查询词典 mutations

Strikingly, mutations in the same genes were associated with clinically different motoneuron syndromes.

这些基因在临床上与各种运动神经原综合症有关。

Multi-window mutations improve the search performance of MRCGA and the new repairing mechanism is applied to the infeasible solutions.

此方法提出了一种新的个体调整方法，可以处理各项约束条件，保证了结果的可行性。

It's normal for genes to mutate and many mutations are completely harmless.

基因突变其实很正常，其中很多的基因突变也是完全无害的。

Results We had 22 deletion mutational cases and 6 point mutations from 35 clinical specimens.

在22例缺失突变病例中，有10例为不完全缺失突变即有低于外显子509 bp的扩增产物。

There are total 8 deletion mutational cases and 4 point mutations from 29 clinical specimens.

结果在29例临床宫颈癌标本中有8例发生缺失突变，4例发生点突变，突变率约41%。

In this study, we want to investigate whether these myotonia congenita-related mutations affect the biogenesis and the subcellular localization of hClC-1 channels.

本篇研究想探讨的主题即是这些与先天性肌肉强直症相关的突变，是否影响了hClC-1通道蛋白之生成以及於细胞中的分布型态。

Previous studies indicate that several mutations alter the voltage dependence of hClC-1 channels. Besides changing the gating property of the Cl- channel, other defects in mutant hClC1 channels may also contribute to the mechanism of myotonia congenita.

前人的研究指出一些与先天性肌肉强直症相关的突变会改变hClC-1通道的电位依赖性，然而除了藉由影响离子通道的门阀开关比例之外，其他由於基因突变造成hClC-1通道的缺失也可能为先天性肌肉强直症的致病机转的成因。

Mutations in the mitochondrial DNA have been observed in human neoplasia.

线粒体DNA的突变已经在很多人类肿瘤中被观察到。

Thus, phenotypically similar conditions may be due to mutations in different genes, nongenetic factors, or both.

因此表型相似可因不同基因的突变和/或非遗传因子所造成。

"Although we did not see any clear surial differences in association with the BRCA mutations we sought, potential important differences emerged when we analyzed the data according to tumor size and the use or nonuse of chemotherapy," the researchers concluded.

虽然我们并没有发现任何明确的与BRCA突变相关的存活差异，但是当我们根据肿瘤大小和是否化疗分析数据时出现了潜在的重要差异。研究者做出以上结论。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。