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癌细胞系
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  cancer cell line
    The Clone of Human p27kiplcDNA and the Study of Its Cellular Biology Effect in Human Tongue Cancer Cell Line Tca8113 Cells
    人p27kiplcDNA克隆及其对人舌癌细胞系Tca8113细胞生物学作用的研究
短句来源
    The Effects on Biological Behaviors of Oral Squamous Cell Cancer Cell Line Tca-8113 Mediated by Stroma Fibroblasts Derived from Oral Normal Mucosa and Oral Squamous Cell Cancer
    间质成纤维细胞对口腔癌细胞系Tca-8113生物学行为影响的实验研究
短句来源
    Effect of Fibronectin on the Invasion Behaviour of Human Tongue Cancer Cell Line (TCa8113) in vitro
    纤连蛋白对人舌癌细胞系TCa 8113细胞体内浸袭行为的影响
    Study on the multidrug-resistance of Tca8113 tongue cancer cell line under chemotherapy
    Tca8113舌癌细胞系在化疗前后多药耐药性(MDR)的研究
    In Vitro Study of the Lytic Activity of Co-cultured DC and CIK to Human Tongue Cancer Cell Line Tca8113
    人DC和CIK共培养细胞对舌鳞癌细胞系Tca8113的体外杀伤实验
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  carcinoma cell line
    The role of TGF-β on Tca83--a tongue squamous cell carcinoma cell line
    转化生长因子β对舌癌细胞系Tca83生长的影响
短句来源
    Effect of c-myc Transfection on fas Expression and Apoptosis in Oral Squamous Cell Carcinoma Cell Line Tca8113
    c-myc转染对舌鳞癌细胞系Tca8113fas表达和凋亡的影响
短句来源
    Transfection of the Exogenous PTEN-induced Growth Inhibition of the Highly Metastatic Mucoepidermoid Carcinoma Cell Line M_3SP_2 in vitro
    PTEN基因转染对粘液表皮样癌细胞系M_3SP_2增殖的抑制作用
短句来源
    Inhibitory effects of the herpes simplex virus-thymidine kinase gene/ganciclovir system on the highly metastatic mucoepidermoid carcinoma cell line M3SP2
    HSV-tk/GCV系统对高转移性粘液表皮样癌细胞系M3SP2的抑制作用
短句来源
    Relationship of Apoptosis and Expression of Fas Gene in Tongue Squamous Cell Carcinoma Cell Line Tca8113
    舌鳞癌细胞系Tca8113 Fas表达水平与凋亡的关系
短句来源
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  carcinoma cell lines
    Objective:To study chemosensitivity and anticancer activity of Cisplatin(CDDP) loaded polylactic acid-polyethylene glycol nanoparticles(CDDP-PLA-PEG-NP) against oral squamous carcinoma cell lines Tca8113(tongue carcinoma) and BcaCD885(buccal carcinoma).
    目的:观察口腔鳞癌细胞系(Tca8113和BcaCD885)对口腔癌靶向顺铂聚乳酸聚乙二醇纳米粒(CDDP-PLA-PEG-NP,或称隐形聚乳酸纳米)的敏感性,并与顺铂(CDDP)对Tca8113和BcaCD885的抗癌活性进行对比观察。
短句来源
    Effects of transforming growth factor β_1 on the malignant phenotypes of oral squamous cell carcinoma cell lines.
    外源性转化生长因子β_1对口腔鳞癌细胞系恶性表型的影响
短句来源
    Hypoxia regulates vascular endothelial growth factor and matrix metalloproteinase-2 in oral squamous cell carcinoma cell lines.
    低氧对口腔鳞癌细胞系血管内皮生长因子和MMP-2的影响
短句来源
    Vascular Endothelial Growth Factors Differently Modulate Activity of Matrix Metalloproteinase-2 and-9 in Oral Squamous Cell Carcinoma and Metastasis Carcinoma Cell Lines
    血管内皮生长因子对口腔鳞癌细胞系基质金属蛋白酶-2和-9活性的影响
短句来源
    Methods: The expression of MMP_2,9, TIMP_1,2 in 30 oral squamous cell carcinoma, two oral squamous cell carcinoma cell lines GNM and TSCCa was detected by in situ hubridization;
    方法 :应用原位杂交法 (insituhybridization ,ISH)检测 3 0例口腔鳞癌组织 ,口腔鳞癌转移细胞系GNM和人舌鳞癌细胞系TSCCaMMP_2 ,9和TIMP_1,2的表达 ;
短句来源
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  “癌细胞系”译为未确定词的双语例句
    Methods: The Tca8113 cell line was exposed to the 60Co irradiation, the dosage of which was 1 Gy for two weeks.
    方法:利用人舌鳞癌细胞株Tca8113,采用单次剂量1Gy,每周2次的60Co照射,诱导其耐放疗性,建立一株耐放疗的人舌鳞癌细胞系
短句来源
    Methods MMP-2,9 expression and β-Dystroglycan degradation status were detected in 30 tongue cancer tissues and cell line SCC-4,9,15,25 by using immunohistochemistry,RT-PCR and western blot.
    方法应用免疫组化、RT-PCR 和Western blot 方法检测30例舌癌组织和舌癌细胞系SCC-4,9,15,25中MMP-2,9的表达情况及β-Dystroglycan 的存在状态,探讨MMP-2,9表达与舌癌颈淋巴结转移的关系。
    Expression of BMP-2/4、-5 and BMPR-Ⅰ、BMPR-Ⅱ in Tca8113 cell line
    骨形成蛋白-2/4、-5及Ⅰ型、Ⅱ型BMP受体在舌癌细胞系Tca8113细胞中的表达及意义
短句来源
    Effect of antisense hTR transfection on Tca8113 cell line
    反义hTR对舌鳞癌细胞系Tca8113作用的初步探讨
短句来源
    Establishment and characterization of a metastatic cell line from spinal cord metastasis induced by injection of Mc3 cells in nude mice
    裸鼠脊髓转移灶粘液表皮样癌细胞系Ms的建立及生物学特性
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  cancer cell line
Additionally, (2) also inhibited the proliferation of human erythroleukemia cancer cell line K562 with IC50 value of 49.1 μg/mL.
      
The aim of this study was to investigate the role of pirh2 (p53-induced RING-H2) protein in the proliferation, apoptosis and cell cycle control of the lung cancer cell line A549.
      
Human mutant-type (mt) p53 cDNA was synthesized and cloned from human lung cancer cell line GL containing mt-p53 gene by using polymerase chain reaction (PCR).
      
The cytotoxicity assays using the mouse cancer cell line L929 proved the cytotoxicity of the TNF in the crude extracts from the transgenic c~anobacteriumAnabaena sp.
      
The RA538 cDNA was transferred into human ovarian cancer cell line SK-OV-3 and human melanoma cell line WM-983A by its recombinant adenoviral vector constructed through homologous recombination.
      
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  carcinoma cell line
In this study, we investigated the effects of two fatty acids, palmitate (PA) and arachidonic acid (AA) on glycogenesis under insulin signaling in HepG2cells, a transformed hepatic carcinoma cell line.
      
With pSIP-ConA-LacZ, p53 activation in response to 12 chemotherapeutic agents was analyzed in human carcinoma cell line HCT116 and its derivatives HCT116/mdm2 and HCT116/ARF, which expressed genes affecting the p53 activity.
      
20,29-Dihydro-20,29-dibromomethylenebetulinic acid inhibited the growth of the Bro melanoma cell line and the CaOv carcinoma cell line practically by 50% at a concentration of 10 μM.
      
Mismatch repair (MMR) efficiency and MSH2 gene mutation in human colorectal carcinoma cell line COLO320HSR
      
Inhibition of metastasis to lung of a human nasopharyngeal carcinoma cell line CNE- 2L2 transfected with pRc/ CMV-antisense 6A8
      
更多          
  carcinoma cell lines
Downregulation of TRIP6 Gene Expression Induces Actin Cytoskeleton Rearrangements in Human Carcinoma Cell Lines
      
The influence on the expression of the c-myc and p53 gene in the human hepatocellular carcinoma cell lines were tested with the TEM and hybridization in situ.
      
We examined retinoic acid receptors (RARs) and retinoids X receptors (RXRs) levels in 6 breast carcinoma cell lines and 18 breast cancer biopsy specimens.
      
Objective: To investigate the expression of Fas ligand in human colon carcinoma cell lines.
      
In present study, we investigated the expression of FasL in SW480 and LS174 human colon carcinoma cell lines and twenty primary colon carcinoma specimens.
      
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The effects of γIFN and TNFα on the proliferation of LAK cells and LAK cytotoxicity against ACC-2 when they act at the induction of LAK cells were atudied in vitro. The results show that TNFα can be a suitable enhancer to augment IL 2 induced LAK cytotoxicity against ACC 2. This synergism has nothing to do with the effect of TNFα on the proliferation of LAK cells; γIFN can lightly inhibit LAK activity. This inhibition on LAK cytotoxicity may be related to the reduction of LAK cells.

通过体外实验观察了当γ干扰素(γlFN)和肿瘤坏死因子α(TNFα)作用于LAK细胞(淋巴因子激活杀伤细胞)诱导阶段时对LAK细胞杀伤涎腺腺样囊性癌细胞系2(ACC-2)活性的影响。结果显示:TNFα可以提高低剂量白介素—2(lL-2)诱导的LAK细胞杀伤活性,且对ACC-2的杀伤活性要高于Raji,增强作用的产生与它对LAK细胞增殖的影响无关。γlFN可以呈剂量依赖性地抑制LAK细胞杀伤活性,并轻度抑制LAK细胞的增殖

tudying the in vitro motility and adhesion of tumor cell is important in understanding the invasion and metastasis mechanisms of malignant tumors.The in vitro motility of two Acc cell lines, hiqh metastatic Acc-M, strain,and Acc-2 line,was measured by Boyden chamber technique.Statistical analysis of the results showed slgnficant differences between the high and low metastatic cells.The ability of motility was higher in Acc-M than that in Acc-2. The cell adhesion test showed that Acc-M had stronger ability of...

tudying the in vitro motility and adhesion of tumor cell is important in understanding the invasion and metastasis mechanisms of malignant tumors.The in vitro motility of two Acc cell lines, hiqh metastatic Acc-M, strain,and Acc-2 line,was measured by Boyden chamber technique.Statistical analysis of the results showed slgnficant differences between the high and low metastatic cells.The ability of motility was higher in Acc-M than that in Acc-2. The cell adhesion test showed that Acc-M had stronger ability of adhesion than Acc-2.The result suggested in vitro motility and adhesion may play an important role in invasion and metastasis of Acc.

研究癌细胞的运动性和粘附性,是探索恶性肿瘤侵袭转移机理的重要方面。本研究应用改良的Boyden小室测得涎腺腺样囊性癌细胞系Acc-2和高转移细胞株Acc-M的体外运动能力,经统计学处理,高转移细胞株的运动能力明显高于Acc-2系细胞株;两种细胞克隆的体外粘附性也有较大的差别,说明在Acc转移过程中,癌细胞的运动性和粘附性起到重要的作用

The cell colony of human adenoid cystocarcinoma of salivary gland was established by the bilaminar soft agar cultivation.The numbers of formative colony were stable and the form was distinct.A ideal model was supplied to study the human adenoid cystocarcinoma of salivary gland further.

应用人涎腺腺样囊性癌细胞系(SACC83),建立了人涎腺腺样囊性癌的细胞集落。所采用的实验方法为双层软琼脂培养法,所形成的集落数目稳定,形态清晰,为深入研究涎腺腺样囊性癌提供了理想模型

 
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