Tumor-augmenting effects of gestational arsenic exposure on F1 and F2 in mice

• 資料種別: 記事
• タイトル: Tumor-augmenting effects of gestational arsenic exposure on F1 and F2 in mice
• 著者・編者: Keiko Nohara; Takehiro Suzuki; Kazuyuki Okamura
• 出版事項: 日本 : Springer Nature
• 出版年月日等: 2017-03-01
• 出版年（W3CDTF）: 2017-03-01
• タイトル（掲載誌）: Genes and environment
• 巻号年月日等（掲載誌）: 39(3)
• 掲載巻: 39(3)
• ISSN（掲載誌）: 1880-7062
• ISSN-L（掲載誌）: 1880-7046
• 本文の言語コード: eng
• DOI: 10.1186/s41021-016-0069-1; https://doi.org/10.1186/s41021-016-0069-1
• 国立国会図書館永続的識別子: info:ndljp/pid/10349116; https://dl.ndl.go.jp/pid/10349116
• コレクション（共通）: 障害者向け資料
• コレクション（障害者向け資料：レベル1）: テキストデータ
• コレクション（個別）: 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > その他; https://dl.ndl.go.jp/collections/B00035
• 収集根拠: オンライン資料収集制度
• 受理日（W3CDTF）: 2017-05-11T11:41:31+09:00
• 保存日（W3CDTF）: 2017-05-10
• 記録形式（IMT）: application/pdf
• オンライン閲覧公開範囲: 国立国会図書館内限定公開
• デジタル化資料送信: 図書館・個人送信対象外
• 遠隔複写可否（NDL）: 可
• 掲載誌（URI）: http://genesenvironment.biomedcentral.com/articles
• 掲載誌（国立国会図書館永続的識別子）: info:ndljp/pid/10265750; https://dl.ndl.go.jp/pid/10265750
• 連携機関・データベース: 国立国会図書館 : 国立国会図書館デジタルコレクション; https://dl.ndl.go.jp

• 要約等: コレクション : 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > その他
• DOI: 10.1186/s41021-016-0069-1; https://doi.org/10.1186/s41021-016-0069-1
• オンライン閲覧公開範囲: インターネット公開
• 関連情報（URI）: http://id.ndl.go.jp/digimeta/10349116; https://dl.ndl.go.jp/pid/10349116; http://link.springer.com/content/pdf/10.1186/s41021-016-0069-1.pdf
• 参照: In vivo evaluation of arsenic-associated behavioral and biochemical alterations in F0 and F1 mice; https://cir.nii.ac.jp/crid/1360005516737150208; Gestational arsenic exposure and paternal intergenerational epigenetic inheritance; https://cir.nii.ac.jp/crid/1360853567764804352; Effects of maternal exposure to arsenic on social behavior and related gene expression in F2 male mice; https://cir.nii.ac.jp/crid/1362820655520958080; Gestational arsenic exposure induces anxiety-like behaviors in F1 female mice by dysregulation of neurological and immunological markers; https://cir.nii.ac.jp/crid/1390015191534788992; Does the prenatal bisphenol A exposure alter DNA methylation levels in the mouse hippocampus？ : an analysis using a high-sensitivity methylome technique; https://cir.nii.ac.jp/crid/2050870367059425536
• 参照: Genome‐wide analysis of <scp>DNA</scp> methylation changes induced by gestational arsenic exposure in liver tumors; https://cir.nii.ac.jp/crid/1360004235487644416; Mutations in the ras proto-oncogene: clues to etiology and molecular pathogenesis of mouse liver tumors; https://cir.nii.ac.jp/crid/1360011144478790016; Genetic and epigenetic effects of environmental arsenicals; https://cir.nii.ac.jp/crid/1360011145442256768; Genetic and Epigenetic Mechanisms in Metal Carcinogenesis and Cocarcinogenesis: Nickel, Arsenic, and Chromium; https://cir.nii.ac.jp/crid/1360011146206793088; Prenatal environmental exposures, epigenetics, and disease; https://cir.nii.ac.jp/crid/1360282589177055488; Late-onset Increases in Oxidative Stress and Other Tumorigenic Activities and Tumors With a Ha-ras Mutation in the Liver of Adult Male C3H Mice Gestationally Exposed to Arsenic; https://cir.nii.ac.jp/crid/1360283692643986688; Epigenetic reprogramming in mouse pre-implantation development and primordial germ cells; https://cir.nii.ac.jp/crid/1360283694068241920; Augmenting effects of gestational arsenite exposure of C3H mice on the hepatic tumors of the F₂ male offspring via the F₁ male offspring; https://cir.nii.ac.jp/crid/1360285705132190464; In vivo mutagenicity of arsenite in the livers of gpt delta transgenic mice; https://cir.nii.ac.jp/crid/1360285707357236608; Arsenic and human health effects: A review; https://cir.nii.ac.jp/crid/1360292618607947008; A human B cell methylome at 100−base pair resolution; https://cir.nii.ac.jp/crid/1360574094696988288; Recent advances in the protocols of transgenic mouse mutation assays; https://cir.nii.ac.jp/crid/1360574094739837568; Epimutagenesis: A prospective mechanism to remediate arsenic-induced toxicity; https://cir.nii.ac.jp/crid/1360574095257263744; Increased Mortality from Lung Cancer and Bronchiectasis in Young Adultsafter Exposure to Arsenic <i>in Utero</i> and in Early Childhood; https://cir.nii.ac.jp/crid/1360574095849704320; Mechanisms Underlying Latent Disease Risk Associated with Early-Life Arsenic Exposure: Current Research Trends and Scientific Gaps; https://cir.nii.ac.jp/crid/1360574096081109888; SREBPs: the crossroads of physiological and pathological lipid homeostasis; https://cir.nii.ac.jp/crid/1360855569807746432; Effects Of Arsenic Exposure On Dna Methylation And Epigenetic Gene Regulation; https://cir.nii.ac.jp/crid/1360855571503984896; Epigenetic protein families: a new frontier for drug discovery; https://cir.nii.ac.jp/crid/1361418518772114048; Developmental origins of non-communicable disease: Implications for research and public health; https://cir.nii.ac.jp/crid/1361418519111644288; Role of Endoplasmic Reticulum Stress in Metabolic Disease and Other Disorders; https://cir.nii.ac.jp/crid/1361699994064949760; Environmentally induced epigenetic transgenerational inheritance of phenotype and disease; https://cir.nii.ac.jp/crid/1361699994629054336; Arsenic Exposure and Toxicology: A Historical Perspective; https://cir.nii.ac.jp/crid/1361699995195175424; Promoting effects of dimethylarsinic acid on <i>N</i>-butyl-<i>N</i>-(4-hydroxybutyl)nitrosamine-induced urinary bladder carcinogenesis in rats; https://cir.nii.ac.jp/crid/1361699996398960128; Arsenic in the aetiology of cancer; https://cir.nii.ac.jp/crid/1361981469038784000; Estrogen Signaling in Livers of Male Mice With Hepatocellular Carcinoma Induced by Exposure to Arsenic In Utero; https://cir.nii.ac.jp/crid/1362262943634726784; Promotion of hepatocarcinogenesis in humans and animal models; https://cir.nii.ac.jp/crid/1362262944608106368; CRELD2 is a novel endoplasmic reticulum stress-inducible gene; https://cir.nii.ac.jp/crid/1362262945563216768; Targeted and genome-scale strategies reveal gene-body methylation signatures in human cells; https://cir.nii.ac.jp/crid/1362544420315636864; The role of microRNAs in metal carcinogen-induced cell malignant transformation and tumorigenesis; https://cir.nii.ac.jp/crid/1362544420849001984; Risk of occupational exposure to asbestos, silicon and arsenic on pulmonary disorders: Understanding the genetic-epigenetic interplay and future prospects; https://cir.nii.ac.jp/crid/1362825893716040832; Role of oxidative stress in the pathogenesis of nonalcoholic steatohepatitis; https://cir.nii.ac.jp/crid/1362825894148042368; The Long (LINEs) and the Short (SINEs) of It: Altered Methylation as a Precursor to Toxicity; https://cir.nii.ac.jp/crid/1362825895650114304; An Emerging Role for Epigenetic Dysregulation in Arsenic Toxicity and Carcinogenesis; https://cir.nii.ac.jp/crid/1362825895835140224; Urinary bladder carcinogenicity of dimethylarsinic acid in male F344 rats; https://cir.nii.ac.jp/crid/1362825896036658432; Dimethylarsinic acid, a main metabolite of inorganic arsenics, has tumorigenicity and progression effects in the pulmonary tumors of A/J mice; https://cir.nii.ac.jp/crid/1363107368406095360; Exposure of hepatocellular carcinoma cells to low-level As2O3‎ causes an extra toxicity pathway via L1 retrotransposition ‎induction; https://cir.nii.ac.jp/crid/1363388843863277568; Cancer epigenetics reaches mainstream oncology; https://cir.nii.ac.jp/crid/1363388845999649536; TET enzymes, TDG and the dynamics of DNA demethylation; https://cir.nii.ac.jp/crid/1363388846134413952; RAS oncogenes: weaving a tumorigenic web; https://cir.nii.ac.jp/crid/1363670319069155968; LINE-1 Elements in Structural Variation and Disease; https://cir.nii.ac.jp/crid/1363670319923419264; Gene Body Methylation Can Alter Gene Expression and Is a Therapeutic Target in Cancer; https://cir.nii.ac.jp/crid/1363670320711629568; Response to “Comment on ‘Effects of <i>in Utero</i> Exposure to Arsenic during the Second Half of Gestation on Reproductive End Points and Metabolic Parameters in Female CD-1 Mice’”; https://cir.nii.ac.jp/crid/1363670321038344448; Kidney Cancer Mortality; https://cir.nii.ac.jp/crid/1363951794078742528; Exposure to dimethylarsinic acid, a main metabolite of inorganic arsenics, strongly promotes tumorigenesis initiated by 4-nitroquinoline 1-oxide in the lungs of mice; https://cir.nii.ac.jp/crid/1363951794443508992; Transgenerational developmental programming; https://cir.nii.ac.jp/crid/1363951794829679744; Transplacental carcinogenicity of inorganic arsenic in the drinking water: induction of hepatic, ovarian, pulmonary, and adrenal tumors in mice; https://cir.nii.ac.jp/crid/1363951795717766784; Mapping of the Hormone-sensitive Lipase Binding Site on the Adipocyte Fatty Acid-binding Protein (AFABP); https://cir.nii.ac.jp/crid/1364233268609738752; 8-Hydroxyguanine: From its discovery in 1983 to the present status; https://cir.nii.ac.jp/crid/1390001204144955648; Genetic susceptibility to arsenic-induced skin lesions and health effects : a review; https://cir.nii.ac.jp/crid/2051714791865681920
• 連携機関・データベース: 国立情報学研究所 : CiNii Research; https://cir.nii.ac.jp/
• 提供元機関・データベース: 雑誌記事索引データベース; https://ndlsearch.ndl.go.jp; Crossref; https://www.crossref.org; 科学研究費助成事業データベース; https://kaken.nii.ac.jp/ja
• 書誌ID（NDLBibID）: 10349116; http://id.ndl.go.jp/bib/10349116