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   人癌细胞系 的翻译结果: 查询用时:0.041秒
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人癌细胞系
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  human cancer cell lines
     In this study, 3 human pancreatic adenocarcinoma cell lines (PC-1, PC-2 and PC-3) and 3 other human cancer cell lines (adenocarcinoma of lung, LE-TP; gastric carcinoma, SGL7901; and breast carcinoma, BCP37) were investigated by adding EGF, anti-EGF antiserum and anti-EGFR monoclonal antibody into culture medium.
     本研究观察了上皮生长因子(EGF)抗EGF抗体和抗EGF受体抗体对3个目建的人胰腺癌细胞系(PC-1,PC-2,PC-3)和3个其它人癌细胞系(肺腺癌LETP,乳腺癌BCP37和胃腺癌SGL7901)生长的影响。
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     To further study the biological effects of this cDNA,an expression plasmid containing an insert of the putative coding fragment(about 0.3kb)of RA538 and neo resistance gene was constructed(designated pRA538-0.3 neo)and transferred into three different human cancer cell lines:EC8712,HL60 and GLC,cell line derived from an adenocarcinoma of the lung.
     为进一步研究这个cDNA的生物学作用,用RA5380.3kb的片段与neo基因构建了一个pRA538-0.3-neo表达质粒,并转入三种不同的人癌细胞系即EC8712、HL60和GLC(一个来自人肺腺癌的细胞系)。
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     Expressions of nm23 gene in eight human cancer cell lines with different metastatic potentials
     8种不同转移潜能人癌细胞系中nm23基因的表达
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     Objective:To study in vitro the anticancer interaction between Ys 96, a bisbenzylisoquinoline compound derived from Stephania tetrandra ,and adriamycin or vincristine against human cancer cell lines.
     目的:研究双苄基异喹啉化合物Ys96与阿霉素或长春新碱联合用药对体外培养人癌细胞系MCF7和KB的抗癌增效作用。
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     Methods The levels of secreted 72000 type IV collagenase in the conditioned media of five human cancer cell lines with different metastatic potential and a normal lung fibroblast strain treated with cancer cell culture media were examined by gelatin zymography and densitometric analysis.
     方法采用明胶酶谱分析法,检测两组5种不同转移潜能的人癌细胞系,分泌72000IV型胶原酶的情况,以及人正常纤维母细胞在不同癌细胞的作用下,分泌的72000IV型胶原酶活性的改变。
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  “人癌细胞系”译为未确定词的双语例句
     Taurine gossypol showed notable cytotoxic activity against two cultured human tumor cell lines,BGC823 and SMMC7721.The IC_(50) values were 19.0 and 23.5 mg/ L,respectively.
     牛磺酸棉酚不同浓度与BGC823和SMMC7721在37℃作用24h用集落形成法检测结果表明,该药对两种人癌细胞系的细胞杀灭作用具有剂量依赖性,IC_(50)浓度分别为19.0和23.5mg/L巴比妥棉酚100mg/kg(ip)对小鼠肝癌和肉瘤180治疗无效。
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     The inhibitory effects of cinobufagin, cinobufotalin and their metabolites on the growth of human tumorcell lines (HCT 8, KB, BGC, BIU and HeLa) were evaluated by bioassay in vitro .
     根据原形化合物和代谢产物的体外抑制人癌细胞系 (HCT 8、KB、BGC、BIU和HeLa)的生长评价其抗肿瘤活性。
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     Study on the cytotoxicity of the elements of Dryopieris Crassirhizoma to the human cancerous cell lines BGC 803 and BCH by MTT
     用MTT法研究贯众有效成份对人癌细胞系BGC 803.BCH细胞毒作用
     According to this reaction the photosensitive inactivation of human tumor cells (HCT,KB and BEL ) were measured by 8-MOP plus UVA radiation.
     的原理,测定了8—甲氧基补骨脂素(8—MOP)对体外培养人癌细胞系HCT、KB和BEL细胞的光敏灭活作用。
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     METHODS Using polymerase chain reaction(PCR) and PCR products restriction fragment length polymorphism(PCR RFLP) methods,mitochondrial cytochrome oxidase subunit Ⅱ (CoⅡ) and ATPase subunit 6(ATPase 6)gene deletions and restriction patterns with Hae Ⅲ were analyzed in 6 human carcinoma cell lines and 16 cases of white blood cells(including tumor patients and normal human beings,8 cases each).
     方法采用PCR和PCR产物HaeⅢ限制性片段长度多态性分析方法,分析了6株人癌细胞系、8例癌患者及8例正常人白细胞线粒体CoⅡ和ATPase6基因的缺失和限制酶谱变化。
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  相似匹配句对
     The Related Problems And Improvement Of Technique For Establishulg Human Oral Cancer Cell Line
     口腔癌细胞建立的相关问题
     Establishment of human lung carcinoma cell line HB-99
     新建1例肺鳞癌细胞
短句来源
     Expression of estrogen receptor in human tongue cancer cells
     雌激素受体在癌细胞中的表达
短句来源
     Establishing of Human Primary Gallbladder Cancer Cell Line SGC-996
     原发性胆囊癌细胞SGC-996的建立
短句来源
     Genetic instability of BGC-823 of human gastric cancer cell line
     癌细胞BGC-823的遗传不稳定性
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  human 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.
      
The transport and uptake of the most common Se compounds, selenate (SeO42-), selenite (SeO32-), selenomethionine, and selenocystine, were investigated using confluent monolayers of Caco-2 cells, a human carcinoma cell line.
      
Both mAb were used to characterize TGFβ-mediated effects on the metastatic potential in nude mice of human carcinoma cell line SLU-1 and its metastatic subline SLU-M1.
      
Cytotoxicity of antitumor platinum complexes withl-buthionine-(R, S)-sulfoximine and/or etanidazole in human carcinoma cell line
      
(2) The microchromosomes of the chicken and double minutes of a human carcinoma cell line also exhibited the core structure.
      
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  human cancer cell lines
32% or less, have been evaluated in a full panel of 60 human cancer cell lines over a 5-log dose range at the National Cancer Institute.
      
To clarify the effect of TPT on SUD4 and DOHH2 cell line in this study, we examined the apoptosis and cell cycle changes of the two human cancer cell lines by exposing to TPT for 18 hours at various concentrations.
      
Gnidimacrin strongly inhibited cell proliferation of human cancer cell lines such as leukemia K562, stomach cancers Kato-III, MKN-28, MKN-45, and mouse leukemia L-1210 by the MTT assay and colony forming assayin vitro.
      
Relationship between telomere length and radiosensitivity in various human cancer cell lines
      
Objective: To investigate the relationship between telomere length and radiosensitivity in various human cancer cell lines with the expectation to find a valid and common predictor of radiosensitivity for different cancers.
      
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  human cancer cell line
In this study, the tumour cell cytotoxic activity of human peripheral blood monocytes was examined by measuring the inhibition of 3H-thymidine uptake in the human cancer cell line, established in our laboratory from human squamous cell lung cancer.
      
ATP levels were linearly related to the number of viable cells and increased with time in human cancer cell line cultures correlating with growth kinetics.
      
Establishment of a human cancer cell line with high potential for peritoneal dissemination
      
Easy stable transfection of a human cancer cell line by electrogene transfer with an Epstein-Barr virus-based plasmid vector
      
The strategy first involves the orthotopic transplantation of a human cancer cell line, such as breast cancer cell line, into the mammary fat pads of immune deficient mice, followed by surgical resection of the resultant primary tumors that develops.
      
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An improved method for the preparation of photosensitizer hematophorphy-rin with hemin from anticoagulated fresh swine or ox blood was reported.The results of UV and IR absorption spectra, fluorescence spectra, and TLC analysis showed that the photosensitizer hematoporphyrin prepared in such a way was the same as reported.The aqueous sodium salt of photosensitizer hematoporphyrin is unstable.A new peak of emission fluorescence spectra (640 nm) appeared at the same excited wave length (395 nm) on exposure to...

An improved method for the preparation of photosensitizer hematophorphy-rin with hemin from anticoagulated fresh swine or ox blood was reported.The results of UV and IR absorption spectra, fluorescence spectra, and TLC analysis showed that the photosensitizer hematoporphyrin prepared in such a way was the same as reported.The aqueous sodium salt of photosensitizer hematoporphyrin is unstable.A new peak of emission fluorescence spectra (640 nm) appeared at the same excited wave length (395 nm) on exposure to sun light.This indicated the presence of photolytic product of the photosensitizer.The experiment of the kinetics of the drug showed that it is unstable both to light and heat.The fluorescence decay of the aqueous sodium salt of hematoporphyrin photosensitizer in accordance with the pattern of first-order reaction of kinetics.The results of biological test showed marked photo-inactivity of human carcinoma cell lines of different species in vitro,and the ability in detection and phototherapy of sarcoma 180 (solid) tumor in mice.

本文报道用新鲜抗凝去血清猪血或牛血制备氯化血红素和用后者制备血卟啉光敏剂的改良方法。所得成品的光谱和薄层色谱与文献值一致。 血卟啉光敏剂钠盐水溶液经日光辐照,于同一激发光波长(395nm)下较照前增加一发射荧光峰(640nm),表明其对光的不稳定性和光解产物的存在。 血卟啉光敏剂钠盐水溶液的稳定性动力学试验表明,它对光和热的不稳定性反映为溶液荧光的迅速衰减,后者符合一级动力学反应模式。 生物试验证明,血卟啉光敏剂对不同种的体外培养人癌细胞系和小鼠5180肉瘤(实体)具有可靠的光灭活作用和实验性光敏诊治效果。

Studies were carried out for examining HpD affinity of different cell lines after 1 h incubation with HpD. HpD uptake of cells was exhibited by relative fluorescence intensity. Our results showed that relative fluorescence intensity was strongly displayed in different human tumor cell lines(esophageal, stomach, lung, liver) , normal human fetal lung fibroblast line and normal human fetal kideny cells after 1 h incubation with HpD 5 μg/ml. The intracellular fluorescence attenuated to the lowest after 16-24 h...

Studies were carried out for examining HpD affinity of different cell lines after 1 h incubation with HpD. HpD uptake of cells was exhibited by relative fluorescence intensity. Our results showed that relative fluorescence intensity was strongly displayed in different human tumor cell lines(esophageal, stomach, lung, liver) , normal human fetal lung fibroblast line and normal human fetal kideny cells after 1 h incubation with HpD 5 μg/ml. The intracellular fluorescence attenuated to the lowest after 16-24 h incubation. The intracellular relative fluorescence intensity and its speed of attenuation between various cell lines showed no significant difference. NO significant increase in relative fluorescence intensity was noticed when human hepatoma cell line (QGY-7703) was used for incubation with HpD 30-50μg/ml, indicating saturation of HpD uptake.

用直接荧光法测定6种人癌细胞系及两种人胚细胞对HpD的亲和力,结果发现,癌细胞系间对HpD的亲和力并无显著差别,但显著低于两种人胚细胞。HpD在细胞内迅速消失。肝癌细胞对HpD的吸收有一饱和浓度。

Rubescensine A (Rub A) was shown to be active against murine tumours in vivo. In the present study, a comparative observation was carried out in 7 lines of human cancer cells, which were exposed in vitro for 1 h to a range of concentrations of Rub A and then cultured for 10 days to assess colony-forming ability. The dosesurvival curves obtained in 6 of the cell lines were of threshold-exponential type, while the most resistant cell line (LTEP-78) derived from a squamous cell carcinoma of the lung only gave a...

Rubescensine A (Rub A) was shown to be active against murine tumours in vivo. In the present study, a comparative observation was carried out in 7 lines of human cancer cells, which were exposed in vitro for 1 h to a range of concentrations of Rub A and then cultured for 10 days to assess colony-forming ability. The dosesurvival curves obtained in 6 of the cell lines were of threshold-exponential type, while the most resistant cell line (LTEP-78) derived from a squamous cell carcinoma of the lung only gave a wide shoulder over the same range of doses up to 60μg/ml. When the parameters calculated from the curves are compared, a stomach adenocarcinema cell line (MGc80-3) and an esophageal cancer cell line (CaES-17) appear to be relatively sensitive to the drug. The results suggest that an evaluation of Rub A in patients with either of these two types of cancer might be worth while and that a high initial dose might be important for the drug to induce clinical response of tumours.

采用体外集落培养技术测定剂量-存活率曲线,比较了七种常见肿瘤的人癌细胞系对冬凌草甲素的敏感性。除在肺鳞瘟LTEP-78仅测及肩段外,其他细胞的存活率曲线均为阈值指数型。对曲线参数的分析表明,食管唐CaES-17和胃腺癌MGc 80-3对冬凌草甲素最敏感。

 
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