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   tumor protein 的翻译结果: 查询用时:0.009秒
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tumor protein
相关语句
  肿瘤蛋白
     N-terminal Acetylation Characterization of Tumor Protein D52 by Nano Electrospray Tandem Mass Mass Spectrometry
     肿瘤蛋白D52N-端乙酰化的纳升电喷雾串联质谱分析
短句来源
     In group B, six clones were isolated, including cytochrome B,upregulated by 1,25-dihydroxyvitamin D_3 (VDUP1), NADH- ubiquinone oxidoreductase 20Kd subunit, μ-calpain large subunit, tumor protein, translationally-controlled 1 (TPT1) and coatomer α subunit.
     B组分离出的 7个上调基因片段包含 6个已知基因 :细胞色素B ,被 1,2 5 二羟维生素D3 上调基因 (VDUP1) ,NADH 泛醌氧化还原酶 2 0Kd亚单位 ,μ 需钙蛋白酶大亚单位 ,转录 调控肿瘤蛋白 1(TPT1) ,外被体蛋白α亚单位。
短句来源
     Isolation and Expression Analysis of the Gene EncodingTranslationally Controlled Tumor Protein(TCTP) in Cabbage
     结球甘蓝转录调控肿瘤蛋白基因(TCTP)的分离与表达特性初步分析
短句来源
     Isolation and expression analysis of the gene encoding translationally ontrolled tumor protein(TCTP) in cabbage
     结球甘蓝转录调控肿瘤蛋白基因(TCTP)的分离与表达特性研究
     Structure and Function of Translationally Controlled Tumor Protein
     受翻译调节的肿瘤蛋白的结构与功能
短句来源
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  “tumor protein”译为未确定词的双语例句
     Tumor Protein D52 Family
     癌蛋白D52家族
短句来源
     In each tumor protein expressions of HIF-1α,bcl-2 and apoptosis were determined by immunohistochemistry and RT-PCR.
     采用免疫组化和RT PCR技术 ,测定肿瘤细胞HIF 1α蛋白、bcl 2mRNA的表达和细胞凋亡指数。
短句来源
     Conclusion The application of C-12 multiple tumor protein chip measurement in diagnosis of lung cancer was helpful in clinic.
     结论C-12多肿瘤标志物蛋白质芯片的应用对肺癌的诊断有较高的临床参考价值。
短句来源
     The positiverection rate of tumor protein extracts and N-linked glycoproteins was 43.3%(26/40)in patients with lungcancer,15%(6/40)in patients with benign resparitory disease, 10.0%(4/40) in normal volunteers, Therewere no significant differences of positive rates in different pathological types of lung cancer patients.
     肺癌病人血清的阳性率43.3%(26/60),非癌性肺病为15.0%(6/40),健康对照组为10.0%(4/40),肺癌病人血清的阳性率与病理类型无相关性。
短句来源
     Sequence analysis of the MS/MS spectrum revealed that the peptide corresponded to the N-terminal peptide (1-10) of tumor protein D52 with the first methionin acetylated. The sequence of this N-terminal peptide is MDRGEQGLLK.
     对未匹配肽段的序列分析表明它对应于TP D52N端1-10氨基酸MDRGEQGLLK,其中N端第1个氨基酸甲硫氨酸M发生了乙酰化。
短句来源
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  相似匹配句对
     Tumor Protein D52 Family
     癌蛋白D52家族
短句来源
     protein.
     protein。
短句来源
     Ezrin protein and its importance in tumor
     Ezrin蛋白及其在肿瘤中的意义
短句来源
     Vascularization and tumor
     血管生成与肿瘤
短句来源
     ,protein etc.
     、蛋白质等控制其质量。
短句来源
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  tumor protein
To study the quantitative tumor protein metabolism ("compartment "tumor") the13C-leucine-tracer-technique was modified.
      
Brain tumor protein synthesis and histological grades: A study by positron emission tomography (PET) with C11-L-Methionine
      
Densimetric analysis of the GFAP stained gels showed that 12-13% of tumor protein was GFAP compared with 2-3% for the non-neoplastic white and gray matter.
      
The Wilms tumor protein is persistently associated with the nuclear matrix throughout the cell cycle
      
The PsCaP23-encoded protein has high homology with an alfalfa callus protein or translationally controlled human or mouse tumor protein P23.
      
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The effects of cytokine interleukin-2 ( IL-2) and its sequential treatment with tumor necrosis factor-α (TNF) on protein metabolism of the malignant tumor and the host were investigated. Sprague-Dawley rats were inoculated subcutaneously with walker 256 carcinosarcoma cells and were randomly divided into three groups as TNF+IL-2, IL-2, and control groups. For the TNF+IL-2 sequential treatment, the rats were injected subcutaneously with recombinant human TNF for 3 days followed by recombinant human IL-2 for 7...

The effects of cytokine interleukin-2 ( IL-2) and its sequential treatment with tumor necrosis factor-α (TNF) on protein metabolism of the malignant tumor and the host were investigated. Sprague-Dawley rats were inoculated subcutaneously with walker 256 carcinosarcoma cells and were randomly divided into three groups as TNF+IL-2, IL-2, and control groups. For the TNF+IL-2 sequential treatment, the rats were injected subcutaneously with recombinant human TNF for 3 days followed by recombinant human IL-2 for 7 days after tumor implantation. The tissue samples were processed, after an intravenous bolus injection of 14C-leucine, for analysis of protein metabolism of the tumor and the host liver, muscle and the whole-body. The results showed that in IL-2 group and TNF+IL-2 group, significant decreases were found in tumor protein fractional growth rate (17.7 ±2.9 and 23.4± 3.0 % /d respectively, compared with control 33.8±3.4%/d, P<0.05) and tumor protein synthesis rate (0.14±.04 and 0.18±0.06 g/d respectively, compared with control 0.56 + 0.14 g/d, P<0.01), while remarkable increases were revealed in protein fractional synthesis rates ofliver ( 107.7 ±7.1 and 105.0 ±9.1%/d respectively, compared with control 79.6±6.9%/d, P<0.05) and muscle (15.8±1.2 and 13.7± 1.1% /d respectively, compared with control 10.7±0.7% / d, P<0.05) . No differences of these parameters were found between IL-2 and TNF+IL-2 groups. There were no changes of tumor protein degradation and whole body protien synthesis. These results indicated that IL-2 leads to decrease in tumor protein synthesis and increase in protein synthesis of host liver and muscle. Sequential treatment of TNF and IL-2 did not siginficantly enhance the effects of IL-2 on protein metabolism of tumor and the host. An investigation of optimal protocol for combination treatment of cytokines may benefit modulation of tumor and host protein metabolism and control of tumor growth.

Sprague-Dawley大鼠皮下接种Walker 256癌肉瘤后随机分为对照组、IL-2治疗组和TNF+IL-2序贯治疗组。分别切取组织分析肿瘤及宿主肝、肌肉和整体蛋白质代谢。IL-2和TNF+IL-2组的肿瘤分段生长率(分别为17.7±2.9和23.4±3.0%/d,与对照组33.8±3.4%/d比较,P<0.05)和蛋白质合成率(分别为0.14±0.04和0.18±0.06g/d,与对照组0.56±0.14g/d比较,P<0.01)均显著降低,两组的肝蛋白质分段合成率(分别为107.7±7.1和105.0±9.1%/d,对照组79.6±6.9%/d,P<0.05)和肌肉蛋白质分段合成率(分别为15.8±1.2和13.7±1.1%/d,对照组10.7±0.7%/d,P<0.05)均增加,两组间无显著差异。三组的肿瘤蛋白质分解和整体蛋白质合成均无显著改变。本文结果表明,IL-2可致肿瘤蛋白质合成减少及宿主肝和肌肉蛋白质合成增加,但TNF与IL-2的序贯治疗并未显著增加IL-2对肿瘤和宿主蛋白质代谢的作用。

Effects of supplementation of arginine on protein metabolism of malignant tumor and the host were investigated in cancer-bearing rats. Sprague-Dawley rats were subcutaneonsly inoculated with Walker 256 carcinos arcoma cells and received 1% arginine solution as drinking water. The rats were injected intraperitoneally with floodIng dose of leucine and14 C-leucine on day 14 after tumor implantation and Specimens of tumor,liver,muscle and whole body were prepared for analysis of protein metabolism,Arginine drinking...

Effects of supplementation of arginine on protein metabolism of malignant tumor and the host were investigated in cancer-bearing rats. Sprague-Dawley rats were subcutaneonsly inoculated with Walker 256 carcinos arcoma cells and received 1% arginine solution as drinking water. The rats were injected intraperitoneally with floodIng dose of leucine and14 C-leucine on day 14 after tumor implantation and Specimens of tumor,liver,muscle and whole body were prepared for analysis of protein metabolism,Arginine drinking resulted in significant decrease of tumor protein synthesis(0.45±0.15g/d d versus control 1.14±0.20g/d,P<0.01),tumor fractional growth rate(26.4±4.%/d versus control 35.8±2.3%/d,P<0.05)in arginine group but no significant change of tumor protein fractional degradation rate.Significant decrease was also found in arginine group for liver protein fractional synthesis rate(100.7±18.4%/d versus control 166.6±19.0%/d,P<0.05)and protein synthesis(1.85±0.35/d versus control 3.36±0.32 g/d P<0.01)as well as whole body protein fractional synthesis rate(39.3±3.8%/d versus control 50.2±2.2%/d,P< 0.05),These results further proved that supplemented arginine decreased tumor protein synthesis and tumor growth,as well as affected host protein synthesis.Thus supplementation of arginine may benefit to anti-tumor therapy.

Sprague-Dawley大鼠经皮下接种Walker256癌肉瘤细胞后以1%精氨酸溶液代替饮用水饲喂大鼠分别进行肿瘤、肝脏、肌肉和整体的蛋白质代谢分析。精氨酸治疗后肿瘤体积和重量显著减少,肿瘤蛋白质合成率、分段生长率均显著减少,而肿瘤蛋白质分段降解率则无明显改变。精氨酸也影响宿主蛋白质代谢。肝脏蛋白质合成率以及整体蛋白质分段合成率也明显减少,但肌肉蛋白质合成则无明显改变。结果表明,补充精氨酸可减少肿瘤蛋白质的合成和抑制肿瘤的生长,同时也使宿主蛋白质代谢发生改变。

In order to evaluate the significance of N- linked glycoproteins in sera in the diagnosis of lungcancer patients, serum samples were collected from 60 patients vvith lung cancer, 40 patients with benignpulmonary disease and 40 normal volunteers.Tumor proteins were extracted from the mixture of neo-plasms of several patients,The tumor protein labled with HRP were used as a probe in ELISA against N-linked glycoproteins in sera. The result was assayed at 490nm with ELISA detector,the mean value of ab-sorbance...

In order to evaluate the significance of N- linked glycoproteins in sera in the diagnosis of lungcancer patients, serum samples were collected from 60 patients vvith lung cancer, 40 patients with benignpulmonary disease and 40 normal volunteers.Tumor proteins were extracted from the mixture of neo-plasms of several patients,The tumor protein labled with HRP were used as a probe in ELISA against N-linked glycoproteins in sera. The result was assayed at 490nm with ELISA detector,the mean value of ab-sorbance of normal volunteers plus two standard deviations was used as the positive threshold. The positiverection rate of tumor protein extracts and N-linked glycoproteins was 43.3%(26/40)in patients with lungcancer,15%(6/40)in patients with benign resparitory disease, 10.0%(4/40) in normal volunteers, Therewere no significant differences of positive rates in different pathological types of lung cancer patients. Theresults suggest that N-linked glycoproteins can react with tumor protein extracts.

为探讨N-糖苷键型糖蛋白在肺癌诊断中的意义。取肺鳞癌、腺癌、大细胞癌、小细胞癌术后切除新鲜癌组织匀浆混匀,提取蛋白质并标记上辣根过氧化物酶,在ELISA板上与血清中N-糖苷键型糖蛋白反应,按常规方法显色。以正常人血清与肺癌蛋白提取物反应,在490nm的吸光度平均值加两个标准差作为阳性阈值。肺癌病人血清的阳性率43.3%(26/60),非癌性肺病为15.0%(6/40),健康对照组为10.0%(4/40),肺癌病人血清的阳性率与病理类型无相关性。结果提示,肺癌病人血清中N-糖苷键型糖蛋白能较特异地与肺癌组织提取蛋白相结合。

 
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