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bud mutation相关的网络例句

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

In this algorithm, inertia weight was nonlinearly adjusted by using population diversity information. Velocity mutation factor and position interchange factor were both introduced and the global performance was clearly improved.

该算法利用种群多样性信息对惯性权重进行非线性的调整,并在算法的后期引入速度变异算子和位置交叉算子,使算法摆脱后期易于陷入局部最优点的束缚。

DMD is caused by a mutation of the gene for dystrophin, a protein in the muscles.

DMD源于肌肉中一种称为肌营养不良蛋白的基因突变。

The dose-effect is relatively ideal,and the HPRT gene mutation can be taken as a radiation biological dosimeter.

克隆法是一种检测放射性核素内、外照射诱发HPRT基因突变的方法,HPRI,基因突变剂量效应关系理想,有可能作为辐射生物剂量计。

In the present experiment, the tender stems of Dracaena cambodiana were used as explants to establish a two-step tissue culture and regeneration system. The effects of types and concentrations of plant hormones on the induction of callus were studied. Based on these, the reactions of callus regeneration to different mutation-induced approaches (60Co irradiation, EMS and colchicines), the regeneration ability of the treated callus as well as the characters diversities (including the appearance traits and cytological observations) of the regeneration plants were investigated.

本试验以龙血树幼嫩茎段为材料,通过对龙血树幼嫩茎段两步培养法再生的研究,建立了龙血树幼嫩茎段离体再生体系,证明了愈伤组织的发生和激素种类与浓度的关系;并在此基础上研究了愈伤组织再生对不同人工诱变方法(60Co辐射、EMS、秋水仙素)的反应、被处理愈伤组织再生能力和再生植株性状多样性、以及再生植株不同生理角度的变异性,得到了2株变异株系。

We can make use of chip to analysis virus gene group; construct mutation detection technique of heredity diseases and become normal detection technique of many heredity diseases; supervise the changes of cell gene expression, research pathogenic theory of virus; differentiate bacteria gene types and identify bacteria strains, provide base data for screening and supervise drug-fast gene.

利用基因芯片可加速对病毒基因组的功能分析;可建立遗传病的突变检测技术,并成为对多种遗传病的常规诊断技术;可用来监测宿主细胞基因表达的改变,研究病毒的致病机理;基因芯片还可用来对细菌基因的分型和菌种鉴定,为筛选和监测细菌的抗药性基因提供基础数据。

We can make use of chip to analysis virus gene group; construct mutation detection technique of heredity diseases and become normal detection technique of many heredity diseases; supervise the changes of cell gene expression,research pathogenic theory of virus; differentiate bacteria gene types and identify bacteria strains,provide base data for screening and supervise drug-fast gene.

目前我国在出入境检验检疫中,已开始在基因芯片技术检测传染病病原方面开展了研究工作,国家质检总局动植物检疫所研制出了检测SARS病毒的全基因芯片,极大的促进了出入境检验检疫检测技术的发展,但目前国内外尚未见到有关新城疫病毒基因芯片的报道。

The mutation means that Duffy receptor proteins are not made in red cells.

变异意味着趋化因子的蛋白质不再由红血球制造产生。

METHODS: We assessed our patients by clinical and electromyographic studies, by intercostal muscle biopsies for in vitro microelectrode analysis of neuromuscular transmission and quantitative electron microscopy EM of 409 end plates, and by mutation analysis, and expression studies of the mutants.

我们通过临床表现及肌电图检查、通过肋间肌活检进行神经肌肉传递的体外微电极分析和对409个运动终板的定量电子显微镜检察,以及运用突变分析和突变体的表达研究对患者进行分析评定。

However,their fluorescence emission intensities decreased by 16-22% and the ellipticity values at the negative trough increased by 13-16% for the mutants,indicating that the conformation of prochymosin was perturbed after mutation.

但它们的荧光强度下降了16-22%,在负谷中的最大椭圆值增加了13-16%,表明突变确实给凝乳酶原的空间结构造成了微扰。

ARID (AT-rich interaction domain) protein is a transcription factor family in higher eukaryotes that regulates cell proliferation, development, and differentiation. Specificity of DNA binding ability in this family prefers AT-rich sequences, but some ARID family proteins are not sequence-specific DNA-binding proteins or they do not bind AT-rich sequences. We found two genes that encode ARID in Giardia lamblia genome database, garid1 and garid2. We analyzed the function of garid1 first. AU1-tagged gARID1 was found to localize to nuclei. During encystation, gARID1 mRNA level decreased emphatically, but protein level increased. We also found that gARID1 can bind AT-rich initiator of the cwp1 promoter by EMSA. Mutation analysis revealed gARID1 binding sequence was AGATC and AATAAAATA. We used ChIP to demonstrate that gARID1 can bind cwp1 gene promoter in vivo.

ARID(AT-rich interaction domain)蛋白质家族是真核生物的一种转因子,在许多同种的真核生物有它的同源基因,这个家族的蛋白质通常与调控细胞的生长、发育和分化的作用有关,而这个家族的蛋白质和DNA的结合能,各种ARID蛋白质的专一性尽相同,过大致上偏好於和AT-rich的序结合;我们已经在形鞭毛虫的基因组中找到个含有ARID 的基因,分别是garid1和garid2,我们首先对於garid1做分析;将AU1标记接到gARID1转染形鞭毛虫,用免疫萤光染色可发现gARID1存在於细胞核中。gARID1的讯息RNA在囊体化后会明显下,过其阳性染色和蛋白质表现有明显增加;EMSA实验中也发现gARID1会明显的与cwp1基因启动子之AT-rich initiator结合,经由突变序分析,也显示gARID1的结合序为AGATC和AATAAAATA,随后我们也用ChIP证明gARID1在细胞内也的确会和cwp1基因的启动子结合。

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Where's Da Bud
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