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   前列腺癌组织 的翻译结果: 查询用时:0.058秒
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前列腺癌组织     
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  prostate cancer tissues
     KDR, Flt1 mRNA were expressed in 48.48%(16/33) and 3.33 %(11/33) prostate cancer tissues respectively, but not in normal prostate tissues.
     KDR、Flt1mRNA在部分前列腺癌组织中表达,分别为48.48%(16/33)和33.33%(11/33),而在正常前列腺组织组织中未见表达;
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     The sequence of DD3 mRNA(the GenBank accession number AY894120)showed complete coincidence among all of the 21 prostate cancer tissues and 99.8% homology with the sequence (AF103907).
     21例前列腺癌组织DD3 mRNA序列之间完全一致(GenBank登陆号为AY894120),与国外报道序列(AF103907)之间有99.8%同源。
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     CONCLUSION: The mRNA expression of VEGF and its receptors KDR, Flt1 were up regulated in prostate cancer tissues, and the mRNA expressions of VEGF is closely related to those of KDR and Flt1 and KDR, Flt1, suggesting VEGF and its receptors KDR, Flt1 play an important role in prostate carcinogenesis.
     结论前列腺癌组织中VEGF121、VEGF165及其受体KDR、Flt1mRNA表达水平升高,且VEGF表达与其受体KDR及Flt1表达密切相关。 提示VEGF及其受体KDR、Flt1在前列腺癌发生发展过程中起重要作用。
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     EXPRESSION OF STAT3 AND PHOSPHORYLATED-STAT3 IN PROSTATE CANCER TISSUES AND CELLS
     前列腺癌组织及PC-3细胞中STAT3及磷酸化STAT3的表达
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     Methods SABC immunohistochemistry and immunocytochemistry were used to detect the expression of STAT3 and phosphorylated-STAT3 proteins in 45 cases of prostate cancer tissues, 20 cases of hyperplastic tissues and PC-3 cell line.
     方法 常规石蜡包埋切片SABC免疫组化法检测45例前列腺癌组织、20例前列腺增生组织中STAT3 及磷酸化STAT3 表达, 细胞免疫化学法检测前列腺癌细胞株PC 3细胞STAT3及磷酸化STAT3表达。
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  prostatic carcinoma tissues
     Results: CXCR4 expression was detected in prostatic carcinoma tissues(the positive rate was 55.5%) but not in prostate hyperplasia. The positive rate of CXCR4 was 61.2% when PSA concentrations >20 ng/ml and was 42.8% when PSA concentrations <20 ng/ml.
     结果:在前列腺癌组织上检测到趋化因子受体CXCR4的表达(表达率55.5%),PSA>20 ng/ml与PSA<20 ng/ml的前列腺癌组织上CXCR4的表达率分别为61.2%和42.8%,而前列腺增生组织中未发现这4种趋化因子受体的表达;
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     Expression of chemokine receptor CXCR4 in human prostatic carcinoma tissues
     CXCR4在前列腺癌组织中的表达与意义
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     Expression and Its Significance of Survivin in Human Prostatic Carcinoma Tissues
     Survivin在前列腺癌组织中的表达及其意义
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     Results:The expression levels of KGF in prostatic carcinoma tissues were higher than those in normal prostate tissues (P<0.05).
     结果:前列腺癌组织中的KGF表达高于正常的前列腺组织(P<0 .0 5 ) ;
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     Methods The expression levels of bFGF mRNA in 22 sample of prostatic carcinoma tissues and normal prostate tissues were detected by semi-quantitive RT-PCR, while the expression level of bFGF protein were detected by immunohistochemical staining and quantitative analysis.
     方法应用半定量RT-PCR技术和免疫组织化学方法,检测22例前列腺癌组织中bFGF的表达,并与正常的前列腺组织进行比较。
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  prostate carcinoma tissue
     The expression and its significance of Smad4 and Smad_3 protein in prostate carcinoma tissue
     Smad_4蛋白和Smad_3蛋白在前列腺癌组织中的表达及意义
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     Expression and significance of Smad_4 protein in prostate carcinoma tissue
     Smad_4蛋白在前列腺癌组织中的表达及意义
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     Expression of NKX3.1 and PTEN in Prostate Carcinoma Tissue and the Studies on Effects of PC3 Cell Line After NKX3.1 Transfection
     NKX3.1与PTEN在前列腺癌组织表达及NKX3.1转染对PC3细胞效应的研究
短句来源
     Expression of NKX3.1 and PTEN Genes in Prostate Carcinoma Tissue and the Studies for PC3 Cell Line Transfected by NKX3.1
     NKX3.1与PTEN在前列腺癌组织表达及NKX3.1转染PC3细胞的效应
短句来源
     Methods Immunohistochemistry ABC method is performed to examine the expression of Smad4 and Smad3protein in normal and prostate carcinoma tissue.
     方法采用免疫组织化学ABC法对正常前列腺组织和前列腺癌组织中Smad3和Smad4蛋白进行检测。
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  prostate cancer tissue
     Expression and significance of CD_(44)V_6 gene in prostate cancer tissue
     CD_(44)V_6基因在前列腺癌组织中的表达及其意义
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     Expression of metastasis-associated gene CD44v6 in prostate cancer tissue
     前列腺癌组织转移相关基因CD44v6的表达意义
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     Results: The positive expression rates of OPN mRNA was 76.1%(35/46). The positive expression rates of OPN and MMP-2 were 71.7% (33/46) and 67.4% (31/46) in prostate cancer tissue, respectively, and the expression of OPN was significantly correlated with MMP-2 expression (P< 0.01 ).
     结果:46例前列腺癌组织中OPNmRNA的表达阳性率为76.1%(35/46),OPN及MMP-2蛋白的表达阳性率分别为71.7%(33/46)和67.4%(31/46),两者表达呈正相关(P<0.01)。
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     Conclusions Th e combination of KLK2,pim-1,AR and IGF-1 which are specific molecular markers of prostate cancer tissue may improve the rate of early diagnosis of prostate ca ncer.
     结论KLK2,pim-1,AR和IGF-1作为前列腺癌组织特异性的分子标记物组合,有望提高前列腺癌早期诊断的准确性。
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     Results:A120bp cDNA was amplified by RT-PCR from prostate cancer tissue and the sequencing result showed it was the domain of the third extron in ODC gene.
     结果:用RT-PCR方法从人前列腺癌组织中扩增出120bp的cDNA片段,经测序证实为ODC基因第三外显子的片段。
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  prostate cancer tissues
Furthermore, BPH and prostate cancer tissues were stained immunohistochemically for p75LNGFR.
      
Staining occurred in glandular epithelial cells in the majority of frozen, and paraffin-embedded prostate cancer tissues and was occasionally seen in prostatic intraepithelial neoplasia (PIN).
      
Although p53 mutations in primary prostate cancer tissues are relatively infrequent, they occur at signif icant levels in metastatic disease.
      
As indicated above, hepsin protein expression was elevated in later stage prostate cancer tissues and prostate cancer bone metastasis.
      
However, not all EGR-1 target genes are up-regulated in prostate cancer tissues.
      
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  prostate carcinoma tissue
To investigate the basics for PDT of prostate cancer, several studies were performed on the optical characteristics of prostate tissue and prostate carcinoma tissue in vitro and in vivo and on the penetration depths of different laser wavelengths.
      
The expression of the oncofetal FN ED-B segment in benign prostatic hyperplasia and prostate carcinoma tissue was investigated by RT-PCR.
      
RT-PCR experiments showed the expression of the oncofetal FN ED-B segment in benign prostatic hyperplasia and prostate carcinoma tissue, with a 3.5-fold higher expression in the prostate carcinoma probes.
      
  prostate cancer tissue
Gene expression studies in prostate cancer tissue: which reference gene should be selected for normalization
      
The suitability of housekeeping genes for that purpose in prostate cancer tissue has not been sufficiently investigated so far.
      
No single molecular parameter is routinely analyzed in prostate cancer tissue.
      
Furthermore, inherent logistical problems result in a shortage of prostate cancer tissue for research purposes.
      
Practical aspects of planning, building, and interpreting tissue microarrays: The Cooperative Prostate Cancer Tissue Resource ex
      
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