查询词典 U-steel

Firstly, full factorial experiment method is implemented to achieve an optimization of longitudinal microstructure design in the incidence plane of a LGP for LED BLUs. There are three control factors involving in the optimization process: the pitch and depth of both V-cut and U-cut, and angle and radius for V-cut and U-cut, respectively. Each individual control factor has three levels. It leads to a total of 27 sets of experiments.

本实验先行讨论全因子实验求取发光二极体背光模组之导光板入光侧纵沟微结构最佳化设计，选定入光侧V-cut纵沟微结构控制因子：V-cut角、V-cut间距、V-cut深及入光侧U-cut纵沟微结构控制因子：U-cut半径、U-cut间距、U-cut深等项目，其中各一因子分别有三个水准变化，依控制因子及其水准的目各进行27组实验。

After regular to faintness library matrix ω undertakes bizarre value is decomposed, the basis is given threshold value abandons bizarre value appropriately, express u σ what get matrix ω approximatelyv(kt, undertake to u and v the standard is mixed processing, use protruding to wrap a technology to undertake is not enjoying a sex and normal state sex processing, use the u after processing,σ and v generate new regular library before after subject function is mixed matrix, library of new and tectonic regulation, the function of new regular library and former regular library are approximate, but regular number decreases significantly.

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WhenPAI-1 level is lower than u-PA level,the tumor cannot protect itself againstthe excess proteolysis of u-PA.Furthermore,high PAI-1 may be associatedwith migration and reimplantation of cancer cells.This hypothesis is supportedby the following observation.

同时基于上述原因，u-PA和PAI-1高表达者，发生周围淋巴结转移的阳性率高于u-PA和PAI-1低表达者。u-PA、PAI-1阳性表达与肝门胆管癌的预后相关，u-PA及PAI-1呈阳性表达者，其生存期较阴性及弱阳性表达者明显减低。

The ubiquitin proteolytic system is an important selective proteolytic system of the celler proteolytic systems, a number of them were identified as a ubiquitin chain assembly factor-E4. The U-box protein is a new family ubiquitin-protein ligase(E3), which determine the substrate specificity of ubiquitination. The U-box is a domain of 70 amino acids that is highly conserved among yeast, plant and animals, but more U-box proteins were found in plants than in animals.

泛素系统是选择性降解细胞内蛋白质的重要系统之一，U-box蛋白质是此系统中决定底物特异性识别的一种新型E3蛋白质，部分U-box蛋白质属于泛素链聚集因子-E4.U-box结构域大约由70个氨基酸残基构成，在酵母、植物和动物等真核生物中保守存在，但植物中的数目远多于动物中。

Crystal structural analysis reveals that, because water molecules bond to Cu atoms, the dhbd ligand can only adopt a hydroxyl oxygen atom to bridge two reversed U-shaped subunits into a novel centrosymmetric dual-U-shaped tetranuclear Cu structure. Each U-shaped frame consists of two crystallographically distinct Cu atoms, two dpphen ligands and one coordinated water molecule.

晶体结构分析表明，由于水的配位阻断， 2，3-二羟基丁二酸根仅通过单羟基氧桥联两个U形双核亚单元形成具有一个对称中心的双U形四核结构，其中U型亚单元包含晶体学上不对称的2个Cu原子、1个2，3-二羟基丁二酸根、2个4，7-二苯基-1，10-邻菲咯啉和1个配位H2O分子。

Based on the energy budget equation, the optimum feeding rate for gibel carp was C〓=G〓+F〓+U〓+R〓(G〓, maximum growth energy, KJ/d; F〓, fecal energy at the optimum feeding rate, KJ/d; U〓, excretion energy at the optimum feeding rate, KJ/d; R〓, metabolism energy at the optimum feeding rate), and F〓=0.077C〓, U〓=0.052C〓 and R〓=k〓 and k is adjusted coefficient.

根据能量收支方程，异育银鲫的最适摄食率可表述为：C〓=G〓+F〓+U〓+R〓（G〓：最大摄食率条件下的生长能，KJ/d；F〓：最适摄食率条件下的排粪能，KJ/d；U〓：最适摄食率条件下的排泄能，KJ/d；R〓：最适摄食率条件下的代谢能，KJ/d），其中F〓=0.077C〓，U〓=0.052C〓，R〓=k*，k为校正系数。

Mean TRACP activity was 3.25 +/- 0.59 U/L in control subjects. Median TRACP activity was significantly greater in patients with HPT (11.97 +/- 8.92 U/L) than those with other types of renal osteodystrophy (ROD; 2.17 +/- 0.61 U/L).

控制组的TRACP活性为 3.25+/- 0.59 U/ L.6个HPT患者的TRACP活性的平均值明显升高(11.97+/- 8.92 U/L)超过其他类型的肾骨发育不良的患者(ROD； 2.17+/- 0.61 U/L)。

The reseach on activity changes of SOD, POD and CAT during the somatic embryogenesis of Y35 showed:(1) The activty of SOD was from 52.98 to 133.20 U·g-1·h-1, and remained a rising trend after early single embryo forming, this revealed that SOD might be positively correlated to the differentiation of embryogenic cell and the development of somatic embryo.(2) The activty of POD was from 0.05 to 0.50 U·mg-1·min-1, ascended firstly and desceded later, and was highest in embryogenic callus and lowest in late single embryo , this revealed that POD might be positively correlated to the division and differentiation of proembryo mass, while negatively correlated to the development of PEMⅢto late single embryo.(3) The activty of CAT was from 0.86 to 2.81 U·mg-1·min-1, showed an up-down-up trend, reaching to the highest peak at the time of early embryo formating and decreasing to the lowest at the time of early cotyledonary embryo formating, this revealed that CAT might be positively correlated to the development of early single embryo, while negatively correlated to the formation of middle single embryo and early cotyledonary embryo.The changes in activty of SOD, POD and CAT indicated these three antioxidant enzymes coregulated the differentiation and development of embryogenic cells during Larix somatic embryogenesis.4. Differentially expressed cDNA libraries of the stages of proembryo mass and somatic embryo maturation were successfully constructed by suppression subtractive hybridization.

对Y35体细胞胚胎发生过程中抗氧化酶活性变化的研究显示：(1)SOD活性在52.98~133.20 U·g-1·h-1之间，并在早期单胚形成后一直保持上升的趋势，表明其与胚性细胞的分化及体细胞胚的发育均具呈正相关；(2)POD活性在0.05~0.50 U·mg-1·min-1之间，呈现出先下降后升高的趋势，在胚性愈伤组织中最高，而在后期单胚形成时降至最低，表明其与原胚团的分裂和分化呈正相关，但与PEMⅢ向后期单胚的发育呈负相关；(3)CAT活性在0.86~2.81 U·mg-1·min-1之间，表现出升-降-升的变化趋势，在早期单胚形成时升至最高，在早期子叶胚形成时降至最低，表明其与早期单胚的发育呈正相关，而与中期单胚和早期子叶胚的发育呈负相关。

In patients with acute PE, if IV UFH is chosen, we recommend that after an initial IV bolus (80 U/kg or 5,000 U), it is administered by continuous infusion (initially at dose of 18 U/kg/h or 1,300 U/h) with dose adjustment to achieve and maintain an APTT prolongation that corresponds to plasma heparin levels of 0.3 to 0.7 IU/mL anti-Xa activity by the amidolytic assay rather than administration as IV boluses throughout treatment, or administration without coagulation monitoring (Grade 1C).

急性PE患者，如果选择IV UFH，我们推荐初始快速注射80U/kg或者5000U，继之以18 U/kg/h 或 1，300 U/h持续静滴。根据APTT延长，或者监测血浆肝素水平在0.3'0.7IU/ml， amidolytic assay 分析抗Xa因子活性来调整UFH剂量，而不能持续静脉注射治疗，或者不监测凝血功能（1C）。

Results By incubating cardiomyocytes with bFGF, ERKs was activated and the cellular viability 〔(70.0±4.6)%in bFGF 10 ng group vs.(53.0±4.5)%in H/R group, P＜0.01） and the ATP content 〔(23.1±2.3) nmol/106 cells in bFGF 10 ng group vs.(12.3±2.1) nmol/106 cells in H/R group, P＜0.01〕 were increased, also the LDH leakage 〔(257.3±51.0) U/L in bFGF 10 ng group vs.(372.5±69.2) U/L in H/R group, P＜0.05〕, was decreased, then attenuation of H/R injury to cardiomyocytes was observed. PD098059, an inhibitor of upstream kinase of ERKs completely abolished the protective effects 〔viability (57.0±5.8)%,ATP content (15.1±2.6) nmol/106 cells,LDH activity in medium (325.5±59.0)U/L in PD098059 group vs. bFGF 10 ng group, P＜0.01, respectively〕.

结果 bFGF激活ERKs，并呈剂量依赖性减轻H/R所致心肌细胞损伤，表现为细胞存活率〔bFGF 10 ng组(70.0±4.6)%，H/R组(53.0±4.5)%，P＜0.01〕和细胞内ATP含量〔bFGF 10 ng组(23.1±2.3)nmol/106细胞，H/R组(12.3±2.1)nmol/106细胞，P＜0.01〕升高，细胞浆酶LDH漏出〔bFGF 10 ng组（257.3±51.0）U/L，H/R组（372.5±69.2）U/L，P＜0.05〕减少；ERKs上游激酶抑制剂PD098059完全消除上述保护作用〔PD098059组细胞存活率（57.0±5.8）%，ATP含量（15.1±2.6）nmol/106细胞，培养液中LDH活性（325.5±59.0）U/L，与bFGF 10 ng组比较均为P＜0.01〕。

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。