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   膀胱癌组织 的翻译结果: 查询用时:1.076秒
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膀胱癌组织     
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  neoplastic tissues
     Results:All normal bladder tissues showed negative staining, the rate of expression of VEGF in neoplastic tissues was 56.5 % .
     结果:正常膀胱移行上皮均为阴性反应,膀胱癌组织中VEGF阳性表达率为56.5%.
短句来源
     Expression of vascular endothelial growth factor (VEGF) in 62 cases of primary transitional cell carcinoma (TCC) and 8 cases of normal bladder tissue was assayed using immunohistochemical technique. The relationship between the expression of VEGF in 30 cases of invasive neoplastic tissues and quantification of angiogenesis was also investigated.
     为了探讨膀胱移行细胞癌中血管内皮生长因子(VEGF)表达及其与血管形成定量关系,应用免疫组织化学方法,对62例原发性膀胱移行细胞癌及8例正常膀胱组织中VEGF进行检测,并对其在30例浸润性膀胱癌组织中表达与血管形成定量关系进行了研究。
短句来源
     All normal bladder tissues showed negative staining while the rate of expression of VEGF in neoplastic tissues was 56%.
     结果发现正常膀胱组织均为阴性反应,膀胱癌组织中VEGF蛋白阳性表达率为56%。
短句来源
     Methods: 62 cases of the TCC was assayed using immunohistochemical technique. The relationship between the expression of bFGF in invasive neoplastic tissues and microvessel quantification was also investigated.
     方法:应用免疫组织化学方法,对62例原发性膀胱移行细胞癌组织中bFGF进行检测,并对浸润性膀胱癌组织中微血管进行定量研究.
短句来源
     Both growth factor were assayed using immunohistochemical technique in 62 cases of TCC. The relationship between the expression of VEGF and bFGF in invasive neoplastic tissues and magnitude of angiogenesis were also investigated.
     应用免疫组织化学方法 ,对 6 2例原发性膀胱移行细胞癌组织中VEGF、bFGF进行检测 ,并对其在 30例浸润性膀胱癌组织中的表达与血管形成的定量关系进行相关性研究。
短句来源
  bladder cancer tissue
     The Significance of the MDR 1 Gene Products GP 170 Expression in the Bladder Cancer Tissue
     膀胱癌组织MDR_1基因产物P-GP_(170)表达的意义
短句来源
     Results There was a significant difference in the P27kipl and CyclinD1 between the normal bladder tissue and the bladder cancer tissue (P< 0.01).
     结果:P27kipl、CyclinD1在正常膀胱组织中的表达率和在膀胱癌组织中的表达差异均具有显著性(P<0.01)。
短句来源
     Methods The fluorescence in situ hybridization(FISH) analyzed the influence of 7 genes,which located in 5p(15.31)-5p(15.1) including TAS2R,ADCY2,DNAH5,CTNND2,TRIO,ANKH and MYO10,in bladder cancer tissue microarray TRIO showed higher rate of amplification.
     方法用原位杂交法(FISH)分析位于5p 15.31~5p 15.1上的7个基因(TAS2R1,ADCY2,DNAH5,CTNND2,TRIO,ANKH和MYO10)在膀胱癌组织微阵列的作用,其中扩增率最高的是TRIO基因。
短句来源
     Relation between failure of chemotherapy and P-GP_(170) glycoprotein expression in the bladder cancer tissue
     膀胱癌组织中P-GP_(170)蛋白表达与化疗失败关系的研究
短句来源
     Optical Properties of Human Normal Bladder and Bladder Cancer Tissue at 532 nm and 808 nm Laser and Their Linearly Polarized Laser Irradiation In vitro
     532nm和808nm激光及其线偏振激光辐照人正常膀胱与膀胱癌组织光学特性
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  bladder carcinoma tissue
     The culture and identity of the fibroblast in the human bladder carcinoma tissue
     人膀胱癌组织中成纤维细胞的培养和鉴定
短句来源
     Conclusion:We can use the examination of ICAM 1 in bladder carcinoma tissue as index in judging immunological function state,therapeutic effect and prognosis.
     结论:膀胱癌组织 I C A M 1 表达检测可以作判定患者机体免疫功能状态、治疗效果及预后观察的客观指标。
短句来源
     Results The expression of nm23 protein was detected in both bladder carcinoma tissue and non-carcinoma mucosa, and the nm23 protein was located in cytoplasm.
     结果 nm2 3蛋白在膀胱癌组织及非癌粘膜中均有表达 ,定位于细胞浆。
短句来源
     Results:Positive rate of ICAM expression in bladder carcinoma tissue was 88% and positive rate of safety limbs was 16%. Difference between them was significant. ICAM 1 expression was negatively correlatal with clinical stages and pathological grading.
     结果:膀胱癌组织中 I C A M 1 表达阳性率为88% ,而安全缘组织中阳性率为 16% ,两者之间差异非常显著,且 I C A M 1 的表达与膀胱癌的临床分期与病理分级呈负相关,即随膀胱癌的临床分期和病理分级的增高 I C A M 1 表达降低。
短句来源
     Objective:To investigate the method of the culture and identity of the fibroblast in the human bladder carcinoma tissue.
     目的:探索人膀胱癌组织中成纤维细胞的培养和鉴定方法,为其功能的研究奠定基础。
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  bladder cancer tissues
     Results The telomerase activity was positive in 34 cases of bladder cancer tissues (82.9%) and 1 case of non cancerous tissues (4.3%);
     结果 :41例膀胱癌组织中端粒酶阳性 34例 ,阳性率 82 9% ,2 3例非癌患者膀胱组织中端粒酶阳性 1例 ,阳性率 4 3%。
短句来源
     Evaluating the effect of intravesical chemotherapy by expressions of P-gp, GST-π and TOPO- Ⅱ in bladder cancer tissues
     膀胱癌组织P-gp,GST-π和TOPO-Ⅱ表达评估灌注化疗
短句来源
     Difference of optical properties of human normal bladder and human bladder cancer tissues at 476.5 nm,514.5 nm and 808 nm radiation respectively in Kubelka-Munk two-flux model was studied.
     研究正常人膀胱和膀胱癌组织在Kube lka-Munk二流模型下对476.5 nm,514.5 nm和808 nm波长的激光的光学特性的差异。
短句来源
     Results:The expression of Her4 in bladder cancer tissues was significantly lower than normal bladder tissues(P<(0.05)),but the average of luminosity is higher(P<(0.05)).
     结果:Her4在膀胱癌组织的表达比正常膀胱组织明显减少(P<0.05),其平均光度显著增高(P<0.05)。
短句来源
     The results of the experiment showed that there werevery significant difference for the absorption,scattering,total attenuation,effective attenuation coefficients of human nor-mal bladder and bladder cancer tissues at the laser wavelength of476.5 nm,514.5 nm and 808 nm radiation respective-ly in Kubelka-Munk two-flux model(P<0.01).
     实验结果表明,正常膀胱和膀胱癌组织在Kube lka-Munk二流模型下对476.5 nm,514.5 nm和808 nm波长的每一个波长的激光的吸收、散射、总衰减、有效衰减系数都有非常显著性的差异(P<0.01)。
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  neoplastic tissues
Neoplastic tissues, marked by Cra Iso 1, showed a higher intensity of staining than normal ones, in comparison withCanavalia ensiformis lectin, Concanavalin A (Con A), conjugated to peroxidase (Con A-Per).
      
Gostjeva then discovered that fetal and neoplastic tissues share a set of cells distinguished by specific nuclear morphotypes that appear to cooperate in creating the elements of the fetal organ, preneoplastic, and neoplastic lesions.
      
Assessment of telomerase activity may help to distinguish normal or hyperplastic from neoplastic tissues.
      
An innovative approach to these formidable lesions is photodynamic therapy that employs a chemotherapeutic photosensitizing agent in combination with wavelength specific light to produce cytotoxic reactions capable of destroying neoplastic tissues.
      
Enzyme activities controlling adenosine levels in normal and neoplastic tissues
      
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  bladder cancer tissue
The-ΔΔCT value of survivin in bladder cancer tissue was 10.2829 (9.0034-11.5624) times that in the adjacent normal tissues.
      
TAA was also isolated and identified on bladder cancer tissue culture line T-24.
      
Bladder cancer tissue was obtained at the time of radical cystoprostatectomy extirpation.
      
We investigated the expression of COX-2 in bladder cancer tissue specimens using immunohistochemistry.
      
Culture of bladder cancer tissue is not convenient; thus, FISH is a useful method for interphase cytogenetic analysis of bladder cancer.
      
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  bladder carcinoma tissue
Local expression of cytokines in rat bladder carcinoma tissue after intravesical treatment withNocardia rubra cell wall skeleton
      
The expression of PAX5, p53 immunohistochemistry and p53 mutation analysis in superficial bladder carcinoma tissue.
      
Human bladder carcinoma tissue was obtained from surgical specimens of 20 different patients.
      
  其他


Density of mast cell and lymphocyte were detected in 30 patients with bladder transitional cell cancer by histochemical methods. The results showed that the density of mast cell and lymphocyte was significantely higher in bladder cancer than that found in normal mucosa and there was also significant correlation between the number of mast cell and lymphocyte.The anti-tumor mechanism of the mast mast cell was discussed too.

我们用组织化学染色技术测定了30例膀胱移行上皮癌组织中肥大细胞和淋巴细胞的密度,结果表明:膀胱癌组织中肥大细胞和淋巴细胞均较正常膀胱粘膜明显增加,且浸润膀耽癌组织的肥大细胞数与淋巴细胞数呈明显的正相关。文中对肥大细胞抗肿瘤免疫机理进行了讨论。

With Northern blot and radioimmunoassay, we first have found the expression of TGF*********a mRNA in bladder carcinoma cells.In bladder transitional cell carcinoma BIU-87 cells, TPA(12-o-tetradecanoylphorol-13-acetate) can increase the levels of TGF **********a mRNA and TGF *********aa, but decrease the level and affinity of EGF receptor, which is also the receptor of TGF************a.These data suggest that TGF*********a is responsible to the abnormal growth of bladder carcinoma and TGF*********a mRNA can be...

With Northern blot and radioimmunoassay, we first have found the expression of TGF*********a mRNA in bladder carcinoma cells.In bladder transitional cell carcinoma BIU-87 cells, TPA(12-o-tetradecanoylphorol-13-acetate) can increase the levels of TGF **********a mRNA and TGF *********aa, but decrease the level and affinity of EGF receptor, which is also the receptor of TGF************a.These data suggest that TGF*********a is responsible to the abnormal growth of bladder carcinoma and TGF*********a mRNA can be modulatde in a protein kinase Cdependent manner.

应用Northern印渍杂交和放射免疫分析技术证明了膀胱癌组织和细胞中TGFαmRNA的表达,并发现TPA能提高人膀胱移行上皮癌BIU-87细胞中TCFαmRNA和TGFα活性分子的水平,但对TGFα的功能受体(EGF受体)具有负调节作用。提示TGFα在膀胱肿瘤细胞的恶性增殖过程中起一定作用,蛋白激酶C的激活可能是调节TGFα基因表达的途径之一。

Using Northern and dot blot analysis, we investigated the expression of c-myc, c-fos abd erbB and regulation of oncogenes by TPA in BIU-87 cells a human bladder transitional cell carcinoma line We found expression of these oncogenes and induc-tion of these genes by TPA.We also found high expression of c-myc, c-fos, erbB, N-ras in human bladder cancer tissues.In contrast, only low level expression of N-ras was detected in normal bladder tissues.These data suggest that the expression of some oncogenes can be modulated...

Using Northern and dot blot analysis, we investigated the expression of c-myc, c-fos abd erbB and regulation of oncogenes by TPA in BIU-87 cells a human bladder transitional cell carcinoma line We found expression of these oncogenes and induc-tion of these genes by TPA.We also found high expression of c-myc, c-fos, erbB, N-ras in human bladder cancer tissues.In contrast, only low level expression of N-ras was detected in normal bladder tissues.These data suggest that the expression of some oncogenes can be modulated in a protein kinase C dependent manner and high level expression of some oncogenes are responsible for the abnormal growth in bladder carcinoma.

本实验应用Northern和斑点印渍杂交技术探测了人膀胱癌细胞株中c-myc、c-fos、erbB等癌基因的表达,以及TPA对这些癌基因表达的调控,发现BIU-87细胞有这些癌基因的表达,并能被TPA所增强,同时也发现人膀胱癌组织有c-myc、c-fos、erbB、N-ras基因的高表达。提示蛋白激酶C的激活可以诱导某些癌基因的表达。多种癌基因的表达异常可能在膀胱癌中起重要作用。

 
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