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Articles by S. Kato
Total Records ( 3 ) for S. Kato
  A. Nishimura , Y. Hayashi , K. Tanaka , M. Hirota , S. Kato , M. Ito , K. Araki and E.J. Hu
  In this study, the environmental load of photovoltaic power generation system (PV) during its life cycle and energy payback time (EPT) are evaluated by LCA scheme. Two hypothetical case studies in Toyohashi, Japan and Gobi dessert in China have been carried out to investigate the influence of installation location and PV type on environmental load and EPT. The environmental load and EPT of a high-concentration photovoltaic power generation system (hcpV) and a multi-crystalline silicon photovoltaic power generation system (mc-Si PV) are studied. The study shows for a PV of 100 MW size, the total impacts of the hcpV installed in Toyohashi is larger than that of the hcpV installed in Gobi desert by 5% without consideration of recycling stage. The EPT of the hcpV assumed to be installed in Gobi desert is shorter than EPT of the hcpV assumed to be installed in Toyohashi by 0.64 year. From these results, the superiority to install PV in Gobi desert is certificated. Comparing with hcpV and mc-Si PV, the ratio of the total impacts of mc-Si PV to that of hcpV is 0.34 without consideration of recycling stage. The EPT of hcpV is longer than EPT of mc-Si PV by 0.27 year. The amount of global solar radiation contributing to the amount of power generation of mc-Si PV is larger than the amount of direct solar radiation contributing to the amount of power generation of hcpV by about 188 kW h/(m2 year) in Gobi desert. Consequently, it appears that using mc-Si PV in Gobi desert is the best option.
  S Sawatsubashi , T Murata , J Lim , R Fujiki , S Ito , E Suzuki , M Tanabe , Y Zhao , S Kimura , S Fujiyama , T Ueda , D Umetsu , T Ito , K. i Takeyama and S. Kato
 

Chromatin reorganization is essential for transcriptional control by sequence-specific transcription factors. However, the molecular link between transcriptional control and chromatin reconfiguration remains unclear. By colocalization of the nuclear ecdysone receptor (EcR) on the ecdysone-induced puff in the salivary gland, Drosophila DEK (dDEK) was genetically identified as a coactivator of EcR in both insect cells and intact flies. Biochemical purification and characterization of the complexes containing fly and human DEKs revealed that DEKs serve as histone chaperones via phosphorylation by forming complexes with casein kinase 2. Consistent with the preferential association of the DEK complex with histones enriched in active epigenetic marks, dDEK facilitated H3.3 assembly during puff formation. In some human myeloid leukemia patients, DEK was fused to CAN by chromosomal translocation. This mutation significantly reduced formation of the DEK complex, which is required for histone chaperone activity. Thus, the present study suggests that at least one histone chaperone can be categorized as a type of transcriptional coactivator for nuclear receptors.

  Y Imai , S Kondoh , A Kouzmenko and S. Kato
 

The osteoprotective action of estrogen in women has drawn considerable attention because estrogen deficiency-induced osteoporosis became one of the most widely spread diseases in developed countries. In men, the significance of estrogen action for bone health maintenance is also apparent from the osteoporotic phenotype seen in male patients with genetically impaired estrogen signaling. Severe bone loss and high bone turnover, including typical osteofeatures seen in postmenopausal women, can also be recapitulated in rodents after ovariectomy. However, the expected osteoporotic phenotype is not observed in female mice deficient in estrogen receptor (ER)- or -β or both, even though the degenerative defects are clearly seen in other estrogen target tissues together with up-regulated levels of circulating testosterone. It has also been reported that estrogens may attenuate bone remodeling by cell autonomous suppressive effects on osteoblastogenesis and osteoclastogenesis. Hence, the effects of estrogens in bone appear to be complex, and the molecular role of bone estrogen receptors in osteoprotective estrogen action remains unclear. Instead, it has been proposed that estrogens indirectly control bone remodeling. For example, the enhanced production of cytokines under estrogen deficiency induces bone resorption through stimulation of osteoclastogenesis. However, the osteoporotic phenotype without systemic defects has been recapitulated in female (but not in male) mice by osteoclast-specific ablation of the ER, proving that bone cells represent direct targets for estrogen action. An aberrant accumulation of mature osteoclasts in these female mutants indicates that in females, the inhibitory action of estrogens on bone resorption is mediated by the osteoclastic ER through the shortened lifespan of osteoclasts.

 
 
 
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