用MUX实现组合逻辑的卡诺图列解法

本文采用卡诺图列解法来处理MUX组件的地址变量少于待发生逻辑函数变量的设计问题。方法简单易行、适用范围广。尤其是对于含有任意项的逻辑函数中任意项的处理,提供了寻找最佳方案的途径。     

与半群的完全不可逆生成集相关的几个性质

讨论了半群环的两个性质以及关于半群的a.c.c.p.（主理想升链条件）的一个结论。     

SW规约下的一些性质

本文进一步分析了SW规约下的SW度结构的一些性质,得到了强可计算实数的两个性质.并且证明了给定可计算可枚举实数,可构造出sw归约下不小于该数的低的可计算可枚举实数.     

丙类功率放大器自给偏置效应产生原因的分析

介绍了丙类谐振功率放大器的工作原理,分析了丙类谐振功率放大器的基极偏置电路,比较了两种丙类谐振功率放大器仿真结果。     

p-可分解群的一个定理

极小子群在有限群的研究中占据着重要的地位．本文利用了极小子群的弱c-正规性刻画了极小子群对有限群构造的影响，得出了p-可分解群的一个结果．     

测定氨氮时浓度及时间对反应的影响

采用纳氏试剂分光光度法，对不同浓度的氨氮标准溶液在各显色时间下的吸光值进行了分析，以了解实验随浓度、时间的变化情况，掌握达到最大显色所需的时间。从而指导实际的检测工作。     

利用图片作为载体实现信息隐藏

采用visual c 6.0作为客户端应用程序的开发工具,利用其集成开发的环境实现对需要保密信息的隐藏.     

实现“（dE／dt）~（－1）－E”倒数示波图的模拟电路参数选择和单板机装置

对实现“（ｄＥ／ｄｔ）－１－Ｅ”倒数示波图的实验装置进行了进一步深入研究：改进了以往的模拟电路，考察了电参数的影响；研制了一台单板机装置．     

In vivo effects of immunostimulating lipopeptides on mouse liver microsomal cytochromes P-450 and on paracetamol-induced toxicity

Summary Immunomodulating lipopeptides lauroyl-L-Ala--D-Glu-LL-A2pmNH2-Gly (RP 44.102) and lauroyl-L-Ala--D-Glu-LL-A2pmNH2 (RP 56.142) were found to protect mice against the hepatotoxicity of paracetamol, which is due to cytochrome P-450 dependent formation of toxic metabolites and radicals. In fact they decreased the amount of hepatic microsomal cytochrome P-450, and the level of CCl₄-induced lipid peroxidation. In contrast lauroyl-L-Ala--D-Glu-DD-A2pmNH2 (RP 53.204), which only differs by the configuration of the two chiral carbons of A2pm (diaminopimelic acid) and is not an immunomodulating agent, failed to protect against poisoning by paracetamol and had no effect on the level of hepatic cytochrome P-450 or the microsomal CCl₄-induced lipid peroxidation. This provides a clear connection between the immunostimulating properties of a compound and its effects on xenobiotic biotransformations.     

The discovery of antidepressants: A winding path

Summary Modern treatment of mental depression started with the availability of monoamine oxidase (MAO) inhibitors and tricyclic antidepressants. These drugs also contributed to the early development of psychopharmacology. Attempts to improve the anti-tuberculous action of the hydrazine derivative isoniazid by developing derivatives thereof led to the synthesis of iproniazid. Its introduction as the first modern antidepressant was based on three unexpected actions of the drug: MAO-inhibition, reversal of reserpine-induced sedation, and the presence of psychostimulation as a clinical side effect in man. However, the initial success of iproniazid and other MAO inhibitors, hydrazides and non-hydrazides, was curtailed by the occurrence of undesirable side effects such as potentiation of the blood-pressure elevating action of food amines. The tricyclic antidepressants were a development of the class of antihistamines, one of which, chlorpromazine, showed neuroleptic activity. A congener of this compound, imipramine, was discovered by clinical observation to have unexpected antidepressant effects. The clinical success of this drug (which is still in use) led to the development of a successful series of other tricyclic and non-tricyclic antidepressants. Progress in the elucidation of possible mechanisms of the action of the tricyclic compounds has helped this development. Recent advances in basic research have also induced a revival of MAO-inhibitors since, due to the discovery of MAO-subtypes, inhibitors with higher specificity and fewer undesirable side effects are now available.