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Samples of conchocelis and gametophytic baldes of both SF-1 and Y-6 (isolated from SF-1 line) lines had a unique allele on PC40 locus, indicating that it can be used as a marker to distinguish these two lines from the others.

在引物PC-40界定的遗传座位上，2个优良品系申福1号和优质6号（以申福1号为母本选育出来的品系）的丝状体和叶状体均出现了区别于其他品系的等位基因，显示对这2个优良品系进行SSR特异性标记是可能的。

In a large, randomly mating population that is free of disturbing forces, allele and genotypic frequencies do not change and are related in a simple way.

在一个大的，随机交配的人口是免费的令人不安的力量，等位基因与基因型频率不改变，并在有关的一个简单的方法。

Results showed that the frequencies of MTHFR T homogenetic type (2.7%), heterogenetic type (51.4%) and T allele (28.4%) in ischemic group were higher than those in control group (1.2%, 39.8% and 21.1%, respectively).

实验检出患者组MTHFR基因T纯合基因型、杂合基因型和T等位基因频率分别为2.7%、51.4%和28.4%，对照组分别为1.2%、39.8%和21.1%。

To study genetic mutations of methylenetetrahydrofolate reductase C677T and cystathioinine-β-synthase T833C related to homocysteine metabolism in patients with ischemic stroke, the MTHFR gene C677T gene mutation and the CBS T833C gene mutation were detected by PCR-RFLP or ARMS method in 74 patients with ischemic stroke and 83 normal people for control. Results showed that the frequencies of MTHFR genet homogenetic type(2.7%), heterogenetic type(51.4%) and T allele(28.4%) in ischemic group were higher than those in control group(1.2%, 39.8% and 21.1%, respectively).

为研究同型半胱氨酸代谢相关酶亚甲基四氢叶酸还原酶基因C677T和胱硫醚-β合成酶基因T833C位点碱基突变与缺血性脑卒中的关系，对74例缺血性脑卒中患者和83例健康对照者，采用聚合酶链反应-限制性片段长度多态性技术检测MTHFR基因C677T基因型，用扩增阻滞突变体系法检测CBS基因T833C突变。

VWF gene is one of the most polymorphism genes. There is a lot of allele in 40th intron of vWF gene, and the heterozygous rate is higher.

vWF基因是人类最具多态性的基因之一。vWF基因40号内含子中的VNTR存在多种等位基因，有较高的杂合频率。

The frequencies of CBS C homogenetic type (13.5%) and C allele (43.9%) in ischemic group were higher than those in control group (6.0% and 38.0%, respectively).

患者组CBS基因C纯合基因型和C等位基因频率分别为13.5%和43.9%，对照组分别为6.0%和38.0%。

The frequencies of CBS gene C homogenetic type (13.5%) and C allele (43.9%) in ischemic group were higher than those in control group(6.0% and 38.0%, respectively).

实验检出患者组MTHFR基因T纯合基因型、杂合基因型和T等位基因频率分别为2.7%、51.4%和28.4%，对照组分别为1.2%、39.8%和21.1%。

Of or relating to a trait that is expressed only when the determining allele is present in the homozygous condition.

隐性性状的属于或与这种性质特点有关的，即在同型接合情况下，只有当决定性等位基因出现时它才会有所表现的特点性质

Such a plant is homozygous for every allele.

这样的植物对每个等位基因来说都是纯合的。

This study intends to investigate the correlation between HBV-GN and HLA-DR allele by testing the frequency of HLA-DR gene in HBV-GN patients, to probe into the effect of immunogenetic factor on the pathogenic mechanism of HBV-GN at the genic level and further explore susceptibility gene and/or resistance gene associated with HBV-GN disease, so as to provide certain experimental basis for diagnosis and treatment of HBV-GN.

本研究拟通过检测HBV-GN患者的HLA-DR的基因频率，对HBV-GN与HLA-DR等位基因相关性进行研究，从基因水平探讨免疫遗传因素在HBV-GN发病机制中的作用，并进一步探索HBV-GN疾病相关的易感基因和/或抗性基因，从而为HBV-GN的诊断和治疗提供一定的实验依据。

Finally, according to market conditions and market products this article paper analyzes the trends in the development of camera technology, and designs a color night vision camera.

最后根据市场情况和市面上产品的情况分析了摄像机技术的发展趋势，并设计了一款彩色夜视摄像机。

Only person height weeds and the fierce looks stone idles were there.

只有半人深的荒草和龇牙咧嘴的神像。