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991.
The structure and properties of solid solutions and the chemical compound Gd2Zr2O7 in the Gd2O3 - ZrO2 system are investigated. Sintering of the initial mixture is studied and the optimum concentration of the stabilizing additive is determined for the production of heat-resistant articles from granular mixtures based on ZrO2 stabilized by Gd2O3 and fired at 1750°C. Properties of specimens prepared by the technology developed are presented. Translated from Ogneupory, No. 3, pp. 12 – 16, March, 1996.  相似文献   
992.
Direct volume display devices (DVDDs), which display 3D volumes and surfaces in a volume by providing depth rather than depth cues, are discussed. The transport theory model is used to illustrate why DVDDs are best able to support fast presentation from arbitrary directions. The technology underlying various DVDDs is described. Specifically, the design and operation of the OmniView rotating-screen DVDD are examined. The air-traffic-control/air-tactics-analysis, satellite orbit mechanics, and time-critical target prosecution applications of DVDDs are also discussed  相似文献   
993.
A metal-insulator-metal (MIM) capacitor structure has been developed for use in field-programmable gate arrays (FPGAs) as a voltage-programmable link (VPL). The structure relies on a combination of a refractory metal and aluminum as the lower electrode, and either a similar combination or aluminum alone as the top electrode. The insulator is prepared by means of plasma-enhanced chemical vapor deposition (PECVD). It comprises a sandwich of nearly stoichiometric silicon dioxide interposed between two like layers of silicon-rich silicon nitride. The structure has displayed characteristics desirable for use in emerging FPGA technology, including high density, low on-resistance, reduced capacitance, and low programming voltage  相似文献   
994.
995.
Optimum (in a maximally flat frequency response error sense) FIR digital differentiators of variable fractional sample delay are derived that calculate the derivative of an input uniformly sampled discrete-time signal with arbitrary centre frequency at an arbitrarily chosen instant of time within each sampling interval. The proposed class of differentiators includes maximally linear differentiators for low frequencies  相似文献   
996.
997.
In the present study we have dissected the transport pathways between the ER and the Golgi complex using a recently introduced (Kuismanen, E., J. J?ntti, V. M?kiranta, and M. Sariola. 1992. J. Cell Sci. 102:505-513) inhibition of transport by caffeine at 20 degrees C. Recovery of the Golgi complex from brefeldin A (BFA) treatment was inhibited by caffeine at reduced temperature (20 degrees C) suggesting that caffeine inhibits the membrane traffic between the ER and the Golgi complex. Caffeine at 20 degrees C did not inhibit the BFA-induced retrograde movement of the Golgi membranes. Further, incubation of the cells in 10 mM caffeine at 20 degrees C had profound effects on the distribution and the organization of the pre-Golgi and the Golgi stack membranes. Caffeine treatment at 20 degrees C resulted in a selective and reversible translocation of the pre- and cis-Golgi marker protein (p58) to the periphery of the cell. This caffeine-induced effect on the Golgi complex was different from that induced by BFA, since mannosidase II, a Golgi stack marker, remained perinuclearly located and the Golgi stack coat protein, beta-COP, was not detached from Golgi membranes in the presence of 10 mM caffeine at 20 degrees C. Electron microscopic analysis showed that, in the presence of caffeine at 20 degrees C, the morphology of the Golgi stack was altered and accumulation of numerous small vesicles in the Golgi region was observed. The results in the present study suggest that caffeine at reduced temperature (20 degrees C) reveals a functional interface between the pre-Golgi and the Golgi stack.  相似文献   
998.
999.
The assay of Complex I activity requires the use of artificial acceptors, such as short-chain coenzyme Q homologs and analogs, because the physiological quinones, such as CoQ10, are too insoluble in water to be added as substrates to the assay media. The medical interest raised in the last years on the pathological changes of Complex I activity has focussed on the requirement of easy reliable assays for its analysis. We have undertaken a systematic examination of the assay conditions of Complex I in mitochondrial membranes, using a series of quinones as electron acceptors, particularly the coenzyme Q homologs CoQ0, CoQ1 and CoQ2, and the analogs duroquinone and decylubiquinone. Our findings have pointed out that the most suitable electron acceptor for the NADH:CoQ reductase assay is the homolog CoQ1. The analog DB, commercially available, although yielding a high activity, nevertheless causes some problems for the standardization of the assay conditions.  相似文献   
1000.
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