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框架序列
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  frame sequence
     At the same time, we study the stability of frame and frame sequence.
     讨论了框架,框架序列等在可逆算子作用下的稳定性问题。
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  “框架序列”译为未确定词的双语例句
     It contains 215 bp, named as ZM908. Biosoftware anlysis sug gests that ZM908 gene properly belongs to the mRNA-like non-coding RNA gene which is purposed to lack of obvious open reading frame (the longest possibly contains 98 AA), contain poly(A) tale and have stable RNA structure in vivo.
     采用生物学软件对ZM908序列和结构进行分析,表明该基因缺乏明显的开放阅读框架,序列中最长可能的开放阅读框架仅编码98个氨基酸,具有poly(A)尾部结构,RNA分子具有稳定的二级结构,符合非编码RNA基因的特点,可能属于类似于mRNA的非编码基因;
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     Conclusion We successfully cloned human interleukin 10 cDNA ORF and constructed the eukaryotic expression vector pcDNA3.1hIL 10.
     结论 成功克隆了人白细胞介素 10cDNA开放阅读框架 ,序列分析证实与GenBank录入序列同源性达 10 0 % ,并成功构建了真核表达载体pcDNA3.1hIL 10。
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     Results The amplified hBMP2 gene of 1.2 kb was completely in accordance with the sequence of its open reading frame in GeneBank. The full-length cDNA was cloned in lentivirus vector.
     结果①扩增出1.2 kb左右的hBMP2全长cDNA与GeneBank中的hBMP2阅读框架序列完全一致;
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     Inheritance of the Foreign Gene 1Ax1 in Transgenic Wheat(Triticum aestivum L.) with Gene Cassettes Lacking Vector Backbone Sequences
     无载体框架序列转基因小麦中外源基因表达框的遗传分析
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     A primary sequence analysis (BlastN search) with the published Xoo genome sequence of KACC 10331 (containing 4,637 protein coding sequences, CDSs) as reference revealed that at least 4,555 (98.23%) CDSs of Xoo KACC 10331 could found homologs in the sequence of PR6, suggesting that the two genomes encode a highly conserved gene content.
     组装序列分析发现,框架序列中能找到4555个(98.23%)编码蛋白基因序列与Xoo KACC 10331菌株序列高度同源。 这为进一步确定和分离Xoo致病基因及其功能基因组学分析奠定了基础。
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  相似匹配句对
     Bessel Sequences and Affine Frames
     Bessel序列和仿射框架
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     p sequences or R.
     p序列和R.
短句来源
     Characterizations of Bessel sequences and frames in a Hilbert space
     Bessel序列框架的若干刻画
短句来源
     It generates 2~~(s·g(n,s)) M sequences of span.
     g(n,s)个n级M序列
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     Then,article also explains Struts' theory and every component.
     —Struts框架
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  frame sequence
For a two-frame sequence reflecting a saccadic displacement, these motion signal maps contain extended patches in which local directions change only little.
      
The reading frame sequence predicts a new class of bHLH family.
      
Image registration based on virtual frame sequence analysis
      
Transient transfection of GADD45 γ cDNA with intact open reading frame sequence into the human hepatoma cells Hep-G2 resulted in dramatic growth suppression in colony formation assays.
      
Average edge frame sequence is obtained by performing Sobel edge detection.
      
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  frame sequences
The method has three steps: the automatic estimation of motion vectors in frame sequences, the description of motions in spatio-temporal space, and the retrieval of sequences of images.
      
The proposed algorithm is based on the fact that most of gradual curves can be characterized by variance distribution of edge information in the frame sequences.
      
An overview of models for frame sequences is given in Section 2.
      
As far as temporal relations are concerned, point and interval data type should be supported to represent frames and frame sequences respectively.
      
Client will have to upload the animation frame sequences to the portal.
      
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The Tat (Twin arginine translocatin) system is a recently defined protein export pathway that serves to translocate folded proteins. The substrates of the Tat pathway contain specific amino terminal signal peptides that exhibit a conserved amino acid consensus motif S/T R R x F L X. Here is the report of knocked out the tatA , tatB and tatC genes of the V. cholerae by suicide plasmid homologous recombination technology. Mutant strains showed obvious changes of growth characteristics....

The Tat (Twin arginine translocatin) system is a recently defined protein export pathway that serves to translocate folded proteins. The substrates of the Tat pathway contain specific amino terminal signal peptides that exhibit a conserved amino acid consensus motif S/T R R x F L X. Here is the report of knocked out the tatA , tatB and tatC genes of the V. cholerae by suicide plasmid homologous recombination technology. Mutant strains showed obvious changes of growth characteristics. The transport of a typical Tat pathway substrate, trimethylamine N oxide reductase (molybdoenzyme), was completely blocked. The physiochemical reactions of the parent and mutant strains were also analyzed. Four physiochemical reactions using D galactose, L asparagine, glyl L aspartic acid and D L α glycerol phosphate as substrates were negative in mutant strains, which might be affected by the inactivation of the Tat dependent system.

Tat(Twin argininetranslocation)双精氨酸转运系统是最新证实的原核生物细菌中运输折叠蛋白的主要途径。是与经典的sec分泌系统完全不同的蛋白运输系统。通过对已测序的O1群霍乱弧菌E1Tol生物型菌株N16 96 1基因组分析 ,并与大肠杆菌TatA、B、C、D同源蛋白进行了氨基酸和基因序列的同源比较 ,对大肠杆菌tatA、tatB、tatC具有同源性的基因采用自杀质粒同源重组原理缺失了这 3个连续排列基因的大部分开放阅读框架序列 ,从而进行了蛋白分泌阻断的初步研究与分析。结果表明 ,该推测基因簇缺失后 ,Tat分泌阻断 ;生长特性易发生粗糙型改变 ,由光滑型菌落或菌苔转化为粗造型 ,且霍乱弧菌粗糙型抗血清凝集实验阳性 ;钼酶 (三甲胺氮氧还原酶 )分泌完全阻断 ;α D半乳糖、天门冬酰氨、甘氨酰 L 天门冬酸及D L α 磷酸甘油等 4项生化反应由阳性转为阴性。此研究在霍乱弧菌中确认了tat基因簇 ,并鉴定了功能 ,为进一步探索Tat分泌对霍乱弧菌蛋白因子分泌的影响奠定了遗传学基础。

Some of properties of frames in a Hilbert space H are given in light of operator theoretic methods, including characterizations,independence and dual frame of frames,and relationship of frames and bounded linear operators from H into l 2 (Z) are obtained.

应用算子论方法研究了 Hilbert空间 H中框架的若干性质 ,包括框架的特征、对偶性、紧性等问题 .建立了框架序列与 H到 l2 ( Z)中的相应算子之间的对应关系与构造框架的统一方法

AIM: To get a better understanding of the thymus development and differentiation,we constructed the gene expression pattern of 100 day foetus porcine thymus(FTY). METHODS: 11712 randomly picked clones from FTY cDNA library were single pass sequenced. After contamination was removed, 7071 cleaned ESTs were used for gene expression analysis. RESULTS: After clustering the 7071 cleaned ESTs by PHRAP, 959 contigs(size>1) and 3074 singletons were obtained. Blast search showed that 806 contigs and 1669 singletons...

AIM: To get a better understanding of the thymus development and differentiation,we constructed the gene expression pattern of 100 day foetus porcine thymus(FTY). METHODS: 11712 randomly picked clones from FTY cDNA library were single pass sequenced. After contamination was removed, 7071 cleaned ESTs were used for gene expression analysis. RESULTS: After clustering the 7071 cleaned ESTs by PHRAP, 959 contigs(size>1) and 3074 singletons were obtained. Blast search showed that 806 contigs and 1669 singletons (totally 5442 ESTs) had homologues in nonredundant nucleic acid database, the Swiss Prot database and Unigene database of human, cattle and mouse. The 1629 ESTs without similarities were considered novel. According to function, the known genes were classified into 7 group and 36.99% of ESTs were classified into the gene expression group. The thymus functional genes were expressed in a certain degree (accounting for 7.55%). Comparative expression analysis showed that the gene expression pattern of FTY was very similar to human infant thymus gene expression profile and different from that of adult human. Blast search found that 58 of 109 novel sequences with both poly A and ORF prediction had homologues to human genome sequence. CONCLUSION: EST strategy is economical and virtual in finding new genes. The 100 day porcine thymus is still at a developmental stage.

目的 :构建家猪 1 0 0d胚胎胸腺基因表达谱 ,为研究胸腺的发育和分化机制奠定基础 .方法 :随机挑取家猪1 0 0d胸腺cDNA文库 (FTY)的 1 1 71 2个克隆 ,进行单向全自动大规模测序 ,去污染后共获得 70 71个高质量的表达序列标签 (EST)用于基因表达分析 .结果 :对 70 71个高质量EST的聚类分析结果获得 95 9个多拷贝基因和 30 74个单拷贝基因 .与非冗余的核酸数据库、Swiss Prot数据库及人、牛和鼠的U nigene数据库进行BLAST ,发现 80 6个多拷贝基因和 1 6 6 9个单拷贝基因 (共计 5 4 4 2个ESTs)与已知序列有同源性 ,1 6 2 9个EST没有发现同源序列被认为是新基因 .根据功能将已知基因归为 7类 ,其中基因表达相关基因占 36 .99% ,胸腺特异的防御功能相关基因有一定程度表达 (占 7.5 5 % ) ,这与人婴儿胸腺基因表达谱相类似而不同于成年人胸腺组织 .将 1 0 9个既发现有ORF又具有PolyA的多拷贝新基因与人类基因组框架序列进行BLAST ,发现其中 5 8个有同源序列 .结论 :EST技...

目的 :构建家猪 1 0 0d胚胎胸腺基因表达谱 ,为研究胸腺的发育和分化机制奠定基础 .方法 :随机挑取家猪1 0 0d胸腺cDNA文库 (FTY)的 1 1 71 2个克隆 ,进行单向全自动大规模测序 ,去污染后共获得 70 71个高质量的表达序列标签 (EST)用于基因表达分析 .结果 :对 70 71个高质量EST的聚类分析结果获得 95 9个多拷贝基因和 30 74个单拷贝基因 .与非冗余的核酸数据库、Swiss Prot数据库及人、牛和鼠的U nigene数据库进行BLAST ,发现 80 6个多拷贝基因和 1 6 6 9个单拷贝基因 (共计 5 4 4 2个ESTs)与已知序列有同源性 ,1 6 2 9个EST没有发现同源序列被认为是新基因 .根据功能将已知基因归为 7类 ,其中基因表达相关基因占 36 .99% ,胸腺特异的防御功能相关基因有一定程度表达 (占 7.5 5 % ) ,这与人婴儿胸腺基因表达谱相类似而不同于成年人胸腺组织 .将 1 0 9个既发现有ORF又具有PolyA的多拷贝新基因与人类基因组框架序列进行BLAST ,发现其中 5 8个有同源序列 .结论 :EST技术是发现新基因的有效手段之一 ;此期家猪胸腺仍处于发育阶段 .

 
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