Haploid development in zebrafish has been applied for genetic screening.
对斑马鱼以开展了单倍体发育的遗传学筛选。
Here we describe haploid mouse embryonic stem cells and show their application in forward genetic screening.
在这里，我们描述单倍体胚胎干细胞显示他们在正向遗传学筛查中的应用。
For women, genetic screening offers the hope of better understanding the likelihood that they'll develop breast cancer.
遗传筛查为妇女提供了一个希望，那就是让她们更好的了解自己患上乳腺癌的几率。
She and her colleagues conclude that, given the cost involved, genetic screening is not worthwhile in a clinical context.
她和她的同事得出结论：考虑到遗传筛查所需费用，现在还不值得在临床上引入。
That has allowed them to get powerful statistical software and hardware for rapid genetic screening not yet in common use.
这样，他们就能获得功能强大但尚未普及的计算软件和硬件，用于快速筛选基因。
Finding tetrachromats through genetic screening is one thing. Proving they can see tens of millions of additional colors is another.
通过基因筛选找到四色视者是一回事，证明她们可以看到千万种更多的色彩则是另一回事。
They may be imaging, they may be biomarkers or genetic screening that would dictate different therapies for different patients.
他们可能是成像、生物标志或者是基因筛选，这些将决定不同患者不同的治疗方法。
Molecular genetic screening in negative autopsy cases can play an important role in explaining the cause of SCD and risk stratification of SCD.
在解剖阴性者中进行分子基因筛查，对解释病因和SCD危险分层有重要作用。
Specialists have a lot more knowledge about genetic screening tools and models, and primary care providers are not necessarily following this literature.
专家们掌握的基因甄别工具及模型方面的知识更多，而基层保健医生不一定会按这些文献去做。
They looked at consumption patterns of beer, wine and liquor, cancer incidence and genetic screening information for the study participants, who were 35 to 70 years old.
调研了35至70岁人群的饮用啤酒、葡萄酒和白酒模式、癌症的发病率和基因谱信息。
It is suggested to utilize this detection for genetic counseling, prenatal diagnosis, and the genetic screening of neonates and the sensorineural hearing loss with unknown reason.
建议将此突变位点检测运用于遗传咨询、产前诊断、新生儿和不明原因感音神经性聋患者的基因筛查中。
Researchers from Boston University employed a widely used genetic-screening technology to find genetic variations that occur more frequently in centenarians — people age 100 and older.
来自波士顿大学的研究人员采用一种广泛使用的遗传筛选技术寻找更多发生在100岁以上的百岁老人身上的遗传变异。
The recent application of recombinant receptors, transgenic animals, genetic probe and other genetic engineering technology in drugs screening is introduced briefly.
简述近年来重组受体、转基因动物、基因探针等基因工程技术在药物筛选中的应用。
And it displays the important theories with the practical value on determining genetic sequence, genetic expressing analysis, drugs screening, gene diagnosis and so on.
在基因测序、基因表达分析、药物筛选、基因诊断等领域显示出重要的理论和实用价值。
Screening human subjects for genetic compatibility with the drugs will save Millennium time and money at this stage.
筛选对药品具有基因适应性的受试人在这一阶段可以节约千年公司时间和金钱。
Investigations into the genetic basis of human obesity are important for understanding the mechanism of obesity formation and for design and screening of anti-obesity drugs.
深入分析人类肥胖的遗传基础，对于阐明肥胖发生的机理以及对于搞肥胖药物的设计和筛选具有重要意义。
PGD is good for screening for specific genetic disorders such as cystic fibrosis and Tay-Sachs disease, and also can be used to select gender.
PGD适用于特殊遗传病的筛查，如囊性纤维化和神经节苷脂病，而且PGD也可以用于性别选择。
Antenatal screening is offered on the NHS, this allows you to undergo a blood test to detect carrier couples and provide genetic counselling.
产前筛查是提供对国民保健服务，这可以让你进行一次血液检测承运人夫妇，并提供遗传咨询。
It can be wide used in maize seed purity identification, genetic background analysis of maize germplasm, fast selection and screening of target gene, maize inbred lines purification, et al.
该项技术可以应用到玉米种子纯度及真伪快速鉴定，玉米种质资源的遗传背景分析、目标基因的快速跟踪筛选、玉米自交系的快速提纯等方面，具有广阔的应用前景。
In this research, random screening of 10 SSR primers from Populus and Salix, respectively, and the genetic relationship among 17 poplar cultivars and 20 willow cultivars were studied.
利用SSR引物的种间通用性，本研究分别从杨属和柳属中各随机筛选出10对SSR引物，对17个杨树品种和20个柳树品种的遗传关系进行了分析。
Conclusions: The gene chip could accurately identify genetic mutations related to pheochromocytoma, which could provide a quick method of screening genetic mutations in pheochromocytoma.
结论：制作的基因芯片可准确识别嗜铬细胞瘤相关的基因突变，为筛查嗜铬细胞瘤基因突变提供一种快速的方法。
Grifo said he wouldn't oppose embryo screening to select a baby with a genetic defect if the parents have been informed of the pros and cons, risks and benefits.
Grifo说他不反对胚胎筛检用于选择有基因缺陷的宝宝，前提是父母已被告知利弊、风险、收益。
In this article, the performance of electrophoretic separations in miniaturized replicated plastic devices is described for applications in genetic analysis and high-throughout screening.
通过基因分析和高通量筛选中的应用，本文介绍了小型化复制的塑料仪器中的电泳分离性能。
This review will address the research advancement in genetic studies of breast cancer susceptibility as well as the screening methods f...
现就近年来乳腺癌易感基因的遗传学研究及基因变异的筛查技术进展作一综述。
The genomic DNA PCR indicated that the genetic homogeneity between NIL-PL01 and NIL-APL01 reached 98.6%, which were being used in screening the molecular marker linked to apetalous trait.
利用随机引物对基因组DNA扩增结果表明，NIL -PL0 1和NIL -APL0 1之间多态性差异较小，遗传同质性达98.6 % ，该材料正用于筛选与无花瓣性状紧密连锁的分子标记。
The genomic DNA PCR indicated that the genetic homogeneity between NIL-PL01 and NIL-APL01 reached 98.6%, which were being used in screening the molecular marker linked to apetalous trait.
利用随机引物对基因组DNA扩增结果表明，NIL -PL0 1和NIL -APL0 1之间多态性差异较小，遗传同质性达98.6 % ，该材料正用于筛选与无花瓣性状紧密连锁的分子标记。
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