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   haplotype 的翻译结果: 查询用时:0.215秒
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haplotype     
相关语句
  单倍型
     The rs1049060-rs129190, rs701831-rs707954, rs1047992-rs1049060-rs129190 , rs701831-rs707954-rs 1047992 and rs701831-rs707954-rs1047992-rs1049060 haplotype systems were associated with schizophrenia ( P<0.05 ).
     rs1049060-rs129190、rs701831-rs707954、rs1047992-rs1049060-rs129190、rs701831-rs707954-rs1047992和rs701831-rs707954-rs1047992-rs1049060单倍型系统与精神分裂症相关联(P<0.05)。
短句来源
     The most common DQA1∶DQB1 haplotype was DQA1*0301/02/03∶DQB1*0303 with a frequency of 12.5%, which was followed by the DQA1*0201- DQB1*0201/02 (10.5%),DQA1*0501-DQB1*0201/02 (9.5%) and DQA1*0501 -DQB1*0301 /09 (7.0%).
     分析得出30种DQA1-DQB1单倍型,DQA1*0301/02/03-DQB1*0303(12.5%)、DQA1*0201-DQB1*0201/02(10.5%)、DQA1*0501-DQB1*0201/02(9.5%)、DQA1*0501-DQB1*0301/09(7.0%)为常见的单倍型
短句来源
     3.Main haplotype pattern is TTT(61.9%),CTC(27.2%) and TCC(7.9%)s.
     ③主要单倍型:TTT(61.9%)、CTC(27.2%)和TCC(7.9%)。
短句来源
     (3) C 829/A 17532/C 20541 (54.3%) was the main haplotype of Zhejiang Han nationality.
     54.3%的C-829/A-17532/C-20541是汉族人群的主要单倍型
短句来源
     The haplotype of CgIVS12-6T-118 was associated with PTC (OR=1.43, 95%CI: 1.02-2.00), compared with TgIVS12-6T-118 haplotype.
     以TgIVS12-6T-118单倍型为参照,CgIVS12-6T-118单倍型可以使PTC的发病风险增加,OR值为1.43(95%CI1.02-2.00)。
短句来源
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  单体型
     Haplotype analysis showed that against TNFα1/TNFβB2,TNFα1/TNFβB1 can significantly enhanced the risk of ESCC(OR=1.30,95%CI=1.03-1.65).
     单体型分析显示,与TNF-α1/TNF-βB2相比,TNF-α1/TNF-βB1可增强ESCC的发病风险(OR=1.30,95%CI=1.03~1.65)。
短句来源
     ⑶ Individuals with M1+-/M2++ haplotype were significantly increased in patients campared with controls ( 0.437 vs 0.314 , P < 0.05 , OR = 1.70 ).
     脑梗组M1+-/M2++单体型基因型频率显著高于对照组(0.437vs0.314,P<0.05,OR=1.70)。
短句来源
     Compared with A_(-1290)-G_(-1195)-G_(-765) containing haplotype, a greater risk of developing
     与单体型A_(-1290)-G_(-1195)-G_(-765)相比较,含有-1195A等位基因的A_(-1290)-A_(-1195)-G_(-765)
短句来源
     Compared with A/T haplotype, A/C and C/C haplotypes significantly increased the risk of developing GCA (OR=1.35 and 1.46, 95% CI=1.01-1.81 and 1.06-2.00).
     与A/T单体型相比,携带A/C、C/C单体型可显著增加GCA的发病风险(OR=1.35和1.46,95%CI=1.01~1.81和1.06~2.00)。
短句来源
     Results The patients with positive Anti U1RNP had significantly increased frequencies of DQA1*0101 alleles and DR15 DQA1*0102 DQB1*0601 haplotype (P=0.040,P=0.000).
     结果 抗U1RNP抗体阳性的SLE病人中DQA1 0 10 1及DR15 DQA1 0 10 2 DQB1 0 60 1单体型频率亦显著增高 (P =0 .0 40 ,P =0 .0 0 0 )。
短句来源
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  单元型
     (4)haplotype 6 contained either single KIR2DL5.1 or both subtypes;
     单元型 6含有单一KIR2DL5 1或二者兼有 ;
短句来源
     Diversity of KIR2DL5 Gene Subtype Content and Haplotype Analysis in Chinese Han Population in Shanghai Arca
     上海地区汉族人群KIR2DL5基因多态性及单元型分析
短句来源
     The overall species haplotype diversity was quite high (h = 0.98?.005), and the nucleotide diversity was also high ( = 0.0303?.0029).
     12个地方种群合并一个大种群分析表明,中国大陆黑斑侧褶蛙的线粒体单元型多样性相当高(h=0.98±0.005),总体核苷酸多样性也较高(0.0303±0.0029)。
短句来源
     The LPL H - carriers and H -S haplotype were significantly associated with dyslipidemia (OR=0.575, 95%CI: 0.358-0.923) in female after multivariate adjustment.
     而H- S单元型与女性血脂异常的OR值为0 .5 35 (95 % CI:0 .2 97~0 .96 1)。
短句来源
     The primers BFP 200 and BFP 201 were designed on the ground of the difference between the SFB4 and SFB4’genes, which only amplify the SFB4’gene. Therefore, using the primers BFP 200 and BFP 201, the difference between the SFB4 and SFB4’genes of sweet cherry was displayed, the self-incompatible S4 haplotype and the self-compatible S4’haplotype were distinguished successfully.
     根据这个缺失差异,设计了一对引物BFP200和BFP201,这对引物只能扩增SFB4’基因, 而不能扩增SFB4基因,从而利用SFB基因区分开了甜樱桃自交不亲和的S4和自交亲和的S4’单元型
短句来源
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  “haplotype”译为未确定词的双语例句
     The most predominant haplotype embracing the two loci was IL1β-31C/-511T(OR, 1.216; 95% CI, 0.763~1.937).
     IL-1β-31C/-511T单倍体型发生IBD的风险增加(OR=1.216,95%CI0.763~1.937)。
短句来源
     G and A allele haplotype frequencies was 71.1% and 28.9% respectively.
     XRCC1G28152ASNPs基因型分布GG、GA、AA分别为49.2%、43.7%、7.1%,G、A等位基因频率分别为71.1%、28.9%。
短句来源
     the frequency of DRB1*15/*16-DQA1*0102 haplotype was 6.80% in self-limited HBV infection subjects, significantly higher than 1.94% in chronic HB patients (P=0.0012) and 1.65% in asymptomatic HBV carriers (P=0.0004);
     DRB1*15/*16-DQA1*0102的频率为6.80%,显著高于慢性乙肝组的1.94%(P=0.0012)和无症状HBV慢性携带者组的1.65%(P=0.004);
短句来源
     TAP2F haplotype might confer the susceptibility to type 1 diabetes mellitus,the pooled OR and 95%CI were 2.51 (1.62,3.90)(P < 0.05).
     TAP2F单倍体型可能是1型糖尿病的易感性单倍体型,其合并OR值和95%置信区间为2.51(1.62,3.90),P<0.05。
短句来源
     The association between HLA DR, DQ antigens, and vulval lichen sclerosus in the UK: HLA DRB1* 12 and its associated DRB1* 12/DQB1* 0301/04/ 09/010 haplotype confers susceptibility to vulval lichen sclerosus, and HLA DRB1* 0301/04 and its associated DRB1* 0301/04/DQB1* 0201/02/03 haplotype protects from vulval lichen sclerosus
     英国HLA DR、DQ抗原与女阴硬化萎缩性苔藓的关系:HLA DRB1*12及其相关的DRB*12/DQB1*0301/04/09/010单倍体对女阴硬化萎缩性苔藓易感,而HLA DRB1*0301/04及其相关性DRB1*0301/04/DQB1*0201/02/03单倍体拮抗女阴硬化萎缩性苔藓
短句来源
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  haplotype
An overview of the haplotype problems and algorithms
      
To gain more information, SNPs on a single chromosome are usually studied together, which constitute a haplotype.
      
In general, four categories of problems are widely researched: the haplotype assembly problem, the haplotype inference problem, the haplotype block partition problem, and the haplotype tagging SNP selection problem.
      
Genetic diversity of ND6 haplotypes was estimated at 0.406, and probability of haplotype random match, at 0.598.
      
Haplotype frequency distributions on wild-type and mutant chromosomes of MFS patients were also significantly different.
      
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The intensity of mixed lymphocyte reaction (MIR) was observed in three goups of human subjects: identical twins, parent-offsprings and unrelated individuals. Lymphocytes from two unrelated individuals cultured together in the same tube generally underwent intensive morphological transformation with increased ~3H-TdR incorporation. Result of MIR between unrelated individuals showed a high degree of stimulation (SI=11.0±6.46). Intensity of MIR between parent and offspring, sharing one haplotype, was lower...

The intensity of mixed lymphocyte reaction (MIR) was observed in three goups of human subjects: identical twins, parent-offsprings and unrelated individuals. Lymphocytes from two unrelated individuals cultured together in the same tube generally underwent intensive morphological transformation with increased ~3H-TdR incorporation. Result of MIR between unrelated individuals showed a high degree of stimulation (SI=11.0±6.46). Intensity of MIR between parent and offspring, sharing one haplotype, was lower (SI=3.25±1.34), The mixed lymphocyte reaction between identical twins, sharing two haplotypes, presented negative result (SI=1.21±0.38). There was a positive quantitative correlation between the intensity of MIR and the degree of difference of histocompatibility in individuals.

本文报道经ABO、Rh、HLA-R·S抗原鉴定核实的9对同卵双生同胞间MLR呈阴性,刺激指数最高不大于2;亲子间MLR呈低强度,刺激指数最高不大于7;一对异卵双生间二个单倍型不同,MLR呈高强度,刺激指数为10.90;无关间MLR强度一般较高,刺激指数大于7,但也有呈低反应者。MLR强度与个体间组织相容程度呈密切的定量关系。

This paper outlined the importance of mathematical methods and computer softwares in the study of leukocyte typing and presented the corresponding software package. Six programs included in this system are as follows:1. HLA-SA-1 Program for clustering analysis. 2. HLA-SA-2 Program for serograph analysis antigen assignment and calculation of posterior probability.3. HLA-SA-3 Program for identication of ferum specificities.4. HLA-SA-4 Program for calculation of genetic parameter and corresponding variances.5....

This paper outlined the importance of mathematical methods and computer softwares in the study of leukocyte typing and presented the corresponding software package. Six programs included in this system are as follows:1. HLA-SA-1 Program for clustering analysis. 2. HLA-SA-2 Program for serograph analysis antigen assignment and calculation of posterior probability.3. HLA-SA-3 Program for identication of ferum specificities.4. HLA-SA-4 Program for calculation of genetic parameter and corresponding variances.5. HLA-SA-5 Program for antigen and haplotype association analysis in HLA and disease study.6. HLA-SA-6 Program for calculation of various parameters of genetic distance in population studies.These methods and softwares have been used in the treatment of experimental data of human and swine leukocyte typing. Satisfactory results were obtained.

本文概述了在白细胞分型研究中数学方法和电子计算机应用软件的重要性,并提出我国自行研制的用于白细胞分型研究的一个应用软件系统,其主要内容和功能为: ①HLA-SA-1聚类分析程序。②HLA-SA-2血清图绘制,抗原指定及后验概率计算程序。③HLA-SA-3血清特异性鉴定程序。④HLA-SA-4遗传参数(包括抗原频率,基因频率,双位点单倍因频率,连锁不平衡参数)及其方差计算程序,⑤HLA-SA-5疾病相关研究中的抗原关联分析及单倍型关联分析程序。⑥HLA-SA-6群体研究中遗传距离分析程序。这些数学方法及计算程序经各单位用于人体和猪白细胞分型实验数据的处理均获得满意结果。

A total of 790 unrelated individuals of Han nationality living in Chengdu,Liuzhao,Shanghai,and Changchun regions and 154 Xinjiang Uighurs were typed for Gm and Km factors.All samples were tested for Gm(1,2,3,5,21) and Km(1) factors.The results obtained from Han populations show an evidence of marked heterogeneity in Gm distribution,with a striking north to south clime in haplotype frequencies.The Gm1,3.5 haplotype frequency increases sharply,and there is a concomitant sharp decrease in Gm1;21 and...

A total of 790 unrelated individuals of Han nationality living in Chengdu,Liuzhao,Shanghai,and Changchun regions and 154 Xinjiang Uighurs were typed for Gm and Km factors.All samples were tested for Gm(1,2,3,5,21) and Km(1) factors.The results obtained from Han populations show an evidence of marked heterogeneity in Gm distribution,with a striking north to south clime in haplotype frequencies.The Gm1,3.5 haplotype frequency increases sharply,and there is a concomitant sharp decrease in Gm1;21 and Gm1,2:21 frequencies.This pattern of Gm distributions may be the result of migration and admixture between two previously distinct mainland populations.The discovery that the Xinjiang Uighur population has Gm3:5 haplotype with frequency 0.3223 suggest that there exist admixture phenomenon between Caucasoids and Mongoloids.The distribution of Km1 frequency appears to be random in the presented populations.

调查了790名成都、柳州、上海、长春地区本地汉族人和154名新疆维吾尔族人的Gm、Km因子分布情况。检查了Gm(1,2,3,5,21)因子和Km(ι)因子。结果表明Gm分布的不均一性,从北方向南方Gm~(1,3;5)单倍型频率急剧升高,而同时Gm~(?)和Gm~(?)频率下降。Gm的这种分布格局可能是早先大陆上的两个群体迁移和混杂的结果。在新疆维吾尔族人中发现Gm~(?)单倍型,频率为0.3223,提示存在白种人与黄种人之间的混杂现象。本文调查群体中Km频率呈随机分布。

 
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