摘要:
The present invention relates to a method of implementing a scatternet over a plurality of piconets using different frequencies in a Wireless Personal Area Network (WPAN). In the scatternet implementation method of the present invention, a master of a first piconet transmits a scatternet request to a shared slave, and the shared slave switches a frequency thereof to a frequency of a second piconet and relays the scatternet request to a master of the second piconet. The master of the second piconet transmits scatternet approval to the shared slave. The shared slave switches the frequency to a frequency of the first piconet, relays the scatternet approval to the master of the first piconet, and is allocated resources, which do not overlap each other, by the masters of the first piconet and the second piconet. The shared slave switches frequencies and relays data between the first piconet and the second piconet while synchronizing with both the first piconet and the second piconet using allocated resources.
摘要:
The present invention relates to a method of continuously producing a phosphor at a supercritical water (SCW) condition and an apparatus used in the method. A phosphor produced according to the method of the present invention has similar luminosity to a phosphor produced according to a conventional solid-state method and the size and shape of particles thereof is also uniform. Accordingly, a phosphor according to the method of the present invention is applicable in various fields such as plasma display (PDP) and field emission display (FED). Also, in the method of producing a phosphor according to the present invention, the total reaction time is within about one minute, which is shorter than in the solid-state method. Also, since a separate heat processing process is not needed to obtain crystallized particles, it is efficient in aspects of time and energy.
摘要:
Provided is an expression vector for gene therapy having a novel combination of transcriptional regulatory elements, including a promoter, an enhancer, an intron, an untranslated region (UTR) and a locus control region (LCR). The expression vector enables sustained expression of a liver tissue-specific gene, and thus, can be effectively used for treating thrombosis, hemophilia, liver cancer, etc.
摘要:
The present invention relates to a novel sulfamide derivative, a pharmaceutically acceptable salt thereof and a pharmaceutical composition for upregulation of lipid metabolism comprising same as an active ingredient.
摘要:
Provided is an expression vector for gene therapy having a novel combination of transcriptional regulatory elements, including a promoter, an enhancer, an intron, an untranslated region (UTR) and a locus control region (LCR). The expression vector enables sustained expression of a liver tissue-specific gene, and thus, can be effectively used for treating thrombosis, hemophilia, liver cancer, etc.
摘要:
Provided is an expression vector for gene therapy having a novel combination of transcriptional regulatory elements, including a promoter, an enhancer, an intron, an untranslated region (UTR) and a locus control region (LCR). The expression vector enables sustained expression of a liver tissue-specific gene, and thus, can be effectively used for treating thrombosis, hemophilia, liver cancer, etc.
摘要:
Provided is an expression vector for gene therapy having a novel combination of transcriptional regulatory elements, including a promoter, an enhancer, an intron, an untranslated region (UTR) and a locus control region (LCR). The expression vector enables sustained expression of a liver tissue-specific gene, and thus, can be effectively used for treating thrombosis, hemophilia, liver cancer, etc.
摘要:
Provided is an expression vector for gene therapy having a novel combination of transcriptional regulatory elements, including a promoter, an enhancer, an intron, an untranslated region (UTR) and a locus control region (LCR). The expression vector enables sustained expression of a liver tissue-specific gene, and thus, can be effectively used for treating thrombosis, hemophilia, liver cancer, etc.
摘要:
A linear double-stranded RNA molecule, which comprises two or more consecutively or convergently linked short interfering RNAs (siRNAs) each reducing the expression of one of different target genes, and a recombinant expression vector comprising double-stranded DNA sequence expressing the linear double-stranded RNA molecule are provided. The linear double-stranded RNA molecule or the recombinant expression vector is useful for a method of reducing expression of target genes in a cell, the method comprising introducing the linear double-stranded RNA molecule or the recombinant expression vector into the cell, whereby the encoded siRNAs target different genes and reduce expression of the target genes. It was also proved that effective gene silencing activity can be induced when each siRNA unit within the linear double-stranded RNA molecule has 18 to 24 nucleotides and, additionally, the gene silencing activity is not affected by inverted orientation of an siRNA.
摘要:
A method for enhancing the serum stability and lowering the immunostimulatory property of a small interfering ribonucleic acid (siRNA) which mediates RNA interference (RNAi) against a viral gene expression of hepatitis B virus (HBV) or hepatitis C virus (HCV) is provided.