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group rate相关的网络例句

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Results:There was no significant difference among A,B,C group in the terms of the incision,abdominal and pulmonic infection incidence rate,but there was significant difference in terms of the pollution rate of incision and abdominal cavity and the operation time.

结果:LC术后切口、腹部、肺部感染发生率,A、B、C各组之间差异无统计学意义,但术中切口、腹腔污染及手术时间差异有统计学意义。

Results:There was no significant difference among A,B,C group in the terms of the incision,abdominal and pulmonic infection incidence rate,but there was significant difference in terms of the pollution rate of incision and abdominal cavity and the operation time.

具有以下因素之一者不列为本组研究对象:急性胆囊炎,术前有黄疸,糖尿病,免疫缺陷性疾病,术前长期服用激素类药物,有慢性呼吸道疾病史,术前3周内胆囊炎急性发作,孕妇肝硬化肝功能失代偿期。

The adipose derived stem cells of inbreds train of rat wereinduced to differentiate into schwann-like cells and the cells were injectedinto the acellular nerve allograff.The proliferation or adhersion of these cells on the graft were observed by inverted microscope or ScanningElectronic Microscope. Activity of cells were detected using MTT. 10mmnerve gap of inbreds train of rats in two group were bridged by tissue-engineered peripheral nerve or autogenous nerve, the effect wereappraised by naked eye, recovery rate of sciatic function index,nerve-electrophysiological, histology, Transmission ElectronMicroscopy and quantitative analysis of recovery rate of myelinated fiberpopulations,diameter of myelinated fiber and thickness of myelin sheat.

按照前述方法培养并诱导近交系大鼠脂肪干细胞向类Sehwann分化,将诱导分化的脂肪干细胞悬液注入已制备的去细胞同种异体神经支架管中,倒置显微镜观察细胞生长情况;扫描电镜下观察细胞在材料上附着情况;四唑盐比色试验测定细胞活性;取两组近交系大鼠,分别用组织工程化神经和自体神经桥接10mm神经缺损,通过大体观察、坐骨神经功能指数恢复率的测定、神经电生理的测定、组织学光镜观察、透射电镜观察、再生有髓神经纤维计数恢复率、神经纤维直径恢复率、髓鞘厚度恢复率的测定等指标评价实验效果。

The overall response rate, the incidence of sequela (cerebral infarction and supranuclear paralysis) and the death rate were analyzed between two griups. Results Compared with Group A, the use of minitrauma and Nimotop resulted in higher response rates 89.7% Versus 52.4%.

对29例脑出血、继发性脑室出血应用尼莫通微创治疗,另有对照组21例单纯应用脱水降颅压、止血剂、控制血压和防止感染等,比较两组临床疗效、后遗症及死亡率。

Result:In the ATRA treatment group, the tumor growth rate was decreased, tumor doubling time was prolonged and tumor inhibitation rate was inereased. Although there was not any significant difference among three groups under light microscope, differentiation and many apoptosis of carcinoma cells were observed under transmissional election microscope.

结果:经ATRA处理后,肿瘤生长速率减慢,倍增时间延长和抑瘤率增高,光镜下治疗组和对照组未见明显变化,透射电镜下可见肿瘤细胞产生一定的分化,出现较多的凋亡细胞。

ANP and CX43 began to express at 2nd week after induction and increased gradually,about 60% of the resulting myogenic cells were positive at 4th week after induction ,they were negative for uninduced cells.hMSCs'surface antigen profiles obtained by Flow Cytometry were negative for CD31\CD34\CD45 before and after induction,but CD90 expressed higher after induction while was weak positive before induction(P.05). Apotosis index was correlated with the cultural time after induction,The apoptosis rate of induced hMSCs was remarkably higher than control group(P.01),and the variation between groups was notable(P.05),the cell cycle analysis showed that the percentages of G_0/G_1phases were reduced significantly after induction. The expresstion levels ofβ-MHC and CTNT mRNA were undetectable before induction,began to increase at 1st、4th week after induction,reached the peak at 6th week and decreased after that,the expression of Bcl-2 and Bax mRNA varied regularly after treated with 5-azacytidine. hMSCs'resting membrane potential、range and rate of depolarization were heightened gradually after being induced.

结果:hMSCs诱导前为纺锤形,诱导后第2天部分细胞即开始发生形变,呈球形或短棒状,1周后胞浆中颗粒增多,约20~30%细胞边缘呈毛刷样变化;hMSCs表面抗原CD31、CD34、CD45在诱导前后差异无统计学意义,CD90未诱导时表达呈弱阳性,诱导后明显增高(P.05);ANP和CX43在诱导前无表达,诱导后第2周开始表达且表达随时间逐渐增强,但CX43在诱导后第5周表达量开始降低。hMSCs诱导后凋亡指数随诱导后培养时间增加,低浓度诱导组低于标准浓度诱导组,组间差异有统计学意义(P.05),G_0/G_1期细胞比例诱导后较对照组显著减少(P.05);β-MHC和CTNT基因分别在诱导后第1周和第4周时表达开始增强,在第6周时均达到高峰,第8周时表达开始衰减,Bcl-2、Bax基因表达呈时间依赖性变化,hMSCs经诱导后随心肌样细胞特征的表达膜静息电位、去极化幅值和去极化速率逐渐增高。

Of CBMC can be purified by Mini-MACS as CD34〓 stem cells. B. The number of CD34〓 stem cells can expand to 40.24±9. 86 fold after 14 days. C. No matter in the expression of CD1a, CD80, CD86, and HLA-DR, or in the function of stimulating xenogenous lymphocyte proliferation, there was no difference between CD34+ stem cell DCs or monocyte DCs. D. The percentage of CD3〓CD56〓 cells is the same in CIK cells co-culture with DCs transfected with SKOV3 RNA, CIK cells co-culture with DCs, and CIK cells. E. The expansion rate of CIK cells can be accelerated by co-culturing with loaded or unloaded DCs. However, the expansion rate between loaded or unloaded group is the same. F. The strongest cytotoxicity against SKOV3 cell line was achieved by CIK cells co-cultured with DCs loaded with SKOV3 RNA.

结果:1、Mini-MACS分选系统可自CBMC中提取0.78±0.31%的CD34〓细胞;2、体外培养14天后可获得原始CD34〓细胞量40.24±9.86倍的细胞;3、不论在CD1a、CD80、CD86及HLA-DR的表达上,或是刺激异体淋巴细胞增生的功能上,脐带血CD34〓细胞与单核细胞来源的DC都没有差别;4、CIK细胞中CD3〓CD56〓双阳性的表达率在与RNA转染DC共培养的CIK细胞组、与DC共培养的CIK细胞组及单纯CIK细胞组3组间比较无差异;5、脐带血CIK细胞增殖显著,培养14天时可扩增18.18±5.59倍,培养21天时可扩增35.02±6.30倍;5、与未转染或转染DC共培养的CIK细胞在培养第14天后增殖速率大于单纯CIK细胞。

D. The function of stimulating xenogenous lymphocyte proliferation was the same between peripheral DCs and ascites PCs. E. The percentage of CD3〓CD56〓 cells was the same in CIK cells co-culture with DCs transfected with SKOV3 RNA, CIK cells co-culture with DCs, and CIK cells. F. The expansion rate of CIK cells can be accelerated by co-culturing with loaded or unloaded DCs. However, the expansion rate between loaded or unloaded group is the same. F. The strongest cytotoxicity against SKOV3 cell line was achieved by CIK cells co-cultured with DCs loaded with SKOV3 lysate.

结果:1、腹水可获得0.83±0.24×10〓个AMC/ml,单核细胞有0.74±0.25×10〓个/ml;2、卵巢癌患者外周血可获得0.87±0.20×10〓个AMC/ml,单核细胞有0.92±0.17×10〓个/ml;3、除CD86外周血单核细胞来源DC表达较高以外,其他表面分子在不同来源DC间没有统计学差异;4、不同来源DC的异基因刺激能力没有差异;5、与负载或未负载卵巢癌抗原的DC共培养并不能提高CIK细胞群中CD3〓CD56〓细胞的数量;6、CIK细胞增殖显著,培养14天时可扩增19.18±4.70倍,培养21天时可扩增35.82±4.36倍;7、与未负载或负载DC共培养的CIK细胞在培养第14天后增殖速率大于单纯CIK细胞。

Cell embryos were cultured in vitro, then viability was observed. The results showed the fertilizing rate in vitro of the group for GV oocytes with cumulus cells after maturating which were conserved at 10℃ for 24 h, 15℃ for 14 h, 20℃ for 8 h and 25℃ for 4 h was 14%, 9%, 10% and 10% respectively, and with the advance of storage temperature and extension of storage time, the rate of 2-cell after maturating-fertilizating of the GV oocytes decreased significantly.

其结果,在10℃下保存24h、15℃下保存14h、20℃下保存8h和25℃下保存4h后,其体内附有卵丘细胞的GV卵的体外成熟-体外受精后的2细胞率分别为14%、9%、10%和10%,随着保存温度的提高和保存时间的延长,带有颗粒细胞GV期卵的比率明显降低,同时其GV期卵经体外成熟及体外受精后的2细胞率明显降低。

More assimilation products were stored in sheathes than those in leaves. 2After rewaterring, net photosynthetic rate and evaporation rate came back quickly, especially D3 and D6 groups whose two photosynthetic indexes were higher than that of control group and then droped back to normal in serveral days.

同化产物在叶片中的含量高于茎鞘,但叶片中的氮素含量低于茎鞘。2恢复灌溉后,受到胁迫的处理组的光合速率、蒸腾速率都迅速升高,干旱3 d和6 d的处理组光合水平超过对照,然后又有所下降,水分利用效率因为蒸腾速率的骤然升高而降低,之后有所恢复。

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