スポンサーリンク
Department of Clinical Genetics, the Tokyo Metropolitan Institute of Medical Science | 論文
- Effect of Apolipoprotein E Genotype on Association of Menopausal Status with Lipid Level in Japanese Women
- Galactonojirimycin derivatives restore mutant human β-galactosidase activities expressed in fibroblasts from enzyme-deficient knockout mouse
- 原子力環境用高性能フッ素樹脂の開発
- Neurological manifestations of knockout mice with β-galactosidase deficiency
- Expression of the Cholera Toxin B Subunit in the Golgi Apparatus of Swiss 3T3 Cells Inhibits DNA Synthesis Induced by Basic Fibroblast Growth Factor
- Localization of Cathepsins B, D, L, LAMP-1 and μ-Calpain in Developing Hair Follicles
- Fabry disease in patients receiving maintenance dialysis
- High Incidence of Thrombosis in Fabry's Disease
- Screening and detection of gene mutations in Japanese patients with Fabry disease by non-radioactive single-stranded conformation polymorphism analysis
- Urinary excretion of the vitron receptor (integrin αυβ_3) in patients with non-insulin dependent diabetes mellitus
- A novel apolipoprotein E5 variant with a 24-bp insertion causing hyperlipidemia
- Typing of Y chromosome single nucleotide polymorphisms in a Japanese population by a multiplexed single nucleotide primer extension reaction
- Extinction of Organelles in Differentiating Epidermis
- Autophagy of mitochondria and apoptosis in terminal differentiation
- Japanese-type adult galactosialidosis. A unique and common splice junction mutation causing exon skipping in the protective protein/carboxypeptidase gene.:A Unique and Common Splice Junction Mutation Causing Exon Skipping in the Protective Protein/Carboxy
- Biological Effect of 9-cis-Retinoic Acid and 9,13-di-cis-Retinoic Acid on Human Acute Promyelocytic Leukemia Cell Line HL-60.