スポンサーリンク
Department of Inherited Metabolic Disease, National Institute of Neuroscience, NCNP | 論文
- Diagnosis of Alexander disease in a Japanese patient by molecular genetic analysis
- Distribution of transient receptor potential vanilloid 1(TRPV1)in the trigeminovascular system of the rat
- Human amniotic epithelial cells are promising transgene carriers for allogeneic cell transplantation into liver
- The role of DC-STAMP in maintenance of immune tolerance through regulation of dendritic cell function
- Role of DC-STAMP in cellular fusion of osteoclasts and macrophage giant cells
- AMELIORATION OF PROLIDASE DEFICIENCY IN FIBROBLASTS USING ADENOVIRUS MEDIATED GENE TRANSFER
- オキシトシンによるヒト羊膜上皮細胞死の誘導 : 移植拒絶反応機序の一つの可能性
- A case of infantile Alexander disease with a milder phenotype and a novel GFAP mutation, L90P
- Effects of immunoglobulin therapy in experimental allergic neuritis (EAN) of the Lewis rat induced by P2 myelin protein
- T Cell Activation in Demyelinating Neuropathy Associated with "Benign" Anti-Myelin Associated Glycoprotein IgM Gammopathy and in MS : Soluble Interleukin-2 Receptor Levels in Serum and Cerebrospinal Fluid
- 1-Alpha, 25-dihydroxy vitamin D_3 inhibits osteoclastogenesis through IFN-beta-dependent NFATc1 suppression