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rs virus
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  rs病毒
     27/35 (77.14%) were shown to be RS virus specific IgM antibody positive in acute phase serum by MAO-ELISA while 23/35 (65.71%) showed≥4 times rising of the neutralizing antibodies in convalescent serum by NT.
     MAC-ELISA测得急性期血清中RS病毒特异性IgM抗体的阳性率为27/35(77.14%),而恢复期血清中和抗体呈≥4倍升高者为23/35(65.71%)。
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  “rs virus”译为未确定词的双语例句
     Methods Rhinovirus type R_ 14 ,Influenza virus type A FM1 strain,RS virus, AD virus type 7 were inoculated into KMB_ 17 、MDCK、Hep-2、Hela cells to observe the action of Lonicerae and Forsythiae Powder on several respiroviruses.
     方法分别接种鼻病毒R_(14)型、流感病毒A型FM1株、呼吸道合胞病毒、腺病毒7型于KMB17、MDCK、Hep-2、Hela细胞,观察银翘散体外对多种呼吸道病毒作用。
短句来源
     It was concluded that MACEIA is a specific, sensitive, rapid, and simple diagnostic method for RS virus infection of infants and children.
     本法特异、敏感、简便,可在早期对RSV感染作出快速诊断,有利于临床治疗。
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     And there is an amino acid substitution located in the antigenic site of the large F 1 subunit of the ZHS13 strain,recognized by neutralizing monoclonal antibodies (McAb) directed against the F protein of human RS virus.
     在北京地方株(ZHS13株)F1亚单位内,由具有中和能力单克隆抗体所识别的抗原表位区中存在一个氨基酸的变异。
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     Three hundred and four positive viral strains,71 cases (23.35%) were RS virus infection, 47 cases (15.46%) were AD virus infection, 74 cases (24.34%) were FLU-A virus infection,50 cases (16.44%) were FLU-B virus infection, 47 cases (15.46%) were PIV1,3 virus infection, and 15 cases (4.93%) were PIV2 virus infection.
     流感病毒B50例 ,占 1 6 .44% ; 副流感 1、3病毒 47例 ,占 1 5 .46 % ;
短句来源
     Both in vivo and vitro Interferon α2a naristilla has the inhibition effect on Influenza virus,RS virus,Parainfluenza virus,Measles virus,Adenovirus, Coxsackie virus B_5 and has some inhibitory activity on the Labialis virus.
     结果显示:在体外有抑制流感病毒、呼吸道合胞病毒、副流感病毒、麻疹病毒、腺病毒、柯萨奇B3病毒的作用,对单纯疱疹病毒有部分抑制作用。
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  相似匹配句对
     Rs expression.
     Rs的表达。
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     (e) infection by virus;
     病毒说:细菌感染或多病原说;
短句来源
     Virus"of Marriage
     捕杀婚姻的“病毒”
短句来源
     Rs, Fc?
     Fc?
短句来源
     Experimentalstudyontherouteofinfectionbyhemorrhagicfeverwithrenalsyndrome(HFRS)virus
     肾综合征出血热病毒感染途径的实验研究
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  rs virus
These results are similar to the immune response observed in children following primary RS virus infection.
      
In contrast, while anti-peptide 205-225 rabbit serum from group A neutralized group A and B strains of RS virus, anti-peptide 205-225 rabbit serum from group B was unable to neutralize a group A virus, although it neutralized a group B strain.
      
In indirect immunofluorescence assays, both anti-peptide rabbit sera recognized human nasal epithelial cells infected with A or B strains of RS virus.
      
A similar pattern was observed with RS virus strains.
      
Immune responses to a synthetic peptide corresponding to amino-acids 205-225 of the fusion protein from group B respiratory syncytial (RS) virus, were studied in mice and rabbits, and compared to a similar peptide from group A RS virus.
      
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A solid-phase IgM antibody capture-ELISA (MAG-ELISA) was set up to test for serum IgM antibody to respiratory syncytial virus (RSV) and was compared with neutralization test (NT).A total of 70 serum samples taking from 35 infants with bronchiolitis were studied. 27/35 (77.14%) were shown to be RS virus specific IgM antibody positive in acute phase serum by MAO-ELISA while 23/35 (65.71%) showed≥4 times rising of the neutralizing antibodies in convalescent serum by NT. All the positive patients proved...

A solid-phase IgM antibody capture-ELISA (MAG-ELISA) was set up to test for serum IgM antibody to respiratory syncytial virus (RSV) and was compared with neutralization test (NT).A total of 70 serum samples taking from 35 infants with bronchiolitis were studied. 27/35 (77.14%) were shown to be RS virus specific IgM antibody positive in acute phase serum by MAO-ELISA while 23/35 (65.71%) showed≥4 times rising of the neutralizing antibodies in convalescent serum by NT. All the positive patients proved by NT were also positive by MAC-ELISA; the negative patients proved by MAC-ELISA were also negative by NT. While the remaining four patients with negative NT result showed positive IgM antibody response. MAO-ELISA was 88.57% correspond with NT.The age dependency of IgM antibody response was also demonstrated clearly in our study. The positive percentage of MAC-ELISA was of much higher as compared with NT until 6 month of age in our observation.The MAC-ELISA was shown to be a reliable technique for rapid

建立酶联免疫吸附试验(MAC-ELISA)检测呼吸道合胞(RS)病毒特异性IgM抗体方法,并与中和试验(NT)进行对比。 取35例患毛细支气管炎婴幼儿的急性期及恢复期双份血清共70份标本进行研究。MAC-ELISA测得急性期血清中RS病毒特异性IgM抗体的阳性率为27/35(77.14%),而恢复期血清中和抗体呈≥4倍升高者为23/35(65.71%)。凡NT阳性病例,MAC-ELISA也呈阳性;凡MAC-ELISA阴性病例,NT也呈阴性。另4例NT阴性而MAC-ELISA呈阳性。两者阳性符合率为88.57%。 本研究也观察了IgM抗体与年龄的关系。在6个月龄以前,MAC-ELISA的阳性率远远高于NT。 实验说明采用MAC-ELISA检测RS病毒特异性IgM是可靠的快速诊断方法。

The anti-RS virus specific IgM antibodies in the serums from 81 infants and children with virus pneumonia were detected by IgM antibody capture assay. The positive rate was 43.21%. The pain sera samples from 30 of the 81 patients were available for indirect fluorescent antibody test (IFA) to confirm the positive results of MACEIA. The results showed that the corresponding rate of these two methods was 83.33% and there were no significant differences between them (χ~2=3.84, P>0.05). It was concluded...

The anti-RS virus specific IgM antibodies in the serums from 81 infants and children with virus pneumonia were detected by IgM antibody capture assay. The positive rate was 43.21%. The pain sera samples from 30 of the 81 patients were available for indirect fluorescent antibody test (IFA) to confirm the positive results of MACEIA. The results showed that the corresponding rate of these two methods was 83.33% and there were no significant differences between them (χ~2=3.84, P>0.05). It was concluded that MACEIA is a specific, sensitive, rapid, and simple diagnostic method for RS virus infection of infants and children.

应用IgM抗体捕获法,检测了81例病毒性肺炎患儿血清中呼吸道合胞病毒(RSV)特异性IgM抗体,阳性率为43.21%。对其中30例病人取双份血清作中和试验,结果发现IgM抗体捕获法与间接荧光抗体(IFA)试验诊断符合率为83.33%。两法经统计学处理无显著差异(P>0.05)。本法特异、敏感、简便,可在早期对RSV感染作出快速诊断,有利于临床治疗。

The ultrastructurai changes ot the cerebral cortex oi suckling mouse brain inl-ected with HFRS virus by intracerebral inoculation and the morphogenesis of HF-RS virus were studied by IBM. The results showed that the nerve cell, neuroglia cell and endothelium cell of the capillary in cerebral cortex were all able to be infected with the virus. Varying degrees of ultrastructurai changes of the infected cell occured and became serious in the process of infection.virons in different stages of assembly...

The ultrastructurai changes ot the cerebral cortex oi suckling mouse brain inl-ected with HFRS virus by intracerebral inoculation and the morphogenesis of HF-RS virus were studied by IBM. The results showed that the nerve cell, neuroglia cell and endothelium cell of the capillary in cerebral cortex were all able to be infected with the virus. Varying degrees of ultrastructurai changes of the infected cell occured and became serious in the process of infection.virons in different stages of assembly and viral precursor labeled with HRP were found in cytoplasma. Most of the virons were spherical or oval with mean diameter 97 nm, and a few of them were rod-like. The virus had a granulofibrilla inner component with an envelope around it, some had an apparent electron-dense coro. Virus matured by budding from the membrane of vesicle or ER labeled with HRP. Many inclusion bodies or some masses of numerous 40-50nm spherical vesicle-like particals labeled with HRP were found in cytoplasma, and a kind of electron-densa material labeled with HRP was occasionally observed beneath the plasma membrane, of which the precise association with the virus wasn't known

本文观察发现乳鼠大脑皮质神经细胞、胶质细胞和毛细血管内皮细胞均对HFRS-V易感,病毒在细胞浆内增殖,可见呈特异性着色反应的不同成熟阶段的病毒颗粒和病毒包涵体,其邻近的膜性结构也常呈特异性着色。感染细胞内,有时可见呈特异性着色的小空泡样颗粒和病毒抗原性物质,其与病毒形态发生的关系尚待进一步研究

 
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