遺伝性ペルオキシソーム欠損症の発症に温度が関わる機序を解明する

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Note (General)：: 出版タイプ： NA研究報告書平成15年度-平成16年度年度科学研究費補助金 (基盤研究(C)(2)　課題番号15591100) 研究成果報告書

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10-13p: Shimozawa N. et al., Genetic Heterogeneity of Peroxisome Biogenesis Disorders Among Japanese Patients: Evidence for a Founder Haplotype for the Most Common PEX10 Gene Mutation. American Journal of Medical Genetics Part A. 2003 120A(1): 40-43
14-27p: Matsumoto N. et al., Mutations in Novel Peroxin Gene PEX26 that Cause Peroxisome-Biogenesis Disorders of Complementation Group 8 Provide a Genotype-Phenotype Correlation. American Journal of Human Genetics. 2003 73(2): 233-246
28-34p: Takemoto Y. et al., Gas Chromatography/Mass Spectrometry Analysis of Very Long Chain Fatty Acids, Docosahexaenoic Acid, Phytanic Acid and Plasmalogen for the Screening of Peroxisomal Disorders. Brain & Development. 2003 25(7): 481-487
35-42p: Kikuchi M. et al., Proteomic Analysis of Rat Liver Peroxisome. Journal of Biological Chemistry. 2004 279(1): 421-428
43-48p: Gootjes J. et al., Novel Mutations in the PEX2 Gene of Four Unrelated Patients with a Peroxisome Biogenesis Disorder. Pediatric Research. 2004 55(3): 431-436

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Material Type: 規格・テクニカルリポート類
Title: 遺伝性ペルオキシソーム欠損症の発症に温度が関わる機序を解明する
Author/Editor: 下澤, 伸行
Publication Date: 2004
Publication Date (W3CDTF): 2004
Target Audience: 一般
Note (General): 出版タイプ： NA
研究報告書
平成15年度-平成16年度年度科学研究費補助金 (基盤研究(C)(2)　課題番号15591100) 研究成果報告書
Access Restrictions: インターネット公開
Data Provider (Database): 国立情報学研究所 : 学術機関リポジトリデータベース（IRDB）（機関リポジトリ）
https://irdb.nii.ac.jp
Original Data Provider (Database): 岐阜大学 : 岐阜大学機関リポジトリ