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死亡细胞
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  dead cells
     The numbers of dead cells in control group and puerarin group were found to be significantly larger than that in normal group(P<0.01) through HE sections, with the number in control group being greater than that in puerarin group(P<0.01).
     HE切片中,对照组和葛根素组死亡细胞数均明显多于正常组(P<0.01),且对照组明显多于葛根素组(P<0.01)。
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     The morphorlogy of PC12 cells were observed under the fluoromi-croscope dyed by acridine orange/ethidium bromide(AO/EB),and the intact cells were green while the damaged or dead cells were orange even red.
     PC12细胞的形态学改变通过荧光显微镜观察(acrid ine orange/eth id ium brom ide染色,AO/EB),完整无损的PC12细胞呈绿色,受损或死亡细胞呈橘黄色和红色。
短句来源
     In the group treated with42mJ/cm 2 UVB irradiation followed by the addition of EGCG,the numbers of apoptotic and dead cells and Fas mRNA were decreased,but bcl-2protein was increased.
     UVB辐照42mJ/cm2立即加入EGCG组较辐照42mJ/cm2未加EGCG组凋亡和死亡细胞数降低(t=7.64,P<0.01;t=3.49,P<0.05),bcl-2增加(t=3.62,P<0.05),FasmRNA表达量减少(t=6.83,P<0.01)。
短句来源
     Results: Numerous round cells, shrinkage of cellular membrane and dead cells were observed 48 hours after 2 μg/ml of TNP_470 was added into the GNM cellular suspension.
     结果 :TNP_4 70 (2 μg/ml)作用于GNM细胞 4 8h ,大量细胞变圆、细胞膜皱缩 ,并出现较多悬浮死亡细胞
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     After treatment of HMME, the dead cells were predominantly necrosis cells.
     流式细胞仪分析结果显示HMME光动力学处理后死亡细胞主要为坏死细胞。
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  “死亡细胞”译为未确定词的双语例句
     dead cell percentage: Group A(1.5±0.6)% and Group B(0.3±0.1)%.
     死亡细胞百分比:A组(1.5±0.6)%,B组(0.3±0.1)%。
短句来源
     The OECs in pH 7.4 group showed productive growth condition, whereas the proliferation of the OECs were suppressed in pH 6.8 and pH 7.0 groups with many necrotic OECs.
     pH7.4组OECs生长旺盛,pH6.8组及pH7.0组OECs生长增殖受到不同程度的抑制,出现死亡细胞;
短句来源
     Furthermore,the incidence of severe apoptotic cells was 0 36±0 09 and 0 12±0 08 at 4 and 24 hours following reperfusion respectively,and the difference was significant ( P <0 01).
     再灌注24小时,重度程序性死亡细胞率为0.12±0.08,与再灌注4小时(0.36±0.09)比较有极显著性差异(P<0.01)。
短句来源
     Expression and distribution of topoisomeraseⅡ in apoptotic cells
     DNA拓扑异构酶Ⅱ在扁桃体程序性死亡细胞中的表达及分布
短句来源
     After adding 1mmol/L of Glu for 2 hours in control group,the survival rate of cells was 44.23%,and the dead cell and non-viable apoptotic rates of cells were 24.90% and 21.63%,respectively.
     用1mmol/L的谷氨酸干预细胞2h后,活细胞比例降为44·23%,而晚期凋亡细胞和死亡细胞分别增为24·90%和21·63%。
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  相似匹配句对
     Mitotic Cell Death
     有丝分裂细胞死亡
短句来源
     Programmed Death in Plant Cell
     高等植物的细胞程序性死亡
短句来源
     MEET DEATH
     遇见“死亡
短句来源
     b) death and funeral;
     b)死亡和葬礼;
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     Tom Clancys Splinter Cell
     细胞分裂
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  dead cells
However, soluble amyloid oligomers of lysozyme caused death of all these cell types, as estimated by flow-cytometry counting dead cells stained with ethidium bromide.
      
Deletion of the gene encoding the cell-wall glucanotransferase Bgl2p in Saccharomyces cerevisiae decreases the number of dead cells in the yeast culture incubated in a liquid nutrient medium for more than two days.
      
The dead cells trigger a complex multicomponent process of wound healing expressed as further proliferation of living tumor cells, angiogenesis, stimulation of cell migration, and other events.
      
Staining with fluorescein diacetate helps distinguish between living and dead cells and also predicts the physiological state of the unicellular alga.
      
Under the type I and type II cells, are a relatively thick layer of secreting material and a layer of mostly dead cells.
      
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The effects of carboxymethyl modified hemicellulose (CMMH) on the growth of the human gastric tubular glandular carcinomatous cell line "NGCC-8310" in vitro were investigated. Although the results showed that the cell growth curve, dead cell enumeration and cell division index of the cells cultured in the medium containing CMMH were essentially the same as compared with those of the controls, changes had been demonstrated by cytochemical studies. It revealed that the activities of the alkaline phosphatase and...

The effects of carboxymethyl modified hemicellulose (CMMH) on the growth of the human gastric tubular glandular carcinomatous cell line "NGCC-8310" in vitro were investigated. Although the results showed that the cell growth curve, dead cell enumeration and cell division index of the cells cultured in the medium containing CMMH were essentially the same as compared with those of the controls, changes had been demonstrated by cytochemical studies. It revealed that the activities of the alkaline phosphatase and acid non-specific esterase were suppressed, and the polysaeeharide content was diminished. In contrast,the activities of the acid phosphatase were enhanced. These suggest that the metabolism of the carcinomatous cells are interfered to some extent after contact with CMMH.

本文研究了CMMH对NGCC-8310的生长和代谢的影响。结果对照组、低浓度组和高浓度组三组间细胞生长曲线、死亡细胞计数和细胞分裂指数都无明显差别(P>0.05)。但细胞的酸性磷酸酶活性增强,硷性磷酸酶、酸性非特异性酯酶活性和糖原含量下降。说明CMMH虽然对NGCC-8310的生长无明显影响,但给药组细胞的代谢已发生一些改变。

This is a report on a research project in which the living cell culture techniquewas employed to observe the effect of the out-aura of Qigong treatment on themalignant cells (LA-795). It was demonstrated that after treatment the malignant cellshad been markedly destroyed or injured in compare with those in the control groups(P<0.01).Meanwhile, the normal cells with the same treatment remained intact.It was shown that the out-aura of Qigong could affect and kill malignant cells,but without harm to normal cells....

This is a report on a research project in which the living cell culture techniquewas employed to observe the effect of the out-aura of Qigong treatment on themalignant cells (LA-795). It was demonstrated that after treatment the malignant cellshad been markedly destroyed or injured in compare with those in the control groups(P<0.01).Meanwhile, the normal cells with the same treatment remained intact.It was shown that the out-aura of Qigong could affect and kill malignant cells,but without harm to normal cells.

本文应用现代细胞培养技术,研究气功外气对传代培养癌细胞(LA-795)及正常细胞(L-929)的作用。气功师用剑指在克氏培养瓶上5~10cm 处,发外气仅5或8秒钟后送回培养室继续传代培养,24小时及48小时用肉眼,倒置相差显微镜及用台盼蓝抗染法观察及计数存活与死亡细胞,并用统计学处理。结果表明发功后48小时时气功外气对癌细胞有明显的杀伤效应(P<0.01)。而对同样处置下的正常细胞无损伤。

Apoptosis is the most common form of cell death in physiological condition,and is an active reac- tion of cells to surrounding signals. There are a series of specific morphological and biochemical events in theprocess. Some genes are expressed in cells undergoing apoptosis or their modulation affects the process. FCM is an important technique for quantitative analysis of apoptosis. To induce apoptosis can open newstrategies for improving cancer chemotherapy. Early detection of apoptosis cells in clinical patient...

Apoptosis is the most common form of cell death in physiological condition,and is an active reac- tion of cells to surrounding signals. There are a series of specific morphological and biochemical events in theprocess. Some genes are expressed in cells undergoing apoptosis or their modulation affects the process. FCM is an important technique for quantitative analysis of apoptosis. To induce apoptosis can open newstrategies for improving cancer chemotherapy. Early detection of apoptosis cells in clinical patient tumorswould be of great value to predict the outcome of treatment protocols.

程序性细胞死亡是细胞生理性死亡最常见的形式,是细胞对其周围环境信号的主动反应。在此过程中细胞发生一系列特征性的变化,一些基因表达参与或调控此过程。FCM是检测研究程序性细胞死亡的重要手段。诱导肿瘤细胞发生程序性死亡是肿瘤治疗的新途径。程序性细胞死亡的检测对肿瘤治疗研究及其临床疗效判断都有其应用前景。

 
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