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
   late gene 的翻译结果: 查询用时:0.177秒
图标索引 在分类学科中查询
所有学科
生物学
感染性疾病及传染病
皮肤病与性病
妇产科学
基础医学
植物保护
更多类别查询

图标索引 历史查询
 

late gene     
相关语句
  晚期基因
     Screening of Positive-expressing Recombinant Yeast Strain for HPV_(16) L_1 Late gene
     HPV_(16)L_1晚期基因阳性表达重组菌株的筛选
短句来源
     2. To obtain HPV6 major capsid protein encoded late gene one (L1) with baculomavirus expression system.
     2.利用昆虫-杆状病毒表达系统获得人乳头瘤病毒6型(human papillomavirus type6,HPV6)晚期基因1(late gene one,L1)编码病毒的主要衣壳蛋白。
短句来源
     16 patients were EBV late gene BcLFI mRNA positive, and 14 of them were HHV 6 positive as well. They had a significant correlation ( x 2=6.788 , P=0.023 ) .
     EBV晚期基因BcLF1 mRNA 16例阳性,其中14例HHV 6阳性,两者有明显相关性(x~2=6.788,P=0.023)。
短句来源
     Gene Cloning and Sequencing of Human Papillomavirus Type 18 Late Gene L 1
     人乳头瘤病毒18型晚期基因L_1的克隆及测序
短句来源
     Construction and identification of late gene L1 of human Papillomavirus type 16
     人乳头瘤病毒16型晚期基因L1的原核表达质粒的构建和鉴定
短句来源
更多       
  “late gene”译为未确定词的双语例句
     A recombinant plasmid pTrc99Am HPV16 L1, which bearing human papillomavirus type 16 (HPV16) late gene L1, had been constructed via subcloning and sequence modiffication strategy for inducible expression of HPV16's main capsid protein L1 in E coli .
     本研究采用亚克隆和序列修饰策略建立了编码人类乳头瘤病毒16型(HPV16)主要结构蛋白L1基因的大肠杆菌可诱导表达质粒pTrc99AmHPV16L1。
短句来源
     △Np63 and MDM2 are an early and a late gene events of TCC, so they can be used to diagnose TCC earlier and to judge the degree of malignancy.
     MDM2和△Np63分别是TCC的早期和晚期事件,因此可以作为膀胱肿瘤早期诊断和判断恶性程度的有效指标。
短句来源
     Conclusion MDM2 and p53 proteins are an early and a late gene events in the occurrence and progress of bladder cancers.
     结论  MDM2和 p5 3蛋白是膀胱癌发生发展的两个早晚基因事件
短句来源
     1 Genes structure were as follows : the odv-e56 gene which coded the occlusion-derived virus envelope fusion protein had a late gene motif TTAAG, its ORF had 1125 bp and encodes 374 amino acides, there were six conserved cysteine residues, a glycosylation site and two hydrophobic domains;
     1在基因结构上,odv-e56基因上游具有晚期调控保守序列TTAAG,是一晚期表达基因,其推定的ORF为1125 bp,共编码374个氨基酸,基因内部有一个保守的糖基化位点、六个半胱氨酸残基和两个疏水区;
短句来源
     (2) Function of IE-1, hr3 on the late and very late gene promoters of baculovirusAbout ubi promoter, in the presence of BmNPV, hr3 could significantly enhance the activity of ubi promoter activity about 62- and 1.4-fold in cis- or in trans-, respectively.
     (2)杆状病毒IE-1及hr3对晚期ubi和极晚期polh启动子的作用 在病毒感染的情况下,顺式连接或反式作用的hr3可分别上调ubi启动子活性达62和1.4倍左右;
短句来源
更多       
  相似匹配句对
     Zip gene is required during the late neurogenesis of Drosophila.
     zip基因为果蝇晚期神经发生所必需。
短句来源
     Potato Late Blight Control using R-gene Polyculture
     利用田间抗病基因近等混合系防治马铃薯晚疫病
短句来源
     On Gene Patenting
     基因的专利问题
短句来源
     The Late Upsurge
     迟来的热潮——关于中国油画艺术及其市场
短句来源
     As to the RYR gene.
     长白猪群中,未发现有该基因存在。
短句来源
查询“late gene”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。
  late gene
The major capsid protein (mcp) gene of Spodoptera exigua ascovirus 5a (SeAV-5a) was confirmed by aphidicolin viral DNA replication inhibition analysis to be a late gene.
      
Temporal transcription analysis revealed that vp39 was a late gene.
      
Early baculovirus gene promoters in general have a resemblance to host promoters while late and very late gene promoters are different from early baculovirus promoters and are more defined.
      
These results together indicated that Ha128 was a late gene.
      
Whereas control of late gene transcription in Mu is becoming well understood, less is known about the phage morphogenetic process.
      
更多          


The characteristics of distribution, strength and time course of Fos expression in the rat hippocampus following transient global cerebral ischemia were investigated by using immunocytochemical method. The results showed that Fos expression was first induced in the dentate gyrus(DG) and subiculum, which appeared at 2h, peaked at 5-8h and decayed at 8h after global ischemia and recirculation (GIR). Fos induction in the CA3 and CA4 fields appeared at 3h, peaked at 5h and disappeared at 24h after GIR. Faint Fos...

The characteristics of distribution, strength and time course of Fos expression in the rat hippocampus following transient global cerebral ischemia were investigated by using immunocytochemical method. The results showed that Fos expression was first induced in the dentate gyrus(DG) and subiculum, which appeared at 2h, peaked at 5-8h and decayed at 8h after global ischemia and recirculation (GIR). Fos induction in the CA3 and CA4 fields appeared at 3h, peaked at 5h and disappeared at 24h after GIR. Faint Fos expression appeard in the CA1 and CA2 fields at 5h and disappeared at 32 -48h after GIR. The sequence of the strength and time course for Fos expression in the hippocampus was DG, CA3, CA4, CA2 and CA1. These characteristics of Fos expression might be involved in mediating the expression of such as late genes dynorphin and nerve growth factor following ischemia insults.

用免疫组化方法,对大鼠暂时性全脑缺血诱导的c-fos原癌基因蛋白(Fos)在海马表达的分布,强度和时间过程等特征进行了观察.结果表明:缺血40min再循环后2h,首先在海马齿状回转折部的颗粒细胞和下托诱导出Fos表达,5~8h达到高峰,8h后锐减并逐步消失.CA4和CA3区的Fos表达在缺血再循环后3h出现,5h达到高峰,持续至24h消失.而在CA2和CA1区,Fos表达最弱,最晚(5h才出现),持续32~48h后消失.Fos在海马表达的强弱和时间发展过程依次为齿状回、下托→CA4、CA3→CA2、CA1区.这种特征性表达可能与介导缺血损伤后强啡肽、神经生长因子等晚期基因的表达有关.

The very late gene (polyhedrin gene) promotor of the tung-oil geometrid Buzura suppressaria nuclear polyhedrosis virus (BsNPV) was cloned into the upstream of the promotor-deficit CAT gene of promotor-probe plasmid PKK232-8 with two methods. One of the recombinants pKB9312 had a high resistence to more than 200 mg/L chloramphenicol. This result indicated that insect baculovirus promotor of very late gene may work well in E. coli like that of some animal viruses (e. g., vaccinia virus,...

The very late gene (polyhedrin gene) promotor of the tung-oil geometrid Buzura suppressaria nuclear polyhedrosis virus (BsNPV) was cloned into the upstream of the promotor-deficit CAT gene of promotor-probe plasmid PKK232-8 with two methods. One of the recombinants pKB9312 had a high resistence to more than 200 mg/L chloramphenicol. This result indicated that insect baculovirus promotor of very late gene may work well in E. coli like that of some animal viruses (e. g., vaccinia virus, adenovirus, etc.). The reason for this phenomenen was discussed.

将油桐尺蠖(Buzurasuppressaria)核多角体病毒晚期基因──多角体蛋白基因启动子及5′端编码区,以两种不同方式置于缺乏启动子的氯霉素乙酰基转移酶(CAT)基因上游,使其分别终止在不同翻译终止位点,其宿主菌具有明显不同的氯霉素抗性,最高达200mg/L LB培养基以上,表明昆虫病毒启动子能启动原核基因表达。对多角体蛋白基因启动子能在大肠杆菌中有效工作的原因进行了讨论。

A polymerase chain reaction(PCR)assay that used two pairs of primers from the immediate early g n s and late genes of human HCMV AD169 strain was used to amplifyHCMV DNA directly from urine of renal transplant recipients. MacELISA and IELISAwere used to detect serum HCMV IgM and lgG of each recipient, while HCMV DNAwas detected by PCR,Of the 65 clinical urine samples, 39 were positive by PCR(60%).Of 33 IgM positive recipients,27 were positive by PCR(81.8%); of 55 IgGpositive recipients,30 were positive...

A polymerase chain reaction(PCR)assay that used two pairs of primers from the immediate early g n s and late genes of human HCMV AD169 strain was used to amplifyHCMV DNA directly from urine of renal transplant recipients. MacELISA and IELISAwere used to detect serum HCMV IgM and lgG of each recipient, while HCMV DNAwas detected by PCR,Of the 65 clinical urine samples, 39 were positive by PCR(60%).Of 33 IgM positive recipients,27 were positive by PCR(81.8%); of 55 IgGpositive recipients,30 were positive by PCR(54.5%).In recent and acute infection pa-tients,the frequency of PCR-positivity was higher than in latent ones(P< 0.01).Dete-ction of serial urine samples from patients whose first PCR result was negative, couldincrease the positive result.PCR technique for detecting HCMV DNA, although promisesa high sensitivity,and has the possibility of detecting latent HCMV infection, but onlyone time detection might lead to false-negative result.PCR in combination with serumHCMV antibody detection,multiple times detection and multiple primers amplifying dif-ferent areas of HCMV genome were necessary to avoid false-negative results. PCR amp-lification is a valuable tool for diagnosing HCMV infcction of rcnal transpiantationrecipients, in combination with MacELISA HCMV-IgM and IELISA HCMV-IgG dete-ction,it may give satisfactory clinical result.

为探讨聚合酶链反应(PCR)技术检测肾移植受者(RTR)尿中人巨细胞病毒(HCMV)DNA在临床工作中的应用及其价值,本组采用HCMV早期及晚期基因组两对引物及HCMV特异性单抗分别建立了PCR技术及捕获、间接酶联法(MacELISA,IELISA)。应用PCR检测RTR尿中HCMVDNA、MacELISA及IELISA法检测各受血者中HCMV-IgM及IgG,并比较其结果,表明:65例RTR尿中HCMVDNA阳性率为60%,lgM及IgG阳性者尿中HCMVDNA阳性率各为81.8%及54.5%。说明PCR应用存在一定局限性,应与血清学等方法相结合,取长补短,才能适应临床需要,充分发挥其应用价值。

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