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RESULTS: Of 49 affected vertebras in 33 cases, 43 were one-off successful, and 5 cases died of tumor metabasis. Finally, 43 vertebras were included in final analysis.

结果: 33例49个椎体中有43个椎体经皮球囊后凸椎体成形均一次成功。5例因肿瘤全身转移死亡。43个锥体进入结果分析。

After contrasting and optimizing this paper gets a set of parameters. Then according to these parameters the paper sets up entity model, and after validating and analyzing with finite element it can save time of calculating. On the other hand, it can provide a good method of design of moldboard plow surface.

通过对这四个阶段中土垡的运动学和动力学分析研究,建立了犁体牵引阻力的数学模型;通过对比分析得到较优的一组参数,然后以该组参数为依据进行参数优化,最后以优化后的参数建立犁体实体模型,应用有限元进行分析,节省了计算时间和提高了计算效率,为今后犁体曲面设计提供了一种方法。

Results (1)ATP could inhibit the proliferation of U937 cells with inhibition rate over 43% after 48hour ATP treatment;(2)ATP treated U937 cells numbers increased obviously in G1 phase,and apoptosis peak appeared before G1 phase,apoptotic cell number was 3.4% for 24hour,and was 22.7% for 48hour of ATP treated U937 cells;(3) Nuclear chromatin condensed into sperical masses bound cytoplasma membrane formed apoptotic bodies which is shed from membrane surface into intercellular medium;(4) Apoptotic bodies were nigrosine staining negtive.

结果 (1)ATP对U937细胞的增殖有按摩明显的阻抑作用,加药48h后增殖的抑制率可达43%以上;(2)ATP处理的U937细胞周期发生改变,G1期细胞数按摩明显增多,ATP作用24h时G1期前出现亚二倍体峰——凋亡峰,凋亡细胞数为3.4%,作用48h时凋亡细胞数增多为22.7%;(3)ATP处理的U937细胞首先在核内染色质浓缩成半月形贴近核膜,逐渐向核膜外移动,进入胞浆内再移向质膜内外面,紧贴质膜外面再逐步脱离细胞体,进入细胞基质中,成为游离的凋亡小体。

Methods Cell culture,flow cytometry,HE staining,Nigrosine staining and electron microscopy were used. Results (1)ATP could inhibit the proliferation of U937 cells with inhibition rate over 43% after 48hour ATP treatment;(2)ATP treated U937 cells numbers increased obviously in G1 phase,and apoptosis peak appeared before G1 phase,apoptotic cell number was 3.4% for 24hour,and was 22.7% for 48hour of ATP treated U937 cells;(3) Nuclear chromatin condensed into sperical masses bound cytoplasma membrane formed apoptotic bodies which is shed from membrane surface into intercellular medium;(4) Apoptotic bodies were nigrosine staining negtive.

结果 (1)ATP对U937细胞的增殖有明显的阻抑作用,加药48h后增殖的抑制率可达43%以上;(2)ATP处理的U937细胞周期发生改变,G1期细胞数明显增多,ATP作用24h时G1期前出现亚二倍体峰——凋亡峰,凋亡细胞数为3.4%,作用48h时凋亡细胞数增多为22.7%;(3)ATP处理的U937细胞首先在核内染色质浓缩成半月形贴近核膜,逐渐向核膜外移动,进入胞浆内再移向质膜内外面,紧贴质膜外面再逐步脱离细胞体,进入细胞基质中,成为游离的凋亡小体。

It was indicated by UV-Vis spectra characterization that the precursor always contains the tetrahedral Ti species and the octahedral Ti species regardless of the Ti content. Calcination of the precursor resulted in a partial condensation of the octahedral Ti species to form the anatase phase.

UV-Vis 光谱表明,Ti-MWW 合成原粉中含有四面体的钛和八面体的钛,而八面体的钛属于一种骨架外钛,未经酸处理而煅烧会使部分八面体钛缩合形成锐钛矿,而经过酸处理和煅烧后的分子筛则几乎不含有锐钛矿。

The dynamic changes of physiological and biochemical indexes of healthy spikes and inoculation ones of the resistant mutants indicated that PAL activity and content and changing tendency of total phenolate and flavoniods and MDA in the healthy spikes of the mutants were similar to that of their susceptible donors, whereas, for the inoculated spikes, content and changing range of these indexes existed significant difference between two kinds of strains, changing from high-resistant variety (Sumai3 ) to their susceptible donors.

以典型抗扩展品种和突变体供体亲本为抗、感对照,对抗赤霉突变体的健康穗及接种穗的生理生化特性研究结果显示,在健康穗中,抗性突变体的PAL活性、总酚、类黄酮及MDA含量及变化趋势与其感病亲本相一致,但在病原菌侵染后,这些生理生化物质的含量与变化程度与其亲本有了明显的差异,其变化范围介于典型高抗品种和感病亲本之间,变化趋势与亲本或抗性品种一致。

Protease treatment of the plasma membranes could abolish the binding but NaIO_4 and glycosidase could not, indicating that nsLTP144 bound to plasma membranes protein without carbohydrate moiety. Using the homobifunctional cross-linking regent bissuberate (BS~3) and rice plasma membranes incubated with ~(125)I-Trx-nsLTP144, we identified, after SDS-polyacrylamide gel electrophoresis and autoradiography, a putative protein receptor on the rice plasma membranes with the molecular mass around 60 kDa. NsLTP144 can not trigger extracelluar alkalization in arabidopsis, but can abolish the extracellular alkalization effect of phytopathogen elicitor cryptogein, suggesting that cryptogein and nsLTP144 may bind to the same membrane protein. In vitro pull-down assay showed that nsLTP144 interacted with OsCaM1, a possible extracellular calmodulin, implying that nsLTP144 and OsCaM1 could function in the same signal transduction pathway. These results shed light on revealing the roles of nsLTP in vivo and make it promising to finally characterize the plasma membranes receptor of nsLTP.

发现~(125)I-Trx-nsLTP144、~(125)I-Trx-nsLTP110与水稻细胞质膜均具有特异性结合,而且结合是饱和性的、可被竞争的,符合配体-受体结合的典型特征,同时用于对照实验的蛋白质~(125)I-Thioredoxin没有此特性,表明水稻细胞质膜上存在nsLTP的受体;利用可氧化糖基的NaIO_4和水解糖基的N\'-糖苷酶F处理水稻细胞质膜,再进行结合实验,结合活性几乎不受影响;而利用胰蛋白酶处理细胞膜则使得结合能力几乎完全丧失,表明其受体为没有经过糖基化修饰的蛋白质;利用交联剂BS~3交联配体一受体后,再进行SDS-PAGE分离和放射自显影,结果显示水稻细胞质膜上的nsLTP受体中有一个60kDa的蛋白质可以与nsLTP144发生特异性的结合,可能是其受体;细胞外碱化实验表明,nsLTP144不能促使拟南芥原生质体细胞培养液的细胞外碱化反应,却能猝灭来自植物病原菌的激发子Cryptogein刺激拟南芥原生质体产生的细胞外碱化反应,表明nsLTP和Cryptogein结合细胞膜上相同的位点,保护了植物细胞免受Cryptogein导致的细胞程序性死亡,并诱导系统获得性抗性的产生;体外Pull-down实验表明,nsLTP144和水稻的OsCaM1具有相互作用,暗示了nsLTP144和OsCaM1可能同在一个信号通路上起作用。

After tail iv injection, the blood exposure time of stealth liposomes and the area under blood drug concentration-time curve were pronouncedly increased, compared with the regular liposomes group and the free doxorubicin group,respectively.

以化学梯度法包封脂质体,用两亲性聚乙二醇-二硬脂酰磷脂酰乙醇胺对脂质体膜进行修饰以制备隐形脂质体;用HPLC-UV法测定给药后小鼠体内组织中的药物浓度。

Secondly, the theory for multi-flexible dynamical systems is introduced and applied, and the simplified system obtained is cubic nonlinear, with 1:3 internal resonance for certain parameter condition.

其次,简要介绍了柔性多体动力学理论,将柔性多体动力学理论应用于一类刚柔耦合系统的建模。该多柔体系统离散化后的简化模型为一个含有1:3内共振关系的立方非线性系统。

There was synergetic effect on toughness of composite between nano-CaCO〓 and elastomer as the sandbag structure was occurred.

纳米碳酸钙或者其团聚体与弹性体形成沙袋结构后,可以消除团聚体对材料韧性的劣化作用,而且在一定程度上通过碳酸钙团聚体的变形吸收能量而提高增韧效果。

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The labia have now been sutured together almost completely.The drains and the Foley catheter come out at the top.

此刻阴唇已经几乎完全的缝在一起了,排除多余淤血体液的管子和Foley导管从顶端冒出来。

To get the business done, I suggest we split the difference in price.

为了做成这笔生意,我建议我们在价格上大家各让一半。

After an hour and no pup, look for continued contractions and arching of the back with no pup as a sign of trouble.

一个小时后,并没有任何的PUP ,寻找继续收缩和拱的背面没有任何的PUP作为一个注册的麻烦。