启动

The early affective priming ERPs effect was characterized by a longer P2 peak latency and decreased P2 peak amplitude for control condition as compared to primed and unprimed conditions; the late affective priming ERPs effect consisted of a shorter P3 latency and attenuated P3 peak amplitude for primed condition as compared to unprimed condition.

5在阈下启动任务中，对于P2、P3成分的潜伏期与波幅，述情障碍组与非述情障碍组之间均不存在显著差异；在阈上启动任务的两个SOA水平中，述情障碍组的P2成分和P3成分波幅均显著小于非述情障碍组的波幅。

The catabolites of acetoin metabolism such as 2,3-butanediol and acetaldehyde as well as other carbohydrates including galactose, lactose, and glycerol did not affect the expression of Paco and PacoK, whereas maltose stimulates the expression of PacoK at 210 min.

其他的乙醯甲基甲醇代谢物如2， 3-丁二醇与乙醛，以及其他糖类包括半乳糖，乳糖和甘油对acoABCD及acoK启动区的表现能力并无明显影响，而在210分钟时，麦芽糖则可刺激acoK启动区的表现。

Tarda AcrAB multidrug resistance system was cloned in this study. Sited-directed mutation was used to determine the promoter sequences of acrAB and acrR and the AcrR binding site.

论文克隆分析了迟缓爱德华氏菌AcrAB耐药系统，采用定点突变确定了acrAB、acrR的启动子序列和AcrR在acrAB启动子的结合位点。

Objective To investigate the characteristics of memory impairment in patients with amnestic mild cognitive impairment.

目的 探讨遗忘型轻度认知障碍患者内隐记忆概念性启动和知觉性启动损害的特征。

The stable clones are further identified by RT-PCR and Western blot; 6 MTT assay is used to investigate the effect of ZNRD1 on the cell growth of cells (AGS, SGC7901, MKN28, NIH3T3, GES-1); 7 Soft agar assay is used to investigate the effect of ZNRD1 on the clonality of cells (AGS, MKN28); 8 Nude mice assay is used to investigate the effect of ZNRD1 on the cell growth of gastric cancer cells (AGS, MKN28); 9 Flow cytometry is used to investigate the effect of ZNRD1 on the cell cycle distribution of cells (AGS, MKN28, NIH3T3, GES-1); 10 Flow cytometry is used to investigate the effect of ZNRD1 on the cell apoptosis of cells (AGS, MKN28, NIH3T3); 11 MTT assay is used to investigate the effect of ZNRD1 on the drug sensitivity of cancer cells (SGC7901, SGC7901/VCR, HL-60, HL-60/VCR) in vitro; 12 SRCA is used to investigate the effect of ZNRD1 on the drug sensitivity of gastric cancer cells (SGC7901, SGC7901/VCR) in vivo; 13 Flow cytometry is used to investigate the effect of ZNRD1 on adriamycin accumulation of cancer cells (SGC7901, SGC7901/VCR, HL-60, HL-60/VCR); 14 Transmission electron microscope is used to investigate the effect of ZNRD1 on the sensitivity of SGC7901 cells towards drug-induced apoptosis; 15 Flow cytometry and DNA ladder assay are used to investigate the effect of ZNRD1 on the sensitivity of cells (SGC7901, SGC7901/VCR, HL-60/VCR) towards drug-induced apoptosis; 16 Microarray is used to investigate the profiling of ZNRD1-responsive genes in gastric cancer cells (AGS, MKN28, SGC7901, SGC7901/VCR); 17 RT-PCR and Western blot are used to identify the results of microarray; 18 Reporter gene assay is used to investigate the effect of ZNRD1 on the transcriptional activity of cyclin D1; 19 Reporter gene assay is used to investigate the effect of ZNRD1 on the transcriptional activity of MDR1; 20 Kinase assay is used to investigate the effect of ZNRD1 on the activity of cyclin E-CDK2 kinase; 21 The antisensenucleic acids of p21 is used to inhibit the expression of p21, and flow cytometry is used to investigate the effect of p21 on ZNRD1-induced cell cycle arrest in gastric cancer cells; 22 The antisensenucleic acids of p27 is used to inhibit the expression of p27, and flow cytometry is used to investigate the effect of p27 on ZNRD1-induced cell cycle arrest in gastric cancer cells; 23 Liposome is used to up-regulate the expression of Skp2, and flow cytometry is used to investigate the effect of Skp2 on ZNRD1-induced cell cycle arrest in gastric cancer cells; 24 Western blot is used to investigate the effect of ZNRD1 on the stability of Skp2 and p27 in gastric cancer cells; 25 MVD assay is used to investigate the effect of ZNRD1 on the angiopoietic activity of gastric cancer cells; 26 ELISA is used to investigate the effect of ZNRD1 on the expression of VEGF165 in gastric cancer cells; 27 The roles of DARPP-32 in MDR of gastric cancer cells are investigated using gene transfection, MTT assay, SRCA, flow cytometry and DNA ladder assay.

应用杂交瘤技术制备ZNRD1的首个单克隆抗体；2）利用RT-PCR、Western blot和免疫组化检测ZNRD1在胃癌组织、胃炎组织、正常胃上皮组织、胃癌细胞和正常胃组织上皮细胞中的表达；3）构建ZNRD1的小干扰RNA载体，并测序鉴定；4）利用脂质体将ZNRD1的真核表达载体及其空载体转染胃癌细胞（AGS、SGC7901、MKN28）和小鼠成纤维细胞（NIH3T3），G418筛选后进行鉴定；5）利用脂质体将ZNRD1的小干扰RNA载体及其空载体转染药敏胃癌细胞（SGC7901）、正常胃组织上皮细胞（GES-1）、对长春新碱耐药的胃癌细胞（SGC7901/VCR）、药敏白血病细胞（HL-60）、对长春新碱耐药的白血病细胞（HL-60/VCR），G418筛选后进行鉴定；6）利用MTT实验检测ZNRD1高/低表达对细胞（AGS、SGC7901、MKN28、NIH3T3、GES-1）生长的影响；7）通过软琼脂克隆形成实验检测上调ZNRD1对AGS、MKN28细胞克隆形成能力的影响；8）通过裸鼠成瘤实验检测上调ZNRD1对AGS、MKN28细胞体内成瘤性的影响；9）通过流式细胞仪分析ZNRD1高/低表达对细胞（AGS、MKN28、NIH3T3、GES-1）的细胞周期的影响；10）通过流式细胞仪分析上调ZNRD1对细胞（AGS、MKN28、NIH3T3）的凋亡的影响；11）通过MTT实验检测ZNRD1高/低表达对细胞（SGC7901、SGC7901/VCR、HL-60、HL-60/VCR）体外药物敏感性的影响；12）通过肾包膜下移植法检测ZNRD1高/低表达对细胞（SGC7901、SGC7901/VCR）体内药物敏感性的影响；13）通过流式细胞仪分析ZNRD1高/低表达对细胞（SGC7901、SGC7901/VCR、HL-60、HL-60/VCR）内阿霉素蓄积和泵出的影响；14）通过透射电镜检测上调ZNRD1对SGC7901细胞凋亡敏感性的影响；15）通过流式细胞仪和DNA梯度试验检测ZNRD1高/低表达对细胞（SGC7901、SGC7901/VCR、HL-60）凋亡敏感性的影响；16）通过基因芯片检测ZNRD1高/低表达对胃癌细胞内基因表达谱的影响；17）利用RT-PCR、Western blot对基因芯片的结果进行鉴定；18）利用报告基因实验检测ZNRD1对cyclin D1的启动子活性的调节作用；19）利用报告基因实验检测ZNRD1高/低表达对MDR1的启动子活性的调节作用；20）利用激酶试验检测ZNRD1对cyclin E-CDK2 激酶活力的影响；21）利用反义核酸技术抑制p21的表达；通过流式细胞仪检测抑制p21对ZNRD1介导的细胞周期阻滞的影响；22）利用反义核酸技术抑制p27的表达；通过流式细胞仪检测抑制p27对ZNRD1介导的细胞周期阻滞的影响；23）利用脂质体转染法上调Skp2的表达；通过流式细胞仪检测上调Skp2对ZNRD1介导的细胞周期阻滞的影响；24）利用Western blot检测ZNRD1对p27和Skp2的蛋白稳定性的影响；25）利用微血管密度实验检测ZNRD1对AGS、MKN28细胞裸鼠移植瘤微血管形成的影响；26）利用ELISA检测ZNRD1对AGS、MKN28细胞培养上清和移植瘤匀浆中VEGF165含量的影响；27）利用脂质体转染法、MTT实验、肾包膜下移植法、流式细胞仪和DNA梯度试验检测新耐药相关分子DARPP-32对细胞（SGC7901、SGC7901/VCR、对阿霉素耐药的胃癌细胞SGC7901/ADR）多药耐药表型的影响；利用脂质体转染法和MTT实验检测下调ZNRD1对DARPP-32介导的胃癌多药耐药的调控作用。

Exhausting : The item resembles anormal psionic item with free activation, but it instead drains theuser of power points whenever she activates its ability.

耗能：该物品类似免费启动的普通灵能物品，但其实在启动能力时会消耗使用者的灵能点。

Rice Tungro bacilliform virus promoter is a phloem specific promoter.

水稻Tungro病毒启动子是一个只在韧皮部表达的启动子。

The invention relates to a processing method of preventing frostbite and restarting of hydrogen electric pile, whose characteristic lies in the treating processes includes: When the electric pile turns off, the unsaturated fuel gas or the nitrogen, through the circle boast to clean the dissociate water; drying the MEA film module to keep the water content below the stipulated temperature which does not ice up; then the recycle gas through a wet exchanger to dry and the dried gas is continue used in the dry pile step; when restarting the electric pile, the recycle gas must heats then through the pile to elevate the temperature, then heats the fuel gas and the oxidant of the gas source, through the weting of the wet exchanger enters to the calefactive pile, enhances the wet step of the film module in the pile, starts the power output of the pile.

本发明涉及一种氢电堆的防冻和重新启动时的处理方法，其特征在于处理过程包括：电堆停机时，将水蒸气不饱和的燃料气体或氮气，通过循环吹扫除去电堆的游离水；干燥其中的MEA膜组件，使膜组件含水量降低到规定低温下不结冰的程度；而后再令循环气体通过一个湿交换机将循环气体干燥，以及被干燥后的循环气体继续用来干燥电堆的步骤；在电堆重新启动时，须将循环气体加热后通过电堆，使电堆升温，然后再将气源的燃料气及氧化剂加热，通过湿交换机加湿后进入已升温的电堆，提高电堆中膜组件的湿度的步骤，开始电堆的功率输出。

All of these attested that there is CBF gene expression-regulated pathway and transcriptional cascade leading to the expression of cold-responsive genes under cold stress in Capsella bursa-pastoris, which ICE1 activate the expression of CBF by binding its promotor and CBF bind the DRE/CRT element in the promoter of the cold-regulated genes and activate transcription of them.

证明在荠菜中存在ICE1通过与CBF启动子部分相结合激活其表达，进而CBF又通过结合抗冻基因启动子部分带有的顺势式作用元件CRT/DRE从而促进抗冻基因表达，提高植物抗冻性的基因表达调控途径，及其它相关转录因子相互作用的级联机制。

The production performance of a gas reservoir idicates that the starting pressure phenomenon occurs in gas flow just as the one occurs in liquid flow and the gas "slippage effect" seems to be contradictious to its starting pressure, therefore it is very necessary to study the generation condition and change law of the both through testing.

实际气藏的生产特征反映出气体渗流与液体一样存在启动压力现象，而气体的&滑脱效应&似乎与气体的启动压力现象相矛盾，所以极有必要通过试验来研究气体二者现象产生的条件及变化规律。

Shop assistant: Please check at the door.

店员：请您到门口柜台交费。

In the end, transportation of PAHs in the environmental matrix was preliminarily investigated and discussed according to PAHs data of soils and sediments from a certain region in Shanghai. The result indicated that there are two or more pathways on PAHs transportation in the environmental matrix.

最后，对上海特定地区内PAHs在环境介质中的迁移径途进行了分析讨论，结果表明上海市土壤和沉积物等环境介质中PAHs的迁移存在多种途径。