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991.
Ming Dai Yu Zhang Yiman Hua Wansun Ni Gonghuan Du 《Electronics letters》1998,34(10):951-953
By active-passive-decomposition synchronisation, the application of the one-way coupled ring map lattice hyperchaotic system in secure digital speech communication is demonstrated. Synchronisation guarantees strong security and recovery without error 相似文献
992.
993.
994.
整个散运系统采用3台FX2-128MRPLC分块控制后,使得控制结构清楚,线路简单,工作可靠性大为提高,对所有控制柜元器件进行数据库管理,极大地提高图表的准确率。 相似文献
995.
矿化剂对氧化铬绿色釉呈色性能的影响 总被引:2,自引:0,他引:2
针对氧化铬绿色釉存在色调暗不够鲜艳的缺点,研究了矿化剂对其呈色性能的影响,经分光光度分析的扫描电镜测试,表明矿化剂具有一定的助熔作用和还原性,从而提高了氧化铬绿色釉的鲜艳度和着色力,增强了装饰性,同时矿化剂还能降低烧成温度,节约能源,具有应用价值。 相似文献
996.
结合实时法全息干涉计量和数字图象处理技术,提出了一种溶液扩散系数的自动测量系统。在干涉图的处理中,采用了相位检测和曲线拟合技术,得到了亚象素的测量精度。 相似文献
997.
Using neutral/neutral and neutral/alkaline two-dimensional (2-D) gel techniques, we previously obtained evidence that initiation can occur at any of a large number of sites distributed throughout a broad initiation zone in the dihydrofolate reductase (DHFR) domain of Chinese hamster ovary (CHO) cells. However, other techniques have suggested a much more circumscribed mode of initiation in this locus. This dichotomy has raised the issue whether the patterns of replicating DNA on 2-D gels have been misinterpreted and, in some cases, may represent such noncanonical replication intermediates as broken bubbles or microbubbles. In an accompanying study (R. F. Kalejta and J. L. Hamlin, Mol. Cell. Biol. 16:4915-4922, 1996), we have shown that broken bubbles migrate to unique positions in three different gel systems and therefore are not likely to be confused with classic replication intermediates. Here, we have applied a broken bubble assay developed from that study to an analysis of the amplified DHFR locus in CHO cells. This assay gives information about the number and positions of initiation sites within a fragment. In addition, we have analyzed the DHFR locus by a novel stop-and-go-alkaline gel technique that measures the size of nascent strands at all positions along each arc in a neutral/neutral 2-D gel. Results of these analyses support the view that the 2-D gel patterns previously assigned to classic, intact replication bubbles and single-forked structures indeed correspond to these entities. Furthermore, potential nascent-strand start sites appear to be distributed at very frequent intervals along the template in the intergenic region in the DHFR domain. 相似文献
998.
本文介绍了广播发射台利用计算机技术、网络技术、遥控遥测技术、现代测试手段,对设备进行自动化控制与管理;实现设备技术指标自动测试,发射台无人值班、有人留守,建立机器的计算机档案制度,确保安全优质播出的方法和经验。 相似文献
999.
V. A. Varlachev A. N. Kuzin S. V. Lykhin E. S. Solodovnikov Yu. P. Usov A. V. Fotin Yu. A. Tsibul'nikov 《Atomic Energy》1995,79(1):447-449
All-Union Scientific-Research Institute of Nuclear Physics at the S. M. Kirov Tomsk Polytechnical University. Translated from
Atomnaya énergiya, Vol. 79, No. 1, pp. 38–40, July, 1995. 相似文献
1000.
The transmembrane proteoglycan NG2 is able to interact both with components of the extracellular matrix and with the actin cytoskeleton. An examination of the distribution of NG2 during cell spreading suggests that NG2 can associate with two distinct types of actin-containing cytoskeletal structures, depending on the nature of the stimulus derived from the substratum. On fibronectin-coated dishes, cell surface NG2 associates exclusively with stress fibers developing within the cell. On poly-L-lysine-coated dishes, cell surface NG2 is associated with radial processes extending from the cell periphery. Spreading on fibronectin/poly-L-lysine mixtures, as well as on matrix components such as laminin, tenascin, and type VI collagen, produces cells with mosaic characteristics, i.e., NG2 is associated with both types of structures. NG2-positive radial processes are distinct from a second population of radial structures that contain fascin. NG2-positive extensions appear to be individual self-contained units (filopodia), whereas fascin is associated with actin ribs within sheets of membrane (lamellipodia). NG2- and fascin-positive structures are often localized to opposite poles of spreading cells, suggesting a possible role for the two classes of cellular extensions in the establishment of cell polarity during morphogenesis or migration. Time lapse imaging confirms the presence of lamellipodia on the leading edges of migrating cells, while numerous filopodia are present on trailing edges. 相似文献