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homogenetic相关的网络例句

查询词典 homogenetic

与 homogenetic 相关的网络例句 [注:此内容来源于网络,仅供参考]

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。

Methods 209 patients with CHD and 101 controls were selected. MTHFR genetic C677T polymorphism was determined by PCR-RFLP, and CBS T833C polymorphism by ARMS method. Plasma homocysteine levels were detected with HPLC. Results The frequencies of MTHFR T homogenetic type and heterogenetic type (27.8%and 45.4%) in case group were higher than those in normal group(22.8%and 34.6%).

对209例冠心病患者和101例健康对照者,采用多聚酶链反应-限制性内切酶片段长度多态性技术检测MTHFRC677T基因型,用扩增阻滞突变体系法检测CBS基因T833C多态性,采用高压液相色谱法测定同型半胱氨酸血浆水平。

Surely western culture is playing a leading part in the process of globalization, but it should not be allowed to shape the world into a homogenetic whole.

全球化时代中国文化建设的中心任务仍是现代性的建构和培育;期望从前现代直接跨入后现代的想法,如果不是出于历史的无知,便是某种虚幻的一厢情愿,见于实践则会是文化建设的延宕甚至挫折。

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%。

A chimeric primer was designated in which segment A near 3' end is complementary to HB plus strand just before the DR2 region gap, and segment B near 5' end is consensus to part of the human immunodefficient irus genomic sequence, without homogenetic relationship to HB genome.

设计一嵌合引物,使之3'端的A片断与HB正链互补,并恰好位于DR2缺口之前;5'端的B片断与人类免疫缺陷病毒的基因序列具有同源性,与乙型肝炎病毒的基因组无同源性。

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