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81.
We study communications under slowly varying channels, and consider three cases of knowledge of the channel impulse response (CIR): full knowledge, no knowledge, and partial knowledge of the CIR. By partial knowledge, we refer to knowing only either the CIR magnitudes or the CIR phases. It is known that obtaining the exact joint maximum‐likelihood estimate (MLE) of the CFO and the SFO requires a two‐dimensional search. Here, we present a new estimation method which uses the Taylor expansion of the MLE cost function, combined with the best linear unbiased estimator, to obtain a method which does not require such a search. The computational complexity of the new method is evaluated. Numerical simulations demonstrate that the new method approaches the corresponding Cramér‐Rao bound for a wide range of signal‐to‐noise ratios, and has superior performance compared to all other existing methods for approximating the solution for the joint MLE, while maintaining a low computational complexity. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   
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Ron Norton 《现代显示》2010,(5):182-187
随着LED产业迅速发展,使其中埋藏着专利危机,随时威胁着企业利润,文章说明了如何利用专利转危为机,并列举了可能采取的应对策略。  相似文献   
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We consider the adjacency operator of the Linial‐Meshulam model for random simplicial complexes on n vertices, where each d‐cell is added independently with probability p to the complete ‐skeleton. Under the assumption , we prove that the spectral gap between the smallest eigenvalues and the remaining eigenvalues is with high probability. This estimate follows from a more general result on eigenvalue confinement. In addition, we prove that the global distribution of the eigenvalues is asymptotically given by the semicircle law. The main ingredient of the proof is a Füredi‐Komlós‐type argument for random simplicial complexes, which may be regarded as sparse random matrix models with dependent entries. © 2017 Wiley Periodicals, Inc. Random Struct. Alg., 51, 506–537, 2017  相似文献   
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Because liver cancer is rarely suitable for surgery, transcatheter arterial chemoembolization (TACE) is used for palliative therapy. In this procedure, an emulsion of doxorubicin in iodized oil is injected directly into liver tumors through a catheter positioned within the artery supplying blood flow to the tumor. At present, there is limited understanding of factors affecting the delivery and dispersion of doxorubicin within treated tumors during TACE. This study addresses the development and application of an ultrahigh‐pressure liquid chromatography–tandem mass spectrometry (UHPLC‐MS‐MS) method for rapid confirmation of drug delivery after TACE in a rabbit VX2 liver cancer model. Doxorubicin levels in liver tumors were measured using UHPLC‐MS‐MS and compared with computed tomography measured levels of iodized oil, a metric used clinically to indicate drug delivery. We found that tissue drug levels determined using UHPLC‐MS‐MS did not correlate with the regional iodized oil concentration (vehicle) within tumors following TACE, suggesting that chemotherapeutic drugs like doxorubicin spread throughout tumors, and that lack of iodized oil staining in portions of a tumor does not necessarily indicate inadequate therapy during TACE. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   
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Summary.  Horseradish peroxidase (HRP), myeloperoxidase (MPO), and manganese peroxidase (MnP) have been shown to catalyze the asymmetric sulfoxidation of thioanisole. When H2O2 was added stepwise to MPO, a maximal yield of 78% was obtained at pH 5 (ee 23%), whereas an optimum in the enantiomeric excess (32%, (R)-sulfoxide) was found at pH 6 (60% yield). For MnP a yield of 18% and a high enantiomeric excess of 91% of the (S)-sulfoxide were obtained at pH 5 and a yield of 36% and an ee of 87% at pH 7.0. Optimization of the conversion catalyzed by horseradish peroxidase at pH 7.0 by controlled continuous addition of hydrogen peroxide during turnover and monitoring the presence of native enzyme as well as of intermediates I, II, and III led to the formation of the sulfoxide in high yield (100%) and moderate enantioselectivity (60%, (S)-sulfoxide). Received November 18, 1999. Accepted January 21, 2000  相似文献   
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