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医药卫生方针政策与法律法规研究
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三甲
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  three-a
     Methods We sampled respectively 30 cases of cholecystitis, cholelithiasis (operation), breast cancer (operation) and hys-teromyoma(operation) in a three - A hospital in 2000. We observed valueless period of hospitalization and costs of three kinds of operation inpatients from hospitalization to discharge and compared period of hospitalization and costs before and after deleting valueless period of hospitalization.
     方法 抽取某“三甲”医院2000年胆囊炎、胆石症(手术)、乳腺癌(手术)、子宫肌瘤(手术)各30份病历,进行数据收集,观察3种手术患者从入院到出院整个住院流程中的无价值住院日及费用,并对去除无价值住院日前后住院日、住院费用进行比较。
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     Sixteen patients were operated firstly in Three-A hospital,64 in Two-A hospital and 9 in One-A hospital.
     第一次手术单位中三甲医院16例,二甲医院64例,一甲医院15例;
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     METHODS:Data concerning the medication of external preparations in 2004 in a“Three-A”hospital were analyzed.
     方法:对某“三甲”医院2004年外用制剂用药数据进行分析。
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  three a
     Quality Control on Case in Grade Three A Hospital
     论三甲医院病案的质量控制
短句来源
     UNDERSTANDING OF NURSING MANAGEMENT IN COMPREHENSIVE “THREE A” CHINESE TRADITIONAL HOSPITAL’S CLINIC
     综合性“三甲”中医医院门诊护理管理工作体会
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     The Research and Evalustion of the Customer Satisfaction of Some Three a Hospital of Jilin City
     吉林市某三甲医院顾客满意度研究与评价
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  “三甲”译为未确定词的双语例句
     The effect of decyltri methyl ammonium bromide C10H21N(CH3)3Br (C10NM3) on the activity of creatine kinase (C.K.)
     测定了溴化十烷基三甲铵(C_(10)H_(21)N(CH_3)_3Br;记为C_(10)NM_3)对肌酸激酶(Creatine Kinase;记为C.K.)
短句来源
     Cluster analyses show a Bi+Hg, As+Sb+Co and Pb+Zn association for the Yinggezhuang gold deposit, a Bi+Hg+As+Sb+Co, Pb+Zn and Ag+Cu+Au one for Sanjia and a Bi+Hg+Sb+Pb+Ag, Cu+Au+Zn+As and Mo+Ni one for Tongxishan.
     聚类分析显示 ,英格庄金矿具Bi+Hg、As+Sb +Co与Pb +Zn组合 ,三甲金矿具Bi+Hg +As +Sb +Co、Pb +Zn与Ag +Cu +Au组合 ,而铜锡山金矿则显示Bi+Hg +Sb +Pb +Ag、Cu +Au +Zn +As及Mo +Ni组合。
短句来源
     The Study and Application of Eosiny NaClO-CTMAB-H_2O_2-Ti(Ⅳ) Chemiluminescence System
     曙红-NaClO-溴化十六烷基三甲铵-H_2O_2-Ti(Ⅳ)化学发光新体系的研究及应用
短句来源
     The effects of sodium alkylsulfate CnH2n+1 SO4Na (CnS; n = 8, 10,12) and decyltrimethyl ammonium bromide C10H21N (CH3) 3Br (C10 NM3) on the activity of creatine kinase (C.K.)
     测定了烷基硫酸钠(CnH_(2n+1)SO_4Na;记为CnS;n=8,10,12)和溴化十烷基三甲铵C_(10)H_(21)(CH_3)Br;
短句来源
     2,9,16,23-Tetracarboxylmetal-phthalocyanies(Fe, Co, Ni) have been synthesized by the hydrolysis of 2,9,16,23-Tetraformamide metal-phthalocyanies(Fe, Co, Ni) in 22.11%, 21.29% and 26.27% yield, respectively, which were prepared by the reaction of trimellitic anhydride with urea and FeCl_24H_2O, CoCl_26H_2O and NiCl_26H_2O, respectively.
     以偏苯三甲酸酐分别与尿素和FeCl_2、CoCl_2以及NiCl_2反应、再水解合成了2,9,16,23-四羧基酞菁化合物(Fe,Co,Ni),收率分别为22.11%、21.29%和26.27%;
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  collidine
The overall yield of these compounds increases upon adding a base (collidine) or an acid (AcOH) into the initial mixture, and the basicity of initial azoles substantially affects the electrosynthesis results.
      
The species in question are complexes of azoles with one another or with collidine generated at the expense of the hydrogen bond, rather than azolate ions.
      
In the second, chemical interaction of this diene with 3-nitro-1,2,4-triazole and tetrazole is performed when heating a mixture of these substances for a long time at 110°C in the presence of additives of collidine.
      
Interfering ions are removed by paper chromatography with a collidine containing solvent.
      
Tissue preparations in each group consisted of immersion fixation in veronal acetate buffered OsO4 and a perfusion technique utilizing s-collidine buffered glutaraldehyde.
      
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  three a
In three a longitudinal evaluation of the cognitive deficit detected no deterioration.
      
of this edition the Christian name Adriaen occurs twice, the first time printed 'Adriaen', the second time 'Aaaa' when pronounced in Dutch 'Adriaen' could be understood to denote 'A three a's'.
      
Of 28 newborns with prolonged jaundice and lowered or subnormal values of alpha-1-antitrypsin in the serum six patients were found to have a Pi-type MZ, three a Pi-type MS and one patient a Pi-type MP.
      
Survival curves of the three A-stages ran close together with median survival times of 58, 51, and 36 months.
      
Three cycles in MVA-A and-MVA-B, and six in MVA-AB were tested during three A and three B growing seasons for evaluation of progress.
      
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A series of 9 compounds of the bis-tolyloxyalkane-bis-quaternary salts were synthesized by Kyi and Huang. Their actions on the nerve-muscle preparation of them. tibialis anticus and the superior cervical ganglion of the cat were investigated. All these compounds possessed neuromusular blocking action, among them AMBA-1 (1, 1-bis-p-tolyloxy-methane bis-trimethyl ammonium dibromide) was the most active with a potency twice that of d-tubocurarine. The mechanisms of their neuromuscular blocking actions were different....

A series of 9 compounds of the bis-tolyloxyalkane-bis-quaternary salts were synthesized by Kyi and Huang. Their actions on the nerve-muscle preparation of them. tibialis anticus and the superior cervical ganglion of the cat were investigated. All these compounds possessed neuromusular blocking action, among them AMBA-1 (1, 1-bis-p-tolyloxy-methane bis-trimethyl ammonium dibromide) was the most active with a potency twice that of d-tubocurarine. The mechanisms of their neuromuscular blocking actions were different. Compounds with trimethyl ammonium methyl groups at para- and meta-positions resembled decamethonium in antagonim to curare, lack of antagonism by prostigmine and persistence of tetanie contraction in spite of the reduction of twitch height; and those with trimethyl ammonium methyl groups at ortho-position resembled d-tubocurarine in potentiation of d-tubocurarine paralysis, antagonism by prostigmine, and rapid decay of tetanic contraction. AMBA-1, 2, 3, 4, 5, possessed feeble ganglion-blocking action at doses higher than those for blocking neuromuscular transmission, but AMBA-11, 21, 22, 23, were not active. Anticholinesterase actions of these compounds were tested manometrically and compared with physostigmine and prostigmine at the equimolar concentration (3×10~(-6) M). AMBA-4 was the most active (40% inhibition), but weaker than physostigmine and prostigmine.

(一)9个双甲苯氧烷季銨盐都具有神經肌肉阻断作用,其中AMBA-1作用最强,約为d-筒箭毒鹼的两倍。在作用机制上,三甲氨甲基附着于苯环对位或間位的化合物AMBA-1,2,3,4,5,11屬于去極化类型,而三甲氨甲基附着于苯环的邻位的化合物AMBA-21,22,23則屬于竞爭性抑制类型。 (二)这几个化合物对神經节的作用很弱。 (三)在抗胆鹼酯酶作用上,这些化合物都有一定的作用,其中以AMBA-4最强,在3×10~(-6)M濃度时抑制酶活力40%。 (四)这9个化合物主要作用点在横紋肌上,其中以AMBA-22比較符合理想的横紋肌松弛藥的要求,因此正在进一步地研究以确定其是否有实际应用的价值。

Nine N-substituted-3-halo-mesidines have been synthesized for the purpose of testing their activities against Schistosomiasis japonica in experimentally infected animals. They were synthesized by the condensation of 3-halo-mesidines with substituted aminoethyl chloride.The 3-halogenated mesidines were obtained from mesitylene via nuclear dinitration,partial reduction to nitro-amines,diazotization to introduce a halogen group,and reduction of the remaining itro group. The halogenated mesidines synthesized by...

Nine N-substituted-3-halo-mesidines have been synthesized for the purpose of testing their activities against Schistosomiasis japonica in experimentally infected animals. They were synthesized by the condensation of 3-halo-mesidines with substituted aminoethyl chloride.The 3-halogenated mesidines were obtained from mesitylene via nuclear dinitration,partial reduction to nitro-amines,diazotization to introduce a halogen group,and reduction of the remaining itro group. The halogenated mesidines synthesized by the above route were of superior yield to those ob- tained by other methods such as monohalogenation,nitration,and reduction,or mononitration, reduction,and direct halogenation.

本文报告了9种 N-取代-3-卤代-2,4,6-三甲苯胺类化合物的合成.它们用作日本血吸虫病的动物治疗突验.这类化合物是由三甲苯用发烟硝酸行二硝基化成2,4-二硝基1,3,5-三甲苯,用硫化钠及硫还原一个硝基得3-硝基-2,4,6-三甲苯胺,重氮化接上卤素,再用铁屑还原得3-卤代-2,4,6-三甲苯胺,再与 N-取代β-氯乙基胺在硝基苯中缩合而得 N-取代-3-卤代-2,4,6-三甲苯胺类化合物.

Starting with p-trimethylsilyltoluene, the methyl group was brominated with N-bromosuc-cinimide into bromomethyl group and thence p-trimethylsilylbenzyl-substituted acetoacetic ester,malonic ester and nitrile were prepared. The bromomethyl group was successfully converted into aldehyde group by means of Sommlet reaction.After the methyl group in p-trimethylsilyltoluene was oxidized into carboxyl group, the amide was prepared through the action of thionyl chloride and ammonia. Similarly, some esters and amides...

Starting with p-trimethylsilyltoluene, the methyl group was brominated with N-bromosuc-cinimide into bromomethyl group and thence p-trimethylsilylbenzyl-substituted acetoacetic ester,malonic ester and nitrile were prepared. The bromomethyl group was successfully converted into aldehyde group by means of Sommlet reaction.After the methyl group in p-trimethylsilyltoluene was oxidized into carboxyl group, the amide was prepared through the action of thionyl chloride and ammonia. Similarly, some esters and amides of p-triphenylsilylbenzoic acid, dimethyldi(p- carboxylphenyl) and diphenyldi(p-carboxyl)silane were synthesized. No cleavage of the carbon-silicon bond was found during the thionyl chloride treatment.

从对(三甲硅基)甲苯开始,将苄基中的甲基溴化成溴甲基,从而制得对(三甲硅基)苄基取代的乙酰乙酸乙酯,丙二酸乙酯和氰化物等,应用Sommlet反应制得醛. 将对(三甲硅基)甲苯氧化成相应的羧酸后,用亚硫酰氯处理,加入氨水即得对(三甲硅基)苯甲酰胺.应用类似方法,制得对(三苯硅基)苯甲酸、二甲基二(对羧基苯基)硅烷和二苯基二(对羧基苯基)硅烷的一些酰胺和酯.在用亚硫酰氯处理时,未发现硅-碳键的断裂现象.

 
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