缺陷

The first 4 defects are formed in machining process, the fifth is created in metallurgic process.

前4种是机械加工形成的缺陷，第5种是冶炼过程中形成的缺陷。

During the period of elementary education, the defects of the teaching contents, methods and assessment standards result in the misguiding of the individual development and the shortcomings of the educational management lead to the suppression of the personality, the compression of the individualized knowledge and the inhibition of the personal ability inclination.

基本结论：在基础教育阶段，来自教学内容、教学训练方法以及教学评价标准的缺陷，构成了对个体发展的误导，而来自教育管理的缺陷则导致了，个性的被压抑、个人化知识的被压缩、个人能力倾向的被压制。

Although the genetic flaw that causes myotonic dystrophy was discovered in 1992, researchers studied the defect for many years before they had a clear understanding of the molecular events that ultimately produce the symptoms of the disease.

尽管引起强直性肌营养不良的基因缺陷在1992年就被发现，研究者在研究该缺陷多年后才清楚理解导致该病症状的分子机制。

MRS2 encode a magnesium transporter protein in Saccharomyces cerevisiae and deletion of MRS2 gene results in decrease in mitochondrial magnesium concentration, Group II RNA splicing defect and growth defect on nonfermentable carbon source.

MRS2 基因编码线粒体镁离子转运蛋白，MRS2缺失会导致酵母线粒体镁离子浓度下降、线粒体内II型内含子剪接缺陷和非发酵碳源上的生长缺陷。

To obtain more information of magnesium homeostasis in mitochondria, mTn-lacZ/LEU2 transposon library was transformed into mrs2 deletion mutant to screen for suppressor genes of MRS2. YMR166C, a member of mitochondrial carrier family, was identified as a suppressor gene of MRS2. Deletion of YMR166C gene can rescue the defects of mrs2 deletion mutant such as the decrease in mitochondrial magnesium concentration, Group II RNA splicing defect and growth defect on nonfermentable carbon source. For the first time we demonstrated YMR166C is involved in mitochondrial magnesium homeostasis.

为了增进对线粒体镁离子代谢调控基因的了解，利用酿酒酵母mTn-lacZ/LEU2转座子文库筛选MRS2的抑制基因，发现线粒体载体家族成员YMR166C基因的缺失可以挽救MRS2基因缺失的突变体的生长缺陷、II型内含子剪接缺陷，并可以调节线粒体镁离子浓度，首次发现YMR166C是线粒体镁代谢相关基因。

CdSe nanoclusters were overcoated with CdS shell in aqueous medium, which resulted in elimination of deep defects on surface of nanoparticles and thus large increase of the emission intensity of CdSe nanoclusters.(4) Based on PL emission and excitation results and the theoretical calculation on fine structure of bandedge exciton, a model of formation of excimer within the small clusters was proposed to explain the large Stokes shift of luminescence from absorption edge observed in PL results.

有机包覆剂虽然可以控制颗粒的长大，但无法同时消除由Ⅱ族和Ⅵ族两种元素的悬挂键在表面形成的无辐射复合缺陷中心，本文实现了在水溶胶中将宽带隙CdS半导体材料外延生长在CdSe纳米颗粒表面，有效的消除了无辐射复合缺陷中心，使得样品在室温就可以测到带边发光。

During the BDST task, areas showing activation in healthy volunteers include bilateral middle frontal gyrus, left superior frontal gyrus, inferior frontal gyrus, precentral gyrus, superior parietal lobe, suprarnarginal gyrus, Inferior temporal gyrus and occipitotemporalis lateralis gyrus, however, the left superior frontal gyrus, inferior frontal gyrus and bilateral posterior parietal cortex in schizophrenic patients showed significantly less activation.

在＊M河的侧m检查中治疗后，IA亚组的左侧额上回及左侧额下口的激活低下明显改善（P＜O.05），H A亚组的左恻额上回及左侧额下回的激活低下明显改善P＜O刀5），右侧领下回的激活降低（P＜0.05）。结论门）首发精神分裂症患者在发病初期就存在认知缺陷症状，工作记忆等与前额区相关的功能缺陷是普遍而严重的。

We generalized the above model of the point defect to Cd〓Zn〓Te, which was taken as ideal cation substituted pseudobinary alloy.

把二元化合物CdTe的点缺陷模型加以推广，建立了三元化合物Cd〓Zn〓Te的点缺陷模型。

In this paper, based on the experimental results of local temperature field and pyromagnetic effect formed in the evolution period of defects, the failure process of time-dependent material containing defects have been studied from a unified standpoint of macro-/meso-/microscopic stratum system.

基于缺陷演化过程中局域温度场和热磁效应的实验研究，从统一的宏、细、微观层次体系出发，研究了与时间相关的缺陷体的失效过程。

Or more round indications in a 3870 mm2 area located at the most defective position, is rejectable

在最多缺陷集中的区域，在3870平方毫米面积内，存在10个或以上圆形缺陷，拒收。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。