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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
Authors :下澤, 伸行
Issue Date :2004
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
49-56p: Nagase T. et al., Peroxisomal Localization in the Developing Mouse Cerebellum: Implications for Neuronal Abnormalities Related to Deficiencies in Peroxisomes. Biochimica et Biophysica Acta-General Subjects. 2004 1671(1-3): 26-33
57-63p: Shimozawa N. et al., Identification of a New Complementation Group of the Peroxisome Biogenesis Disorders and PEX14 as the Mutated Gene. Human Mutation. 2004 23(6): 552-558
64-69p: Morita M. et al., Baicalein 5,6,7-Trimethyl Ether, a Flavonoid Derivative, Stimulates Fatty Acid β-Oxidation in Skin Fibroblasts of X-Linked Adrenoleukodystrophy. FEBS Letters. 2005 579(2): 409-414
Abstract :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
Type Local :研究報告書
Appears in Collections:Grants-in-Aid for Scientific Research - Research Centers