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
   two deletion 的翻译结果: 查询用时:0.178秒
图标索引 在分类学科中查询
所有学科
更多类别查询

图标索引 历史查询
 

two deletion
相关语句
  碱基缺失
     Conclusion: There were two deletion sites in Fcgr2 b gene promoter region in NZB mice and the deletions could induce hypergammaglob ulinemia.
     结论 :NZB小鼠Fcgr2b基因启动子区存在碱基缺失 ,且该缺失突变可能与血清总IgG水平升高有关
短句来源
     Conclusion:There were two deletion sites in Fcgr2b gene promoter region in NZB mice and the deletions could induce decreasing of the expression of Fcgr2b mRNA that lead to hyper-IgG.
     结论:NZB小鼠Fcgr2b基因启动子区存在碱基缺失,且该缺失突变可引起其表达的降低而导致高IgG血症
短句来源
  “two deletion”译为未确定词的双语例句
     Polymorphism of the ACE gene was categorized into three genotypes: two deletion alleles (genotype DD), heterozygous alleles (genotype ID), and two insertion alleles (genotype II): Serum ACE levels were 28.34±9.88U/ml, 24.82±8.39U/ml, 19.18±4.8U/ml for DD, ID, II respectively.
     血清ACE水平在DD、DI、I型分别为28.3±9.9U/ml、24.5±8.4U/ml、19.2±4.8U/ml,即DD>DI>ⅠⅠ。
短句来源
     Primers were designed according to that, then two deletion fragments JP58B(1093 bp) and JP58S(462 bp) were obtained by PCR using Oryza sativa (japonica cultivar-group) etiolated seedling total DNA as template. The sequencing result showed that they possessed conservative elements of most higher plants promoter.
     在此基础上设计引物,以粳稻日本晴Oryza sativa (japonica cultivar-group)黄化苗总DNA为模板采用DNA聚合酶链式反应(PCR)的方法扩增出基因上游1093bp和462bp两个不同长度的启动子缺失片段(分别命名为JP58B和JP58S),测序结果显示其具有大多数高等植物启动子的保守元件。
短句来源
     The result showed that the I/D polymorphism in intron 16 of the ACE gene was categorized into three genotypes: two deletion alleles (genotype DD),heterozygous alleles (genotype ID),and two insertion alleles (genotype II).
     结果位于ACE基因内含子 16的I/D多态性经PCR扩增后呈三种基因型 :纯合子插入型 (II)、纯合子缺失型(DD)和杂合子插入或缺失型 (I/D)。
短句来源
     Primers were designed, and then two deletion fragments, JP58B (1 093 bp) and JP58S (462 bp), were obtained by PCR using total DNA of O. sativa etiolated seedling as template. The sequencing result showed that they possessed conservative elements of most higher plants′ promoters.
     在此基础上设计引物,以粳稻Oryzasativa(japonicacultivar-group)日本晴黄化苗总DNA为模板,采用DNA聚合酶链式反应(PCR)的方法扩增出基因上游1093bp和462bp两个不同长度的启动子缺失片段(分别命名为JP58B和JP58S),测序结果显示,其具有大多数高等植物启动子的保守元件.
短句来源
     (2) The I/D polymorphism in intron 16 of the ACE gene was categorized into three genotypes: two deletion alleles (genotype DD), heterozygous alleles (genotype ID) and two insertion alleles (genotype II). There was no significant different in genotype pattern of DD, ID.
     (2) 位于ACE基因第16内含子的 I/D多态性经PCR技术扩增后分为三种基因型:纯合子缺失型(DD),纯合子插入型(Ⅱ)及杂合子插入/缺失型(ID)。
短句来源
更多       
  相似匹配句对
     Two.
     二.
短句来源
     Two.
     二、末日意识
短句来源
     TWO NODE DELETION ALGORITHMS FOR BALANCED TREES
     二个关于平衡树的结点删除算法
短句来源
     Identification of Deletion Genotype by Two Different Methods
     缺失突变的两种检测方法
     The Deletion in Translation
     翻译中的除赘
短句来源
查询“two deletion”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。
  two deletion
As the two deletion mutants interacted successfully with the wildtype protein, while they failed to self-interact, we suggest that the N-terminal amino acids interact with amino acids of the C-terminal region.
      
To assess whether these regions substantially function as signals for nuclear localization of the IE180 molecule, we then constructed two deletion mutants lacking each region.
      
The extent of these deletions was examined in seven of these mutants and, for comparison, in two deletion mutants that were induced by UV irradiation.
      
Charge differences between the two deletion analogs and MCD peptide may explain some of the differences in activity.
      
The regions of EBNA-1 which interact with this protein were studied using two deletion clones and mapped to EBNA-1 residues 1-102 and 325-357.
      
更多          


AVL trees are a kind of balanced binary trees in height. If the order of the nodes in the trees is the same as that of binary search trees, then it is the better form of binary search trees. In the worst case the time to search an AVL tree for a node is only O(log_2n). But it takes O(n) to search a general binary search tree for a node. So it is necessary to explore modification problem to AVL trees. The deletion problem is discussed in this paper. First, the two deletion methods, direct deletion...

AVL trees are a kind of balanced binary trees in height. If the order of the nodes in the trees is the same as that of binary search trees, then it is the better form of binary search trees. In the worst case the time to search an AVL tree for a node is only O(log_2n). But it takes O(n) to search a general binary search tree for a node. So it is necessary to explore modification problem to AVL trees. The deletion problem is discussed in this paper. First, the two deletion methods, direct deletion and indirect deletion, are put forward. With respect to the algorithm both deletion methods are handled under the same circumstance. Here a new kind of deletion tecbnigue is presented. Then the rebalance method has been dealt with in detail and it has been shown that the rebalance is recursive. The recursive algorithm on rebalance is given.

AVL树是一种在高度上平衡的二叉树。如果其各结点在树中的次序(位置)与排序二叉树相一致,则它是一种较好形式的查找二叉树。在最坏情况下的查找时间只是O(log_2n),而一般的查找二叉树在最坏情况下的查找时间为O(n)。因而有必要对AVL树的各种修改进行探讨。本文专就删除问题进行讨论。首先提出了直接删除和间接删除两种方法,而在算法中又对这两种删除算法进行了统一处理,提出了一种新的删除技巧,然后详细地论述了重新平衡的各种情况,并讨论了其中各个细节,确定了重新平衡的速归性,并给出了递归算法。

Steroid sulfatase deficiency is a common genetic disorder, with a prevalence of approximately one in every 3500 males world wide.About 90% of these patients have complete gene deletions, which appear to result from recombination between members of a low-copy repeat family (CR1-232 is the prototype) that flank the gene. RUI and RU2 are two VNTR elements found within each of these family members.The RU1 consists of 30bp repeating units and its length shows minimal variation among individuals. The RU2 element consists...

Steroid sulfatase deficiency is a common genetic disorder, with a prevalence of approximately one in every 3500 males world wide.About 90% of these patients have complete gene deletions, which appear to result from recombination between members of a low-copy repeat family (CR1-232 is the prototype) that flank the gene. RUI and RU2 are two VNTR elements found within each of these family members.The RU1 consists of 30bp repeating units and its length shows minimal variation among individuals. The RU2 element consists of repeating sequences which are highly asymmetric, with about 90% purines and no C's on one strand, and range from 0. 6kb to over 23kb among different individuals. We conducted a study to determine if the RU1 and RU2 elements can promote recombination in an in vivo test system.We inserted these elements adjacent to the neo gene in each of two pSV2neo derivatives. One of which has a deletion in the 5' portion of neo gene and the other having a deletion in the 3'portion. These plasmids were combined and used to transfect EJ human bladder tumor cells. Survival of cells in G418 indicates restoration of a functional neo gene by recombination between two deletion constructs. Thus counting G418 resistant colonies gives a quantitative measure of the enhancement of recombination by the inserted VNTR elements.The results showed no effect on recombination by the inserted RU1 element(compared to the insertion of a nonspecific sequence), while the RU2 element stimulated.recombination by 3. 5-fold (P< 0.01). A separate set of constructs placed RU1 or RU2 within the nitron of an exon trapping vector. Following transfection of cells, recombination events were monitored by a quantitative PCR assay that detected the approximation of primer banding sites (as a result of recombination).These studies showed that, as in the first set of experiments, the highly variable RU2 element is capable of stimulating somatic recombination in tnammalian cells.

AVNTRELEMENTASSOCIATEDWITHSTEROIDSULFATAESGENEDELETIONSSTIMULATES RECOMBINATIONIN CULTURED CELLSGongYan;X.M.Li,L.J.Shapiro(De...

The angiotensin converting enzyme(ACE) insertion/deletion (I/D) polymorphism found in intron 16 was shown to segregate with serum levels and proposed as independent risk factor for a subgroup of myocardial infarction survivors in the Caucasian and Japanese population. This study is designed to find whether it is also true in Chinese population. A 287 bp I/D polymorphism in intron 16 of the ACE gene was examined by polymerase chain reaction in a cross sectional study of 96 healthy subjects and 103 patients...

The angiotensin converting enzyme(ACE) insertion/deletion (I/D) polymorphism found in intron 16 was shown to segregate with serum levels and proposed as independent risk factor for a subgroup of myocardial infarction survivors in the Caucasian and Japanese population. This study is designed to find whether it is also true in Chinese population. A 287 bp I/D polymorphism in intron 16 of the ACE gene was examined by polymerase chain reaction in a cross sectional study of 96 healthy subjects and 103 patients with myocardial infarction, whose serum ACE levels were measured. Polymorphism of the ACE gene was categorized into three genotypes: two deletion alleles (genotype DD), heterozygous alleles (genotype ID), and two insertion alleles (genotype II): Serum ACE levels were 28.34±9.88U/ml, 24.82±8.39U/ml, 19.18±4.8U/ml for DD, ID, II respectively. In the study, the frequency of deletion alleles was higher(0.62) in the myocardial infarction group than in healthy control subjects (0.48) ( P <0.01).

旨在探讨中国人中血管紧张素转化酶(ACE)基因的插入/缺失(insertion/deletion,I/D)多态性与血清中ACE水平及心肌梗塞的关系。心肌梗塞患者103例;正常对照96例。位于ACE基因第16内含子的I/D多态性经PCR扩增可分为三种基因型:纯合缺失型(DD),纯合插入型(I),杂合子型(ID)。血清ACE水平在DD、DI、I型分别为28.3±9.9U/ml、24.5±8.4U/ml、19.2±4.8U/ml,即DD>DI>ⅠⅠ。结果显示,心肌梗塞患者的D等位基因的频率(0.61)高于正常对照组(0.48),P<0.01。认为:ACE基因的缺失多态性与中国人血清ACE水平及心肌梗塞相关。

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