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991.
Yang W. Kelly D. Mehr L. Sayuk M.T. Singer L. 《Solid-State Circuits, IEEE Journal of》2001,36(12):1931-1936
This paper describes the design of a 14-b 75-Msample/s pipeline analog-to-digital converter (ADC) implemented in a 0.35-μm double-poly triple-metal CMOS process. The ADC uses a 4-b first stage to relax capacitor-matching requirements, buffered bootstrapping to reduce signal-dependent charge injection, and a flip-around track-and-hold amplifier with wide common-mode compliance to reduce noise and power consumption. It achieves 14-b accuracy without calibration or dithering. Typical differential nonlinearity is 0.6 LSB, and integral nonlinearity is 2 LSB. The ADC also achieves 73-dB signal-to-noise ratio, and 85-dB spurious-free dynamic range over the first Nyquist band. The 7.8-mm2 ADC operates with a 2.7- to 3.6-V supply, and dissipates 340 mW at 3 V 相似文献
992.
993.
994.
M Harmsen TA Oosterlaken C Tangerman H Snippe CA Kraaijeveld 《Canadian Metallurgical Quarterly》1993,43(2):137-146
3-Hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase (EC 1.1.1.34) is the rate limiting step in the mevalonate pathway that produces isoprenoids and cholesterol. Inhibitors of HMG-CoA reductase are teratogenic in vivo and induce neural tube defects in rat embryo culture, effects which appear unrelated to cholesterol deficiency. This study is the first to localize HMG-CoA reductase mRNA by in situ hybridization (ISH). Expression of reductase mRNA was examined in post-implantation rat embryos, and for control purposes in rat liver and UT-1 cells, using a digoxigenin-11 (dig-11) labelled cRNA probe. Eighteen-day fetal liver showed heavy but patchy hybridization, and adult rat liver showed strong hybridization only on some periportal hepatocytes, which was absent in livers of fasted animals. UT-1 cells stimulated to overexpress HMG-CoA reductase mRNA were strongly positive with the same probe. Control hybridizations with sense strand RNA probe, or with cRNA probe on pre-RNased tissue were negative. Strong hybridization signal for HMG-CoA reductase mRNA was observed in all tissues of the post-implantation rat embryo, from egg cylinder to 30 somite stages (7 to 12 days). Heavy signal was noted in primitive ectoderm and neural tube. The wide embryonic and extraembryonic distribution and abundance of HMG-CoA reductase mRNA may reflect developmental requirements for products of the mevalonate pathway, e.g., isoprenoids for post-translational farnesylation of p21ras. 相似文献
995.
X Meng X Lu Z Li ED Green H Massa BJ Trask CA Morris MT Keating 《Canadian Metallurgical Quarterly》1998,103(5):590-599
Williams syndrome (WS) is a contiguous gene deletion disorder caused by haploinsufficiency of genes at 7q11.23. We have shown that hemizygosity of elastin is responsible for one feature of WS, supravalvular aortic stenosis (SVAS). We have also implicated LIM-kinase 1 hemizygosity as a contributing factor to impaired visual-spatial constructive cognition in WS. However, the common WS deletion region has not been completely characterized, and genes for additional features of WS, including mental retardation, infantile hypercalcemia, and unique personality profile, are yet to be discovered. Here, we present a physical map encompassing 1.5 Mb DNA that is commonly deleted in individuals with WS. Fluorescence in situ hybridization analysis of 200 WS individuals shows that WS individuals have the consistent deletion interval. In addition, we identify three novel genes from the common deletion region: WS-betaTRP, WS-bHLH, and BCL7B. WS-betaTRP has four putative beta-transducin (WD40) repeats, and WS-bHLH is a novel basic helix-loop-helix leucine zipper (bHLHZip) gene. BCL7B belongs to a novel family of highly conserved genes. We describe the expression profile and genomic structure for each of these genes. Hemizygous deletion of one or more of these genes may contribute to developmental defects in WS. 相似文献
996.
997.
分析国际、国内高浓度磷复肥的需求与产能形势,贵州发展磷化工产业的优势条件;提出对贵州省磷化工产业发展的若干建议,认为我国磷复肥产能虽然过剩,但作为全国磷复肥建设基地的贵州省磷化工产业仍具有广阔的发展前景. 相似文献
998.
999.
综述了近年来稀土配合物杂化材料的制备和性能.按基质的不同,稀土配合物杂化材料可分为稀土配合物,无机杂化材料,稀土配合物,有机杂化材料以及稀土配合物,混合基质杂化材料。本文对以上3种杂化材料的优缺点进行了较为详细的分析,并提出一步法制备稀土配合物杂化材料,以简化合戍步骤,提高稀土配合物在基质分布的均匀性,因而该方法有望戍为制备稀土配合物杂化材料的一个重要发展方向。 相似文献
1000.