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

• Material Type: 文書・図像類
• 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
• Author Heading: 下澤, 伸行
• Publication Date: 2004
• Publication Date (W3CDTF): 2004
• Text Language Code: jpn
• Target Audience: 一般
• Note (General): 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
• 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

Table of Contents

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