2026-03-15T02:41:31Z https://gifu-u.repo.nii.ac.jp/oai

oai:gifu-u.repo.nii.ac.jp:00077052 2024-02-06T05:12:45Z 2092:2213:2214

モデル動物を用いたペルオキシソーム代謝障害に基づく発生異常と生活習慣病の病態解明 下澤, 伸行 metadata only access ペルオキシソーム 生活習慣病 先天異常 ペルオキシソーム病診断システム 7-12p: 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 13-19p: Hashimoto K. et al., Molecular Mechanism of a Temperature-Sensitive Phenotype in Peroxisomal Biogenesis Disorder. Pediatric Research. 2005 58(2): 263-269 20-24p: Suzuki Y. et al., Natural History of X-Linked Adrenoleukodystrophy in Japan. Brain & Development. 2005 27(5): 353-357 25-37p: Kashiwayama Y. et al., Role of Pex19p in the Targeting of PMP70 to Peroxisome. Biochimica et Biophysica Acta. 2005 1746(2): 116-128 38-47p: Ito R. et al., Identification of Pex5pM, and Retarded Maturation of 3-Ketoacyl-CoA Thiolase and Acyl-CoA Oxidase in CHO Cells Expressing Mutant Pex5p Isoforms. Journal of Biochemistry. 2005 138(6): 781-790 48-53p: Funato M. et al., Aberrant Peroxisome Morphology in Peroxisomal beta-Oxidation Enzyme Deficiencies. Brain & Development. 2006 28(5): 287-292 54-66p: Shiozawa K. et al., The Common Phospholipid-Binding Activity of the N-Terminal Domains of PEX1 and VCP/p97. FEBS Journal. 2006 273(21): 4959-4971 67-71p: Shimozawa N., Molecular and Clinical Aspects of Peroxisomal Diseases. Journal of Inherited Metabolic Disease. 2007 30(2): 193-197 研究報告書 平成17年度-平成18年度科学研究費補助金 (基盤研究(C)　一般　小児科学　課題番号17591079) 研究成果報告書 2007-03 jpn research report NA http://hdl.handle.net/20.500.12099/22370 https://gifu-u.repo.nii.ac.jp/records/77052