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
   加压对照 的翻译结果: 查询用时:0.174秒
图标索引 在分类学科中查询
所有学科
更多类别查询

图标索引 历史查询
 

加压对照
相关语句
  “加压对照”译为未确定词的双语例句
     The left in uncomprssion operation group was 32.2±2.3,3 2.2±4.3,32.2±3.1/mm2;
     手术不加压对照组左侧为(32.2±2.3),(32.2±4.3),(32.2±3.1)/mm2;
短句来源
     Methods: The retinal neuron of postnatal SD rats were cultured in vivo, the elevatedpressure was produced after 7days, and the total RNA was extracted after another 2 days,expression of p53、MDM2 and Ref1 gene were analyzed with RT-PCR.
     方法:新生SD大鼠视网膜神经细胞体外培养,倒置相差显微镜观察细胞的生长情况,细胞分单纯加压组、实验加压组(加入维生素B1)及未加压对照组,于加压后2 d(培养第9~10天)行苔盼兰染色检查计数细胞成活率,p53免疫组化检查并提取细胞总RNA,用逆转录聚合酶链反应法检测p53、MDM2及Ref1基因的表达。
短句来源
     RESULTS:The expressions of IL-6 after continuous pressure-loading for 16 and 24 hours in the pressure-loading group were(143.1±0.42) and(49.46±1.01) ng/L,which were obviously higher than those in the pressure-loading control group [(18.36±0.43),(18.78±0.50) ng/L,P < 0.05].
     结果:加压组细胞经持续加压16,24h后的白细胞介素6表达量分别为(143.1±0.42),(49.46±1.01)ng/L,明显高于加压对照组[(18.36±0.43),(18.78±0.50)ng/L,P<0.05];
短句来源
     Part I : The cartilages were pressed at 100KPa and 300KPa for different duration. The thickness of proliferative zone and transitional zone were measured by computer.
     第一部分:建立髁突软骨组织的体外培养模型,对体外培养的乳鼠髁突软骨施加100KPa、300KPa的静压力,在加压4、8、12h取材,使用电子测量尺测量软骨增殖层、过渡层厚度变化,设不加压对照组。
短句来源
     METHODS:Fifty pure breed healthy male New Zealand rabbits were devided into th ree groups randomly: non-treatment group(10 rabbits); non-compression control g roup(10 rabbits) and trial group(30 rabbits).
     方法:纯种健康雄性新西兰兔40只,按随机数字表法分为3组,非手术对照组10只,手术不加压对照组10只,模型组30只;
短句来源
更多       
  相似匹配句对
     (G)normal control;
     G ,正常对照 ;
短句来源
     F, as control.
     F,对照组。
短句来源
     COLD PRESSOR ECHOCARDIOGRAPHY IN NORMAL CHILDREN AND CASES WITH MYOCARDITIS
     健康儿童超声心动图冷加压试验(附6例心肌炎对照)
短句来源
     Pressure conversion of sulphur dioxide to sulphur trioxide
     二氧化硫的加压转化
短句来源
     E.
     加压二氧化碳对E.
短句来源
查询“加压对照”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。
  compression control
Compression control and its significance in the manufacture and effects on properties of poplar LVL
      


Twenty—four rabbits, after artificial fracture, were randomly allocated into the nut—stress control group and the five groups in which the forces of one times. two times, three times, four times and five times of their body weights were respectively adopted to do the experiment of nut—stress on the artificial fractures. Judging from the 6 healing data of the stability of the broken ends, the gaits in the sixth week, x—ray examination, histology the calcium deposition and curve intensity, it proved that the healing...

Twenty—four rabbits, after artificial fracture, were randomly allocated into the nut—stress control group and the five groups in which the forces of one times. two times, three times, four times and five times of their body weights were respectively adopted to do the experiment of nut—stress on the artificial fractures. Judging from the 6 healing data of the stability of the broken ends, the gaits in the sixth week, x—ray examination, histology the calcium deposition and curve intensity, it proved that the healing effect is the best favorable under the compression of three times and four times of body weights and that the best shearing stress of nut—stress on the artificial fractures of the rabbits:σ=3.45MPa

采用24只家免,人工骨折后随机分不加压的对照组和用体重的1、2、3、4、5倍的力进行骨折加压实验的5组,而后通过骨断端的稳定性、6周后的步态、X光片、钙盐沉积及弯曲强度等6项愈合指标判定。结果以体重的3倍及4倍加压骨折愈合最佳,得出家兔骨折加压最佳应力值:σ=3.45MPa。

AIM:To study the pathological mechanism of sensory disturbance caused by cauda equina nerve damage.METHODS:Fifty pure breed healthy male New Zealand rabbits were devided into th ree groups randomly: non-treatment group(10 rabbits);non-compression control g roup(10 rabbits) and trial group(30 rabbits).At the following time points(1/4,1/ 2,3,7 and 15 days).According to the of the compressor screw the sagittal diamete r of vertebral canal,the model group was divided into 1/9,2/9,1/2.The compressio n devices were...

AIM:To study the pathological mechanism of sensory disturbance caused by cauda equina nerve damage.METHODS:Fifty pure breed healthy male New Zealand rabbits were devided into th ree groups randomly: non-treatment group(10 rabbits);non-compression control g roup(10 rabbits) and trial group(30 rabbits).At the following time points(1/4,1/ 2,3,7 and 15 days).According to the of the compressor screw the sagittal diamete r of vertebral canal,the model group was divided into 1/9,2/9,1/2.The compressio n devices were fixed between S2 and S3 to compress cauda equina.Posterior root g anglion was removed from the model with cauda equina nerve syndrome at different time point,and stained with HE.The number of normal sensory neuron cells were c ounted.RESULTS:After cauda equina nerve syndrome occurred for 1/2 day,there was isch emia and edema in two sides of posterior root ganglion and cellular necrosis of neurons in ganglion.The number of normal cells in posterior root ganglion was 3 and 7.The left in unoperation control group at time point of 30d was 32.2±4.2,3 2.2±4.3,32.2±4.3/mm2; The left in uncomprssion operation group was 32.2±2.3,3 2.2±4.3,32.2±3.1/mm2;The left in experiment group was 17.2±3.3,14.2±3.2,14. 1±2.3/ mm2.There was significant difference between groups(P< 0.05).CONCLUSION:Sensory neurons in posterior root ganglion are very sensitive and e asily suffer necrosis,which is one of the important pathological changes of dire ct degeneration in cauda equina nerve damage and also explain why the numbness o f sella turcica region and sensory disturbance are hard to recover.

目的:初步探讨马尾神经损害导致马尾神经综合征,引以感觉障碍的原因。方法:纯种健康雄性新西兰兔40只,按随机数字表法分为3组,非手术对照组10只,手术不加压对照组10只,模型组30只;模型组再根据加压螺丝进入椎管矢状径的深度分为进入1/9,2/9,1/2。模型组加压装置置于S2~3压迫马尾神经组。取不同时间段的马尾神经综合征的模型的神经根的后根节,作HE染色对其内正常感觉神经元细胞记数。结果:临床出现马尾神经综合征1/2d,将导致双侧后根节缺血水肿,节内神经元细胞坏死。后根节的正常细胞记数:3,7,30d时非手术对照组左侧为(32.2±4.2),(32.2±4.3),(32.2±4.3)/mm2;手术不加压对照组左侧为(32.2±2.3),(32.2±4.3),(32.2±3.1)/mm2;实验组左侧为(17.2±3.3),(14.2±3.2),(14.1±2.3)/mm2;差异有显著性意义(P<0.05)。结论:背根结内的感觉神经元极敏感,极易坏死,是马尾神经损害顺行溃变的重要病理变化之一,是导致鞍区麻木、感觉障碍,难以恢复的重要原因。

Purpose: To investigate the expression of p53、MDM2 and Ref1 gene in cultured retinaneurons of SD rats treated with Vitamine B1 and (or) elevated pressure.Methods: The retinal neuron of postnatal SD rats were cultured in vivo, the elevatedpressure was produced after 7days, and the total RNA was extracted after another 2 days,expression of p53、MDM2 and Ref1 gene were analyzed with RT-PCR.Results: The expression level of p53 and MDM2 gene were increased in elevatedpressure group, normal with Ref1 gene expression.But...

Purpose: To investigate the expression of p53、MDM2 and Ref1 gene in cultured retinaneurons of SD rats treated with Vitamine B1 and (or) elevated pressure.Methods: The retinal neuron of postnatal SD rats were cultured in vivo, the elevatedpressure was produced after 7days, and the total RNA was extracted after another 2 days,expression of p53、MDM2 and Ref1 gene were analyzed with RT-PCR.Results: The expression level of p53 and MDM2 gene were increased in elevatedpressure group, normal with Ref1 gene expression.But the expression of p53 and MDM2gene were decreased significantly in elevated pressure group treated with vitamine B1compare to the elevated group.Conclusion: Apoptosis seem to be a mechanism of cell death in retinal neurons of SDrats with elevated pressure.Vitamine B1 have protect effects against elevated pressure.

目的:探讨压力及压力加维生素B1联合作用下SD大鼠视网膜神经细胞p53、MDM2及Ref1基因的表达情况。方法:新生SD大鼠视网膜神经细胞体外培养,倒置相差显微镜观察细胞的生长情况,细胞分单纯加压组、实验加压组(加入维生素B1)及未加压对照组,于加压后2 d(培养第9~10天)行苔盼兰染色检查计数细胞成活率,p53免疫组化检查并提取细胞总RNA,用逆转录聚合酶链反应法检测p53、MDM2及Ref1基因的表达。结果:单纯压力组p53/MDM2基因的表达较正常未加压组增强,Ref1基因表达无增强;而维生素B1作用后的加压组,其p53/MDM2基因的表达较单纯加压组明显减弱。结论:压力作用下视网膜神经细胞的损害有凋亡机制参与,维生素B1对压力作用下视网膜神经细胞具有保护作用。

 
<< 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加压对照的内容
在知识搜索中查有关加压对照的内容
在数字搜索中查有关加压对照的内容
在概念知识元中查有关加压对照的内容
在学术趋势中查有关加压对照的内容
 
 

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