查询词典 The Gene Generation

Without giving thought to from any angle looks, he will by without doubt delimit " successful Chinese businessman " that a flock of, but if be in earlier before, someone dare say he will make an ideological mark, use corroborant if businessman of this generation China can bring active gene for the body with this giant country, so OK and affirmative, the person that gives out this to say or state with certainty will be earlier than Ma Yun be surrounded to be in controversy.

不管从任何的角度看，他都将会被毫无疑问的划入"成功的中国商人"那一群，但如果在更早之前，有人敢说他将会成为一个意识形态的符号，用来确证这一代中国商人能够为这个国家庞大的躯体带来积极基因的话，那么可以肯定，发出这个断言的人会比马云更早的被包围在争议之中。

Genomic PCR of T0 generation plants revealed that the DNAj gene from foxtail millet was integrated into one wheat plant by repeated assay.

对转化获得的703株T0小麦植株提取DNA进行分子检测，有1株小麦稳定扩增到了预期的1 260 bp的目的基因片段。

Objective To study the relationship between tumor suppressor gene p16 and the generation and development of gynecologic malignancies.

目的：探讨抑癌基因p16与原发性妇科恶性肿瘤发生发展的关系。

Some of this genetic heterogenetics unfortunately leads to the development of disease. The genetics of many diseases are passed from one generation to the next by inheriting a single gene. An example is Huntingdon's disease.

很不幸的，部分的这种基因异种性导致疾病的发展，而许多疾病的这些基因藉由遗传的方式一代传给下一代，例如亨丁顿氏症(Huntingdon's disease)。

In order to further investigate the pathologic role of HOXD13 p.Q317R mutation during embryonic development and elucidate the molecular mechanism of typeⅤsyndactyly,we constructed mouse Hoxd13 Q50R replacement gene targeting vector,which will contribute to future generation of mouse model carrying the corresponding mutation.

为进一步研究HOXD13 p.Q317R突变体的功能及其导致V型并指的致病机制，我们成功构建了针对此点突变的小鼠Hoxd13 Q50R置换型基因打靶载体，为建立此点突变的小鼠模型奠定了基础。

This research was carried out on T2 generation of transgenic BoCAL cauliflower lines, which as main material, to study the expression and genetics of BoCAL gene.

本研究以T_2代的转BoCAL基因花椰菜株系为主要试材，对BoCAL基因的表达及其遗传进行研究。

These male sterile transgenic plants with TA29 Barnase gene have the same horticultural characters which can be also inherited steadily by plants in next generation as non transgenic ones. But their flowers bear fully catagenetic stamen lacking pollens, normal fragrant nectaries and strong pistils able to receive pollens from other plants or different cultivars and set seeds. At the meantime, the sterility i...

带有TA 2 9 Barnase基因的雄性不育植株的园艺学性状与未转化植株相同，并且其性状在后代中稳定不变；不育植株的花朵表现雄蕊完全退化，但蜜腺和雌蕊健全，能接受外来花粉，杂交结实率较高；同时，雄性不育植株的不育性在后代中出现分离，不育株率占 12 。5%～ 85.7%；此外，不育性状具有镶嵌性

During the process of nuclear reprogramming, the zygotes of the normal embryos and the donor nuclei of thecloned embryos cease their unique repertoire of gene expression and reset their gene expression to the totipo-tent status, and then the normal and cloned embryos redifferentiate from the totipotent status to variousdifferentiated states for tissue generation or organogenesis.

通过细胞核重编程，首先，受精卵和克隆胚胎的供体核停止其特有的基因表达程序，恢复为全能状态的基因表达程序；然后，受精胚胎和克隆胚胎的细胞再从全能状态重新进入分化状态，最终形成各种组织和器官。

In this study, genetic analyses were conducted to determine the genetic basis in an elite resistant inbred line Siyi with complete resistance to maize dwarf mosaic. A new genetic model, two dominant complementary genes conditioning the resistance, were found by Mendelian genetic analysis based on parents, F1, F2 and backcrosses in three successive years' field trails. The two genes were further mapped near the centromere of chromosome 3 and 6, respectively by tightly linked microsatellite markers using 242 plants from F2 generation. The resistance gene on chromosome 3 is 1.0 cM apart from the flanking markers phi053 and umc1527, respectively. Whereas the linkage distance between two flanking markers bnlg1600 and phi075 and resistance gene on chromosome 6 was 1.0 and 4.0 cM, respectively. Genotypic analysis of the plants from testcross and F3 populations supported the new genetic manners.

课题组通过连续三年的抗病鉴定，在国内种质资源中筛选出一份综合农艺性状优良、配合力较高的自交系四一，三年的表型遗传研究和两年的分子标记工作，发现四一中的玉米矮花叶病抗性是由两对显性互补基因控制的，进而利用F2作图群体，把发现的两个基因定位在第三和第六染色体的着丝点附近，并获得了双侧紧密连锁的分子标记连锁图谱，其中第三染色体上的分子标记UMC1527和phi053从抗病基因双侧逼近1 cM，而第六染色体上的分子标记phi075、bnlg1600从抗病基因双侧分别逼近4 cM和1 cM；利用B2群体、F2：3家系、BC3F1群体和带有第三、第六染色体抗病基因以及两个抗病基因的近等基因系，进一步证实了四一中成株期抗性是由两个显性互补基因控制的。

Results were shown as followings:(1) Sodium selenite at 0～2.5 μmol/L significantly increased the antioxidative capacity of L-02 cells without having remarkable impact on SMMC-7721 cells;(2) Sodium selenite at concentrations above significantly increased telomerase activity, hTERT gene expression and telomere length of L-02 cells without significant impact on SMMC-7721 cells;(3) Sodium selenite at higher concentrations (larger than 5 μmol/L) resulted in peroxidation of L-02 cells, while scutellarin significantly counteracted its effect;(4) Selenium-rich amino acids from silkworm pupas in the range of 0.5～2.5 μmol/L Se significantly inhibited SMMC-7721 cell growth, induced apoptosis and cell cycle change, and the generation of reactive oxygen species. In contrast, sodium selenite and selenomethionine only had weak impact on them at the same concentrations;(5) A new selenium-containing protein was found from selenium-rich silkworm pupas, which is worthy to be study further;(6) An expression vector containing ansense RNA of hTERT gene were constructed and used to transfect SMMC-7721 cells. They were observed to inhibit hepatoma cells.

结果如下：（1）0～2.5μmol/L亚硒酸钠显著性增强L-02细胞的抗氧化能力；而对SMMC-7721细胞的作用不显著；（2）该浓度硒显著性提高L-02细胞端粒酶活性、增强hTERT基因表达和延长细胞端粒长度；而对SMMC-7721细胞的作用均不显著；（3）高浓度硒（5μmol/L以上）显著性抑制L-02细胞生长、致细胞过氧化，灯盏花素能拮抗硒所致过氧化、降低硒毒性；（4）0.5～2.5μmol/L富硒蚕蛹氨基酸显著性抑制肝癌细胞SMMC-7721生长、导致细胞凋亡和周期改变、诱导细胞产生活性氧，同浓度亚硒酸钠和硒代蛋氨酸对其抑制不显著；（5）富硒蚕蛹蛋白经分离纯化和鉴定后发现存在一新含硒蛋白，其结构和功能有待研究；（6）通过已有的含hTERT基因质粒，成功构建hTERT反义RNA表达质粒，转染SMMC-7721细胞后对其生长具有抑制作用。

It has been put forward that there exists single Ball point and double Ball points on the symmetrical connecting-rod curves of equilateral mechanisms.

从鲍尔点的形成原理出发，分析对称连杆曲线上鲍尔点的产生条件，提出等边机构的对称连杆曲线上有单鲍尔点和双鲍尔点。

The factory affiliated to the Group primarily manufactures multiple-purpose pincers, baking kits, knives, scissors, kitchenware, gardening tools and beauty care kits as well as other hardware tools, the annual production value of which reaches US$ 30 million dollars.

集团所属工厂主要生产多用钳、烤具、刀具、剪刀、厨具、花园工具、美容套等五金产品，年生产总值3000万美元，产品价廉物美、选料上乘、质量保证，深受国内外客户的青睐