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治疗
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  1 therapy
     3 Astragalus Panax Notoginseng 2:1 therapy group: treated the rats with quercetin 0.1 g·kg-1·d-1,tPNS 0.05 g·kg-1·d-1;
     3黄芪三七2:1治疗组:给予槲皮素 0.1 g·kg-1·d-1三七总皂甙0.05 g·kg-1·d-1灌胃;
短句来源
     4 Astragalus Panax Notoginseng 3:1 therapy group: treated the rats with quercetin 0.15 g·kg-1·d-1,tPNS 0.05 g·kg-1·d-1;
     4 黄芪三七3:1治疗组:给予槲皮素 0.15 g·kg-1·d-1三七总皂甙0.05 g·kg-1·d-1灌胃;
短句来源
     3 There was no significant difference in TC、TG between Astragalus Panax Notoginseng 3:1 and 2:1 therapy group .
     3黄芪三七3:1与2:1治疗组之间TC、TG无明显差异。
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     Echocardiographic evaluation of prostaglandin E_1 therapy on pulmonary hypertension secondary to left heart failure in 20 patients
     前列腺素E_1治疗左心衰竭伴肺动脉高压患者20例的超声学评价
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     A meta-analysis of PGE_1 Therapy for Survival and Incidence of Complications in Patients with Liver Failure
     PGE_1治疗对肝衰竭患者生存及并发症发生率影响的荟萃分析
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  “1治疗”译为未确定词的双语例句
     (16.2 ± 1.7)%,(294.7 ± 18.5)%,(15.9 ± 2.8)% in ST + Rg1 group.
     ST+Rg1治疗组为(16.2±1.7)%、(294.7±18.5)%、(15.9±2.8)%。
短句来源
     (9.8 ± 0.9)%, (179.5 ± 11.3)%, (10.4 ± 0.94)% in Rg1 group;
     Rg1治疗组为(9.8±0.9)%,(179.5±11.3),(10.4±0.94)%;
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     However,the expression of CD 4 +,CD 8 + and CD 4 +/CD 8 + was significantly decrease while TGF β 1 was added after the surgery.
     术后经 TGF-β1 治疗 ,CD4+ 、 CD8+ 以及 CD4+ / CD8+ 明显受到抑制。
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     In the fake operated group/ the ischemic reoperfusion damage group and the GM1 treatment group neonatal rats,the levels of ET were:(41.6±4.06)ng/L,(63.45±6.91)ng/L,(50.67±5.20)ng/L;
     假手术组\缺血再灌注组和GM1治疗组新生大鼠血浆的内皮素含量(ng/L)分别为:41.6±4.06,63.45±6.91和50.67±5.20;
短句来源
     The combination treatment with Tα1 increased liver inflammation degree (9.0±5.2).
     拉米夫定治疗可减轻肝细胞变性(3.2±0.8vs4.6±0.5)和炎症反应程度(6.2±3.3vs8.6±2.8),联合Tα1治疗后肝脏炎症反应有所加强(9.0±5.2)。
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  相似匹配句对
     The total courses were 24 weeks.
     d-1,治疗24w。
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     The interval of treatment is 1 year.
     治疗时间1年。
短句来源
     (390.29±53.20)mg·L~(-1)h;
     L-1.h;
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     L~-1 were perfect exterior qualification.
     L~(-1)。
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  1 therapy
A multiple dose IL-1 therapy was evaluated for its capability to stimulate hematopoiesis in normal primates and to restore hematopoiesis after autologous bone marrow transplantation.
      
IL-1 therapy had its greatest effect on the restoration of platelet counts after transplantation, reaching >amp;gt;100 x 10e9/l by day 21, two weeks earlier than control.
      
This work demonstrates that IL-1 therapy stimulates myelopoiesis but its most promising clinical application is the stimulation of platelet production.
      
Effect of insulin-like growth factor-1 therapy on erythropoetin concentrations in extreme insulin resistance
      
Moreover urinary iron excretion due to L1 therapy has been monitored by measuring urine Fe-(L1)3 complex concentrations using reverse phase HPLC and subsequent detection at 450 nm.
      
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Three new 4-amino-2-alkylsulfonyl benzoic acids, namely, 4-amino-2-methylsulfonyl benzoic acid, 4-amino-2-ethylsulfonyl benzoic acid and 4-amino-2-n-propylsulfonyl benzoic acid, have been studied for in vitro in human tuberculosis, hoping that they would surpass the p-amino- salicylic acid in activity. Contrary to our expectations, however, these new compounds have been found to be far less active than the p-amino-salicylic acid itself. The 4-amino-2-n-propyl- sulfonyl benzoic acid possesses an activity in the...

Three new 4-amino-2-alkylsulfonyl benzoic acids, namely, 4-amino-2-methylsulfonyl benzoic acid, 4-amino-2-ethylsulfonyl benzoic acid and 4-amino-2-n-propylsulfonyl benzoic acid, have been studied for in vitro in human tuberculosis, hoping that they would surpass the p-amino- salicylic acid in activity. Contrary to our expectations, however, these new compounds have been found to be far less active than the p-amino-salicylic acid itself. The 4-amino-2-n-propyl- sulfonyl benzoic acid possesses an activity in the order of 10~(-3) in concentration, while the other two compounds require still higher concentrations. Besides, we have prepared five other new compounds: 4-nitro-o-tolyl-methyl sulfide, 4- nitro-2-methylsulfonyl benzoic acid, 4-nitro-o-tolyl-ethyl sulfide, 4-nitro-o-tolyl-n-propyi sulf- fide and 4-nitro-2-n-propylsulfonyl benzoic acid.

對-氨基柳酸為現在常用的一種結核病治療藥劑。我們將其中的羥基代以-SO_(2)R,希望能增強其抑制結核桿菌的性能。我們合成了4-氨基-2-甲磺醯苯甲酸,4-氨基-2-乙磺醯苯甲酸和4-氨基-2-正丙磺醯苯甲酸三種新的化合物。在試管中試驗的結果,除最後一種化合物能在千分之一濃度的溶液中具抑制結核桿菌的性能外,其餘兩種化合物抑制結核桿菌的性能則是更低。我們在製備上述三種化合物時,曾附带合成另外五種新的化合物。

A series of 8 new compounds with the dithia-dihydrostibiol structure has been compared for the therapeutic activities against schistosomiasis japonica in white mice. Each drug, thoroughly mixed with the finely powdered food, was fed to healthy mice for 14 days, and the LD_(10) and LD_(50) were evaluated. At the dosages of LD_(10) and LD_(50), each drug was fed to treat diseased mice (beginning on the 36th day after percutaneous infection on abdomen with 40 cercariae per mouse) for 14 days. After a holding period...

A series of 8 new compounds with the dithia-dihydrostibiol structure has been compared for the therapeutic activities against schistosomiasis japonica in white mice. Each drug, thoroughly mixed with the finely powdered food, was fed to healthy mice for 14 days, and the LD_(10) and LD_(50) were evaluated. At the dosages of LD_(10) and LD_(50), each drug was fed to treat diseased mice (beginning on the 36th day after percutaneous infection on abdomen with 40 cercariae per mouse) for 14 days. After a holding period of another 14 days mice were killed. Both portal system and liver were carefully scrutinized for worms. Basing on the average number of worms remained in each mouse, the therapeutic effects of out of the 8 compounds were better than that of tartar emetic administered orally.

用小白鼠试验8种二硫锑五环化合物,在同一毒性水平上比较对於日本血吸虫病的疗效。每种药物与饲料粉混匀喂饲健康小鼠14天,求出LD_(10)及LD_(50)。以这两个剂量,分别治疗病鼠(每鼠腹部皮肤感染40条尾蚴,5周後开始给药)14天,然後停药14天解剖,详细检查门静脉系统与肝内的余存虫。根据平均每鼠余存虫数,以吐酒石为标准,比较各药的疗效。结果发现Sb-1及Sb-19口服疗效较吐酒石为优。

Acute toxicity experiment consisted of one single intraperitoneal injection, while subacute toxicity experiment consisted of one injection daily for 14 days, of tartar emetic and a subsequent 3-day holding period. The mortality of mice from tartar emetic was observed after concomitant injections of 5 testing drugs (procaine-HCl, sodium phenyl acetate, sodium α α'-dimercaptoadipate, sodium mercaptosuccinate and sodium thiosulfate). The effective detoxicants were mixed up with tartar emetic and then injected intraperitoneally,...

Acute toxicity experiment consisted of one single intraperitoneal injection, while subacute toxicity experiment consisted of one injection daily for 14 days, of tartar emetic and a subsequent 3-day holding period. The mortality of mice from tartar emetic was observed after concomitant injections of 5 testing drugs (procaine-HCl, sodium phenyl acetate, sodium α α'-dimercaptoadipate, sodium mercaptosuccinate and sodium thiosulfate). The effective detoxicants were mixed up with tartar emetic and then injected intraperitoneally, once daily for 14 days, to infected mice. The mice were killed after a holding period of another 14 days. Basing on the average number of worms remained in each mouse, the effects of detoxicants on the antibilharzial activity of tartar emetic were compared. The results were as follows: (1) In mice the acute and subacute LD_(50) after intraperitoneal injection of tartar emetic were found to be 38 and 35 mg/kg/day respectively. (2) The mortality of mice from tartar emetic could be markedly reduced by simultaneous injection of procaine, sodium phenyl acetate, sodium α α'-dimercaptoadipate and sodium mercaptosuccinate, while sodium thiosulfate did not afford any protection. (3) Procaine, sodium phenyl acetate, sodium α α'-dimercaptoadipate and sodium mercaptosuccinate did not decrease the therapeutic. activity of tartar emetic, and, moreover, procaine could significantly augment its therapeutic activity against schistosomiasis japonica.

本文叙述了5种药物(盐酸普鲁卡因、苯乙酸钠、aa′-二巯基己二酸钠、巯基丁二酸钠及硫代硫酸钠)对小白鼠腹腔注射吐酒石急性(注射1次,观察3天)及亚急性(注射14天,观察3天)中毒死亡的影响;并将其中有效解毒药分别和吐酒石混合後腹腔注射小鼠14天以治疗日本血吸虫病,然後停药14天解剖,根据平均每鼠余存虫数比较各药对於吐酒石疗效的影响。结果如下: (一)小白鼠腹腔注射吐酒石急性及亚急性LD_(50)分别为38及35毫克/千克/天。 (二)普鲁卡因、苯乙酸钠、aa′-二巯基己二酸钠及巯基丁二酸钠能使小鼠腹腔注射吐酒石急性及亚急性中毒死亡率明显地减低,而硫代硫酸钠则无效。 (三)普鲁卡因、苯乙酸钠、aa′-二巯基己二酸钠及巯基丁二酸钠4种解毒药并不减低吐酒石之疗效,其中普鲁卡因尚能提高吐酒石治疗日本血吸虫病之疗效。

 
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