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deletion     
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  缺失
     Establishment of an Oil Body-based Expression System and Deletion Analysis of a Vascular-specific Profilin2 Promoter
     植物油体表达体系的建立及Profilin2维管束特异表达启动子的区段缺失分析
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     Construction of Pseudorabies Virus SH Strain Mutant with gE-gI Gene Partial Deletion Inserting GFP-LacZ Reporter Gene and Primary Study Its Immunogenicity
     伪狂犬病病毒上海株gE~-/gI~-/GFP~+/LacZ~+缺失株的构建及其免疫原性初步研究
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     Study on a New Domain in Rat Ribosomal RNA and the Deletion Mutation of Cinnamomin A-chain
     大鼠核糖体RNA一个新的结构域以及辛纳毒蛋白A链缺失突变的研究
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     The Association Between the Infection of Mycobacterium Tuberculosis and the FHIT Gene Deletion of Lung Cancers with Pevious Pulmonary Tuberculosis
     结核杆菌感染与肺结核相关肺癌FHIT基因缺失的研究
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     Homozygous Deletion, Methylation, Expression and Microsatellite Instability of FHIT Gene in Laryngeal Squamous Cell Carcinoma
     喉鳞癌中FHIT基因纯合性缺失、甲基化、表达及其微卫星不稳定性研究
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  删除
     Cre/LoxP Mediated Report Gene Deletion from Pseudorabies Virus
     从伪狂犬病病毒中删除Cre/LoxP介导的报告基因
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     10 are deletion mutations.
     10个为删除突变;
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     In order to reveal its physiological function, human MFE2, MFE2ΔSCP2 (deletion of SCP2 in MFE2), dehydrogenase domain, hydratase domain, hydratase domain plus SCP2 homologous domain and SCP2 domain were separately expressed in E.
     为了研究SCP2结构域在MFE2中的功能 ,将人MFE2、MFE2ΔSCP2 (删除MFE2中的SCP2 )、脱氢酶结构域、水合酶结构域以及SCP2结构域分别在E .
短句来源
     A Study of Deletion Algorithm in AVL Trees
     AVL树删除算法的研究
短句来源
     It took 51.19 days from report to deletion of repeated cards, and the timeliness rate of checking repeated cards was 22.24%.
     报告到重卡删除51.19d,及时查重率22.24%。
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  中间缺失
     Results All 10 exons could be detected in the 40 RhD-positive and 2 weak D samples. Out of the 120 RhD-negative samples, 28 (23.33%) carried 10 exons, 19 (15.83%) lost most of the 10 exons (with mainly intermediate deletion), and 73 (60.83%) had deletion of all the 10 exons;
     结果40例RhD阳性和2例弱D型样本均检出RHD 基因的10个外显子,120例RhD阴性样本中28例样本的10个外显子全存在(占23.33%),19例样本10个外显子部分存在(占15.83%),大部分为中间缺失型,73例样本10个外显子全缺失(占60.83/%)。
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     Clinical and molecular characterization of a patient with an interstitial deletion of chromosome 12q15-q23 and peripheral corneal abnormalities
     染色体12q15-q23中间缺失和周边角膜异常患者的临床和分子特征
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     ObjectiveTo construct a phosphatidylinositol 4-kinase beta (PI4K-β) mutant with the 325th to 373rd amino acid codons deleted, and try to develop a simple method for constructing middle fragment deletion mutant.
     目的 构建缺失第 32 5~ 373位氨基酸密码子的磷脂酸磷酸化激酶β(phosphatidylinositol 4 - kinase beta,PI4 K-β)基因 ,以探索一种简便的构建中间缺失突变体的方法。
短句来源
     Of 76 RhD negative blood donors,22(28.95%)carried the intact RHD genes,9(11.84%)had the major deletion of RHD genes,the type of which was an intermediate deletion one,45(59.21%)had complete deletion of RHD genes.
     76名RhD(- )供者中 ,2 2名供者(2 8 95 % )存在完整RHD基因 ,9名供者 (11 84% )缺失大部分RHD基因 ,并全为中间缺失型 ; 45名供者(5 9 2 1% )完整缺失RHD基因。
短句来源
     Construction of middle fragment deletion mutant with improved gene splicing by overlap extension
     用改进的重叠区扩增基因拼接法构建中间缺失突变体
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  删除部分
     The experimental results show that the proposed algorithm is robust to the attack of rotation,translation,entities addition and deletion.
     实验结果证明这种方法对平移、旋转、添加及删除部分实体等攻击具有良好的鲁棒性。
短句来源
     The experimental results show that the proposed algorithm is robust to the attack of rotation,translation,scaling,mirroring and entities addition and deletion.
     实验结果证明这种方法对平移、旋转、缩放、镜像以及添加或删除部分实体攻击具有良好的鲁棒性。
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      deletion
    The case deletion model is equivalent to mean shift outlier model, as well as case weights model.
          
    A diagnostic based on case-deletion approach in estimating equations is proposed.
          
    It is shown that the case deletion model is equivalent to the mean shift outlier model.
          
    By constructing an interval extension of adjustable entropy function and some region deletion test rules, a new interval algorithm is presented.
          
    Differentiation of Indica-Japonica rice revealed by insertion/deletion (InDel) fragments obtained from the comparative genomic s
          
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    A procedure of simultaneous calculations for correcting regression coefficients due to deletion and/or addition of observations is developed, which includes the Plackett result as a special case. Considerations with respect to deleting observations in relation to the missing values problem in the factorial experiment lead to a different, yet feasible, approach to the correction problem. That is, with the deleted observations being first estimated, the correct regression coefficients turn up naturally.As...

    A procedure of simultaneous calculations for correcting regression coefficients due to deletion and/or addition of observations is developed, which includes the Plackett result as a special case. Considerations with respect to deleting observations in relation to the missing values problem in the factorial experiment lead to a different, yet feasible, approach to the correction problem. That is, with the deleted observations being first estimated, the correct regression coefficients turn up naturally.As for estimation of missing values, the principle of least squares may be worked into a tabular form equivalent in the wide sense to the method of cross-contrasts as was proposed in a previous paper by one of the authors.

    本文导出关于舍去或(并)加入数据的回归计算公式(包括了Plackett的结果作为特例)。并在舍去数据方面,结合析因试验中缺数的估计问题,得到回归计算的另一种可行方法——先补缺,后回归。 根据交互对比法与最小二乘法的等效性,按最小二乘法补缺,可表格化为一般意义的交互对比法。

    Chromosome abnormalities were studied in a girl with multiple congenital anomalies. Trisomy of the short arm of chromosome 9 (9p +) and distal deletion of the long arm of X-chromosome were found with G banding and C-banding techniques. The clinical features included psychomotor and growth retardation, short stature, moderate microcephaly, hypertelorism and enophtha mos, prominent nose with inverted nostrils, short upper lip, low-set ears, low posterior hairline, anomalies of phalanges and vertebrae, widely-spaced...

    Chromosome abnormalities were studied in a girl with multiple congenital anomalies. Trisomy of the short arm of chromosome 9 (9p +) and distal deletion of the long arm of X-chromosome were found with G banding and C-banding techniques. The clinical features included psychomotor and growth retardation, short stature, moderate microcephaly, hypertelorism and enophtha mos, prominent nose with inverted nostrils, short upper lip, low-set ears, low posterior hairline, anomalies of phalanges and vertebrae, widely-spaced hypoplastic nipples, undeveloped breasts, delayed onset of menar-che and dermatoglyphic abnormalities.

    本文报告一例多发性先天畸形女子的细胞遗传学研究。用G带和C带技术鉴定为第9号染色体短臂三体(9p+)和一条X染色体长臂远端部分缺失(xq—)。其临床征状为:严重的智力和发育障碍,身材矮小,头略小,两眼距稍宽并内陷,鼻圆,鼻梁高而鼻孔内翻,上唇短,耳位和后发线低下,指骨和脊椎骨异常,两乳头距远,乳房发育差,月经延迟,皮纹异常。

    Transposon Tn233 (CH) contains sir sul-resistant genes which are originally located on drug-resistant plasmid DR233 (Tcr Cmr Smr Sur) harbored by Shigella flexneri strain 233.Plasmid E144drd3: :Tn233 (CH) was constructed previously by transposition of Tn233 (CH) from DE233 into R144drd3 (Km1) and was then transferred to E.coli C600/pBK322 (Apr Tcr),so that strain with two coexisting plasmids was constructed.The plasmid DNA prepared from this coexisting strain was used to transform E.coli C600 cells and was selected...

    Transposon Tn233 (CH) contains sir sul-resistant genes which are originally located on drug-resistant plasmid DR233 (Tcr Cmr Smr Sur) harbored by Shigella flexneri strain 233.Plasmid E144drd3: :Tn233 (CH) was constructed previously by transposition of Tn233 (CH) from DE233 into R144drd3 (Km1) and was then transferred to E.coli C600/pBK322 (Apr Tcr),so that strain with two coexisting plasmids was constructed.The plasmid DNA prepared from this coexisting strain was used to transform E.coli C600 cells and was selected for Tc resistant transformants on L-broth plate containing 12.5ug Tc per ml.After the transformants had grown on Tc containing plates,E.coli C600/pBR322::Tn233 (CH) strain was selected from these colonies on the same medium containing 12.5ug/ml Sm by replica method.Then plasmid DNA was extracted from E.coli C600/pBR322:: Tn233 (CH) cells.The purified plasmid DNA preparations were digested by restriction endonuclease BamHI,EcoRⅡ,PstI,HindⅢ,PvuII and subjected to electrophoresis through agarose horizontal gel slabs and polyacrylamide gel in Tris-Acetate or Loening bouffer using DNA digested by both BamHⅠ and EcoRI,T5 DNA digested by Hindlll and M13 DNA digested by HaeⅢ as mobility markers.The molecular weight of these DNA fragments were measured.The molecular weight of plasmid pBR322:: Tn233 (CH) calculated by summation of all the bands to be of approximately 15.93×106 daltons,assuming that there is no deletion on pBR322 during the transposition experiment.If we take pBR322 as 2.87X106 daltons,the molecular weight of Tn233 (CH) is 13.06×106 daltons.The electrophoresis results also indicated that the number of substrate site of restriction endonuclease BamHI,EcoRI,PstI,HindⅢ and PvuⅡ on the Tn233 (CH) DNA sequence were 5,9,1,6 and 2 respectively.

    转座子Tn233(CH)带有str sul抗性基因,最早是在痢疾杆菌的抗药质粒DR233(Tc~r Cm~r Sm~r Su~r)中发现的。现在通过菌株间的配对,将插入了Tn233(CH)转座子的质粒R144drd3::Tn233(CH)转移到E·coli C600/pBR322(Ap~r、Tc~r)细胞中,组成两种质粒共存的菌株。从此菌株中提取出质粒DNA,用转化方法使它转移到E.coli C600菌株,再从所得到的转化子中用复印方法筛选出Tn233(CH)转座到pBR322质粒的转化子E.coli C600/pBR322::Tn233(CH),然后提出此质粒DNA,经限制性内切酶BamHⅠ、EcoRⅠ、PstⅠ、HindⅢ与PvuⅡ等酶切后,在琼脂糖凝胶平板与聚丙烯酰胺凝胶柱上进行电泳分析,分别以BamHⅠ与EcoRⅠ双重酶解的λDNA、HindⅢ酶解的T5DNA、HaeⅢ酶解的M13 DNA与HaeⅢ酶解的pBR322 DNA作为泳动的标记,计算出质粒酶解片段的分子量,用此方法算出各片段分子量的总和为15.93×10~6道尔顿,此即为所求的pBR322::Tn233(CH)分子量,将此值减去pBR322...

    转座子Tn233(CH)带有str sul抗性基因,最早是在痢疾杆菌的抗药质粒DR233(Tc~r Cm~r Sm~r Su~r)中发现的。现在通过菌株间的配对,将插入了Tn233(CH)转座子的质粒R144drd3::Tn233(CH)转移到E·coli C600/pBR322(Ap~r、Tc~r)细胞中,组成两种质粒共存的菌株。从此菌株中提取出质粒DNA,用转化方法使它转移到E.coli C600菌株,再从所得到的转化子中用复印方法筛选出Tn233(CH)转座到pBR322质粒的转化子E.coli C600/pBR322::Tn233(CH),然后提出此质粒DNA,经限制性内切酶BamHⅠ、EcoRⅠ、PstⅠ、HindⅢ与PvuⅡ等酶切后,在琼脂糖凝胶平板与聚丙烯酰胺凝胶柱上进行电泳分析,分别以BamHⅠ与EcoRⅠ双重酶解的λDNA、HindⅢ酶解的T5DNA、HaeⅢ酶解的M13 DNA与HaeⅢ酶解的pBR322 DNA作为泳动的标记,计算出质粒酶解片段的分子量,用此方法算出各片段分子量的总和为15.93×10~6道尔顿,此即为所求的pBR322::Tn233(CH)分子量,将此值减去pBR322的分子置2.87×10~6道尔顿,得到Tn233(CH)的分子量为13.06×10~6道尔顿。电泳结果还表明在Tn233(CH)DNA分子上,BamHⅠ、EcoRⅠ、PstⅠ、HindⅢ与PvuⅡ分别有5、9、1、6、2个切点数。

     
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