safety and Health Association
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Fujiwara Yushi
Department Of Surgery Osaka City Juso Hospital
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KAKEHASHI Anna
Department of Pathology, Osaka City University Medical School
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Kinoshita Anna
Department Of Pathology Osaka City University Medical School
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Wanibuchi H
Department Of Pathology Osaka City University Medical School
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Fukushima Shoji
中央労働災害防止協会日本バイオアッセイ研究センター
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Wei Min
Department Of Food Science Obihiro University Of Agriculture And Veterinary Medicine
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Fukushima Shoji
Japan Bioassay Research Center
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Fukushima Shoji
Dept. Pathol. Osaka City University Medical School
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Fukuhara Kennichirou
Department Of Gastroenterological Surgery Osaka City University Graduate School Of Medicine
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Min Wei
Department Of Pathology Osaka City University Medical School
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Fukushima Shoji
Department Of Gastroenterological Surgery Osaka City University Graduate School Of Medicine
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Kakehashi Anna
Department Of Pathology Osaka City University Medical School
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Fukushima Shoji
Japan Bioassay Res. Center Japan Industrial Safety And Health Assoc.
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Wanibuchi Hideki
Department Of Pathology Osaka City University Graduate School Of Medicine
関連論文
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- Lack of changes in the levels of liver and kidney cytochrome P-450 isozymes in p53(+/-)knockout mice treated with N-butyl-N-(4-hydroxybutyl)nitrosamine.
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- Aberrant expression of E-cadherin and β-catenin in association with transforming growth factor-β1 in urinary bladder lesions in humans after the Chernobyl accident
- Dose-dependence of promotion of 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline-induced rat hepatocarcinogenesis by ethanol : Evidence for a threshold
- Examination of the Rat Model of Liver Injury via Thioacetamide (TAA) or Carbon Tetrachloride (CCl_4)
- Significance of overexpression of metallothionein in mouse urinary bladder focal lesions induced by treatment with N-butyl-N-(4-hydroxybutyl)-nitrosamine
- Biphasic Increase of Epithelial DNA Synthesis in the Urinary Bladder of Rats Treated with a Tumor Promoter, Sodium L-ascorbate
- Influence of Strain and Diet on Hepatocarcinogenicity of N-Butyl-N-(4-hydroxybutyl)nitrosamine (BBN) in Rats : Slight Inhibition of Preneoplastic Liver Lesion Development by Uracil
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- Self-Expandable Metallic Stent for Unresectable Malignant Strictures in the Esophagus and Cardia
- Lack of Inhibitory Effects of Coumaperine from Pepper on the Promotion Stage of Chemical Hepatocarcinogenesis in the Rat
- Inhibitory effect of phenobarbital at low dose on rat hepatocarcinogenesis : the evidence for hormesis (CARCINOGENICITY) (GENERAL SESSION BY POSTER PRESENTATION) (Proceedings of the 30th Annual Meeting)
- Thresholds for Carcinogenicity of Environmental Carcinogens (SYMPOSIUM3: RECENT TOPICS ON THE RISK ASSESSMENT OF CHEMICAL CARCINOGENS) (Proceedings of the 30th Annual Meeting)
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- Strain Differences in Sensitivity to the Promoting Effect of Sodium L-Ascorbate in a Two-stage Rat Urinary Bladder Carcinogenesis Model
- Characteristic Upregulation of Glucose-Regulated Protein 78 in an Early Lesion Negative for Hitherto Established Cytochemical Markers in Rat Hepatocarcinogenesis
- Increased susceptibility to spontaneous lung cancer in mice lacking LIM-domain only 7
- Ambulatory intraesophageal bilirubin monitoring in Japanese patients with gastroesophageal reflux
- Lack of Enhanced Epithelial Cell Proliferation in the Urinary Bladder of Heterozygous p53 Knockout Mice Given Sodium Ortho-phenylphenate or Uracil
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