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  tcp
     β TCP1/rhBMP 2, β TCP2/rhBMP 2, β TCP1, β TCP2 and β TCP3 were used to repair 15 mm radial segmental defects in 81 Chinese rabbits.
     选择81只中国家兔,制成15mm长的双侧桡骨节段性缺损动物模型,分别用βTCP1/rhBMP2、βTCP2/rhBMP2、βTCP1、βTCP2、βTCP3修复桡骨缺损区。
短句来源
     Methods Three kinds of β tricalcium phosphate(β TCP) with different degradation rate (β TCP1-3) were prepared by means of different techniques. β TCP/rhBMP 2 composites with different degradation rate(β TCP1/rhBMP 2 and β TCP2/rhBMP 2)were obtained by combining β TCP1, β TCP2 with recombinant human bone morphogenetic protein 2(rhBMP 2), respectively.
     方法以不同工艺制备出三种不同降解率的βTCPβTCP1~3βTCP1、βTCP2分别与rhBMP2复合制备生成不同降解率的βTCP1/rhBMP2和βTCP2/rhBMP2复合人工骨。
短句来源
     Although degradation occurred to some extent in β TCP alone the degradation were faster in β TCP/rhBMP 2 composites. At 24 weeks the degradation rate in β TCP1/rhBMP 2 group and β TCP2/rhBMP 2 group were 97.4%and 73.4%, respectively.
     复合人工骨移植材料与单纯βTCP相比,降解速度更快,24周时βTCP1/rhBMP2和βTCP2/rhBMP2两组的降解率分别为97.4%和73.4%。
短句来源
     The quantity and rate of new bone formation in β TCP1/rhBMP 2 group and β TCP2/rhBMP 2 group were higher than those in group of β TCP alone. The ability of new bone formation in β TCP1/rhBMP 2 group was strongest.
     βTCP1/rhBMP2和βTCP2/rhBMP2两组的成骨数量和成骨速度均高于单纯βTCP组,其中以βTCP1/rhBMP2组成骨能力最强,术后24周时骨缺损已完全修复,骨髓腔出现;
短句来源
     Objective To examine the segmental bone defects healing by β TCP/rhBMP 2 composites with different degradation rate and discuss the relationship between osteogenesis and degradation of β TCP in vivo.
     目的检测不同降解率βTCP/rhBMP2复合人工骨修复节段性骨缺损的能力,探讨成骨与βTCP体内降解的关系。
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  “tcp”译为未确定词的双语例句
     In this paper, energy dispersive X ray spectroscopy and element ratio of implanted bioceramic, interface and rabbit femur when the bioceramic implanted into femur were measured by two different scan electron microscopy (SEM) EDXA modes.
     采用两种不同的扫描电镜与X射线能谱仪测量了多孔磷酸三钙(βTCP) 生物陶瓷骨内植入后植入陶瓷、界面和兔股骨的X射线能谱和元素比。
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  相似匹配句对
     Gly.
     Gly。
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     A Summarization of TCP Congestion Control
     TCP拥塞控制综述
短句来源
     The Analysis of TCP Congestion Control Algorithms
     TCP拥塞控制算法
短句来源
     Conclusion β TCP/rhBMP 2 composites with different degradation rate could repair segmental bone defects, and osteogenesis could accelerate the degradation of β TCP in vivo.
     结论不同降解率βTCP/rhBMP2人工骨具有修?
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     Some gene model for mammalian sex determination such as Zgene model and DSSgene model etc.
     X连锁的DAX基因;
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  tcp
Based on a linearized TCP/AQMmodel, a new proportional integral (PI) controller design approach is proposed.
      
This analytical approach applies H∞ optimization and internal model control (IMC) theory to design active queue management (AQM) routers that support transmission control protocol (TCP) flows.
      
The results show the advantages of the new PI controller design approach for AQM routers supporting TCP flows.
      
Virtual Interface (VI) protocol has been proposed to overcome the software overhead of the TCP/IP.
      
Then, we can take advantage of VI's superior performance over TCP/IP in LAN environment.
      
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In this paper the as-cast microstructure, the rules of phase precipitation, the change of microstructure and minor phase content and the degeneration of aluminide coating after thermal exposure at temperature range from 850℃ to 1100℃ for 1000-3000 hours have been studied in comparison between two kinds of low chromium-high tungsten cast nickel-base superalloys.The experimental results have shown that these alloys have high structural stability, the alloys of normal composition did not precipitate TCP phase...

In this paper the as-cast microstructure, the rules of phase precipitation, the change of microstructure and minor phase content and the degeneration of aluminide coating after thermal exposure at temperature range from 850℃ to 1100℃ for 1000-3000 hours have been studied in comparison between two kinds of low chromium-high tungsten cast nickel-base superalloys.The experimental results have shown that these alloys have high structural stability, the alloys of normal composition did not precipitate TCP phase in all thermal exposure conditions and the total amount of minor phase in K002 and K19H after thermal exposure at 1050℃/1000 hr. only increased by 89%and 18% respectively. The following reactions have been proposed:Because the above reactions pick up residual carbon in γ-matrix, the formation of M6C and M23C6 is restricted.Besides, large quantity of niobium containing in MC carbide of K19H mates MC stabilize, therefore slows down the following reaction

本文对比地研究了两种低铬-高钨系列的铸造镍基高温合金的铸态显微组织,在850~1100℃范围内热暴露1000~3000小时后的相析出规律,显微组织和微量相的变化及铝化物涂层的蜕化。 试验结果表明这些合金具有高的组织稳定性,标准成份的合金在所有热暴露条件下不析出TCP相,经1050℃/1000小时后K002和K19H合金中微量相总量只分别增加了89%和18%。 提出了下列反应:由于上述反应夺取γ中残余的碳,抑制了M_6C和M_(23)C_6的形成。 此外,在K19H的MC碳化物中含有大量Nb使MC稳定,因此减缓了下列反应;

pharmacokinetic process of DS-36 was studied in the 6 adult normal milk goats. Ds-36 was administrated intravenously at a dose of 100 mg/kg of boody weight (single dose).Blood samples were collected within the 12-hour period after the drug was given.The blood concentration-time curves of the drug were fitted for a single-compartment pharmacokinetic model.The pharmacokinetic values of the milk goats are described as follows:β0.0089±0.0027min~(-1).;B 26.12± 2.78(mg/100ml);T(1/2)1.45h,V_d 3.91±0.47 (100ml/kg);AUC...

pharmacokinetic process of DS-36 was studied in the 6 adult normal milk goats. Ds-36 was administrated intravenously at a dose of 100 mg/kg of boody weight (single dose).Blood samples were collected within the 12-hour period after the drug was given.The blood concentration-time curves of the drug were fitted for a single-compartment pharmacokinetic model.The pharmacokinetic values of the milk goats are described as follows:β0.0089±0.0027min~(-1).;B 26.12± 2.78(mg/100ml);T(1/2)1.45h,V_d 3.91±0.47 (100ml/kg);AUC 3186.15±943.78 mg·min/100ml;cl_B0.034±0.0009(100ml/kg·min.)Tcp(ther.)3.3h.Theresults obtained showed that DS-36 is a short action drng of sulfonamides for the milk goats.

本文初步分析了 DS-36在8只健康成年奶山羊体内的代谢动力学过程。静脉推注100毫克/公斤,血药浓度—时间曲线符合一室开放模型,不符合二室开放模型;按一室模型算出 DS-36的药代动力学参数如下:消除速率常数(β)0.0089(分钟~(-1));初始浓度(B)26.12(毫克/100毫升);生物半衰期(T(1/2))1.45(小时);表观分布容积(Vd)3.91(100毫升/公斤);廓清率(Cl_B)0.034(100毫升/公斤·分钟)维持有效浓度的时间(Tcp[ther])3.3(小时),上述结果表明 DS-36对奶山羊为短效药物。

This papar described pharmaco, kinetics process of weekly-acting sulfonamide in four healthy adult horses. Some parameters of pharmacokinetics on weeklyacting Sulfonamide were calculated by mathematical equation associated with twocompartment open model. The t 1/2 of weekly-acting Sulfonamide was 14.13±2.15 hours and the TCP(ther) was 10.03±3.50 hours. The weekly-acting Sulfonamide for the horses was not weekly-acting, it was only medium sulfanamide. Following post-intravenous administrastion (Bolus)(50mg/kg...

This papar described pharmaco, kinetics process of weekly-acting sulfonamide in four healthy adult horses. Some parameters of pharmacokinetics on weeklyacting Sulfonamide were calculated by mathematical equation associated with twocompartment open model. The t 1/2 of weekly-acting Sulfonamide was 14.13±2.15 hours and the TCP(ther) was 10.03±3.50 hours. The weekly-acting Sulfonamide for the horses was not weekly-acting, it was only medium sulfanamide. Following post-intravenous administrastion (Bolus)(50mg/kg body weight)its loading dose was 115mg, and its interval of the adbministration was 10 hours.

本文报告了周效磺胺在四匹健康成年马体内的药代动力学过程。根据二室开放式模型的数学公式,算出了周效磺胺有关的一些药代动力学参数。周效磺胺的生物半衰期为14.13±2.15小时,其有效浓度维持时间为10.03±3.50小时。周效磺胺对马不是周效,而是属于中效磺胺。静脉推注50mg/kg体重,其负荷剂量(突击剂量)为115mg,给药间隔时间为10小时。

 
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