查询词典 Gene

In order to analyze gene sequence of the bovine Theileria annulata in Xinjiang, a pair of primers was designed, Tamsl gene fragment was amplified by PCR, sequence of positive clones was showed that the gene fragment has a total length of 846 bp, which encoded 281 amine acids.

采用PCR技术，从新疆焦虫病疫区感染牛的全血中扩增到Tamsl基因，该基因长度为846 bp，编码281个氨基酸。

The p53 gene structural abnormality and mdm2 protein overexpression might be two factors causing p53 protein overexpresion in NPC. The function of p53 proteins produced by various structural anormality of p53 gene might be different in activating MDM2. The overexpression of p53 or mdm2 protein, particularly both cooperation, might play an important role during NPC genesis.Key words: Nasopharyngeal neoplasms; p53 gene; p53 protein; mdm2 protein

p53基因结构改变和mdm2蛋白过度表达是影响NPCp53蛋白过度表达的两个因素；不同类型p53基因结构改变所产生的p53蛋白激活MDM2的功能并不相同；p53和mdm2蛋白过度表达，尤其两蛋白协同作用，可能在NPC发生中起重要作用。

That means Pho85 kinaseand calcineurin were involved in salt tolerance with an identical target protein or in 中科院上海生化与细胞所博士学位论文摘要 the same pathway. Inhibition of calcineurin decrease the YPH499, pho80? mutant,and pap1 (pcl7)? mutant Mn2+ tolerance but not that of pho85? mutant and thepho85? mutant was more sensitive to Mn2+ than YPH499, pho80? mutant, and pap1(pcl7)? mutant even with the addition of cyclosporin A. Therefore, the conclusioncould be drawn that PHO85 gene played a dominant role in Mn2+ homeostasisregulation in compare with calcineurin. As for Ca2+ tolerance, cyclosporin A canincrease the tolerance to Ca2+ of all the mutant mention above, that means Pho85kinase and calcineurin function antagonistically in regulation of Ca2+ homeostasis.In Bioinformatics, BRI3 gene is a novel gene without any function clue but givehigh conservation in mammalian.

我们通过钙调磷酸酶的特异抑制剂环孢菌素A研究了YPH499、+2+pho85缺失株、pho80缺失株、pap1缺失株在钙调磷酸酶失活后对Na、Mn、2+Ca金属离子敏感性的变化，结果显示Pho85蛋白激酶和钙调磷酸酶通过直接+或间接激活同一个靶蛋白或途径来增强细胞对Na的耐受；和钙调磷酸酶相比，2+PHO85的缺失对酵母细胞Mn耐受性的破坏是相对控制性的，钙调磷酸酶的失2+活不能进一步降低pho85缺失株对Mn的耐受能力；Pho85和钙调磷酸酶在对2+Ca的耐受调节中是相互拮抗的，钙调磷酸酶的失活能增加pho85缺失株和2+pho80缺失株的Ca耐受。i中科院上海生化与细胞所博士学位论文摘要对本实验室克隆的人新基因BRI3进行系统的生物信息学分析，发现它是一个在哺乳动物中保守的，但功能未知的基因。

Methods PCR-SSCP and PCR product cloning, sequencing were performed to detect mutation of p16 gene exon 2 in peripheral blood of 60 patients with arseniasis caused by coal-burning pollution,at the same time,PCR-based methylation assay was performed to analyze the methylation of p16 gene exon 1. Results No p16 gene exon 2 mutation was found in 60 cases.

采用聚合酶链反应-单链构象多态性分析和PCR产物克隆测序技术对60例砷中毒患者外周血中p16基因第2外显子突变情况进行检测，同时采用甲基化敏感的限制性内切酶方法对p16基因第1外显子甲基化情况进行分析。

The expression of Pax-6 gene in the different stages was demonstrated by RT-PCR (Real - Time PCR):(1) The mRNA of Pax-6 gene expression was positive in Bufo raddei Strauch embryo at 16 stage; and the gene expression was also detected at 20 stage.

2荧光定量PCR结果显示在花背蟾蜍的晶状体再生的第7天Pax-6基因的表达量达到最高，表明此时期Pax-6基因在晶状体再生的过程中起到调控细胞增殖的作用。

Therefore, the identification and characterization of floral organ identity genes in Buxaceae is critical in elucidating the gene evolution related to floral organ formation. Floral organ identity gene homologues of Buxus microphylla ssp. sinica were screened, and nine gene homologues of B.

根据前人的谱系关系研究，黄杨科很接近真双子植物基群第二次主要复制事件的时间点，因此鉴定黄杨科植物的花部基因，将有助於厘清调控花部器官形成基因的演化情形。

DATA SYNTHESIS:①Technical choice of gene therapy for bone defect: Human bone morphogenetic protein was the most often used objective gene in the gene therapy for bone defect at present, which had been identified in the models of rabbit, murine, caprine and dog in the application of plerosis of bone defect.

资料综合：①基因治疗骨缺损的技术选择：人骨形态发生蛋白基因是目前骨缺损基因治疗中应用最多的目的基因，已在兔、鼠、羊和狗模型中证实其对骨缺损的修复作用。

The real-time quantitative PCR results showed that the expression level of two genes did not be affected by HHO obviously, whereas, the expression level of CHS gene had down regulation of different degree, except in 1.0 mM of HHO's concentration. It meaned that CHS gene is probably related with the metabolism of allelochemical.4. The Chalcone synthase gene (EaCHS1) of E.

荧光定量PCR的结果表明，萜类代谢途径中的两个关键酶基因的表达水平，没有因为羟基泽兰酮的诱导而表现出显著的差异；CHS基因的表达水平，除了在羟基泽兰酮处理浓度为1.0 mM时的差异不显著之外，在其他处理浓度均有不同程度的下调，说明该基因与化感物质的代谢途径相关。4。

The TC gene was screened from cDNA library of adult Clonorchis sinensis, cloned, expressed and purified. The purified protein of TC gene will be of importance for further research on the biological function of the gene.

通过生物信息学方法由华枝睾吸虫成虫cDNA文库中筛选出TC基因，并成功予以克隆，表达及纯化。

By using wheat with recessive ph gene as parents in wide crosses, new wheat lines with alien chromosome segments, such as TKL1, were obtained. Gene phKL and its combinant have new usefulness for studying on genetic mechanism of homoeologous chromosome pairing and alien gene transfer.

phKL基因及其重组体在染色体配对的遗传作用机制和外源基因转移方面存在新的应用价值。

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。