| 1 | Self-assembly of ZnO nanoparticles and preparation of bulk ZnO porous nanosolids显示文摘Novel bulk ZnO porous nanosolids were pre- pared by a unique solvothermal hot-press method, using ZnO nanoparticles and several kinds of solvents as the start- ing materials. It was found from the experiments that ZnO nanoparticles underwent a “self-assembly process” under some specific hydrothermal hot-press conditions. As a result, some “nanoflowers” formed. The results showed that porous nanosolids with uniform pore diameters could be obtained when water distributed uniformly among the ZnO nanopar- ticles. On the contrary, if the uniformity of the distribution of water was poor, “nanoflowers” would appear in the wa- ter-rich region. It was also found that the photoluminescence of ZnO porous nanosolids was affected by the self-assembly phenomenon. In addition, the results also showed that, both the volume and diameters of the pores could be adjusted by changing either the hot-press temperature, pressure or the kinds of solvents. | LIUXiulin XUHongyan YULili LIMei WANGChengjian CUIDeliang JIANGMinhua | 2005 | Chinese Science Bulletin2005，50，7： | 5 |
| 2 | Cloning and characterization of a mouse liver-specific gene mfrep-1,up-regulated in liver regeneration显示文摘Human fibrinogen-related protein-1/liver fibrinogen-related protein-1 (HFREP-1/LFIRE-1), a liver-specificprotein, is a member of fibrinogen superfamily that exerts various biological activities. However, the func-tion of HFREP-1/LFIRE-1 in liver remains unknown. Here we isolated its mouse ortholog gene-mousefibrinogen-related protein-1 (mfrep-1), which encoded 314 amino acids, exhibiting 80.4% similarity toHFREP-1/LFIRE-1. Northern blot analysis revealed that 1.2-kb mfrep-1 mRNA was detected selectivelyin mouse liver. To explore the function of MFREP-1, we examined the levels of mfrep-1 mRNA duringregeneration after 70% partial hepatectomy (PHx) in mice. mfrep-1 mRNA increased in the regeneratingliver and reached the first shoulder peak at 2-4 h after PHx. Cycloheximide pretreatment could suppress theinduction of mfrep-1, indicating the up-regulation of this gene need de novo protein synthesis. Its mRNAcontinued to elevate at 6 h thereafter and reached the second peak at 24 h. The enhanced expression ofmfrep-1 maintained high until 72 h and then declined slowly to the basal level. Immunohistochemistryassessment confirmed the up-regulated expression of MFREP-1 protein in parenchymal cells during liverregeneration. These data suggested that MFREP-1 might play an important role in liver regeneration andbe involved in the regulation of cell growth. | JUNYAN HAOYING FEIGU JINHE YuLILI HuIMINLIU YONGHUAXU | 2002 | Cell Research2002，12，5： | 5 |
您所在的机构暂未开通此部分的功能，请联系管理员