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人前列腺癌细胞     
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  human prostate cancer cell
     Experimental Study of the Growth Inhibition in Vitro on Human Prostate Cancer Cell Line PC-3M by TRAIL
     TRAIL抑制人前列腺癌细胞PC-3M体外生长的实验研究
短句来源
     Establishment of Highly Metastatic Models of Human Prostate Cancer Cell and Expression of Tumor Metastasis Suppressor Genes CD44s and Nm23-H1
     转移性人前列腺癌细胞模型的优化及CD44s和nm23-H1基因的表达
短句来源
     To study the expression of Omi/HtrA2 in human prostate cancer cell line (PC-3M), construct siRNA expressing vector and investigate the effect of Omi/HtrA2 on PC-3M apopto-sis.
     目的检测人前列腺癌细胞(PC-3M)中Omi/HtrA2的表达情况,并构建其小干扰 RNA(siRNA)表达载体,探讨Omi/HtrA2对PC-3M凋亡的影响。
短句来源
     Result: 1. Both α-ANO and β-ANO monomers effectively inhibited human prostate cancer cell proliferation, and the suppression effect of α-monomer was stronger than that of β-monomer.
     结果:1.α-ANO和β-ANO均能有效抑制人前列腺癌细胞DU145、PC-3、LNCaP、L1A和CWR22-RV1的增殖,α-ANO抑制作用强于β-ANO;
短句来源
     Methods Cell counts and MTT method were used to detect the influence of ATP on the growth of 1E8 (metastatic) and 2B4 (non metastatic) cells derived from human prostate cancer cell line PC3M.
     方法 用细胞计数及MTT法检测外源性P2嘌呤受体激动剂ATP对人前列腺癌细胞PC 3M亚系 1E8(高转移 )和 2B4(低转移 )体外生长的影响。
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  human prostatic cancer cell
     Conclusion:The vector pDR2-TK carried the objective HSV-TK gene and could be efficiently transferred by liposome into human prostatic cancer cell.
     结论 :pDR2 TK质粒含有目的基因HSV TK ,阳离子脂质体法可将 pDR2 TK导入人前列腺癌细胞并获得较高效率的表达
短句来源
     Objective To study the effect of hyperthermia on growth of human prostatic cancer cell lines PC-3m and LNCaP in vitro.
     目的 探讨高温对人前列腺癌细胞株PC - 3m和LNCaP生长的影响。
短句来源
     The Inhibitive effect of NS398 on the proliferation of human prostatic cancer cell lines in vitro
     还氧合酶-2抑制剂NS398对人前列腺癌细胞系PC-3的增殖抑制作用
短句来源
     Methods: The protein coding region of pc 1 cDNA was amplified using nested PCR technology from the primary cloning plasmid and subcloned into the eukaryotic expressing vectors pEGFP N1 and pCDNA3.1( )/myc his containing EGFP and MYC tag,respectively,then transfected into the human prostatic cancer cell line C4 2.The location of its expression product in C4 2 was observed with immunocytochemistry and laser confocal scanning microscopy.
     方法 :采用巢式PCR技术 ,从原始克隆质粒中扩增出可编码蛋白分子的pc 1cDNA片段 ,分别将其克隆入含EGFP和MYC标签的真核表达载体中 ; 用脂质体介导法将其转染入人前列腺癌细胞C4 2中 ;
短句来源
     Effect of lycium barbarum polysaccharides on human prostatic cancer cell growth
     枸杞多糖对人前列腺癌细胞生长影响
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  human prostate carcinoma cell
     Cloning and Sequencing of PTI-1 cDNA in Human Prostate Carcinoma Cell Line PC-3
     人前列腺癌细胞系PC-3中PTI-1 cDNA的克隆及序列分析
短句来源
     Objective To observe the change characteristics of TGF-β 1 mRNA expression in human prostate carcinoma cell strain (PC-3) in vitro.
     目的 观察人前列腺癌细胞株 (PC- 3) TGF-β1 m RNA表达变化特点。
短句来源
     To obtain a new member of the human prostate carcinoma tumor inducing gene ( PTI 1) family in human prostate carcinoma cell line PC 3, human PTI 1 cDNA was synthesized from human prostate carcinoma cell line PC 3 by RT PCR, which was then subcloned into pUC19 vector and sequenced.
     为获取人前列腺癌诱导基因家族新成员 ,以人前列腺癌细胞系PC 3的总RNA为模板 ,用RT PCR方法扩增人前列腺癌诱导基因 1(PTI 1) ,将其亚克隆至克隆载体pUC19,进行测序 .
短句来源
     Methods After treatment of 1×10 -9 ? mol/L for 24 h, expression of cell cycle regulation molecules including CDK2, CDK4, CDK6 and p27 kipl in human prostate carcinoma cell line LNCaP and PC 3 was detected by using immunoprecipitation and Western blot analysis after 0, 8 and 24 h of withdrawal of androgen.
     方法 在人前列腺癌细胞株LNCaP和PC 3中 ,先加 1× 10 -9mol/L双氢睾酮 (DHT)维持培养 2 4h后分别于去除DTH 0、8和 2 4h行免疫沉淀和WesternBlot分析检测细胞周期素依赖激酶CDK 2、CDK4、CDK6和p2 7kip1的表达。
短句来源
     To obtain a new member of the human prostate carcinoma tumor-inducing (PTI-1) gene family in human prostate carcinoma cell line PC-3. The human PTI-1 cDNA was synthesized from human prostatic carcinoma cell line PC-3 by RT-PCR, then subcloned into pUC19 vector and sequenced.
     为获取人前列腺癌诱导基因家族新成员,以人前列腺癌细胞系PC-3的总RNA为模板,用RT-PCR方法扩增人前列腺癌诱导基因1(PTI-1),将其亚克隆至克隆载体pUC19,进行测序。
短句来源
更多       
  human prostate cancer cell line
     Experimental Study of the Growth Inhibition in Vitro on Human Prostate Cancer Cell Line PC-3M by TRAIL
     TRAIL抑制人前列腺癌细胞PC-3M体外生长的实验研究
短句来源
     To study the expression of Omi/HtrA2 in human prostate cancer cell line (PC-3M), construct siRNA expressing vector and investigate the effect of Omi/HtrA2 on PC-3M apopto-sis.
     目的检测人前列腺癌细胞(PC-3M)中Omi/HtrA2的表达情况,并构建其小干扰 RNA(siRNA)表达载体,探讨Omi/HtrA2对PC-3M凋亡的影响。
短句来源
     Methods Cell counts and MTT method were used to detect the influence of ATP on the growth of 1E8 (metastatic) and 2B4 (non metastatic) cells derived from human prostate cancer cell line PC3M.
     方法 用细胞计数及MTT法检测外源性P2嘌呤受体激动剂ATP对人前列腺癌细胞PC 3M亚系 1E8(高转移 )和 2B4(低转移 )体外生长的影响。
短句来源
     Expression and Biological Effect of Pituitary Tumor Transforming Gene 1 On Human Prostate Cancer Cell Line LNCaP
     垂体瘤转化基因1(PTTG1)的表达变化对人前列腺癌细胞LNCaP生长增殖的影响
短句来源
     In human prostate cancer cell line PC-3, soluble fibronectin caused morphological change from polygonal to round and antibody against α5β1 integrin prevented the change.
     在人前列腺癌细胞系PC-3中,可溶性纤维连接蛋白可引起细胞从多角形向圆形的形态改变,α5β1整合素的抗体可阻断这一改变。
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  human prostate cancer cell
Following incubation, the cultured cells containing immature DCs were concentrated and transfected with tumour mRNA from human prostate cancer cell lines employing a highly efficient electroporation procedure.
      
Screening of differently expressed genes in human prostate cancer cell lines with different metastasis potentials
      
It was concluded that two subtractive libraries of human prostate cancer cell lines with different metastasis potentials were constructed successfully.
      
Effect of tumor necrosis factor-α and interferon-γ on the growth of human prostate cancer cell lines
      
Endopeptidase 24.11 activity in the human prostate cancer cell lines LNCaP and PPC-1
      
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  human prostatic cancer cell
Androgen receptors and hormone sensitivity of a human prostatic cancer cell line (PC-3) are modulated by natural beta-interferon
      
Effects of BFA (30?ng/ml) were examined on the growth of three human prostatic cancer cell lines, PC-3, DU-145, and LNCaP cells.
      
Effect of keratinocyte growth factor and activin on cell growth in the human prostatic cancer cell line LNCaP
      
In addition, the biological effects of NGFβ addition to the human prostatic cancer cell cultures were investigated.
      
Lectin-induced alterations on the proliferation of three human prostatic cancer cell lines
      
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  human prostate carcinoma cell
Normal genital skin fibroblasts (GSF) and the human prostate carcinoma cell line LNCaP have been used widely as cell culture models of genital origin to study androgen receptor (AR) signaling.
      
Antiproliferative effect of interferons on human prostate carcinoma cell lines
      
The effect of purified human fibroblast beta-interferon (B-IFN) and recombinant alpha-2b-interferon (A-IFN) on cell proliferation was investigated in two human prostate carcinoma cell lines, named PC-3 and DU-145.
      
High mannose-type glycans were sought on the human prostate carcinoma cell surface.
      
Results: BE-4-4-4-4 was shown to be approximately 4 to 86 times more cytotoxic in clonogenic assays than DENSPM in both rat and human prostate carcinoma cell lines.
      
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  human prostate cancer cell line
Monoclonal antibody-defined antigens of human prostate cancer cell line PC3
      
Cell cycle perturbations and radiosensitization effects in a human prostate cancer cell line
      
Unchecked DNA synthesis and blocked cell division induced by methionine deprivation in a human prostate cancer cell line
      
In order to establish an animal model of bone metastasis, cells from a human prostate cancer cell line (PC-3) were injected into the tail veins of athymic nude mice while the inferior vena cava was occluded.
      
To evaluate the role of MKP-1 in regulating cell death and tumor growth in prostate cancer, MKP-1 was conditionally overexpressed in the human prostate cancer cell line DU145.
      
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