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family data
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  家系资料
     MCMC method is recommended to small sample family data due to its steadiness.
     小样本家系资料,MCMC法可得到比REML法更稳健的估计,推荐使用。
短句来源
     Methods To apply linear mixed models to the nuclear family data, to set up the genetic variance component model in term of familial genetic relationship, and to estimate parameters by WinBUGS and the PROC Mixed in SAS in order to analyze the effects of risk factors.
     方法 将线性混合模型应用于核心家系资料 ,根据核心家系成员的遗传关系建立遗传方差分量模型 ,运用SAS软件中的Mixed模块和WinBUGS软件进行参数估计 ,分析各影响因素作用大小。
短句来源
     Objective To study the method for measuring familial correlations of quantitative trait and analyzing family data set of body height.
     目的 研究数量性状家庭相关的测量方法 ,并对身高家系资料进行分析。
短句来源
     A new statistical method on familial correlation dealing with family data from case-control studies
     一种病例对照家系资料的家庭相关统计分析方法
短句来源
     Conclusion This model can be used to practical family data to analyze the effects of genetic factors and environmental factors to quantitative phenotype.
     结论 该模型可应用于实际家系资料 ,分析遗传因素和环境因素对数量表型的影响大小
短句来源
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  家庭数据
     The system composed of Remote Data Center (RDC) and Family Data Terminal.
     系统由远程数据管理中心(RDC)和家庭数据终端两部分组成.
短句来源
     Family Data Terminal included Main Control Unit (MCU), Wireless Data Transmission Module, Digital Water Meter, Digital Gas Meter and Digital Ammeter.
     家庭数据终端由主控单元(MCU)、无线数据收发模块和带有无线传输模块的水、电、气表组成,各表与MCU通过无线调频方式进行数据通信;
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  “family data”译为未确定词的双语例句
     The realization of I~2C-Bus to MCS51 Single Chip Microcontroller family data gather system
     I~2C总线在MCS51系列单片机数据采集系统中的实现
短句来源
     The estimated gene fre-quencies for BFS,BFF,BF S07,BF SGI and BF FG2 were 0.8668 0.1197,0.0077,0.0019 and 0.0039 respectively Family data confirmed the existence of the variant BF FG2 and de-monstrated the mode of codominant inheritance of it.
     计算出的基因频率分别为:FB~*S∶0.8668,BF~*F∶0.11979 BF~*S07∶0.0077,BF~*SG1∶0.0019,BF~*FG2∶0.0039。 家系调查证实BF FG2确系一独立的变异型,并显示常染色体共显性遗传方式。
短句来源
     Haplotype Frequency Estimation for Tightly Linked Loci from Family Data
     家系数据紧密连锁位点的单体型频率估计
短句来源
     A test via flood ping and iperf is launched to this project, in which a lowest byte rate of 16.1MBps in the described case can be realized and thus fulfill demands of all types of family data transmission.
     通过floodping和iperf对其测试,在论文所述的测试条件下,速率最低到16.1.MBps,满足家庭各种信息的传输要求。
短句来源
     (1) This paper researched on the interrelated concepts of mass customization, product configuration, product family data management, and analyzed the present situation of domestic and international of product configuration design.
     (1)研究了大规模定制、产品配置、产品族数据管理的相关概念,分析了国内外产品配置设计研究的现状。
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  family data
Results are presented for demographic data, select legal/criminal data, select drug and alcohol use data, employment data, health, parent/family data, education data, social data, and "other".
      
We describe the resources and the methods needed to achieve such a task, including extensive collection of family data, semiautomated genotyping technology, and specialized statistical approaches for linkage analysis of complex traits.
      
Analysis of the family data, for each probe, revealed no significant departure from Mendelian inheritance.
      
Extensive family data verified autosomal codominant inheritance.
      
Insufficient family data were available to confirm autosomal inheritance of the 6PGD polymorphism, but the electrophoretic patterns of variant types (putative heterozygotes) suggested the codominant expression of alleles at an autosomal locus.
      
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The present paper is concerned with genetic studies on Chinese families regarding the Gm and Km allotypes and is meant to resolve the problem, how the haplotypes are designated in Chinese population.A total of 203 individuals from 35 Chinese families of Han nationnality was examined for Gm(1), (2), (3), (5), (21), and Km(1) factors. Six different Gm phenotypes were identified and Gm 1,3;5, Gm1, Gm1,2;21 and Gm1:21 haplotypes were proposed from the segregation patterns in the family data. These four Gm...

The present paper is concerned with genetic studies on Chinese families regarding the Gm and Km allotypes and is meant to resolve the problem, how the haplotypes are designated in Chinese population.A total of 203 individuals from 35 Chinese families of Han nationnality was examined for Gm(1), (2), (3), (5), (21), and Km(1) factors. Six different Gm phenotypes were identified and Gm 1,3;5, Gm1, Gm1,2;21 and Gm1:21 haplotypes were proposed from the segregation patterns in the family data. These four Gm haplotypes are commonly found among the Mongoloid populations.The random distribution of Km(1) factor in various Gm phenotypes suggests that Gm and Km factors are inherited independently.

本文研究了Gm和Km在我国汉族家庭中的遗传情况,以便确定中国人的Gm单倍型究竟如何组成。对35个汉族家庭的203名成员检查了Gm(1),(2),(3),(5),(21)和Km(1)因子。发现有6种不同的Gm表型。根据分离格局提示存在Gm(?),Gm(?),Gm~1和Gm(?)等4种Gm单倍型,它们在蒙古人种群体中较为常见。 Km(1)因子在各种Gm表型中呈随机分布,说明Gm和Km因子相互独立遗传。

The distribution of genetic polymorphism of properdin factor B(BF) was investigated in 259 unrelated healthy adults liying in Guangzhou,by means of high voltage agarose gel electrophoresis followed by immunofixation.Besides SS,FS,FF and SS07.twp rare heterozy-gous phenotypes,tentatively named SSGI and SFG2,were observed.The estimated gene fre-quencies for BFS,BFF,BF S07,BF SGI and BF FG2 were 0.8668 0.1197,0.0077,0.0019 and 0.0039 respectively Family data confirmed the existence of the variant BF FG2 and...

The distribution of genetic polymorphism of properdin factor B(BF) was investigated in 259 unrelated healthy adults liying in Guangzhou,by means of high voltage agarose gel electrophoresis followed by immunofixation.Besides SS,FS,FF and SS07.twp rare heterozy-gous phenotypes,tentatively named SSGI and SFG2,were observed.The estimated gene fre-quencies for BFS,BFF,BF S07,BF SGI and BF FG2 were 0.8668 0.1197,0.0077,0.0019 and 0.0039 respectively Family data confirmed the existence of the variant BF FG2 and de-monstrated the mode of codominant inheritance of it.

本文应用高压琼脂糖电泳,继以免疫固定技术,对259名居住在广州市无亲缘关系的健康成年人进行了BF多态性分析。除了SS、FS、FF和SS07外,还观察到2种罕见杂合型,暂命名为SSGI和SFG2。计算出的基因频率分别为:FB~*S∶0.8668,BF~*F∶0.11979 BF~*S07∶0.0077,BF~*SG1∶0.0019,BF~*FG2∶0.0039。家系调查证实BF FG2确系一独立的变异型,并显示常染色体共显性遗传方式。

Allotypes and complotypes of Bf, C4A and C4B in 42 families with myasthenia gravis (MG) were determined by means of high voltage agarose gel elect rophoresis of EDTA plasma and subsequent immunofixation, in an attempt to determine whether specific allotypes and/or complotypes were associated with this disease. From the family-data, 108 complotypes were obtained, which could be classified into 28 kinds of complotypes. We found that there are positive linkage disequilibra in S42, S31 and S40,and...

Allotypes and complotypes of Bf, C4A and C4B in 42 families with myasthenia gravis (MG) were determined by means of high voltage agarose gel elect rophoresis of EDTA plasma and subsequent immunofixation, in an attempt to determine whether specific allotypes and/or complotypes were associated with this disease. From the family-data, 108 complotypes were obtained, which could be classified into 28 kinds of complotypes. We found that there are positive linkage disequilibra in S42, S31 and S40,and negative linkage disequilibra in S32 and S41. Compared of these results with those of normal controls, the frequency of S42 is significantly increased in MG(P 0.05).Furhter analysis showed that the MG associated S42 may result from that C4A4 is strongly associated with MG, while C4A4 is in linkage disequilibrium with Bf S and C4A2. Preliminary association mechanism between C4A4 and MG was analysed and discused.

对42个无血缘关系的重症肌无力(MG)患者家庭及36个健康献血员家庭成员的EDTA血浆用琼脂糖高压电泳及免疫固定的方法对属于HLA-Ⅲ的Bf,C4A及C4B的遗传多态性及其构成的补体型进行了检测。通过家系分析及对比发现,MG的Bf基因频率与正常人无差异;C4A~*4的基因频率病人远大于正常人,而C4A~*2则较常人为小。在补体型方便,MG患者与正常人亦不相同:患者以S42的频率最高,常人则以S31最高。MG患者的S42、S31及S40之间存在着正向连锁不平衡,S32和S41之间存在着负向连锁不平衡。进一步分析显示,S42与MG密切相关,这主要是由于C4A~*4与MG强烈相关,而Bf~*S和C4A~*2又与C4A~*4连锁不平衡的结果。

 
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