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   genotypes 在 公安 分类中 的翻译结果: 查询用时:0.063秒
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genotypes
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  基因型
    Results The length of PCR products were 807 bp and 962 bp respectively. Seven genotypes in each locus were detected. AAAACCCCCTCCCC allele amounted to 87.72% of all nt16180 genotype,while AAAACCCCCCCCCCCCC was firstly reported in Han population.
    结果两对引物扩增长度分别为807bp和962bp,nt16180位点检测到7种基因型,其中AAAACCCCCTCCCC基因型占87.72%,AAAACCCCCCCCCCCCC基因型在汉族人群中首次报道;
短句来源
    Primary Study on the Influence of Blood Transfusion on the STR Genotypes of Recipient's Blood
    输血对受者血液基因型的影响
短句来源
    The number of alleles and genotypes of D3S1358 ,VWA, FGA, D8S1179, D21S11, D18S51, D5S818, D7S820, D13S317 were 6,8,14,8,12,18,8,9,8and 13,19,38,26,36,50,19,19,23 respectively .
    D21S11基因座上有12个等位基因,36种基因型:D18S51基因座上有18个等位基因,50种基因型; D5S818基因座上有8个等位基因,19种基因型
短句来源
    Since HLA polymorphisms is derived from single base difference and each base associate at random ,the number of HLA genotypes is over 10 . This provides an ideal genetic maker for personal identification and paternity testing.
    由于HLA多态性是由单个碱基差异造成的序列多态性(即单核苷酸多态性),各个位点碱基组合又是随机的,故人群中HLA基因型可达10~8种之多,这为法医学个人识别和亲子鉴定提供了理想的遗传标记。
短句来源
    8 alleles and 17 genotypes of CSF1PO locus, 6 alleles and14 genotypes of TPOX locus,and 6 alleles and 19 genotypes of TH01 locus were observed.
    TPOX基因座,观察到6个等位基因,14个基因型; TH01基因座,观察到6个等位基因,19个基因型
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  种基因型
    Results The length of PCR products were 807 bp and 962 bp respectively. Seven genotypes in each locus were detected. AAAACCCCCTCCCC allele amounted to 87.72% of all nt16180 genotype,while AAAACCCCCCCCCCCCC was firstly reported in Han population.
    结果两对引物扩增长度分别为807bp和962bp,nt16180位点检测到7种基因型,其中AAAACCCCCTCCCC基因型占87.72%,AAAACCCCCCCCCCCCC基因型在汉族人群中首次报道;
短句来源
    The number of alleles and genotypes of D3S1358 ,VWA, FGA, D8S1179, D21S11, D18S51, D5S818, D7S820, D13S317 were 6,8,14,8,12,18,8,9,8and 13,19,38,26,36,50,19,19,23 respectively .
    D21S11基因座上有12个等位基因,36种基因型:D18S51基因座上有18个等位基因,50种基因型; D5S818基因座上有8个等位基因,19种基因型
短句来源
    The PCRproducts were analyzed by polyacrylamide gel(PAG)vertical electrophoresis. Results 9 allelesand 23 genotyp es werefound at D1S549locus,9 allelesand 15 genotypeswere found at D3S1754 locus ,10 alleles and 30 genotypes werefound at D22S683 locus.
    D3S1754 共检出9 个等位基因, 15 种基因型; D22S683共检出10 个等位基因, 30 种基因型
短句来源
    Results 5 alleles and 15 genotypes for D10S1432 locus , and 9 alleles and 31genotypes for D10S1213 were obtained in the two populations.
    在D10S12 13位点上观察到 9个等位基因 ,31种基因型。 两位点的基因型频率在调查的两个群体中的分布符合Hardy -Weinberg平衡定律 (P >0 .0 5 )。
短句来源
    Using PCR and PAG, followed by silver staining, the tetrameric STR D2S441 locus was studied in 260 unrelated Chinese individuals living in Chengdu. 9 alleles and 26 genotypes were observed. The range of fragment size was 131bp to 155bp.
    为研究 STR位点 D2S441的遗传多态性,为法医学应用提供基础数据,应用 PCR及 PAG电泳技术对 260名成都地区汉族无关个体进行了调查,共检出 9个等位基因及 26种基因型,首次获得汉族群体频率分布 ,其等位基因片段大小范围为 131~ 155bp。
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  “genotypes”译为未确定词的双语例句
    Objective To investigate the probability of siblings testing by the 9 autosomal STR loci such as D3S1358.Methods These 9 STR loci were amplified by multiplex PCR,and then the genotypes were detected by ABI 310 genetic analyzer.
    目的探讨D3S1358等9个常染色体STR基因座用于鉴定两个体间同胞亲缘关系的可行性。
短句来源
    Compared with conventional PAGIEF, 1+2- and 1-2+ cant be differentiated and the rare genotypes also cant be detected by this method. The advantage of this method was PGM1 genotyping successfully in bloodstains stored for 25 years and with 0 1ng genomic DNA.
    与传统的PAGE酶型检测比较 ,本法不能区分 1+ 2 -和 1-2 +型 ,不能检测出PGM 1稀有基因 ,但克服了IEF无法分析微量、陈旧材料的缺点 ,对保存 2 5年陈旧血痕及 0 1ng模板DNA均能成功分型。
短句来源
    VWA*20-0 014.A total of 29 genotypes was observed in 214 individuals.
    VWA * 2 0 - 0 .0 14。 个体识别率 :0 .932 ,杂合度0 .82 1,多态信息含量 0 .814,非父排除率 0 .6 0 3。
短句来源
    Results We observed 5 genotypes in Uygur, 4 in Li, 3 in Yao, and 2 in Han and Zang ethnicals.
    结果 维族人群发现5种等位基因,黎族4种,瑶族3种,而汉族、藏族只观察到两种等位基因。
短句来源
    Results The genotypes of 270 bloodstains, 20 mix stains, 20 hair roots, 12 saliva stains were compatible with their serotypes.
    结果对270例血斑、20例混合斑、20根毛发(有毛囊)、12份唾液斑等不同的生物检材进行了分型,与血清学方法检验结果相符。
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  genotypes
The distributions of GNB3 C825T genotypes were CC (27.2%), TT (42.9%), and CT (29.9%) in the hypertensive subjects and CC (27.7%), TT (42.4%), CT (29.9%) in the normotensive subjects.
      
Further analysis shows that there is no association between C825T genotypes and age, body mass index (BMI), Glucose (GLU), Triglyceride (TG), Cholesterol (CHO), systolic blood pressure (SBP) and diastolic blood pressure (DBP).
      
Compared to individuals with EPHX1 rs1051741 CC or rs2234922 AA genotype in the drinkers, the risk of CBP in those carrying genotypes of EPHX1 rs1051741 CT+TT or rs2234922 AG+GG was decreased, respectively (P = 0.04, P >amp;lt; 0.01).
      
Karyotypic analysis on the metaphase plates from the root meristem demonstrated different genotypes.
      
Effects of Genotypes at the Unspecific Esterase (Est) and Leucine Aminopeptidase (Lap) Loci on the Temporal Dynamics of Morpholo
      
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Allelic frequencies of the D1S80 locus were determined by using the PCR followed by a high-resolusion PAGE technique and silver staining. In a sample of 175 unrelated individuals of Han nationality in Xi' an, 22 alleles and 64 Renotypes were found. The distribution of genotypes was in agreement with expected values according to the Hardy-weinberg equilibrium. The helerozygosity was 82. 3% and the probability of diserimination (DP) was 0. 9588. Pedigree analysis confirmed Mendelian inheritance of the Amp-FLP...

Allelic frequencies of the D1S80 locus were determined by using the PCR followed by a high-resolusion PAGE technique and silver staining. In a sample of 175 unrelated individuals of Han nationality in Xi' an, 22 alleles and 64 Renotypes were found. The distribution of genotypes was in agreement with expected values according to the Hardy-weinberg equilibrium. The helerozygosity was 82. 3% and the probability of diserimination (DP) was 0. 9588. Pedigree analysis confirmed Mendelian inheritance of the Amp-FLP alleles, and the exeluding probability of paternity (EPP) was 0. 6704.

利用PCR技术、小型聚丙烯酰胶凝胶电泳及银染法,检测D1S80位点的VNTR扩增片段长度多态性(Amp-FLP)。在175名无关的西安地区汉族人群中发现了22个等位基因,片段大小分布于320~750bp之间,频率分布为0.0057~03314,杂合度为82.3%,个人识别率(DP)为0.9588,非父排除率(EPP)为0.6704。对7个家系23名相关个体分析,证实DIS80位点的遗传符合孟德尔方式。已发现的64种基因型分布符合Hardg-Weinberg定律。

Amp FLP analyses of Apo B 3′ VNTR locus in human blood stain, saliva(stain),semen, mixed stain and hair have been carried out. The genotypings have been achieved. The genotypes of Apo B 3′ locus can be detected accurately in blood stains kept at room temperature within 15 weeks and at -20℃ within two years. In a series of paternity testing on 34 cases, 8 false alleged fathers were excluded; of them, 6 were excluded by Apo B 3′ locus alone or by Apo B 3′ locus combined with other genetic markers. 3 rape...

Amp FLP analyses of Apo B 3′ VNTR locus in human blood stain, saliva(stain),semen, mixed stain and hair have been carried out. The genotypings have been achieved. The genotypes of Apo B 3′ locus can be detected accurately in blood stains kept at room temperature within 15 weeks and at -20℃ within two years. In a series of paternity testing on 34 cases, 8 false alleged fathers were excluded; of them, 6 were excluded by Apo B 3′ locus alone or by Apo B 3′ locus combined with other genetic markers. 3 rape cases were investigated; 2 suspects were excluded.

用扩增产物片段长度多态性分析方法测出人类血痕、精液、精液与阴道分泌液混合斑、唾液(斑)与毛发的ApoB3′VNTR位点的DNA遗传多态性,探讨了不同保存温度血痕中ApoB3′位点DNA多态性的可检出时限,发现室温保存15周以内,-20℃保存两年以内的血痕均可测出ApoB3′位点的DNA多态性。用该法作34例亲子鉴定,其中8例否定了错误被控父亲,8例中6例ApoB3′位点参与了否定。对3例强奸案的混合斑进行个人鉴定,否定了2例的嫌疑对象。

In this report, DNA extraction from the blood and the multiplex amplification of CSF1PO,TPOXand TH01 were carried out. By using denaturing polyacrylamide gel electrophoresis and silver stain,the distribution of allele frequencies of CSF1PO TPOX and TH01 loci in Miao ethnie group living inYunnan province in China was investigated. 8 alleles and 17 genotypes of CSF1PO locus, 6 alleles and14 genotypes of TPOX locus,and 6 alleles and 19 genotypes of TH01 locus were observed.

在同一反应体系中,对CSFIPO,TPOX和TH01三个STR基因座做复合扩增,采用高分辨率的聚丙烯酸胺凝胶电泳分离、银染法显影技术,对云南苗族的3个基因座基因频率分布进行调查。CSFIPO基因座,观察到8个等位基因,17个基因型;TPOX基因座,观察到6个等位基因,14个基因型;TH01基因座,观察到6个等位基因,19个基因型。

 
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