用数据选择器和译码器的组合优化逻辑设计

介绍一种用数据选择器和译码器的组合优化逻辑设计的方法.该方法可减少数据选择器芯片及门电路使用的数量.文中给出几个实例.     

抽水引起岩土体内应力变化分析

针对开采地下水这一特定问题,以在抽水实践中地下水水位面是一以井心为顶点的旋转抛物面为出发点,研究了地下水开采过程中岩土体应力变化的时空规律。通过分析影响内部应力变化的宏观物理量—开采影响半径、井心水位下降和空间位置,可以方便的得到随着时间变化岩土体内部应力变化的全程规律。同时,分析了影响边界、下沉位置等因素对计算结果的影响。     

一类广义Liénard系统的正半轨线与特征曲线相交的条件

获得了广义Li啨ｎａｒｄ系统dxdt =p(y) -F(x) ,　 dydt =-g(x)q(y)过平面上任意一点的正半轨线与特征曲线p(y) =F(x)相交的充分条件 .     

论网络教育对传统教育的影响

本主要论述了网络教育的时代性、网络教育的特点和目前存在不足，以及网络教育的未来发展趋势。本最后得出结论认为：网络教育作为一种辅助方式，对传统方式影响很大，但仍不能动摇其主导地位。     

电子期刊及其服务

论述了电子期刊的各类及其主要特点，分析了电子期刊对传统图书馆服务的影响，提出了图书馆工作的应对对策。     

试论"代表先进社会生产力发展要求"是对历史唯物主义的新发展

中国共产党始终代表中国先进生产力的发展要求的论断,是站在历史唯物主义的角度,揭示出我们党兴旺发达的根本动力.     

Nuclear localization and signalling activity of phosphoinositidase C beta in Swiss 3T3 cells.

The hydrolysis of phosphatidylinositol 4,5-bisphosphate (PtdInsP2) is a widespread receptor-coupled signalling system at the plasma membrane of most eukaryotic cells. The existence of an entirely separate nuclear phosphoinositide signalling system is suggested from evidence that purified nuclei synthesize PtdInsP2 and phosphatidylinositol 4-phosphate (PtdInsP) in vitro and that a transient decrease in the mass of these lipids occurs when Swiss 3T3 cells are cultured in the presence of insulin-like growth factor-1 (IGF-1). These IGF-1-dependent changes in inositol lipids coincide with an increase in nuclear diacyglycerol and precede translocation to the nucleus and activation of protein kinase C (refs 5, 6). Circumstantial evidence that links these changes with mitosis comes from the isolation of a 3T3 clone that expresses the type-1 IGF receptor and binds IGF-1 peptide but does not respond mitogenically or show transient mass changes in nuclear inositol lipids. A key question is how IGF-1 initiates the rapid breakdown of PtdInsP and PtdInsP2 in the nucleus. Here we present evidence that nuclei of 3T3 cells contain the beta-isozyme of phosphoinositidase C, whereas the gamma-isozyme is confined to the cytoplasm and that IGF-1 treatment stimulates exclusively the activity of nuclear phosphoinositidase C.     

Prediction of the structure of a receptor-protein complex using a binary docking method.

To validate procedures of rational drug design, it is important to develop computational methods that predict binding sites between a protein and a ligand molecule. Many small molecules have been tested using such programs, but examination of protein-protein and peptide-protein interactions has been sparse. We were able to test such applications once the structures of both the maltose-binding protein (MBP) and the ligand-binding domain of the aspartate receptor, which binds MBP, became available. Here we predict the binding site of MBP to its receptor using a 'binary docking' technique in which two MBP octapeptide sequences containing mutations that eliminate maltose chemotaxis are independently docked to the receptor. The peptides in the docked solutions superimpose on their original positions in the structure of MBP and allow the formation of an MBP-receptor complex. The consistency of the computational and biological results supports this approach for predicting protein-protein and peptide-protein interactions.     

Targeted disruption of the mouse transforming growth factor-beta 1 gene results in multifocal inflammatory disease.

Transforming growth factor-beta 1 (TGF-beta 1) is a multifunctional growth factor that has profound regulatory effects on many developmental and physiological processes. Disruption of the TGF-beta 1 gene by homologous recombination in murine embryonic stem cells enables mice to be generated that carry the disrupted allele. Animals homozygous for the mutated TGF-beta 1 allele show no gross developmental abnormalities, but about 20 days after birth they succumb to a wasting syndrome accompanied by a multifocal, mixed inflammatory cell response and tissue necrosis, leading to organ failure and death. TGF-beta 1-deficient mice may be valuable models for human immune and inflammatory disorders, including autoimmune diseases, transplant rejection and graft versus host reactions.