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。     

Periodic paralysis in quarter horses: a sodium channel mutation disseminated by selective breeding.

We recently reported on a linkage study within a Quarter Horse lineage segregating hyperkalaemic periodic paralysis (HYPP), an autosomal dominant condition showing potassium-induced attacks of skeletal muscle paralysis. HYPP co-segregated with the equine adult skeletal muscle sodium channel alpha subunit gene, the same gene that causes human HYPP. We now describe the Phe to Leu mutation in transmembrane domain IVS3 which courses the horse disease. This represents the first application of molecular genetics to an important horse disease, and the data will provide an opportunity for control or eradication of this condition.     

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。     

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。     

求Ramsey数最优下界值的递归算法

要确定每个具体的Ramsey数的数值是相当困难的,至今人们只求出了为数很少的几个Ramsey数的数值.人们在研究Ramsey数性质的同时,也在估计Ramsey数的数值,得出了某些Ramsey数的下界值,但工作进展缓慢.本文提出了一种计算Ramsey数最优下界值的递归算法,该算法利用当今关于Ramsey数的最新结果,能得出Ramsey数的目前最优下界值.1 算法描述不妨将本算法定名为G,参数个数为1个以上(可变化),算法允许递归调用,其输出值为Ramsey数的目前最优下界值.C(k_1,k_2…,k_n)表示以k_1,k_2…,k_n作为输入,通过算法G所得到的输出结果,即C(k_1,k_2…,k_n)表示的是G算出的Ramsey数N(k_1,k_2,…,k_n;2)的目前最优下界值,其中N(k_1,k_2…,k_n;2)的含意与文献[2]中有关含意相同.算法G:     

用栅板剪切干涉法确定应力强度因子

本文介绍了一种用栅板剪切干涉法确定应力强度因子的新方法,阐明了该方法的基本原理与实验技术,通过三点弯曲梁确定了Ⅰ型裂纹应力强度因子,实验结果与理论上近似计算结果相符合。     

Short alanine-based peptides may form 3(10)-helices and not alpha-helices in aqueous solution.

Short alanine peptides, containing 16 or 17 residues, appear to form alpha-helices in aqueous solution. But the main spectroscopic analyses used on helical peptides (circular dichroism and nuclear magnetic resonance) cannot distinguish between an alpha-helix (in which the ith residue is hydrogen-bonded to residue i + 4; ref. 9) and the next most common peptide helix, the 3(10)-helix10 (i-->i + 3 hydrogen-bonding). To address this problem we have designed single and doubly spin-labelled analogues of alanine-based peptides in which the nitroxide spin label forms an unbranched side chain extending from the sulphur atom of a cysteine residue. Here we report the circular dichroism, Fourier-transform infrared and electron-spin resonance spectra of these peptides under helix-forming conditions. The infrared absorbance gives an amide I' band with a frequency that is substantially different from that observed for alpha-helices. The electron-spin resonance spectra of doubly labelled helices show that the ranking of distances between side chains, around a single turn (residues 4-8), is inconsistent with an alpha-helical structure. Our experiments suggest that the more likely peptide geometry is a 3(10)-helix.