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   genotypes frequency 的翻译结果: 查询用时:0.011秒
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genotypes frequency
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  基因型频率
     Objective To investigate the alleles and genotypes frequency of 10 short tandem repeat (STR) loci (DXS101,DXS6789,DXS6799,DXS6804,DXS7130,DXS7132,DXS7133, DXS7423, HPRTB, DXS8378)on X chromosome of Chinese Hui nationality population.
     目的研究宁夏回族群体X染色体上的10个短串联重复序列(DXS101、DXS6789、DXS6799、DXS6804、DXS7130、DXS7132、DXS7133、DXS7423、HPRTB、DXS8378)的基因及基因型频率分布。
短句来源
     AIM:To investigate the geographic distribution of T102C genotypes frequency of 5-hydroxytryptophan 2A(5HT2A) receptor in schizophrenia patients in different areas.
     目的:调查中国不同省区精神分裂症患者5-羟色胺2A(5-hydroxytryptophan2A,5HT2A)受体基因T102C基因型频率在地理上的分布。
短句来源
     Objective To investigate the alleles and genotypes frequency of 6 short tandem repeat (STR)loci (DXS8378、DXS7132、DXS6789、DXS101、HPRTB and DXS7423) on the X chromosome in Han popu-lation.
     目的调查西安汉族人群6个位于X染色体上的短串联重复序列:DXS8378、DXS7132、DXS6789、DXS101、HPRTB和DXS7423的基因及基因型频率分布。
短句来源
     Objective To investigate the geographic distribution of 5-HT2A T102C genotypes frequency in the PLA schizophrenia patients.
     目的 调查不同省区军人精神分裂症患者5-HT2A受体基因T102C基因型频率在地理上的分布。
短句来源
     Results No significant association was noted between- 159 C/T polymorphism of CD14 and allergic asthma or total serum IgE. The C/C, C/T and T/T genotypes frequency of CD14 in Control was 0.139, 0.583 and 0.278 respectively.
     结果 患儿组CD14-159位C/C、C/T和T/T基因型频率分别是0.189、0.469和0.343,与对照组的0.139、0.583和0.278的差异无显著性,两组3种基因型间血清IgE水平差异亦无显著性。
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  “genotypes frequency”译为未确定词的双语例句
     But there were statically significantly different genotypes frequency and allele frequency of C311S polymorphism in the normoalbuminuria and microalbuminuria (incipient nephropathy) . The CC+CS genotype frequency and C allele frequency were significantly higher in incipient nephropathy than in nomoalbuminuria group, (P=0.02, P=0.009).
     但在2DM肾病正常白蛋白尿和微量白蛋白尿组间PON2C311S基因型和等位基因频率分布差异有显著性,微量白蛋白尿组CC+CS基因型和C等位基因频率显著高于正常白蛋白尿组(分别为P=0. 02,P=0. 009) 。
短句来源
     In primer FSHRP1 product, we detected C-528T mutation and the genotypes frequency differed among different sheep breeds (P<0.05).
     6.绵羊FSHR基因5'调控区C-528T突变与超排处理后卵巢上黄体数量的表型变异存在显著相关(P<0.05);
短句来源
     The difference of genotypes frequency of HLA-C3,HLA-B55,71,72,54 between the patients and the healthy subjects reached statistical significance(/><0.05).
     乙肝患者中HLA-C3基因阳性率高于健康人,并且经统计学处理后均有显著性差异(P<0.05);
短句来源
     Results we found no statically significant difference of genotypes frequency and allele frequency of PON2C311S gene polymorphism among 2DMJGT and NOT groups and among diabetic retinopathy groups.
     结果 2DM、IGT、NGT三组间PON2C311S基因型和等位基因频率分布差异无显著性; 糖尿病视网膜病变组间不同基因型和等位基因频率分布也无显著性差异。
短句来源
     There werestatically significantly different genotypes frequency and allele frequency of 4A/13polymoiphism of eNOS gene in three diabetic groups defined by ophthalmoscopy andNGT group. The eNOS A allele frequency was higher in proliferate retinopathy groupthan in two other groups(p=O.007).
     在NGT组与2DM视网膜病变分组间eNOS基因的VNTR(4A/B)位点BB基因型和A、B等位基因频率分布差异有显著性,A等位基因频率随糖尿病视网膜病变程度加重而增多(P=0.007)。
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  相似匹配句对
     FREQUENCY
     生死频率
短句来源
     Frequency and Genotypes of Thalassemia in Shenzhen Area
     深圳地区地中海贫血患病率调查及其基因分型
短句来源
     the regeneration frequency was different for calli from different genotypes.
     愈伤组织的质量对芽的分化有重要影响,不同基因型来源的愈伤组织其植株再生频率有很大差异。
短句来源
     Biograding frequency of C.
     在四种菌株降解胆固醇的比较中,C.
短句来源
     1RS genotypes.
     1RS易位系的平均籽粒蛋白质含量极显著高于非易位系。
短句来源
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  genotypes frequency
Population-specific patterns of the polymorphic alleles and genotypes frequency distribution were established.
      
In the region examined the population-specific patterns of the apoE alleles and genotypes frequency distribution were established.
      
HBV genotypes frequency in health-care workers and their controls at haemodialysis units is shown in Table 7.
      


AIM To observe the polymorphism of YNZ22 gene on atherosclerosis people in Shaanxi province and toassess the possible association between polymorphism and suceptibility of atherosclerosis so as to provide clues for genetic marker of atherosclerosic. METHODS Polymorphism at YNZ22 VNTR locus was studied by PCR in 94 cases of atheroclerosis and 75 cases of normal old people of Shaanxi. RESULTS 20 genotypes, 9 alleles ranging from 168 bp to 798 bp were revealed in normal old people of Shaanxi. The heterozygosity...

AIM To observe the polymorphism of YNZ22 gene on atherosclerosis people in Shaanxi province and toassess the possible association between polymorphism and suceptibility of atherosclerosis so as to provide clues for genetic marker of atherosclerosic. METHODS Polymorphism at YNZ22 VNTR locus was studied by PCR in 94 cases of atheroclerosis and 75 cases of normal old people of Shaanxi. RESULTS 20 genotypes, 9 alleles ranging from 168 bp to 798 bp were revealed in normal old people of Shaanxi. The heterozygosity of YNZ22 was 24.0%, PIC 0.9372; 23 genotypes, 9 alleles ranging from 168 bp to 798 bp were revealed in atherosclerosis cases. The heterozygosity of YNZ22 was 24.5%, PIC 0.8067. There was difference in distribution of allele frequency; and obviously between atherosclerosis and normal people in allele and genotypes frequency. CONCLUSION YNZ22 locus can be the polymorphic genetic marker of the atherosclerosis.

目的 研究 YNZ2 2基因多态性在陕西地区老年动脉粥样硬化 (atherosclerosis,AS)人群中分布规律及其该位点与 AS遗传易感性的关系 .方法 应用多聚酶链反应(polymerase chain reaction,PCR)对 94例老年 AS患者及 75例非 AS老年人 YNZ2 2 - VNTR(可变数目串联重复序例variable number tandem repeats)位点进行多态性分析 .结果 在正常人群中 YNZ2 2位点共检测出 2 0种基因型 ,9个等位基因 ,其片段大小在 16 8~ 798bp之间 ,杂合度为 2 4.0 % ,多态信息量 (polymorphism inform ation content,PIC)为 0 .8372 ;AS人群中 YNZ2 2基因点共检测出 2 3种基因型 ,9个等位基因 ,其片段大小在 16 8~ 72 8bp之间 ,杂合度为 2 4.5 % ,多态信息量 (PIC)为 0 .80 6 7.它们的基因频率分布有差异 .另外 ,在正常人群与 AS人群中 ,小片段的频率有显著差异 .最重要的是发现基因频率和基因型频率在两群体中不同 .结论...

目的 研究 YNZ2 2基因多态性在陕西地区老年动脉粥样硬化 (atherosclerosis,AS)人群中分布规律及其该位点与 AS遗传易感性的关系 .方法 应用多聚酶链反应(polymerase chain reaction,PCR)对 94例老年 AS患者及 75例非 AS老年人 YNZ2 2 - VNTR(可变数目串联重复序例variable number tandem repeats)位点进行多态性分析 .结果 在正常人群中 YNZ2 2位点共检测出 2 0种基因型 ,9个等位基因 ,其片段大小在 16 8~ 798bp之间 ,杂合度为 2 4.0 % ,多态信息量 (polymorphism inform ation content,PIC)为 0 .8372 ;AS人群中 YNZ2 2基因点共检测出 2 3种基因型 ,9个等位基因 ,其片段大小在 16 8~ 72 8bp之间 ,杂合度为 2 4.5 % ,多态信息量 (PIC)为 0 .80 6 7.它们的基因频率分布有差异 .另外 ,在正常人群与 AS人群中 ,小片段的频率有显著差异 .最重要的是发现基因频率和基因型频率在两群体中不同 .结论  YNZ2 2位点可能可以作为 AS的遗传标记

Objective To study the genetic polymorphisms of two new STR loci D7S817, D18S865 in Chinese Han and Dongxiang populations. Methods EDTA-blood samples were collected from unrelated individuals and DNA samples were extracted by “CHELEX-100” method. The products of the polymerase chain reaction (PCR) were analyzed by nondenaturing polyacrylamide gels electrophoresis and silverstaining. Results On D7S817 locus, 9 alleles and 23 genotypes were found in Wuhan area Han population, 8 alleles and 20 genotypes were...

Objective To study the genetic polymorphisms of two new STR loci D7S817, D18S865 in Chinese Han and Dongxiang populations. Methods EDTA-blood samples were collected from unrelated individuals and DNA samples were extracted by “CHELEX-100” method. The products of the polymerase chain reaction (PCR) were analyzed by nondenaturing polyacrylamide gels electrophoresis and silverstaining. Results On D7S817 locus, 9 alleles and 23 genotypes were found in Wuhan area Han population, 8 alleles and 20 genotypes were found in Ganshu province Dongxiang population. Therewith, at D18S865 locus, 7 alleles and 17 genotypes were identified in Wuhan area Han population, 6 alleles and 15 genotypes were identified in Ganshu province Dongxiang population. The heterozygosity and discrimination powers (DP) of D7S817 were 0.738 and 0.931respectively, in Wuhan Han population; 0.752 and 0.917 respectively, in Ganshu province Dongxiang population. The heterozygosity and DP of D18S865 were 0.72 and 0.906 respectively, in Wuhan Han population; 0.814 and 0.898 respectively in Ganshu Dongxiang population. The distribution of genotypes frequency in both loci were accorded with Hardy-Weinberg equilibrium. There were no significantly differences on distribution of allele frequency between the two populations. Conclusion These results suggest that STR system D7S817 and D18S865 loci are useful markers in forensic haemogenetics.

目的 调查D7S817、D18S86 5两个STR位点的遗传多态性 ,获得群体遗传学基本数据。 方法 采用PCR和PAG垂直电泳技术、银染显色方法。结果 D7S817位点在成都汉族群体中发现 9个等位基因 ,2 3种基因型 ,杂合度为 0 .738,个人识别机率为 0 .931。在甘肃东乡族群体中发现 8个等位基因 ,2 0种基因型 ,杂合度为 0 .75 2 ,个人识别机率为 0 .917。D18S86 5位点在成都汉族群体中发现 7个等位基因 ,17种基因型 ,杂合度为 0 .72 ,个人识别机率为 0 .90 6 ;在甘肃东乡族群体中发现 6个等位基因 ,15种基因型 ,杂合度为 0 .814,个人识别机率为 0 .898。基因型频率分布符合Hardy -Weinberg平衡定律。等位基因频率的分布在 2个群体之间无显著性差异。 结论 D7S817、D18S86 5位点的扩增效率高 ,重复性好 ,个人识别能力强 ,在法医学个人识别和亲子鉴定应用中有较高的价值。

Objective To determine whether the promoter polymorphism of CD14 affects the allergic asthma susceptibility and total serum immunoglobulin E. Methods Unrelated childhood allergic asthma cases and controls were studied. The polymorphism at promoter- 159 of CD14 was genotyped by polymerase chain reaction-restriction endonuclease digestion. Results No significant association was noted between- 159 C/T polymorphism of CD14 and allergic asthma or total serum IgE. The C/C, C/T and T/T genotypes frequency of...

Objective To determine whether the promoter polymorphism of CD14 affects the allergic asthma susceptibility and total serum immunoglobulin E. Methods Unrelated childhood allergic asthma cases and controls were studied. The polymorphism at promoter- 159 of CD14 was genotyped by polymerase chain reaction-restriction endonuclease digestion. Results No significant association was noted between- 159 C/T polymorphism of CD14 and allergic asthma or total serum IgE. The C/C, C/T and T/T genotypes frequency of CD14 in Control was 0.139, 0.583 and 0.278 respectively. Conclusion The polymorphism at promoter- 159 of CD14 is not related with the pathogenesis of allergic asthma and serum total IgE.

目的 探讨CD14基因启动子区-159位基因多态性与变应性哮喘易感性的关系,以及对血清总IgE水平的作用。方法 采用聚合酶链反应-限制性片段长度多态性技术检测CD14基因启动子区-159位C/T基因多态性,共检测143例变应性哮喘息儿(患儿组)和72例正常儿童(对照组)。结果 患儿组CD14-159位C/C、C/T和T/T基因型频率分别是0.189、0.469和0.343,与对照组的0.139、0.583和0.278的差异无显著性,两组3种基因型间血清IgE水平差异亦无显著性。结论 CD14基因启动子区-159位C/T基因多态性与变应性哮喘发病无关,与血清IgE水平亦不相关。

 
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