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凋亡
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  apoptosis
    THE STUDY ON AUTOPHAGIC APOPTOSIS INDUCED BY VINCRISTINE IN HUMAN LIVER CELL LINE L02
    长春新碱诱导人肝细胞系L02细胞自噬性凋亡的研究
短句来源
    Molecuar Dissection of Relationship Between Autophagy and Apoptosis
    自噬与凋亡分子水平相关关系的探讨
短句来源
    The Action of IL-12 Inducing T Lymphocyte Apoptosis and Effect on Graft-Versus-Host Disease.
    白介素12对T淋巴细胞的凋亡诱导作用及对移植物抗宿主病的影响
短句来源
    Effects of DNA Damage on Cell Cycle and Apoptosis of Mammalian Cells
    DNA 损伤对哺乳动物细胞周期和凋亡的影响
短句来源
    Effects of Tripchlorolide on Proliferation and Apoptosis of Mammalian Cells
    雷公藤氯内酯醇对哺乳动物细胞周期和凋亡的影响
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  and apoptosis
    Molecuar Dissection of Relationship Between Autophagy and Apoptosis
    自噬与凋亡分子水平相关关系的探讨
短句来源
    Effects of DNA Damage on Cell Cycle and Apoptosis of Mammalian Cells
    DNA 损伤对哺乳动物细胞周期和凋亡的影响
短句来源
    Effects of Tripchlorolide on Proliferation and Apoptosis of Mammalian Cells
    雷公藤氯内酯醇对哺乳动物细胞周期和凋亡的影响
短句来源
    Study on the Molecular Mechanism of P2X7 Receptor Mediates Activation and Apoptosis in Human HEK293 Cells
    P2X7受体介导的HEK293细胞活化与凋亡机理研究
短句来源
    Regulation of Proliferation and Apoptosis of Smooth Muscle Cell in Atherosclerosis
    动脉硬化平滑肌细胞增殖和凋亡及其调节
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  “凋亡”译为未确定词的双语例句
    Roles of Apoptosis-inducing Ligands and, Th1/Th2 Like Subsets in Pathological Injury in the Patients with Hemorrhagic Fever with Renal Syndrome
    凋亡诱导配体及Th1/Th2样细胞亚群在HFRS免疫病理损伤中的作用
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    Studyonproapoptoticeffectofaribozymeagainstbcl┐2onHL┐60celsZhao
    抗bcl-2核酶在HL-60细胞中的表达及促进其凋亡的研究
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    CHARACTERIZATION OF A CELL SURFACE MOLECULE RECOGNIZED BY PF18-3, AN APOPTOSIS-INHIBITING MONOCLONAL ANTIBODY TO MOUSE THYMIC STROMAL CELL LINES
    小鼠胸腺基质细胞单抗PF18-3的凋亡抑制作用及其识别分子的特征分析
短句来源
    Objective: To investigate the pro-apoptotic effect of Her 2-targeted recombinant caspase-6 fusion protein on osteosarcoma SOSP-9607 cells.
    目的:探讨Her2靶向重组的caspase-6融合蛋白对骨肉瘤SOSP-9607细胞的促凋亡作用。
短句来源
    Objective:To construct 3 eukaryotic expression vectors of short hairpin RNA(shRNA) against livin gene and then transfect into HCT-8/V cells,and to pave the way to research that gene-silencing of livin in HCT-8/V on trait of vincristine resistance.
    目的:构建3个针对凋亡蛋白抑制因子livin基因mRNA的小干扰RNA(siRNA)表达载体,然后转染HCT-8/V细胞。 为研究livin基因沉默对HCT-8/V细胞耐长春新碱特性的影响奠定基础。
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  apoptosis
Prodigiosin also could induce apoptosis of pancreatic cancer cells at low concentration and results in the fragmentation pattern of DNA.
      
All these results demonstrate that prodigiosin can obviously inhibit the proliferation of pancreatic cancer cells H8898 by arresting the cell cycle and inducing apoptosis.
      
Detection of the apoptosis of Jurkat cell using an electrorotation chip
      
The apoptosis of cells is one of the fields that attract increasing attention in biology today.
      
Usually, the cells are treated with chemicals when detecting apoptosis.
      
更多          
  and apoptosis
Cell cycle control and apoptosis were analyzed by flow cytometry.
      
Relationship between expression of hepatocyte grow factor and apoptosis of trophoblasts in hypertensive disorder complicating pr
      
It needs to be further verified whether microgranulomas, lipogranulomas and apoptosis bodies could be used as histopathological markers of development of NAFLD.
      
The Causes of Necrobiosis and Apoptosis of Cornea Epithelial Cells during Primary Acquired Keratoconus Cornea
      
Effect of Bilirubin on Lipid Peroxidation, Sphingomyelinase Activity, and Apoptosis Induced by Sphingosine and UV Irradiation
      
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The present paper described the radiation effect of EL一4 on the cell cycle

采用流式细胞术(FCM)研究了0.5、1、2、4GyX射线照射后,小鼠淋巴瘤细胞EL一4的凋亡与细胞周期的剂量效应关系。结果表明:以上剂量照射后24h,G1期细胞呈剂量依赖性增加,出现明显的G1阻滞;而S期细胞则剂量依赖性减少;G2期出现明显的G2阻滞;细胞凋亡亦呈剂量依赖性增力。该结果提示:EL一4细胞经较高剂量x射线照射后,出现明显的DNA合成抑制和G2阻滞,致使EL一4细胞的有丝分裂延迟。统计分析表明:G1阻滞与细胞凋亡高度相关r=0.91。

Programmed cell death(PCD), or apoptosis, is a conceptuallydifferent way of cell death from necrosis. PCD plays an important role in immunologic regulation. PCD in thymocytes was analyzed by flow cytometry following invitro X-irradiation. It was found that culturing of thymocytes could induce PCDwhich showed a time dependent increase. Four hours after culturing, 16% of thymocytes was found in the Ac region (PCD is shown in the Ao region of the histogram of flow cytometry). PCD in thymocytes showed a time dependent...

Programmed cell death(PCD), or apoptosis, is a conceptuallydifferent way of cell death from necrosis. PCD plays an important role in immunologic regulation. PCD in thymocytes was analyzed by flow cytometry following invitro X-irradiation. It was found that culturing of thymocytes could induce PCDwhich showed a time dependent increase. Four hours after culturing, 16% of thymocytes was found in the Ac region (PCD is shown in the Ao region of the histogram of flow cytometry). PCD in thymocytes showed a time dependent increaseafter 2.0 Gy X-irradiation, being significantly higher than that in the control atthe same culturing time. 24 hours after X-irradiation in vitro, it was found thatwith doses below 100 mGy PCD was not significantly differrent from the controlat the same culturing time. but when the doses were above 100 mGy, PCD showeda dose dependent increase, being significantly higher than that of the control atthe same culturing time. These tesults are important in the understanding of thebiological effects of low dose radiation.

用流式细胞计数仪检测不同辐射剂量诱导的小鼠胸腺细胞程序性死亡苏旭,张迎春,刘树铮(白求恩医科大学卫生部放射生物实验室,长春130021)关键词程序性细胞死亡,流式细胞术,胸腺细胞,X射线自Wyllie等’‘’对程序性细胞死亡(PCD),又名细胞凋亡(...

Cell death is currently divided into two catogories,apoptosis necrosis. We investigated DNA strand breaks(DSB)in apoptotic and necrotic cells by gel electrophoresis and labeling of extracted DNA by nonradioactive nick translation and TdT tailing reaction,As models of apoptosis and necrosis,rat thymus with an i.p.injection of hydrocortisone(10 mg/100g BW)and rat livers treated with CCl4(1 00μl/1 00 g BW)were used respectively. The DNA from the hydrocortisontreated thymus revealed a typical ladder from of DNA...

Cell death is currently divided into two catogories,apoptosis necrosis. We investigated DNA strand breaks(DSB)in apoptotic and necrotic cells by gel electrophoresis and labeling of extracted DNA by nonradioactive nick translation and TdT tailing reaction,As models of apoptosis and necrosis,rat thymus with an i.p.injection of hydrocortisone(10 mg/100g BW)and rat livers treated with CCl4(1 00μl/1 00 g BW)were used respectively. The DNA from the hydrocortisontreated thymus revealed a typical ladder from of DNA fragments in gel electrophoresis,When the same amount of DNA from the CCl4-treated liver was analyzed by gel electrophoresis,nonregular pattern of banding was detected.The labeling density of the extracted DNAs by nick translation was at the same level,while the DNA from the necrotic tissue was labeled by TdT was much denser than that of from the apoptotic tissue.These results indicate that 1.Although DSB occured both in apoptosis and in necrosis,the types of DSB was different;2.DSB in apoptosis is oligonucleosomal fragments and DSB in necrosis was non regular fragments;3.DSB occured more frequently or more densely in necrotic cells than that of in apoptotic cells.

用琼脂糖凝胶电泳法、非放射性缺口翻译标记法(nicktranslation,NT)和末端脱氧核苷酸转移酶(terminaldeoxynucleotidyltransferase,TdT)标记法研究细胞凋亡(apoptosis)和坏死时细胞总DNA的DNA断裂(DNAstrandbreaks,DSB)状态。细胞凋亡标本取自皮下注射氢化可的松(10mg/100g体重)的大鼠胸腺;坏死标本采用CCl_4(100μ1/100g体重)的大鼠肝脏。结果表明:经激素处理的胸腺组织DNA在琼脂糖凝胶电泳呈现清晰、规则的“梯子”状(ladder)带纹,而CCl_4处理后的肝脏组织DNA则呈现不规则的带纹。缺口翻译标记时,凋亡和坏死组织的DNA显色无差别,但TdT末端标记时,坏死组织的DNA显色较凋亡组织的DNA显色速度快,着色深。以上结果提示:1.细胞凋亡和坏死时均存在DSB,但DSB类型不同。2.凋亡时DNA降解成寡聚核小体而出现规则的“ladder”,坏死时DNA降解成长短不等的片段。3.TdT末端标记法显示,细胞凋亡DSB显色特性不同于坏...

用琼脂糖凝胶电泳法、非放射性缺口翻译标记法(nicktranslation,NT)和末端脱氧核苷酸转移酶(terminaldeoxynucleotidyltransferase,TdT)标记法研究细胞凋亡(apoptosis)和坏死时细胞总DNA的DNA断裂(DNAstrandbreaks,DSB)状态。细胞凋亡标本取自皮下注射氢化可的松(10mg/100g体重)的大鼠胸腺;坏死标本采用CCl_4(100μ1/100g体重)的大鼠肝脏。结果表明:经激素处理的胸腺组织DNA在琼脂糖凝胶电泳呈现清晰、规则的“梯子”状(ladder)带纹,而CCl_4处理后的肝脏组织DNA则呈现不规则的带纹。缺口翻译标记时,凋亡和坏死组织的DNA显色无差别,但TdT末端标记时,坏死组织的DNA显色较凋亡组织的DNA显色速度快,着色深。以上结果提示:1.细胞凋亡和坏死时均存在DSB,但DSB类型不同。2.凋亡时DNA降解成寡聚核小体而出现规则的“ladder”,坏死时DNA降解成长短不等的片段。3.TdT末端标记法显示,细胞凋亡DSB显色特性不同于坏死。

 
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