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   人膀胱癌细胞系 的翻译结果: 查询用时:0.547秒
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人膀胱癌细胞系
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  human bladder cancer cell line
     Effects of PTEN Gene Transfection on Proliferation and Invasion of Human Bladder Cancer Cell Line BIU87
     PTEN基因转染对人膀胱癌细胞系BIU87增殖及侵袭活性的影响
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     Expression of MTS1 in Human Bladder Cancer and Inhibitory Effects of Wild-type MTS1 on Human Bladder Cancer Cell Line
     MTS1在膀胱癌中的表达及野生型MTS1对人膀胱癌细胞系生长抑制作用的研究
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     Objective To investigate the role of protein kinase C- alpha (PKCα) in regulating multidrug resistance (MDR) in human bladder cancer cell line T24.Methods Plasmid green fluorescent protein -PKCα (GFP/PKCα) carrying PKCα gene was transfected into a human T24 bladder cancer cell line.
     目的探讨蛋白激酶C-α(PKCα)对人膀胱癌T24细胞多药耐药的调节作用。 方法将载有PKCα基因的表达质粒GFP-PKCα导入人膀胱癌细胞系T24。
短句来源
     To study the resistance mechanism of human bladder cancer cell line, an adriamycin(ADM) resistance bladder cancer cell line, BIU 87/A and an etoposide (VP 16) resistance cell line, BIU 87/V were established by exposing the BIU 87 parent cells to a culture medium with a persistent increase of concentration of ADM or VP 16 respectively over a period of 10 months.
     为研究人膀胱癌细胞株耐药机制,应用阿霉素(ADM)、足叶乙甙(VP-16)低浓度持续递增法,在体外持续培养10个月,逐步诱导人膀胱癌细胞系BIU-87,获得具有多重抗药性的BIU-87/A、BIU-87/V细胞。
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     Cyclooxygenase Inhibitor Suppressed COX-2 Expression and Induced Apoptosis in Human Bladder Cancer Cell Line T24
     环氧化酶抑制剂诱导人膀胱癌细胞系T24凋亡作用研究
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  “人膀胱癌细胞系”译为未确定词的双语例句
     A human RT4 bladder cancer cell line stably expressing green fluorescent protein(GFP)-PKCα (RT4/PKCα) was established.
     应用人浅表膀胱癌细胞系RT4细胞,建立能够稳定表达PKCα绿色荧光蛋白(GFP)的人膀胱癌细胞系RT4/PKCαGFP。
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     Method:Morphological characteristics of T24 cell nucleus induced by SFN were observed by AO/EB fluorescein staining .
     方法:以人膀胱癌细胞系T24细胞为离体研究对象,通过AO/EB荧光染色观察SFN诱导T24细胞凋亡核形态改变;
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     Inhibition of human bladder tumor cell line EJ by adenovirus mediated over expression of human p27 KIP1
     Adp27~(KIP1)基因的过度表达对人膀胱癌细胞系EJ的抑制作用
短句来源
     Objective To investigate the influence of over expression of p27 KIP1 on the malignant phenotype of EJ human bladder carcinoma cell line.
     目的 探讨p27KIP1 的过度表达对人膀胱癌细胞系EJ的影响。
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     Effects of adenovirus intervening exterior p16 gene on human cell lines RT112 of carcinoma of urinary bladder
     腺病毒介导外源性p16基因对人膀胱癌细胞系RT112的作用
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  相似匹配句对
     CHROMOSOME STUDY ON A NEWLY ESTABLISHED HUMAN BLADDER CANCER CELL LINE BIU-87
     新建膀胱癌细胞BIU-87的染色体分析
短句来源
     Establishment and biological characteristics of a human bladder cancer cell line BC-6
     膀胱癌细胞BC-6的建立及其生物学特性
短句来源
     Establishment of a human bladder cancer cell line with multidrug resistance──BIU-87/ ADM
     膀胱癌BIU-87细胞多重抗药性的形成
短句来源
     KARYOTYPIC CHARACTERISTICS OF THREE NEW ESTABLISHED HUMAN BLADDER TRANSITIONAL CELL CARCINOMA LINES
     三株新建膀胱癌细胞染色体畸变特点
短句来源
     Application of Electroporation in Transducing Plasmid Plasmid DNA into Human Bladder
     电穿孔质粒DNA转染膀胱癌细胞的应用研究
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  human bladder cancer cell line
Preliminary study of the in vitro growth inhibition of human bladder cancer cell line BIU-87 by arsenic trioxide
      
The growth inhibition rates of human bladder cancer cell line BIU87 by various concentrations of As2O3 were detected by using MTT method.
      
Comparison of the cytotoxic activities of chemotherapeutic drugs using a human bladder cancer cell line
      
A human bladder cancer cell line was exposed to a range of concentrations of the four drugs commonly used to treat superficial bladder cancer (adriamycin, epodyl, mitomycin-c, thiotepa) for periods of 30, 60 and 120 min.
      
Drug sensitivity of the human bladder cancer cell line J-82 was assessed using monolayer, stem cell and [3H]thymidine incorporation assays.
      
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A newly established cell line, derived from human bladder carcinoma, was designated as BIU-87.Its chromosome G-banding karyotype and clinical implication were studed. The chromosome number ofthe BIU-87 was characterized as hetertetraploid. By analysing 100 mitosis cells, the modal count was101 and the structure was quite diffrent from that of normal cell. A total of 12 marker chromosomeswas discovered. Notably. the M 1 and M 2 marker chromosomes are related to No. 1 chromosome. Weconclude that it could be of...

A newly established cell line, derived from human bladder carcinoma, was designated as BIU-87.Its chromosome G-banding karyotype and clinical implication were studed. The chromosome number ofthe BIU-87 was characterized as hetertetraploid. By analysing 100 mitosis cells, the modal count was101 and the structure was quite diffrent from that of normal cell. A total of 12 marker chromosomeswas discovered. Notably. the M 1 and M 2 marker chromosomes are related to No. 1 chromosome. Weconclude that it could be of help to dignosis of bladder carcinoma. The presence of some doubleminute (DM) may imply the relationship between malignant cell and the oncogene.

新建的人膀胱癌细胞系命名为BIU-87,本文研究其染色体及其G带的变化及临床意义。BIU-87细胞有明显的超4倍体特点,分析100个中期细胞得出染色体众数平均为101条。染色体形态结构与正常细胞相比有很大不同,可检出12个异常的标记染色体。其中最为明显的M_1和M_2标记染色体都与1号染色体有关。这将有助于临床辅助诊断膀胱癌。双小体的存在提示了细胞癌变和癌基因变化之间的关系。

Based on the high level of human granulocyte—macrophage colony—stimulating factor(HGM—CSF)re-

本文应用人髓样白血病细胞系 HL60在了 DMSO 诱导下可表达高亲和力 HGM—CSF 受体的特点,建立了 HGM—CSF 生物学检测方法。结果表明:未经诱导的 HL60细胞对 HGM—CSF 只有很低的反应性,经 DMSO 诱导的 HL60细胞对 HGM—CSF 反应性明显增加,最适诱导时间为3~5天,检测时间为36小时,细胞密度以3~6×10~4/孔为宜,检测敏感性至少可达0.3ng/ml。TPA 和细胞因子 IL—1、IL—6、IL—8.均不能促进 DMSO 诱导的 HL60细胞对 HGM—CSF 的反应性。本文还应用此检则方法对人膀胱癌细胞系U5637培养上清中 GM—CSF 的生物学活性进行了检测。

The cDNA for human G-CSF was cloned from total RNA of human bladder carcinoma 5637 cells following PCR amplification. Sequencing data proved that the cloned cDNA contained the intact coding region of human G-CSF gene which was 612 bp in length, encoding 30 amino acids of signal peptide and 174 amino acids of the mature protein. One base mutation was found in the 43rd codon of the cDNA (CAC→TAC) resulting in the replacement of histidine by tyrosine. The gene products proved having G-CSF aetivity after its preliminary...

The cDNA for human G-CSF was cloned from total RNA of human bladder carcinoma 5637 cells following PCR amplification. Sequencing data proved that the cloned cDNA contained the intact coding region of human G-CSF gene which was 612 bp in length, encoding 30 amino acids of signal peptide and 174 amino acids of the mature protein. One base mutation was found in the 43rd codon of the cDNA (CAC→TAC) resulting in the replacement of histidine by tyrosine. The gene products proved having G-CSF aetivity after its preliminary expression in SP2/0 cells following retroviral transfer.

利用多聚酶链反应技术,从人膀胱癌细胞系5637细胞中快速扩增并克隆了人粒细胞集落刺激因子cDNA,序列分析证明,该cDNA包含人粒细胞集落刺激因子的全部编码基因,全长612bp,编码30个氨基酸的信号肽和174个氨基酸的成熟蛋白。其中第43位codon出现一个碱基的突变(CAC→TAC)导至第43位氨基酸的改变(组氨酸→酪氨酸)。经逆转录病毒导入SP2/0细胞并初步表达。结果表明:该基因产物具有G-CSF活性。

 
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