助手标题  
全文文献 工具书 数字 学术定义 翻译助手 学术趋势 更多
查询帮助
意见反馈
   expression strength 的翻译结果: 查询用时:0.009秒
图标索引 在分类学科中查询
所有学科
肿瘤学
内分泌腺及全身性疾病
更多类别查询

图标索引 历史查询
 

expression strength
相关语句
  表达强度
     the frequency of PCNA positivity was 45%(14/31),65%(13/20),and 91%(10/11). The P53 protein,PCNA positivity and expression strength showed a significant statistical difference among the three differentiations (P<0.05).
     PCNA阳性率分别为45%(14/31)、65%(13/20)、91%(10/11),在三组间P53蛋白、PCNA的阳性率及表达强度差异均有统计学意义(P<0.05)。
短句来源
     The positive rate of caspase 3 in 88 cases HCC was significantly lower than that in pericarcinomatous liver tissue(18. 5% vs 38. 6% ,P<0. 01) ,the expression strength of caspase 3 protein in HCC was remarkably related to differentiation degree of HCC, the poorer differentiation,the weaker the expression of caspase 3 protein(F= 8. 651 ,P <0. 01).
     88例肝癌组织caspase3蛋白的阳性表达率明显低于癌旁肝组织(18.5%vs38.6%,P%0.01),caspase3蛋白的表达强度与HCC的分化程度相关,分化愈差,caspase3蛋白表达愈弱(F=8.651,P<0.01);
短句来源
     TGF βRⅡ positive rates increased as p27 protein positive expression strength( P <0.05).
     随 p2 7蛋白表达强度增加 ,TGF βRⅡ阳性率增高 (P <0 .0 5 ) ;
短句来源
     The positive expression percentage and expression strength of VEGF, Flt-1 and TGF-β1 in NSCLC cases were related to lymph node metastasis (P<0.05).
     NSCLC组织中VEGF、Flt-1、TGF-β1的阳性表达率和表达强度均与肿瘤淋巴结转移密切相关;
短句来源
     b) Different drug resistance factors had different expression characteristics in various lung cancers, specifically, there was a significant difference in the expression strength between the non-small cell lung cancer (NSCLC) and small-cell lung cancer (SCLC) (P<0.05).
     2)不同耐药因子在不同肺癌的表达具有不同的特点,特别是在表达强度方面NSCLC(非小细胞肺癌)与SCLC(小细胞肺癌)存在显著差异性(P<0.05);
短句来源
更多       
  表达程度
     ②The positive rate and expression strength of TGF-β 1 and -β 2 proteins were more elevated in SD,which suggested that TGF-β 1 and -β 2 proteins were associated with skin fibrosis of SD.
     ②SD组TGF -β1 、β2 蛋白表达阳性率和表达程度均明显增高 ,显示TGF -β1 、β2 蛋白与SD皮肤纤维化有密切关系。
短句来源
     While the expression strength and the strong positive rate of TGF β2 were higher than TGF β1 in SD (P<0.05).
     TGF β2在SD组中的表达程度和过度表达率明显高于TGF β1(P <0 .0 5 )。
短句来源
     Conclusion ①The positive rate and expression strength of TGF-β 1 mRNA in SD patients increased, which implied that TGF-β 1 mRNA may play an important role in fibrosis of SD.
     结论 ①SD组TGF -β1 mRNA表达阳性率和表达程度均增高 ,表明TGF -β1 mRNA在SD纤维化过程中起重要作用。
短句来源
     The positive rates and the expression strength of TGF β1 and β2 in SD were much higher than that in controls (P<0.01);
     SD组TGF β1、β2表达阳性率和表达程度均明显高于对照组 (P <0 .0 1) ;
短句来源
     Results The positive rates and the expression strength of TGF- β1 mRNA in lesions of SD were much higher than those in controls (P < 0.05).
     结果:TGF-β1mRNA在SD组表达阳性率和表达程度均高于对照组(P<0.05);
更多       
  “expression strength”译为未确定词的双语例句
     (3) On expression strength of telomerase and HPV16: cervical cancer>CIN>chronic cervicitis(P<0.05).
     (3)宫颈组织中HPV16及端粒酶协同阳性表达率为:宫颈癌>CIN>慢性宫颈炎(P<0.05);
短句来源
     On expression strength of telomerase and HPV16: cervical cancer> CIN> chronic cervicitis;
     宫颈组织中HPV16及端粒酶协同表达率为:宫颈癌>CIN>慢性宫颈炎,各组之间具有显著性差异(P<0.05);
短句来源
     Conclusions: The expression strength of ET-1 and SCF is related to the ability of DPC inducing hair follicle regeneration.
     结论 :毛乳头细胞诱导毛囊再生的能力与其表达 ET- 1和 SCF的强度相关
短句来源
     There was significantly linearly negative correlation between apoptosis density and expression strength of p53 protein.
     骨肉瘤和良性骨肿瘤组织中p5 3蛋白表达与凋亡细胞密度呈明显的线性负相关 (r =- 0 .895 4,P <0 .0 1) ,其表达增强则凋亡细胞密度逐渐降低。
短句来源
     Finally,FBG was measured and pancreas specimen was collected from all the rats. Pancreas were compared among each groups by reverse transcription polymerase chain reaction(RT PCR) to semi quantify the expression strength of insulin gene.
     最后,测空腹血糖并取胰腺标本,用反转录多聚酶链式反应(reverse-transcriptionpolymerasechainreaction,RT-PCR)方法半定量比较各组胰岛素基因表达的强弱。
短句来源
更多       
查询“expression strength”译词为用户自定义的双语例句

    我想查看译文中含有:的双语例句
例句
为了更好的帮助您理解掌握查询词或其译词在地道英语中的实际用法,我们为您准备了出自英文原文的大量英语例句,供您参考。
  expression strength
Expression strength and tissue specificity were maintained over five transgenic generations.
      
A novel interrupted palindromic sequence, ACATGTCATCATGT, was required for ES specificity and substantially contributed to expression strength of the?AsGlo1 promoter.
      
For example, in sugar-cane the nopaline synthase and CaMV 35S promoters were of equivalent strength, and insertion of Adh1 intron 1 into the 5' transcribed region decreased expression strength.
      
Various chimaeric promoter regions coupled to the uidA β-glucuronidase gene were evaluated for transient expression strength following electroporation into sugar-cane (monocot) and carrot (dicot) protoplasts.
      
The total color intensity of a spot determines the expression strength.
      
更多          


Using in situ hybridization technique with Dig Labeled DNA probe, we studied the expression of cyclin D1, PCNA, P21, p16, and cdc2 gene in the ovary in kunming mice being 3, 5, 7 days pregnant. The results shows that a) The expression strength of PCNA and p16 gene were descendent as pregnancy progress; b)The expression strength of P21,cdc2 and cyclin D1 gene were variational like waves, i. e. being strong in third and seventh day, while being weak in fifth day. The expression pattern of PCNA...

Using in situ hybridization technique with Dig Labeled DNA probe, we studied the expression of cyclin D1, PCNA, P21, p16, and cdc2 gene in the ovary in kunming mice being 3, 5, 7 days pregnant. The results shows that a) The expression strength of PCNA and p16 gene were descendent as pregnancy progress; b)The expression strength of P21,cdc2 and cyclin D1 gene were variational like waves, i. e. being strong in third and seventh day, while being weak in fifth day. The expression pattern of PCNA gene above mentioned do not constrast with the view that tis gene functions as a cell growth-promotive gene. Since the expression of cyclin D1,cdc2, P21 and p16 above described are inconsistent with role of them as the cell growth-promotive and the cell growth-inhibitory genes respectively, these genes may be related to the expression regulution of those genes except cell cycle-related genes. The waves-like variation of the expression of cdc2 and cyclin D1 genes suggests that the physiological change of mice ovarr during early stage pregnant is very complex and activation.

以怀孕为3,5,7d的昆明种小鼠的卵巢为材料,利用质粒扩增的、地高辛标记的基因探针在组织切 片上进行DNA-mRNA分子原位杂交,研究了 cyclinD1,PCNA. cdc2,p21和 p16基因共 5种细胞周期调控基因 在怀孕早期小鼠卵巢中的表达.结果发现:p21基因在怀孕的 3, 5和 7 d的表达都较弱; PCNA基因和 p16基因 的表达强度随孕期的延长而减弱; p21和 cdc2基因和cyclin D1基因的表达强度以 3, 7 d的为强,而怀孕 5 d的 极弱,其表达强度呈现了高(3d)→低(5d)→高(7d)的波浪型变化;PCNA基因的表达变化与其在离体细胞中 的 DNA合成功能一致,而cyclin D1, cdc2,p21和 p16基因表达变化与其细胞周期变化无关,因此它们在孕鼠卵 巢中的功能可能不是作为细胞周期调控因子,而可能与某些基因的表达激活或关闭有关.这些事实一方面表明 细胞周期调控因子在卵巢中的作用可能与细胞周期调控无关,另一方面也说明卵巢组织在怀孕初期在生理上 极为活跃,变化复杂.

Objective To study the effects of psychological stress on the somatostatin mRNZ (SSmRNA) positive cells of gastro sinus. Methods Situ hybridization combined with computer image analysis was used to exame the expression, volume density (Vv) and numerical density (Nv) of the SSmRNA positive cells in three groups of model rats, ie the regular electric and irregular flashing light stimulating group (group A), the regular electric and regular flashing light stimulating group (group B) and the only irregular flashing...

Objective To study the effects of psychological stress on the somatostatin mRNZ (SSmRNA) positive cells of gastro sinus. Methods Situ hybridization combined with computer image analysis was used to exame the expression, volume density (Vv) and numerical density (Nv) of the SSmRNA positive cells in three groups of model rats, ie the regular electric and irregular flashing light stimulating group (group A), the regular electric and regular flashing light stimulating group (group B) and the only irregular flashing light stimulating group (group C). Results Group A>group B>group C in the expression strength of the SSmRNA, the Vv and Nv of the SSmRNA positive cells of the gastro sinus mucosa. Conclusion Psychological stress may increase the somatostatin synthesis and secretion of the gastro sinus mucosa D cells in rats.

目的 探讨心理因素对胃窦粘膜生长抑素m RNA 阳性反应细胞的影响。方法 采用心理应激大鼠模型A、B、C三组, 以原位杂交组织化学和微机图像分析技术, 检测大鼠心理应激后胃窦粘膜生长抑素mRNA 阳性反应细胞的表达强度和细胞体积密度(Vv) 、单位体积数密度(Nv) 的变化。结果 在生长抑素m RNA 的表达程度和Vv、Nv 等方面, 三组相比, 闪光间期长短不均加电刺激组(A 组) > 闪光间期恒定加电刺激组(B 组) > 单纯闪光间期长短不均组(C组) 。结论 此结果表明, 心理应激明显增加大鼠胃窦粘膜D 细胞合成和分泌生长抑素

To investigate the role of transforming growth factor a(TGF- a) in cell proliferation in the pathogenesis of condyloma acuminatum(CA). Methods :The TGF-a expression in situ in lesions of 30 patients with CA and in normal prepuce tissue of 20 healthy men was detected by immunohistochemistry assay.Results:The positive rates of TGF-a expression in two groups were the same, but the expression strength and the strong positive rates in pos- itive TGF-a expression lesions of CA was much higher than those...

To investigate the role of transforming growth factor a(TGF- a) in cell proliferation in the pathogenesis of condyloma acuminatum(CA). Methods :The TGF-a expression in situ in lesions of 30 patients with CA and in normal prepuce tissue of 20 healthy men was detected by immunohistochemistry assay.Results:The positive rates of TGF-a expression in two groups were the same, but the expression strength and the strong positive rates in pos- itive TGF-a expression lesions of CA was much higher than those in normal prepuce tissue (P < 0.001 and P< 0.005 respectively).Conclusions:The cells in CA lesions may synthesize and secrete more TGF-a,which result in its prolif erative effects as a medium in the pathogenesis of the disease.

目的:探讨TCF-α在尖锐湿疣(CA)发病中致细胞增生的作用。方法:采用免疫组化SP法检测30例CA损害中IGF-α的原位表达,并以20例健康男性正常包皮组织作为对照。结果:两组TCF-α表达阳性率相同;CA组TGF-α表达阳性者中的表达程度显著高于对照组(P<0.001);其过度表达率也明显高于对照组(P<0.005)。结论:CA组织细胞可合成与分泌较多的TGF-α,在其发病中作为中间介质发挥致细胞增生的作用。

 
<< 更多相关文摘    
图标索引 相关查询

 


 
CNKI小工具
在英文学术搜索中查有关expression strength的内容
在知识搜索中查有关expression strength的内容
在数字搜索中查有关expression strength的内容
在概念知识元中查有关expression strength的内容
在学术趋势中查有关expression strength的内容
 
 

CNKI主页设CNKI翻译助手为主页 | 收藏CNKI翻译助手 | 广告服务 | 英文学术搜索
版权图标  2008 CNKI-中国知网
京ICP证040431号 互联网出版许可证 新出网证(京)字008号
北京市公安局海淀分局 备案号:110 1081725
版权图标 2008中国知网(cnki) 中国学术期刊(光盘版)电子杂志社