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   膀胱癌细胞 在 泌尿科学 分类中 的翻译结果: 查询用时:0.079秒
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膀胱癌细胞     
相关语句
  bladder cancer cell
    Expression of Human Telomerase Reverse Transcriptase Gene (hTERT) in Bladder Cancer and Reversal of the Malignant Phenotype of Bladder Cancer Cell Line T24 by the Antisense Gene Therapy Targeted Against Telomerase
    端粒酶逆转录酶基因hTERT在膀胱癌组织中的表达及端粒酶反义基因治疗逆转T24膀胱癌细胞恶性表型的研究
短句来源
    Study of Photodynamic Inhibitory Action on Human Bladder Cancer Cell Lines BIU-87 with BPD-MA and Its Mechanisms
    BPD-MA对人膀胱癌细胞株BIU-87光动力抑制作用及其机制研究
短句来源
    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
短句来源
    Inhibitory effects of c-Ha-ras antisence oligodeoxynucleotide on the human bladder cancer cell line
    c-Ha-ras反义寡聚脱氧核苷酸对人膀胱癌细胞生长增殖的抑制作用
短句来源
    MECHANISM OF RESISTANCE TO MITOMYCIN C IN a HUMAN BLADDER CANCER CELL
    人体膀胱癌细胞对丝裂霉素耐药机制的研究
短句来源
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  bladder cancer cells
    Antisense Inhibition of COX-2 and NSAIDs Reduce Malignant Phenotype of Bladder Cancer Cells
    COX-2反义RNA与NSAIDs抑制膀胱癌细胞恶性表型的实验研究
短句来源
    Transfection of wild-type p53 gene and growth of bladder cancer cells
    野生型p53基因导入对膀胱癌细胞生长抑制和H-ras基因表达调控
短句来源
    Objective:To investigate the influence of trichostatin A(TSA),a histone deacetylase(HDAC) inhibitor,on the growth of human bladder cancer cells and on the expression of related genes,and to explore the mechanism involved.
    目的:观察组蛋白去乙酰化酶(HDAC)抑制剂曲古霉素A(TSA)对体外培养膀胱癌细胞生长情况及相关基因表达的影响,并探讨其可能的作用机制。
短句来源
    Influence of Fibronectin gene transfection on BCG adherence to bladder cancer cells
    纤维粘连蛋白的导入对BCG与膀胱癌细胞粘附的影响
短句来源
    Experimental Study on High Focused Ultrasound in the Treatment of Bladder Cancer Cells and Vx2 Rabbit Kideny Tumors
    高强度聚焦超声对膀胱癌细胞及兔移植性肾肿瘤的实验研究
短句来源
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  bladder carcinoma cells
    The Study of Tumor Suppression Function of RB1 Gene in Human Bladder Carcinoma Cells in Vitro
    RB_1抑癌基因对人膀胱癌细胞抑癌作用的体外研究
短句来源
    A study of tumor suppression effect of RB_1 gene on human bladder carcinoma cells in vitro
    RB_1抑癌基因对人膀胱癌细胞抑癌作用的研究
短句来源
    An experimental study of microwave radiation on the bladder carcinoma cells in vitro
    微波对膀胱癌细胞杀伤的体外实验研究
短句来源
    After successful cell transfection indicated by GFP expression, GCV and hydroxycamptothecin are respectively added into the cell culture with normal T-24 cells serving as the blank control group. The growth inhibition rate of hunman bladder carcinoma cells in response to HCPT treatment for 72 h and the cell survival rate of 24 h, 48 h and 72 h after transfection with different protocols were observed by MTT assay.
    以正常T-24细胞为空白对照,转染成功后分别加入GCV、GCV+HCPT,采用MTT法测定单纯HCPT作用于人膀胱癌细胞72h细胞增殖抑制率、各组治疗转染后人膀胱细胞24、48、72h细胞存活率;
短句来源
    Controlled expression and significance of p16 protein in bladder carcinoma cells transfectioned wild type MTS1
    转染野生型MTS1基因的膀胱癌细胞中p16蛋白的可控表达及意义
短句来源
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  bladder carcinoma cell
    Exptessions of TGFα gene and oncogenes in human bladder carcinoma cell line BIU-87
    TGFα基因和某些癌基因在人膀胱癌细胞系BIU-87中的表达
短句来源
    IL-6 expression in the renal and bladder carcinoma cell lines
    白细胞介素6在肾癌和膀胱癌细胞系中的表达
短句来源
    Methods Hunman bladder carcinoma cell line T-24 was transfected with adenovirus expression vector containing TK gene and green fluorescent protein (GFP) gene, and the transfection efficiency was observed and TK expression detected by PCR.
    方法使用含有HSV-TK基因、绿色荧光蛋白(GFP)基因的复制缺陷腺病毒转染人膀胱癌细胞T-24细胞,表达GFP为转染成功标志,同时观察转染率,PCR检测TK表达。
短句来源
    The role of Clusterin in preventing bladder carcinoma cell death
    Clusterin对膀胱癌细胞抗死亡作用的研究
短句来源
    Study of the antiapoptosis mechanism of clusterin in EJ bladder carcinoma cell line.
    Clusterin对膀胱癌细胞抗凋亡作用机制的研究
短句来源
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  bladder cancer cell
Study of recombinant human IFN-α-2b bacilli calmette-guerin activated killer cells and against bladder cancer cell in vitro
      
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.
      
Adenovirus-mediated transfer of p53 and p16 inhibiting proliferating activity of human bladder cancer cell EJin vitro andin vivo
      
Under the induction of Lipofectamine 2000, the recombinant was transfected into Uroplakin II negative bladder cancer cell line EJ.
      
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  bladder cancer cells
Conclusion: The constructed chimeric antibody was expressed successfully in eukaryotic cells, and the chimeric antibody had desired affinity against human bladder cancer cells.
      
Effect of photodynamic therapy with BPD-MA on the proliferation and apoptosis of human bladder cancer cells
      
OBJECTIVE This study was conducted to explore the effect of Rg3 on inhibition of proliferation and induction of apoptosis in bladder cancer cells.
      
On Day 21 the tumors were resected and examined pathologically to see the immune response.Results: The observation of morphology of MBT-2 cells in vitro and MTT assay indicated that Allicin has apparent direct cytotoxicity to bladder cancer cells.
      
To study the effects of arsenic trioxide (As2O3) on the in vitro growth of human bladder cancer cells and the mechanisms.
      
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  bladder carcinoma cells
The in vitro growth of bladder carcinoma cells was analyzed by MTT colorimetry, and the apoptosis rate was assayed by TUNEL methods.
      
Using this in situ assay method, we detected the reduced permeability to HRP in aortic and brain microvascular endothelial cells after 4-5 days culture with conditioned media of human astrocytes or bladder carcinoma cells.
      
In line with these data, expression of either p63RhoGEF or GEFT in J82 human bladder carcinoma cells induced the formation of actin stress fibres.
      
Nucleic acid metabolism of bladder carcinoma cells in vitro
      
Nucleic acid metabolism was investigated to determine the metabolic activity of bladder carcinoma cells.
      
更多          
  bladder carcinoma cell
Expression of a mutant hTERT in human bladder carcinoma cell line T24 and its clinical significance
      
After transfecting the fusion gene into bladder carcinoma cell line T24 by calcium phosphate-DNA coprecipitation, the steady expression of GFP-hTERT fusion protein was tested by fluorescent light microscopy.
      
The proliferation changes of bladder carcinoma cell line T24 were detected by light microscopy and senescence correlated β-galactosidase staining.
      
Conclusion: The mutant-type hTERT gene suppresses the proliferation of bladder carcinoma cell line T24 by competitive effect on telomerase activity.
      
Apoptosis induced by ginsenoside Rg3 in a human bladder carcinoma cell line
      
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