The failure of two major formaldehyde catabolism enzymes (ADH5 and ALDH2) leads to partial synthetic lethality in C57BL/6 mice
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DOI[10.1186/s41021-020-00160-4]to the data of the same series
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- Material Type
- 記事
- Author/Editor
- Jun NakamuraDarcy W. HolleyToshihiro Kawamoto
- Publication, Distribution, etc.
- Publication Date
- 2020-06-03
- Publication Date (W3CDTF)
- 2020-06-03
- Periodical title
- Genes and environment
- No. or year of volume/issue
- 42(21)
- Volume
- 42(21)
- ISSN (Periodical Title)
- 1880-7062
- ISSN-L (Periodical Title)
- 1880-7046
- Text Language Code
- eng
- DOI
- 10.1186/s41021-020-00160-4
- Persistent ID (NDL)
- info:ndljp/pid/11520477
- Collection
- Collection (Materials For Handicapped People:1)
- Collection (particular)
- 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
- Acquisition Basis
- オンライン資料収集制度
- Date Accepted (W3CDTF)
- 2020-08-03T12:00:21+09:00
- Date Captured (W3CDTF)
- 2020-08-03
- Format (IMT)
- application/pdf
- Access Restrictions
- 国立国会図書館内限定公開
- Service for the Digitized Contents Transmission Service
- 図書館・個人送信対象外
- Availability of remote photoduplication service
- 可
- Periodical Title (URI)
- Periodical Title (Persistent ID (NDL))
- info:ndljp/pid/11467640
- Data Provider (Database)
- 国立国会図書館 : 国立国会図書館デジタルコレクション
- Summary, etc.
- 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/s41021-020-00160-4
- Access Restrictions
- インターネット公開
- Related Material (URI)
- Is Referenced By
- Fanconi anemia and Aldehyde Degradation Deficiency Syndrome: Metabolism and DNA repair protect the genome and hematopoiesis from endogenous DNA damageALDH2 polymorphism rs671 is a predictor of PD-1/PD-L1 inhibitor efficacy against thoracic malignanciesAnalysis of disease model iPSCs derived from patients with a novel Fanconi anemia–like IBMFS <i>ADH5/ALDH2</i> deficiencyPotential Doxorubicin-Mediated Dual-Targeting Chemotherapy in FANC/BRCA-Deficient Tumors via Modulation of Cellular Formaldehyde Concentration
- References
- Variant ALDH2 is associated with accelerated progression of bone marrow failure in Japanese Fanconi anemia patientsKinetic Mechanism of Human Glutathione-Dependent Formaldehyde DehydrogenaseFormaldehyde catabolism is essential in cells deficient for the Fanconi anemia DNA-repair pathwayDNA-protein crosslink formation by endogenous aldehydes and AP sitesEndogenous formaldehyde is a memory-related molecule in mice and humansThe formaldehyde metabolic detoxification enzyme systems and molecular cytotoxic mechanism in isolated rat hepatocytesGenotoxic consequences of endogenous aldehydes on mouse haematopoietic stem cell functionSubstrate specificity of human and yeast aldehyde dehydrogenasesNon-P450 aldehyde oxidizing enzymes: the aldehyde dehydrogenase superfamilyCells Deficient in the FANC/BRCA Pathway Are Hypersensitive to Plasma Levels of FormaldehydeFHR5 Binds to Laminins, Uses Separate C3b and Surface-Binding Sites, and Activates Complement on Malondialdehyde-Acetaldehyde SurfacesAldehyde dehydrogenase (ALDH) 2 associates with oxidation of methoxyacetaldehyde; in vitro analysis with liver subcellular fraction derived from human and <i>Aldh2</i> gene targeting mouseThe association of mitochondrial aldehyde dehydrogenase gene (ALDH2) polymorphism with susceptibility to late-onset Alzheimer's disease in ChineseKinetics of Cytochrome P450 2E1-Catalyzed Oxidation of Ethanol to Acetic Acid via AcetaldehydeEvidence that endogenous formaldehyde produces immunogenic and atherogenic adduct epitopesDeficiency in Mitochondrial Aldehyde Dehydrogenase Increases the Risk for Late-Onset Alzheimer's Disease in the Japanese PopulationMammals divert endogenous genotoxic formaldehyde into one-carbon metabolismToxicological and Metabolic Consequences of Methanol PoisoningALDH2 polymorphisms and bone mineral density in an elderly Japanese populationFormaldehyde Dehydrogenase from Human LiverActive DNA demethylation: many roads lead to RomeEndogenous Formaldehyde Is a Hematopoietic Stem Cell Genotoxin and Metabolic CarcinogenA Novel Mechanism for Endogenous Formaldehyde Elevation in SAMP8 MouseLymphocyte Development Requires <i>S</i>-nitrosoglutathione ReductaseThe Janus face of alcohol dehydrogenase 3Reduction of <i>S</i>-nitrosoglutathione by alcohol dehydrogenase 3 is facilitated by substrate alcohols via direct cofactor recycling and leads to GSH-controlled formation of glutathione transferase inhibitorsOxidation-specific epitopes restrain bone formationEffects of Aldehyde Dehydrogenase-2 Genetic Polymorphisms on Metabolism of Structurally Different Aldehydes in Human LiverAcid-specific formaldehyde donor is a potential, dual targeting cancer chemotherapeutic/chemo preventive drug for FANC/BRCA-mutant cancer
- Data Provider (Database)
- 国立情報学研究所 : CiNii Research
- Original Data Provider (Database)
- 雑誌記事索引データベースCrossref科学研究費助成事業データベースCrossrefCrossrefCrossrefCrossref
- Bibliographic ID (NDL)
- 11520477