查询词典 mutation

Alternatively, four-leaf clovers could be caused by somatic mutation or a developmental error of environmental causes.

寓意着，有可能你付出了，希望了，爱了，但不一定会找到幸福的时候，只有拥有了四叶草，才有了真正的幸福与幸运。

Furthermore, the very significant/nearly identical increase in the ratio of doubling times in dmdm medium in the presence/absence of high concentration of paromomycin was observed in symptomatic or asymptomatic cybrid cell lines carrying the c1494t mutation as compared with the average rate in control cell lines.

结果 来自听力下降者的融合细胞系的线粒体dna标记速率分别比对照组4名成员的12个融合细胞系下降了38％和43％，这一缺陷显然造成了携带c1494t突变的融合细胞（不论来自听力正常者还是来自听力下降者）的细胞总体呼吸率下降，或苹果酸/谷氨酸、琥珀酸/3-磷酸甘油及tmpd/抗坏血酸所始动的呼吸率下降。

We found 1 RTT case simultaneously exist MeCP2 gene mutation and decreased mitochondrial oxygen consumption in cybrids.

首次发现1例患儿同时存在MeCP2突变和融合细胞线粒体氧耗率下降。

Mosquito is a communicator. And communication is a process of mutation. It is all about deceits and lies. In the context of my work, mosquito plays a role as the joint.

蚊子是传播者，传播的过程是一个变异的过程，在这个过程中满是欺骗与谎言，在我的作品体系中，蚊子应该是一种承接者，起了一个转折的作用。

That's that the old "win on Sunday, sell on Monday" adage fades with every NASCAR body mutation that makes the various stock-car models look as androgynous as Indy Cars or NHRA dragsters.

这是旧的&胜利日，出售星期一&格言消失每纳斯卡突变，使身体的各种股票车型看起来雌雄同体的印地汽车或全国改装高速汽车协会dragsters 。

His concept is that you use the dugs which may induce mutation as early as several weeks or sometimes several months, that's why he has to measure the DNA, but there are now some drugs available who are OK for 5 years, they don't have to measure the DNA, because no mutations.

Keefe教授的概念指的是你所用的药在使用几周或者几个月后会引起突变，因此，在这种情况下就很有必要检测HBV DNA。但是，目前已经有一些药物，其5年内的突变率很低，因此没有必要检测病毒水平。

Software Description: About DWEEBS 2 - The New Breed, Mutation, the original creators and developers of Dweebs, now bring you those super cute furry dudesin this sequel.

DWEEBS 2 - The New Breed Dweebs 是一款带有动作性质的解谜游戏，挑战性相当高，玩家除了必须动脑思考、反应快速之外，操作技巧也要高明迅速。

Results The two patients with primary dystonia were found to have the gene mutation of SCA3, the CAG repeat were 80 and 75 respectively.

结果 2例原发性肌张力障碍患者SCA3基因突变，其异常等位基因的CAG重复数为80和75；SCA1、SCA2基因无突变。

Objective To investigate in Chinese population the relationship between GTP cyclohydrolase 1 gene mutation and phenotypes of dopa-responsive dystonia.

目的 分析国人多巴敏感性肌张力障碍患者三磷酸鸟苷环羟化酶1（GCH-1）基因突变与表现型的关系。

Results The two patients with primary dystonia were found to have the gene mutation of SCA3,the CAG repeat were 80 and 75 respectively.

方法采用聚合酶链反应方法对一家父子2例原发性肌张力障碍患者及其21名家系健康成员SCA1~3型基因CAG重复数进行检测。

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。