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
   in in 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
金属学及金属工艺
材料科学
文艺理论
更多类别查询

图标索引 历史查询
 

in in
相关语句
  在in
     STUDY OF Zn, Zn-Cd DIFFUSION IN In_xGa_1-xAs
     Zn、Zn-Cd在In_xGa_(1-x)As中扩散的研究
短句来源
     THERMODYNAMIC CALCULATION AND PRECIPITA- TION BEHAVIOR OF α-Cr PHASE IN IN718 ALLOY
     α-Cr相在IN718合金中的析出及其热力学计算
短句来源
     The temperature dependence of the quadrupole interaction of 111Cd in In0 95 Ag0 045 Ga0.005 alloy is determined by the time differential perturbed angular correlation (TDPAC) method from 80 to 422K.
     本文采用时间微分扰动角关联方法,测量了80—422K温度范围内~(111)Cd在In_(0.95)Ag_(0.043)Ga_(0.005)合金中的四极相互作用随温度的变化,进而导出晶格电场梯度的温度变化。
短句来源
     The gas sensing properties of doping Pd,Fe2O3,SnO2,CaO, MgO in In2O3 material were reported in this paper. The experimental results showed that the doping and sintering temperature had the big influence for gas sensitive properties of In2O3 material. 
     报道了在In2O3材料中分别掺杂一定比例的Pd,Fe2O3,SnO2,CaO和MgO材料后敏感材料的气敏特性.实验结果表明,掺杂及烧结温度对In2O3材料的气敏特性有较大的影响.
短句来源
     INFLUENCES OF BORON, SULFUR AND ALUMINUM ON THE EFFECTS OF PHOSPHORUS IN IN718 ALLOYS
     硼、硫和铝对磷在IN718合金中作用的影响
短句来源
更多       
  “in in”译为未确定词的双语例句
     AES STUDY OF THE COMPOSITIONAL TRANSITION LAYER IN In_1-_xGa_xAs_yP_(1-y)-InP HETEROJUNCTION INTERFACE
     In_(1-x)Ga_xAs_yP_(1-y)—InP异质结界面组分过渡层的俄歇电子能谱研究
短句来源
     Electric quadrupole interactions in In_(0.95) Ag_(0.045) Ga_(0.005) alloy
     In_(0.95)Ag_(0.045)Ga_(0.005)合金中的电四极相互作用
短句来源
     GENETIC TOTIPOTENCY OF PLANT CELLS AND CONTROLOF MORPHOGENESIS IN IN VITRO CULTURES
     植物细胞的遗传全能性与组织培养形态发生控制
短句来源
     WATER SUPPRESSION IN in VIVO ~1H NMR SPECTROSCOPY
     体内~1H NMR中的水峰抑制
短句来源
     STUDY OF PICOSECOND SPECTRA OF HOT CARRIER DISTRIBUTION IN In_xCa_(1-x)As/GaAS STRAINED SINGLE QUANTUM WELL STRUCTURES
     In_xCa_(1-x)As/GaAs应变量子阱结构中热载流子分布的皮秒光谱研究
短句来源
更多       
查询“in in”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。
  in in
It was shown that the IN efficiency in a liposomal form decreased depending on the liposome composition and concentration as compared with the IN in water solution.
      
The differences in in vitro antiesterase activity of cyclic thionic and the corresponding oxo derivatives of phosphorinane were revealed.
      
The majority of data accumulated in in vitro models and discussed in this review are in good agreement with the results of in vivo observations.
      
In etiolated seedlings of Pisum sativum and leaves of Arabidopsis thaliana, in vivo ethylene treatment resulted in an increase in in vitro phosphorylation of 17 kD (P.
      
However, the deletion of the first 17 N-terminal residues results in functionally active protein that can complete the 11--defective phage particles in in vitro complementation assay.
      
更多          


Short-term cultures of human leukemic cells were utilized to study the antitumour effect of eight drugs commonly used in clinical medicine. Cytotoxic effect was demonstrated with nitrogen mustard, nitromin, sarcolysin, thio-TEPA and myleran at concentrations of 7, 10, 25, 35, 100, and 100μg/ml respectively. No effect on the leukemic cells was observed with 6 MP and aminopterin. With the same culture technic twenty four compounds of various structures were screened for antitumour activity. Among these nine were...

Short-term cultures of human leukemic cells were utilized to study the antitumour effect of eight drugs commonly used in clinical medicine. Cytotoxic effect was demonstrated with nitrogen mustard, nitromin, sarcolysin, thio-TEPA and myleran at concentrations of 7, 10, 25, 35, 100, and 100μg/ml respectively. No effect on the leukemic cells was observed with 6 MP and aminopterin. With the same culture technic twenty four compounds of various structures were screened for antitumour activity. Among these nine were found to have an injurious action on the leukemic cells in vitro, and besides, they were shown in in vivo experiments to possess also an inhibitory action on the growth of several transplantable animal tumours. The remaining fifteen compounds exhibited no effect on the leukemic cells in the culture, nor did they affect the growth of transplanted tumours. The close parallelism between the results of the in vivo and in vitro experiments indicates that this tissue culture method could be used effectively for screening antitumour drugs.

本文应用人的白血病細胞短期培养的方法,对常用的8种抗肿瘤药物进行了观察。氮芥及氧化氮芥在7—10微克/毫升,溶肉瘤素和新恩必恨于25—35微克/毫升,三乙酰硫代磷酰胺和丁二醇二甲磺酸酯在100微克/毫升,都出現了显著的細胞毒作用,使細胞很快死亡溶解;但6-巯基嘌吟和氨基喋吟未表現作用。在24种不同类型药物的研究中:9种对白血病細胞有明显的毒性作用,这些药物对动物移植性肿瘤也有抑制作用;15种体外无效,体內也无作用(表1)。結果証明,本方法可作为抗肿瘤药物篩选方法之一。

A method of extraction,separation and determination of the residual rogor (O,O-dimethyl S-(N-methyl-carbomoylmethyl) phosphorothionate) in vege- tables and fruits is described.The residual quantities of the rogor retained in the cabbages of different growing stages,in two-varieties of rapes and in leaves and fruits of peach tree were determined successively at intervals of the first,third,fifth and seventh day after the spraying of the insecticide. The insecticidal effects against the aphids as measured by lethal...

A method of extraction,separation and determination of the residual rogor (O,O-dimethyl S-(N-methyl-carbomoylmethyl) phosphorothionate) in vege- tables and fruits is described.The residual quantities of the rogor retained in the cabbages of different growing stages,in two-varieties of rapes and in leaves and fruits of peach tree were determined successively at intervals of the first,third,fifth and seventh day after the spraying of the insecticide. The insecticidal effects against the aphids as measured by lethal rate (in %) in respective period were recorded. It is found that at the first day after spraying the residual rogor in buds and stem of the cabbages at budding stage is about 2.5 times as that of the leaves of the same plant,while the amount of the insecticide in the whole plant at seedling stage is between the latter two.The rogor residue in Sun-li rape (cabbage type) is higher than that of the Pai-go rape (Chi- nese cabbage type).For the peaches,the rogor retained in the leaves is about 5 times as that of the fruits.The insecticidal effect agrees very well with the residual rogor in the tested samples. All the rogor residues retained in the tested samples are below I ppm. which is far below the recognized safety margin,2 ppm.

1.作者描述了一个效果较好而又节省有机溶剂的提取及分离乐果的方法。2.不同生育期青菜(四月慢)中乐果残留量的测定指出:在同株孕蕾抽苔期青菜上,苔莢中乐果含量为菜叶的2.5倍(施药一天后);同时也大于小菜期全株的含量。3.所试两种不同类型的油菜中,甘蓝型(胜利油菜)的乐果残留量大于白菜型(白果油菜)。这种差具可能由于生态的而非生理的原因所致。4.施药一天后,同株桃树上,桃叶中的乐果残留量为桃子的5倍。5.施药五天后,所测各样品的乐果残留量均小于1ppm,这个数值低于规定的安全限量2ppm。

Thioacetamide is a hepatotoxic agent.In this paper,the effects of thioacetamide on the pentobarbital sleeping time and the rate of hepatic drug metabo- lism in mice and rats are reported. Mice treated with a dose of thioacetamide (60mg/kg s.c.) 48 hours prior to an in- jection of pentobarbital slept much longer than untreated animals.Similar results were obtained in rats treated 12-72 hours previous to injection.One hour after pentobarbital administration,whole-body levels of the hypnotic in thioacetamide-treated...

Thioacetamide is a hepatotoxic agent.In this paper,the effects of thioacetamide on the pentobarbital sleeping time and the rate of hepatic drug metabo- lism in mice and rats are reported. Mice treated with a dose of thioacetamide (60mg/kg s.c.) 48 hours prior to an in- jection of pentobarbital slept much longer than untreated animals.Similar results were obtained in rats treated 12-72 hours previous to injection.One hour after pentobarbital administration,whole-body levels of the hypnotic in thioacetamide-treated mice were significantly higher than those in control animals.The rate of biotransformation of pentobarbital in vitro by liver slices from rats pretreated with thioacetamide was found to be less rapid than those from control animals.These facts indicate that the hepatic metabolism of pentobarbital was lowered by thioacetamide pretreatment,and thus may explain,at least in part,the prolonging effect of thioacetamide on pentobarbital sleeping time.On the other hand,at the time of recovery from narcosis,the whole body levels of pentobarbital in thioacetamide pretreated mice as well as the concentrations of bar- biturate in the brain of rats pretreated similarly,were significantly lower than those in control animals.In addition,it was found that the ED-50 of pentobarbital action was decreased,and that the diethylbarbital sleeping time was increased by pretreatment with thioacetamide.It appears,therefore,that an extra-hepatic mechanism of the effect of thioacetamide on pentobarbital action is also involved. In in vitro experiments using liver slices from rats treated with thioacetamide 48 hours previously,only a slight decrease in the rate of metabolism of chlorpromazine was observed,while the rate of biotransformation of p-nitrobenzoic acid was not sig- nificantly affected.When added in vitro,thioacetamide was shown to exert no inhibitory effect on pentobarbital metabolism.The decrease in the pentobarbital-metabolizing ability of liver slices from rats pretreated with thioacetamide was found to correlate to a certain extent with the fall of hepatic glycogen and aseorbic acid contents,as well as with the histological changes induced by this hepatotoxic agent. Thioacetamide was shown not to block completely the shortening of phenobarbital sleeping time or the increase in hepatic aseorbio acid content induced by phenobarbital pretreatment.

给小鼠皮下注射硫代乙酰胺60毫克/公斤后48小时戊巴比妥钠睡眠时间明显延长;同剂量的硫代乙酰胺给大鼠后在12—72小时内戊巴比妥钠睡眠时间也都明显延长,而以48小时者最为明显。进一步实验发现48小时前接受一剂硫代乙酰胺处理的小鼠,戊巴比妥钠自体内消失的速率比正常动物者明显减慢;12—72小时前曾接受一剂硫代乙酰胺的大鼠肝切片转化戊巴比妥钠的速率比正常动物肝切片者小,此与戊巴比妥钠睡眠时间的延长相一致。可见,经硫代乙酰胺处理的动物的戊巴比妥钠睡眠时间延长的原因之一,是由于硫代乙酰胺抑制了肝脏对戊巴比妥钠的转化。另一方面,48小时前曾接受过硫代乙酰胺处理的小鼠,睡眠刚醒时,体内戊巴比妥钠含量明显地低于对照组;曾经硫代乙酰胺处理的大鼠刚醒时,脑组织的戊巴比妥钠含量明显低于对照组者。在经硫代乙酰胺处理后的小鼠,戊巴比妥钠引起睡眠的 ED_(50)明显减小;二乙基巴比妥钠的睡眠时间亦明显延长。这些结果说明硫代乙酰胺处理也增加了动物中枢对戊巴比妥类药物的敏感性。

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