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白血病细胞     
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  leukemia cells
     Effects of Lovastatin on Leukemia Cells HL-60,KG-1,K562 in Vitro
     洛伐他汀对HL-60、KG-1、K562白血病细胞体外作用的研究
短句来源
     while the residual leukemia cells were not increased in one year, from 5.90±5.09 % before and 5.82±2.42% after treatment (P>0.05).
     而残留白血病细胞1年来未见增加[治疗前为(5.90±5.09)%,治疗后为(5.82±2.42)%,P>0.05];
短句来源
     Analysis of CD_(117) expression on leukemia cells
     CD_(117)在白血病细胞上的表达分析
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     Cloning and functional analysis of P2X7 receptor from J6-1 leukemia cells
     J6-1白血病细胞P2X7受体基因的克隆和功能初步分析
短句来源
     Expressions of MIP-1α,MCP-1 and Their Receptors CCR-1,CCR-2 in Chronic Myeloid Leukemia Cells
     趋化因子MIP-1α和MCP-1及其受体CCR-1和CCR-2在慢性髓系白血病细胞中的表达
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  leukemia cell
     The anticancer activity in vitro showed that Ⅱ_7, and Ⅲ_8 had the strongest inhibition and their IC_(50) against L1210 Leukemia cell were 3.910×10~(-3) μg/ml and 6.172×10~(-3) μg/ml.
     体外抗肿瘤活性以Ⅱ_7和Ⅳ_8最强,对L1210白血病细胞株的IC_(50)分别为3.910×10~(-3)μg/ml和6.172×10~(-3)μg/ml,与MTX相当。
短句来源
     Furthermore, a variety of leukemia cell lines including HEL, HL-60, K562, U937, DAMI, MEG-01, HUT78 and CA were found to express mRNAs for TGFβ_1 and its receptor.
     白血病细胞系(HEL、HL-60、K562、U937、DAMI、MEG-01、HUT78)及CA均表达TGFβ_1及其受体mRNA。
短句来源
     Objective:It is to investigate the effect of rhIL-13(recombinant human interleukine-13) on the differentiation of Dami cells,a megakaryocytic leukemia cell line, and the expression of IL-13Rα1(interleukine-13 receptor alpha 1)on Dami cells, and to elucidate the mechanism of IL-13-induced differentiation of Dami cells.
     目的:研究重组人白细胞介素13(recombinant human interleukine-13,rhIL-13)对巨核细胞白血病细胞株Dami细胞分化的影响,以及Dami细胞白细胞介素13受体α1(Interleukine-13receptor alpha1,IL-13Rα1)的表达,探讨IL-13诱导Dami细胞分化的机制。
短句来源
     After the treatment of leukemia cell line K562 and its multidrug-resistant cell line K562/A02 by thapsigargin, intracellular calcium concentrations ([Ca~ 2+]i) in K562 and K562/A02 were measured by fluorescence spectrophotometer with calcium sensitive fluorescence indicator Fura-2/AM;
     应用Ca2+荧光指示剂Fura2/AM通过荧光分光光度计测定白血病细胞系K562及其多药耐药细胞株K562/A02经thapsigargin作用前后细胞内Ca2+浓度([Ca2+]i)变化;
短句来源
     This study was designed to investigate the molecular mechanism of apoptosis and G2/M arrest in leukemia cell line HL-60 induced by proteasome inhibitor MG132 (Z-Leu-Leu-Leu-CHO).
     本研究旨在探讨蛋白酶体抑制剂MG132(Z-Leu-Leu-Leu-CHO)诱导白血病细胞HL-60凋亡和G2/M期阻滞的机制。
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  leukemic cells
     The Antisense Oligodeoxynucleotides of bcl-2 Oncogene Enhances the Sensitivity of K562 Leukemic Cells to As_2O_3
     bcl-2反义寡核苷酸增强K562白血病细胞对As_2O_3药物敏感性
短句来源
     Deficiency of TGF-β_1 in leukemic cells and the effects of exogenous TGF-β_1 gene on HL-60 cells
     白血病细胞TGF-β_1含量减少及外源性TGF-β_1基因对HL-60细胞的作用
短句来源
     Conclusions B lymphoblastic leukemic cells can be represented by CD10 + CD22 + CD45 -or ± cells.
     结论 CD10 + CD2 2 + CD45 -或± 表现型细胞代表了B细胞性白血病细胞
短句来源
     Expression of mRNA of TGF-beta,TNF-alpha and LIF in leukemic cells
     TGF-β、TNF-α和LIF mRNA在白血病细胞中的表达
短句来源
     Investigation of Purging Effect of CD3AK/iNOS on Leukemic Cells in Vitro
     CD3AK/iNOS细胞对白血病细胞体外净化的研究
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  leukemic cell
     The data Showed that when LAK: BMMNC: leukemic cell was 20 : 10 : 1, the colony formation of U937, HL60 and K562 were 1.21% ±2.10% , 1.56% ±1.65% and 0.26 ±0.19% of control resectively after 12 hours preincubation.
     结果显示,当LAK细胞:骨髓单个核细胞:白血病细胞为20:10:1,预孵育12小时,U937、HL60和K562集落生成分别为对照组之1.21%±2.10%,1.56%±1.65%和0.26%±0.19%。
短句来源
     Results The ligation efficiency detected in leukemic cell lines NB4U937K562SHI-1Jurkat was 10.6%~32.9% and 5.2%~20.0% in normal marrow or peripheral blood cells.
     结果 白血病细胞株NB4、U937、K5 6 2、SHI 1、Jurkat的连接能力为10 .6 %~32 .9% ,正常骨髓或外周血细胞的连接能力为5 .2 %~2 0 .0 %。
短句来源
     Conclusion AsI3-Tu can effectively induce the cell apoptosis of the leukemic cell line HL-60,the combined application of RNA and AsI3-Tu can enhance the action of AsI3-Tu.
     结论AsI3-Tu能有效诱导白血病细胞系HL-60细胞凋亡,RNA与AsI3-Tu联合应用能增强AsI3-Tu的作用。
短句来源
     Methods The difference was confirmed among four leukemic cell lines, NB4, HL60, K562, U937 , concerning their sensitivity to apoptosis induction by 2μmol/L of As2O3;
     方法 用2μmol/L As2O3作用于四种髓系来源的人白血病细胞株(NB4、HL60、K562、U937),证实As2O3促凋亡敏感性在四种细胞之间的差异。
短句来源
     Study on the Functional Expression of P2X_7 Receptor in Human Leukemic Cell Line KG1a
     人白血病细胞系KG1a中P2X_7受体的表达和功能研究
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  leukemia cells
To investigate the expression of JWA after hemin and (or) thermal stress exposure, we treated K562 (chronic myelogenous leukemia cells) cells with different doses of hemin and thermal stress using different exposure times.
      
The seven-day leukemia cells feature lower proliferative potential and higher sensitivity to oxidative stress and platidiam.
      
Apoptosis in P388 Leukemia Cells Induced by Specific Inhibitors of 5- and 12-Lipoxygenase and the Product of Cyclooxygenase, Pro
      
We studied the effect of specific inhibitors of 5- and 12-lipoxygenases as well as the product of cyclooxygenase activity, prostaglandin E2?, on proliferation and death of P388 leukemia cells.
      
The cytotoxins were considerably different in cytotoxicity and cooperativity of the effect on human promyelocytic leukemia cells HL60, mouse myelomonocytic cells WEHI-3, and human erythroleukemic cells K562.
      
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  leukemia cell
HLDF has been isolated from the culture medium of human promyelocytic leukemia cell line HL-60.
      
It was shown that the full-size neurotrophic factor from pigment epithelium (PEDF) induces the cell differentiation of the human promyelocyte leukemia cell line HL-60.
      
Liposomal formulation of a methotrexate diglyceride conjugate: Activity toward a culture of methotrexate-resistant leukemia cell
      
The results of the biologic tests of the complexes of arsenic show that the biologic effect of these complexes of arsenic to leukemia cell (HL-60) is higher than arsenic only by MTT colorimetric assay.
      
In autodigestion assays, endonucleaw activity in non-apoptotic HL-60 promydocytic leukemia cell nuclei cleaved the chromatin of he autologous cells to an oligonucleosomal length pattern.
      
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  leukemic cells
Effects of mycelial fungus (Pleurotes ostreatus) extracts used separately and in combination with the cytostatic drugs doxorubicine and cyclophosphamide on cultured transformed human cells (HeLa and myeloid leukemic cells) were investigated.
      
Effects of inhibition of ubiquitin-proteasome pathway on human primary leukemic cells
      
Though there were a lot of reports about the totally different responses to the inhibition of ubiquitin-proteasome pathway in different kinds of cell lines, much less has been known about the responses in primary human leukemic cells.
      
Various tolerances to arsenic trioxide between human cortical neurons and leukemic cells
      
Homoharringtonine (HHT) has currently been used successfully in the treatment of acute and chronic myeloid leukemias and has been shown to induce apoptosis of different types of leukemic cells in vitro.
      
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  leukemic cell
Membrane bound macrophage colony-stimulating factor (m-M-CSF) and its receptor (M-CSF-R) were shown in human leukemic cell line J6-1 as autojuxtacrine mechanism.
      
We investigated the anti-angiogenesis potential of HHT with the human umbilical vein endothelial cell line (ECV304) and leukemic cell line (K562) in vitro.
      
EPR study of the effect, induced by zidovudine (AZT), on the membrane lipid dynamics in leukemic cell
      
In the present study, the sensitivity to photodynamic inactivation of 3 leukemic cell lines was compared with their counterpart normal hematopoietic cells.
      
Characterization of a human herpes virus-6 (HHV-6) and epstein-barr virus (EBV) associated leukemic cell line, J6-1
      
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