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inversion chromosome
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  “inversion chromosome”译为未确定词的双语例句
     The study of inversion chromosome 9 influencingfertility.
     9号染色体臂间倒位对生育影响的研究
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  相似匹配句对
     13 cases of inversion of Y chromosome;
     倒位染色体13例;
短句来源
     The study of inversion chromosome 9 influencingfertility.
     9号染色体臂间倒位对生育影响的研究
短句来源
     2 chromosome.
     2染色体有一对随体,No.
短句来源
     The third is inversion;
     第三是数据的解释以及反演。
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     Artificial Chromosome
     人工染色体
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  inversion chromosome
The efficiency of an inversion-based mutagenesis screen can be substantially enhanced provided that the inversion chromosome and its wild-type (WT) homologue are both visibly tagged by two different coat color markers.
      
To positively identify the rudimentary gene we in situ hybridized the various phage recombinants obtained in this walk to an inversion chromosome that has one breakpoint at 15A1 which inactivates the gene.
      
- In the saliva of heterozygotes (FM1/H) carrying one inversion chromosome In(1) FM1 and one X chromosome from Hikone, protein 4h could not be detected.
      
Additionally, it is argued that it is the gene sequence on only the inversion chromosome that is important in Trimerotropis.
      


The analyses of chromosome aberrations and micronuclei in peripheral blood lymphocyte were performed in 3 cases exposed to 60 Co radiation accident in 6(7) years and 11(12) years after irradiation The results show that the frequencies of chromosome aberrations in exposed cases were 4 29% in 6(7) years and 3 63% in 11(12) years after irradiation, respectively, and the difference was not significant in the two times follow-up study Most of the chromosome aberrations were acentric...

The analyses of chromosome aberrations and micronuclei in peripheral blood lymphocyte were performed in 3 cases exposed to 60 Co radiation accident in 6(7) years and 11(12) years after irradiation The results show that the frequencies of chromosome aberrations in exposed cases were 4 29% in 6(7) years and 3 63% in 11(12) years after irradiation, respectively, and the difference was not significant in the two times follow-up study Most of the chromosome aberrations were acentric and dicentric chromosomes in first time follow-up study, and translocation, deletion and inversion chromosomes in second time follow-up one The frequencies of micronuclei in exposed group were 4 17‰ and 1 17‰ in the two times follow-up study, respectively, and the rates of micronuclei in second time follow-up study were much lower than that in first one The results indicated that the unstable type aberrations were gradually lost as time goes on ,and the level of stable type aberration was of high degree

对三例钴源事故受照人员照后6 (7) 年和11 (12) 年两次细胞遗传学随访结果表明, 两次随访受照者染色体畸变率分别为429 % 和363 % , 均显著高于对照组 ( P< 001) , 但两次随访间未见显著差异 ( P> 005) , 而且第一次随访染色体畸变是以双+ 环和无着丝粒断片为主, 第二次随访是以易位、缺失和倒位为主; 两次随访受照者微核率分别为417 ‰和117 ‰, 第二次随访微核率明显下降( P< 001) 。提示随着照后时间推移, 非稳定性染色体畸变逐渐丢失, 稳定性染色体畸变仍保持在较高水平。

Objective: To investigate the relationship between sterility,spontaneous abortion and abnormal chromosome karyotypes,and that would be help for clinical diagnose for hereditary disease.Methods: 922 reproduction abnormality patients′ were performed by peripheral blood lymphocytes cultivating to make chromosome G-banding.Results: 66 of 922 cases of patients(7.16%) were abnormal chromosome karyotypes.Among 21 cases are chromosome translocations,21 cases are inversion chromosomes,18...

Objective: To investigate the relationship between sterility,spontaneous abortion and abnormal chromosome karyotypes,and that would be help for clinical diagnose for hereditary disease.Methods: 922 reproduction abnormality patients′ were performed by peripheral blood lymphocytes cultivating to make chromosome G-banding.Results: 66 of 922 cases of patients(7.16%) were abnormal chromosome karyotypes.Among 21 cases are chromosome translocations,21 cases are inversion chromosomes,18 cases are Klinefelter′s syndromes,1 case is Turner′s syndromes and deletion X-chromosome,1 case is Y-chromosome deletion,1 case is ring 21-chromosome,1 case is marker chromosome,63 cases are polymorphism of Y-chromosome accounting for 13.35%.Conclusion: Chromosome abnormalities are the important factors resulting in female/male infertilities.we advocate that should try to do chromosome investigation for reproduction abnormality patients.

目的探讨不孕不育及自发流产与染色体核型异常的关系,指导临床对这些疾病的诊断。方法采集922例生殖异常患者外周静脉血,进行淋巴细胞培养,常规方法收获细胞,低渗、固定、制片、经G显带处理、镜检,进行观察研究。结果922例患者共检出异常核型66例,总检出率7.16%。其中,易位21例,倒位21例,克氏综合征18例,X-三体综合征2例,Turner综合征伴X染色体缺失1例,Y染色体缺失1例,环状21号染色体1例,额外标记染色体1例,及常见染色体多态性大Y染色体63例,发生率13.35%。结论染色体异常是导致不孕不育及自发流产的重要原因之一,对生殖异常患者进行染色体检查可为临床诊断和优生优育提供依据。

 
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