拟—幂零群的一组性质

我们引入拟－幂零群的概念，主要得到了拟－幂零群Ｇ的中心Ｚ（Ｇ０与极小正规子群之间的关系。     

平面弹性连杆机构的KED分析

本文放弃了文献中引用的运动学假设和瞬时结构假定,考虑了刚体运动和弹性变形运动之间的耦合项,分析了梁的横向位移对轴向应变的影响。利用虚位移原理和达明贝尔原理,建立了构件和系统的运动微分方程式。以四杆较接机构为例,进行了KED分析。从所得结果可以看出,本文更好地反映出弹性对机构动态误差的影响。     

DNA fingerprinting transforms the art of cell authentication.

The increasing diversity of new cell cultures is seriously stretching the capabilities of traditional methods of identification. DNA fingerprinting is set to play an important role in increasing confidence in the authenticity of cultures in research and industry.     

我院申请国家自然科学基金项目情况分析

本文分析了“八五”以来国家自然科学基金项目的现状、前景及我院申报国家自然科学基金项目的获得资助率，并从六个方面探讨提高我院申报国家自然科学基金项目获得资助率的措施与方法．     

用钼蓝反应动力学方法作微量磷的分光光度测定

提出用ｄ－葡萄糖试剂做钼蓝反应的还原剂测定磷的动力学方法。用吸光度监测反应速度，用假一级反应的关系式测定了反应速度与磷浓度的线性范围为０．６～２．５μｇ／ｍＬ。用内标法计算五种土壤样品中的含磷量，分析结果与常规方法比较，符合程度令人满意。     

单电极直流电弧炉电热特性理论研究

运用电磁理论与流体静压力原理,导出了电弧自身的电磁向心压缩力以及电弧对熔池冲力的解析式。又运用辐射传热原理,导出了单电极电弧对熔池与炉衬辐射传热的解析式。解析式揭示出电弧自身电磁向心压缩力、电弧对熔池冲力,单电极电弧对熔池以及对炉衬辐射传热的规律。     

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.     

混合氯化稀土催化合成DOP,DOM和DOA

本文报道:价廉的混合氯化稀土,对合成DOP等增塑剂有明显的催化效果。产品精制简单,转化率高,有应用前景。