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
   1基因启动子 的翻译结果: 查询用时:0.02秒
图标索引 在分类学科中查询
所有学科
呼吸系统疾病
更多类别查询

图标索引 历史查询
 

基因启动子
相关语句
  1 promoter
     RESULTS: Treatment of MC3T3 E1 cells with FGF 9(from 1× 10- 9 to 1 × 10- 5 mol/L) followed by 24 hours of growth in serum free medium decreased the transcription from the Cbfa1 promoter(P< 0.05).
     结果:MC3T3-E1细胞中,FGF-9(1×10-9~1×10-5mol/L)作用24h能够降低Cbfa1基因启动子活性(P<0.05)。
短句来源
     In C2C12 cells, FGF 9 (1× 10- 5 mol/L) decreased the expression of luciferase reporter plasmid driven by Cbfa1 promoter(P< 0.05). Addition of PD98059 had no effect on the FGF 9 induced expression of Cbfa1 promoter activity(P< 0.01).
     C2C12细胞中,1×10-5mol/L的FGF-9处理后亦可以降低小鼠Cbfa1基因启动子活性(P<0.05),且未见到PD98059的阻断作用(P<0.01)。
短句来源
     In contrast, treatment of these cells with 10 μ M PD98059 blocked the FGF 9 induced expression of Cbfa1 promoter activity(P< 0.01).
     加入PD98059(10μmol/L)后阻断了FGF-9所诱导的Cbfa1基因启动子活性的降低(P<0.01)。
短句来源
     Lovastatin in regulation of mesangial cell proliferation and activity of TGF-β1 promoter in rats
     洛伐他汀对大鼠系膜细胞增殖及TGF-β1基因启动子活性的调控
短句来源
     Objective: To investigate the correlations of transforming growth factor(TGF)-β_1 promoter polymorphism C-509T with the phenotype and severity of asthma, and the relationship between TGF-β_1 gene promoter polymorphism C-509T and the serum protein levels of TGF-β_1 in asthmatics.
     目的:探讨转化生长因子-β_1(TGF-β_1)基因启动子C-509T 多态性与支气管哮喘发病、哮喘病情程度的关系以及支气管哮喘患者TGF-β_1基因启动子C-509T 多态性与血清中TGF-β_1蛋白水平的相关性。
短句来源
更多       
  “1基因启动子”译为未确定词的双语例句
     Analysis of methylation status of the promoter of mdr1 gene in K562 and K562/DNR cells
     K562和K562/DNR细胞中mdr1基因启动子甲基化状态的分析
短句来源
     Hypermethylation of FHIT, CDH13, CRBP1 and LKB1 Genes in Hepatocellular Carcinoma
     肝细胞癌中FHIT、CDH13、CRBP1和LKB1基因启动子异常甲基化
短句来源
     Association of the TGF-β_1 gene promoter -800G/A、-509C/T polymorphisms with esophageal cancer
     TGF-β_1基因启动子-800GA、-509C/T多态性与食管癌的研究
短句来源
     ConclusionThe promoter polymorphism (-1385 A/G) of FGF-1 gene was associated with LOAD.
     结论FGF1基因启动子(-1385A/G)多态性与LOAD显著相关。
短句来源
     CONCLUSION: FGF 9 can decrease the promoter activity and the expression of Cbfa1 gene in MC3T3 E1 and C2C12 cells in mice through the MAPK signal conduction pathway partly.
     结论:FGF-9部分通过MAPK信号传导通路抑制MC3T3-E1和C2C12细胞中小鼠Cbfa1基因启动子活性及mRNA的表达。
短句来源
更多       
  相似匹配句对
     We forecast more twenty cis-elements in 0sW19p from PLACE website.
     1 OsWRKY19基因启动子的分析
短句来源
     Activity of Clb1 Gene Promoter From Bombyx mori
     家蚕CIb1基因启动子活性分析
短句来源
     The complex methylation patterns of BRCA1 promoter
     BRCA1基因启动子复杂甲基化模式
短句来源
     1. Cloning and sequence analysis of nap in gene promoter from Brassica napus.
     1.napin基因启动子的克隆和序列分析
短句来源
     FUNCTIONAL VERIFICATION ON PROMOTER OF ARF1 GENE FROM GOSSYPIUM HIRSUTUM
     棉花arf1基因启动子的功能验证
查询“1基因启动子”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。
  1 promoter
To this end a family of recombinant plasmids based on Gal10Cyc1 promoter and neomycin phosphotransferase gene NPTII were created.
      
Insertion polymorphism Ins96 of the CYP2E1 promoter region was for the first time studied in three ethnic groups of Bashkortostan.
      
The activity of the LTR 22-19 fragment accounted for about 0.34% of the activity of the inducible GAL1 promoter and for 0.25% of the activity of the constitutive TDH promoter.
      
Isolation of Mitochondrial DNA-Binding Proteins Specific to the Maize cox1 Promoter
      
Mobility shift competition data confirm the assumption that the protein under study is specific to the cox1 promoter.
      
更多          


PstI,Bglll double digested DNA fragments from Streptomyces griseus have been cloned into promoter-probe plasmid pGA46 digested with the same enzymes.Transfor-ments were selected on the medium that allowed the selection of Tcr gene promoter-bearing plasmids.Electrophoresis showed that common vector bands were found in PstI,Bglll cleavage patterns of vector and recombinant plasmids.Hybridization studies revealed that recombinant plasmids shared homology with both vector and 8.griseus DNA while there was no detectable...

PstI,Bglll double digested DNA fragments from Streptomyces griseus have been cloned into promoter-probe plasmid pGA46 digested with the same enzymes.Transfor-ments were selected on the medium that allowed the selection of Tcr gene promoter-bearing plasmids.Electrophoresis showed that common vector bands were found in PstI,Bglll cleavage patterns of vector and recombinant plasmids.Hybridization studies revealed that recombinant plasmids shared homology with both vector and 8.griseus DNA while there was no detectable hybridization of vector to S.griseus DNA.HindIII fragments of 8.griseus DNA have been cloned into another promoter-probe plasmid pPV33-H and functioned as promother of Tc' gene.Streptomyces insert in recombinant plasmid No.8 was reduced by Hindlll complete digestion and subcloning into pGA46.It activated the Tc' gene of pGA46.Our results indicated that some Stveptomyces derived inserts really have promoter function in E.coli.

灰色链霉菌(streptomyces griseus)No.45是链霉素产生菌,用于工业规模的链霉素生产,其启动子结构及基因表达的调控尚未揭示。本文报道了S.riseus启动子在大肠杆菌(Escherichia coil)中的克隆和表达,证实了S.griseus中也存在E.coli类型的启动子。我们已将S.griseus DNA的PstⅠ、BglⅡ酶切片段克隆到启动子探测质粒pGA46上,在大肠杆菌中表达四环素抗性基因启动子的功能。S.griseus DNA的Hin dⅢ酶切片段也已经克隆到另一个启动子探测质粒pPV33-H上,在E.coli中表达四环素抗性基因启动子的功能。为了进一步验证和分析,将重组质粒和载体以限制性内切酶酶切,从电泳图谱中可以重新找到共同的载体区带。以DNA分子杂交的方法进行DNA同源性分析,结果表明载体pGA46或pPV33-H和S.griseus DNA没有可察觉的杂交区带,而重组质粒和S.griseus DNA及载体均有明显的杂交区带。这说明重组质粒中的外源插入序列确是来自S.griseus,这些DNA片段携带了四环素抗性基因的启动子。为了进一步分析启动子功...

灰色链霉菌(streptomyces griseus)No.45是链霉素产生菌,用于工业规模的链霉素生产,其启动子结构及基因表达的调控尚未揭示。本文报道了S.riseus启动子在大肠杆菌(Escherichia coil)中的克隆和表达,证实了S.griseus中也存在E.coli类型的启动子。我们已将S.griseus DNA的PstⅠ、BglⅡ酶切片段克隆到启动子探测质粒pGA46上,在大肠杆菌中表达四环素抗性基因启动子的功能。S.griseus DNA的Hin dⅢ酶切片段也已经克隆到另一个启动子探测质粒pPV33-H上,在E.coli中表达四环素抗性基因启动子的功能。为了进一步验证和分析,将重组质粒和载体以限制性内切酶酶切,从电泳图谱中可以重新找到共同的载体区带。以DNA分子杂交的方法进行DNA同源性分析,结果表明载体pGA46或pPV33-H和S.griseus DNA没有可察觉的杂交区带,而重组质粒和S.griseus DNA及载体均有明显的杂交区带。这说明重组质粒中的外源插入序列确是来自S.griseus,这些DNA片段携带了四环素抗性基因的启动子。为了进一步分析启动子功能区域的结构,已将重组质粒No.8中4.24kb的S.griseus插入序列缩短到1.89kb。插入序列的继续缩小正在进行中。

A series of programs for the nucleic acid data treatment on Apple Ⅱ microcomputer have been reported.With these programs,we can store the nucleic acid data,alter the data structure,compare the homology of the related DNA or RNA sequences,tentatively study the promoter region of the gene,predict the reading frame,translate the DNA sequence into the amino acid sequence and calculate the frequency of codons used in the different hosts.

本文报道了在AppleⅡ型微机上实现核酸数据处理的一系列工作程序。应用这些程序,可进行核酸数据的贮存、对指定的核酸数据结构的改造、限制性内切酶识别位点的检索、核酸序列至蛋白序列的翻译、相关核酸序列及蛋白序列的同源性比较、氨基酸密码使用频率的统计和基因的启动子结构的初步探索等方面的工作。

Two subclones (pHh8c and pHh9a) were obtained by inserting 8c and 9a DNA fragments containing human histone H1 gene into cloning vector pUC8.Comparison of their 5'-flankjng sequences has revealed some promoter elements and consensus sequence motifs,the Hogness box TATA at position-85,the CCAAT sequences at -105,the GC rich regions and TC pyrimidine clusters.

从人基因库中分离得到的两个含有不同变种组蛋白H_1基因的λ克隆(λHh8和λHh9),分别把它们含有该基因的片段(8c和9a)插入载体puc8质粒中,得到了亚克隆pHh8c和pHh9a。对这两个人组蛋白H_1基因的启动子(Promoter)和部份编码蛋白质的区域作了核苷酸顺序的分析和比较,确定了它们的启动要素和同系顺序。

 
<< 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1基因启动子的内容
在知识搜索中查有关1基因启动子的内容
在数字搜索中查有关1基因启动子的内容
在概念知识元中查有关1基因启动子的内容
在学术趋势中查有关1基因启动子的内容
 
 

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