查询词典 qualified expression

Objective To examinate the expression of GFAP and S - 100 protein between cerebral infarction and diabetes combined cerebral infarction by immunohistochemistry method. To detect the expression of GFAP and S -100 protein in diabetes.

目的 通过免疫组化方法，检测单纯脑梗塞、糖尿病合并脑梗塞时GFAP及S-100蛋白的表达特点以及糖尿病对GFAP及S-100蛋白表达的影响。

Objective To investigate the expression of angiotensin-converting enzyme 2 (ACE2) in rat endocrine and exocrine tissue of pancreas and to compare its expression level with that in other visceral tissues.

目的 检测SARS冠状病毒S蛋白的功能性受体血管紧张素转换酶2(ACE2)在大鼠内脏尤其在胰腺内、外分泌腺的表达。

Exogen ous c-fos antibody could decrease the area density ratio of bFGF mRNA to 4.60± 0.86 at the first day post-burn. The bFGF mRNA expression was increased little without significant difference after exogenous treatment with bFGF. Treatment of c-fos antibody could significantly decrease the expression of PCNA. Through th e re-epithelial process was almost completed at 14th d post-burn, the thicknes s of basal cells was thinner than that in controls.

给予外源性c-fos抗体能抑制bFG F mRNA的表达，伤后1 d其mRNA表达的面密度降为4.60±0.86，伤后14 d创面皮肤虽然基本完成了再上皮化过程，但其基底细胞排列成薄层细胞，PCNA数密度明显低于对照组，同时皮肤全层变薄。

RESULTS We successfully obtained human caspase-3 gene, the genes and expression vectors of reversed caspase-3 and its fusion protein with part of the translocation domain of Pseudomonas exotoxin A. Compared with the control group, the expression of both genes caused in a similar degree the decrease of living cell numbers and massive occurrence of apoptosis.

结果成功获得了caspase-3基因，构建了重构型caspase-3基因和重构型caspase-3与绿脓杆菌外毒素转膜结构域部分肽段的融合蛋白基因及其表达载体，与对照组相比，在转染后1～4 d内，两种基因的表达均导致HeLa细胞存活数减少，大量细胞发生凋亡，且二者活性相当。

On the other hand, it is expressible as a Boolean expression if you accept including function calls in the Boolean expression.

但换个角度，如果你允许在布尔表达式中植入包含函数调用，则它就是一个布尔表达式可表述的属性。

If more than one operand of an expression raises an error, the implementation may choose which error is raised by the expression.

如果一个表达式有一个以上的操作数引发错误，实现可以选择哪一个错误被该表达式引发。

Making gfp fusion protein is a convenient method to mark the expression of interesting proteins, but it may interfere the expression of interesting proteins, since gfp is a quite big protein itself.

一方面，作为标记与目的蛋白融合可以方便的标示目的蛋白的表达情况，但gfp本身是个相当大的蛋白，会降低目的蛋白的表达；另一方面，进一步分离时需使用抗gfp的单克隆抗体进行免疫共沉淀，既不经济又不方便。

Above all, we take color part mediumly to do a specification to the graph, the small rectangle that brings facial expression is representing the communication port that can be sent and receives broadcast data package, have ' S ' the expression of the mark this port basically sends broadcast data package outwards, have ' R ' state this port receives broadcast data package only.

首先，我们对图一中的带颜色部分做一个说明，带颜色的小矩形都代表着能发送和接收广播数据包的通讯端口，有'S'标志的表示该端口主要向外发送广播数据包，有'R'表示该端口只接收广播数据包。

Objective: The purpose of our studies are gaining a better insight into the effect of genistein on mesangial cell"s phenotype change and ECM expression plus degradation under DN circumstances.We add genistein with different concentrations in high glucose cultured rat mesangial cells;feed DM rats with the single concentration genistein for different days;to explore the expression of SMemb,the mark of mesangial cell"s hypertrophy phenotype change;to examine the synthesis of Fn as well as the change of the balance between MMP-2 and TIMP-l;to comprehend its effect on renal pathological changes of DM rats and some related factors;trying toexplore the possible mechanisms.Through these studies,we will have some information about the experimental value of genistein in DN field.

目的：为了研究金雀异黄素对DN环境下大鼠MC肥大表型转换标志物SMemb和ECM分泌及降解的影响，我们拟在细胞水平以不同浓度的金雀异黄素作用于高糖培养下大鼠MC，在动物水平以同一浓度的金雀异黄素作用于DM大鼠不同时间，观察细胞表型转换标志物SMemb、ECM主要成分Fn、ECM降解酶系统基质金属蛋白酶—2(MMP-2)／基质金属蛋白酶抑制剂—1(TIMP-1)表达的变化，同时观察金雀异黄素对DM大鼠肾脏病理及影响肾脏病进展的糖脂代谢紊乱的影响，并进一步探讨金雀异黄素发挥作用的可能机制；为明确金雀异黄素在DN治疗中的地位及意义提供实验依据。

Three RNAi target sites (named as Abil1, Abil2, Abil3) targeting the E3B1 (NCBI: NM-024397), an identified target sites and positive control GAPDH-A were selected. The pGenesil-1 eukaryotic expression vectors with the neoR mark and GFP green fluorescent mark were selected to construct E3B1 RNAi plasmid. The effect of RNAi targeting various sites on E3B1 genes expression was evaluated by testing the transfection efficiency with fluorescence microscope and western blot. The most effective siRNA in inhibiting E3B1 genes were screened. The most effective siRNA in inhibiting E3B1 genes screened and used to transfect the neuronal cells. After that, the inhibitor of axon growth was added and the axon growth was observed. Result: The siRNA expressing plasmids targeting the E3B1 were constructed successfully.

选择针对E3B1(NCBI： NM-024397)RNAi的3个靶位点Abil1、Abil2、Abil3和1个不针对任何mRNA的RNAi靶位点以及甘油醛－3-磷酸脱氢酶，用带有neoR选择标志和GFP绿色荧光标志的真核表达载体pGenesil-1构建E3B1 RNAi质粒，分别转染培养的神经元，在荧光显微镜下观测转染率，经G418筛选得到单一的转染细胞，并用Western blot法检测各转染组神经元E3B1蛋白的表达情况，选出具有最佳抑制效应的siRNA转染神经元，加入轴突生长抑制物，观测轴突生长情况。

In the chapter 2, the theoretic knowledge about the photosensitive resin and the grinding tools was firstly introduced.

第二章阐述了光固化树脂结合剂磨具的相关理论研究。

Do not use the program's indenting or margin-setting features; these will be added during typesetting.

不要使用缩排，页面边缘设置之类的选项，偶看不大懂。