沥青路面玻璃纤维加劲格栅的理化性能研究

通过沥青路面玻璃纤维加劲格栅的理化性能试验 ,给出了格栅的耐热性、耐腐蚀性、材料属性、抗张强度、弹性模量、温度对强度的影响等试验结果 ,为产品的应用提供了科学依据。     

高校后勤社会化改革的现实意义

高等学校后勤社会化改革是适应市场经济体制与日益发展的高等教育需要之间的唯一出路，也是我国高等教育发展史上的一场深刻革命。     

核动力装置模拟器就地系统中双机通讯的实现

利用微机软仿真实现模拟器就地系统中仪表的动态实时显示和开关的实时控制，可以节省的大量外部设备，提高系统可扩充性。本文介绍了该技术实现的方法，即服务器与客户机之间数据双向通讯的实现途径。经实践验证，本文的方法是正确、可行的。     

马铃薯脱毒种薯生产二级体系的理论与实践

对目前西南地区脱毒马铃薯种薯生产四级体系进行分析，总结存在的问题，对南方马铃薯研究中心近几研究成功的二级体系作了概述性的介绍，对操作技术要点系统的进行说明，描述和展望了该体系巨大的经济前景和社会效益，得出“马铃薯种苗二级体系替代四级体系是21世纪马铃薯产业发展重要趋势”的初步结论。     

从中西方文化冲突看文化对司法制度的影响

一个国家，一个民族在长期的历史发展中，形成了自己特定的文化传统，人们的思想观念，价值取向甚至法律制度都植根于其文化传统之中，本文从律师在社会生活中的作用，司法公正的价值取向，证人出庭作证制度，打官司与打“关系”等方面分析了文化传统对司法制度的影响。     

虚拟共享型MIMD的几个问题

并行处理是提高计算机性能的有效手段，也是新一代计算机的结构特征。本文论述虚拟共享型处理机的特点、实现机制、可伸缩性和负载平衡。     

噬菌体展示禽流感病毒抗原变异性基因片段文库的构建

构建T7噬菌体展示禽流感病毒抗原变异性基因片段文库. 首先， 从Gene Bank中查找筛选禽流感病毒抗原变异性基因, 将其截短、 修饰、 简并后得到禽流感病毒抗原变异性基因微阵列. 其次， 将合成的禽流感病毒抗原变异性基因片段文库扩增、 酶切, 链接到双酶切后的T7噬菌体载体基因上, 构成重组噬菌体DNA. 最后， 重组噬菌体DNA经体外包装和扩增, 得到T7噬菌体展示文库, 并进行T7噬菌体展示文库滴度、 重组率和免疫活性测定. 实验结果表明, 从Gene Bank中查找、 筛选、 剪切和修饰共获得96 258条序列构建T7噬菌体展示文库, 原始文库滴度为3.6×107个菌落/mL, 重组率大于90%. 用禽流感病毒H5N1抗体进行捕获, 经聚合酶链式反应(PCR)鉴定, 得到理想目的条带, 证明噬菌体表面展示蛋白具有抗原活性, 可用于禽流感病毒感染患者的快速检测及抗原表位筛选.     

CALIS分布式联合虚拟参考咨询系统（CDCVRS）使用之我见

介绍了CALIS分布式联合虚拟参考咨询系统CDCVRS,在调查排名前50位的大学图书馆使用CDCVRS的情况基础上,总结了CDCVRS使用过程中存在的问题,提出了相应的解决办法。     

Specific anti-tumor effect induced by attenuated Salmonella typhimurium vaccine expressing extracellular region of vascular endothelial growth factor receptor 2

The purposes of this research were to study the stable expression of exogenous gene encoding therapeutic protein in attenuated Salmonella typhimurium, observe the metabolism of oral gene vaccine carried by attenuated Salmonella typhimurium in BALB/c mouse, and investigate the feasibility of prevention and treatment of tumors by the recombinant bacteria. Recombinant plasmid pcDNA3.1 VEGFR2(n1-7) was transformed into competent attenuated Salmonella typhimurium SL3261 to develop oral DNA vaccine SL3261-pcDNA3.1 VEGFR2(n1-7). To observe whether the exogenous gene can be expressed in the recombinant bacteria, PCR was performed to amplify the CMV promoter of the eukaryotic expression vector as the proof of stable expression of exogenous protein; transmission elec- tron microscopy (TEM) was applied to observe the morphology of the recombinant bacteria to confirm that the exogenous gene has no impact on the growth of the bacteria, and then BALB/c mice were immunized with the gene vaccine. After inoculation of the gene vaccine, the recombinant bacteria SL3261 could be detected in the tissues such as small intestine, colon, liver and spleen. And then, mice in each group were challenged with tumor cells. The results of animal experiment showed that tumor growth of the mice in experimental group was inhibited and survival time of immunized mice was prolonged compared with control groups. A higher lymphocyte infiltration in tumors from animals treated with DNA vaccine was observed. Immunohistochemical analysis of tumor samples revealed an en- hanced accumulation of CD8 cytotoxic T lymphocytes, as well as an increase in CD4 cells in the tumors of animals treated with the oral gene vaccine compared to tumors from control group mice. Ultrastructure of the tumor tissue showed that tumor cells in the samples of the immunized mice were well-differentiated. Our research confirmed that the exogenous gene can be stably expressed in the attenuated Salmonella typhimurium and has no impact on the growth of the recombinant bacteria; the exogenous gene can de delivered to the host by attenuated Salmonella typhimurium to produce anti-tumor effect with no obvious cytotoxity to the host. In this study, it is established that attenuated Salmonella typhimurium could be used as a vector for oral gene vaccine, and our study provided a theoretical basis for the body distribution and the metabolism of the recombinant bacteria. This strategy may provide a simple, safe and effective way for the prevention and treatment of tumors.     

基于MATLAB的控制系统CAI设计

基于MATLAB开发平台，利用其可视化编程能力的GUI，对控制系统进行分析、设计与仿真，开发了控制系统CAI应用软件，它具有较强的教学、实验、工程应用价值。