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1.
Glycosylphosphatidylinositol-anchored proteins (GPI-APs), which are anchored at the outer leaflet of plasma membranes (PM) only by a carboxy-terminal GPI glycolipid, are known to fulfill multiple enzymic and receptor functions at the cell surface. Previous studies revealed that full-length GPI-APs with the complete GPI anchor attached can be released from and inserted into PMs in vitro. Moreover, full-length GPI-APs were recovered from serum, dependent on the age and metabolic state of rats and humans. Here, the possibility of intercellular control of metabolism by the intercellular transfer of GPI-APs was studied. Mutant K562 erythroleukemia (EL) cells, mannosamine-treated human adipocytes and methyl-ß-cyclodextrin-treated rat adipocytes as acceptor cells for GPI-APs, based on their impaired PM expression of GPI-APs, were incubated with full-length GPI-APs, prepared from rat adipocytes and embedded in micelle-like complexes, or with EL cells and human adipocytes with normal expression of GPI-APs as donor cells in transwell co-cultures. Increases in the amounts of full-length GPI-APs at the PM of acceptor cells as a measure of their transfer was assayed by chip-based sensing. Both experimental setups supported both the transfer and upregulation of glycogen (EL cells) and lipid (adipocytes) synthesis. These were all diminished by serum, serum GPI-specific phospholipase D, albumin, active bacterial PI-specific phospholipase C or depletion of total GPI-APs from the culture medium. Serum inhibition of both transfer and glycogen/lipid synthesis was counteracted by synthetic phosphoinositolglycans (PIGs), which closely resemble the structure of the GPI glycan core and caused dissociation of GPI-APs from serum proteins. Finally, large, heavily lipid-loaded donor and small, slightly lipid-loaded acceptor adipocytes were most effective in stimulating transfer and lipid synthesis. In conclusion, full-length GPI-APs can be transferred between adipocytes or between blood cells as well as between these cell types. Transfer and the resulting stimulation of lipid and glycogen synthesis, respectively, are downregulated by serum proteins and upregulated by PIGs. These findings argue for the (patho)physiological relevance of the intercellular transfer of GPI-APs in general and its role in the paracrine vs. endocrine (dys)regulation of metabolism, in particular. Moreover, they raise the possibility of the use of full-length GPI-APs as therapeutics for metabolic diseases.  相似文献   
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移动OFDM水声通信系统中,基于压缩感知的稀疏信道估计方法计算量较大,不适用于实时通信.针对这一问题,该文基于一致多普勒信道模型提出一种扩展路径识别(GPI)算法.该方法首先使用信道多普勒扩展矩阵构造等效发射序列,将多普勒信道转化为等效线性时不变信道.然后使用GPI算法估计信道多普勒及各路径的时延及幅度参数,实现低复杂...  相似文献   
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This article describes the design of an observer based robust linear output feedback controller for the regulation and output reference trajectory tracking tasks in switched ‘buck’ converter circuits feeding a completely unknown time-varying load. The state-dependent perturbation effects of the unknown load resistance are on-line estimated by means of a generalised proportional integral (GPI) observer, which represents the dual counterpart of GPI controllers introduced in Fliess, Márquez, Delaleau and Sira-Ramírez (Fliess, M., Márquez, R., Delaleau, E., and Sira-Ramírez, H. (2002), ‘Correcteurs Proportionnels-intégraux Géneralisés’, ESAIM: Control, Optimisation and Calculus of Variations, 7, 23–41). The reconstructed perturbation complements the controller in a cancellation effort which allows the core of the feedback controller to become a traditional proportional derivative (PD) controller. The designed average feedback controller is then implemented via a sigma–delta-modulator, which effectively translates the designed continuous average feedback control input signal into a discrete valued switched input signal driving the converter's input switch and preserving all relevant features of the average design. The Appendix collects some generalities about GPI observers.  相似文献   
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In many applications involving a robot in contact with a surface it is important to control the interaction between the manipulator and its environment, usually by employing force sensors. However, sometimes it is desirable to remove them due to a variety of reasons, e.g. high costs, noisy measurements and a narrow bandwidth. To overcome these drawbacks, in this work it is proposed as a velocity/force observer based on the Generalized Proportional Integral (GPI) technique. Joint velocities and contact forces are estimated with only position measurements and then used in a force/position control scheme. Ultimate boundedness of the observation errors is formally proven and an arbitrarily small ultimate bound is then achieved. Simulation results are used to validate the proposed approach.  相似文献   
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The effect of free and liposomal forms of phenolic lipids isolated from rye grains, cashew nut-shell liquid (CNSL) from Anacardium occidentale, and Merrulius tremellosus fruit body on the glycosyl-phosphatidylinositol (GPI)-anchor-deprived erythrocyte-ghost acetylcholinesterase activity was studied. It was shown that the observed effect distinctly depends on the form of the phenolic lipids available for interaction with the enzyme. The free form of the phenolic lipids decreased the enzymatic activity of GPI-anchor-deprived acetylcholinesterase less than the acetylcholinesterase anchored in erythrocytes ghosts, whereas the same phenolic lipids present in the medium in liposomal form, increased it.  相似文献   
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基于时间-数字转换的精密时差测量系统设计   总被引:3,自引:0,他引:3  
精密时差测量在激光测距、无源时差定位、航空遥控遥测等领域有着广泛的应用.提出时间-数字转换技术的时差测量方法,设计一种基于TDC-GPl的高精度时差测量系统,并介绍测量系统设计方法和软、硬件实现原理.所设计的系统具有配置灵活、可靠性高、功耗低等优点.通过对实际测量数据的分析表明,系统可以实现纳秒级的时间间隔测量.  相似文献   
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The GGP1/GAS1/CWH52 gene of Saccharomyces cerevisiae encodes a major exocellular 115 kDa glycoprotein (gp115) anchored to the plasma membrane through a glycosylphosphatidylinositol (GPI). The function of gp115 is still unknown but the analysis of null mutants suggests a possible role in the control of morphogenesis. PHR1 gene isolated from Candida alibicans is homologous to the GGP1 gene. In this report we have analysed the ability of PHR1 to complement a ggp1Δ mutation in S. cerevisiae. The expression of PHR1 controlled by its natural promoter or by the GGP1 promoter has been studied. In both cases we have observed a complete complementation of the mutant phenotype. Moreover, immunological analysis has revealed that PHR1 in budding yeast gives rise to a 75–80 kDa protein anchored to the membrane through a GPI, indicating that the signal for GPI attachment present in the C. albicans gene product is functional in S. cerevisiae.  相似文献   
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