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mendelian     
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  孟德尔的
     3.Genetic analysis and ^detecting showed that the majority of T] generation (Tn selfed seed) accorded with Mendelian segregation (3:1) , the genes could inherit into its descendances as single gene .
     3.通过遗传分析并经过x~2测验结果表明,转基因水稻多数株系T_1代(T_0代自交种子)遗传分离符合孟德尔的3:1遗传规律,其能以单基因遗传给后代,T_2代(T_1代自交种子)就可以得到纯合株系。
短句来源
     The results suggested that the 13/17 translocation chromosomes weretransmitted according to the Mendelian law, and homozygous boar for the 13/17Robertsonian translocation has a normal fertility.
     此结果表明,13/17易位染色体的遗传完全符合孟德尔的遗传规律,13/17易位纯合子公猪具有正常的繁殖力.
短句来源
     Conclusion:Familial type 2 diabetes had a familial aggregation. It was not inherited in the manner fully as polygene inheritance,butir seems to be of Mendelian autosomal dominant inheritance.
     结论 :有家族史的 2型糖尿病患者有明显的家族聚集性 ,其发病与遗传密切相关 ,其遗传方式不完全支持多基因遗传 ,而支持孟德尔的常染色体显性遗传。
短句来源
  孟德尔
     The 356 (73.40%) of polymorphic markers with Mendelian segregation ratio (P=0.01) were obtained. 247(69.38%)of the 356 loci were 1:1 segregation, 109(30.62%)of the 356 loci were 3:1 segregation.
     共有356(73.40%)个多态性位点符合孟德尔分离比例(P=0.01),其中发生1:1分离的位点为247(69.38%)个,发生3:1分离的位点为109(30.62%)个。
短句来源
     Markers Deviated from Mendelian segregation ratios were observed to be 15.0% (P<0.05) and (27.5%) (P<0.01) respectively.
     255个AFLP位点中偏离孟德尔遗传的比率(P<0.05)为15 0%和27 5%(P<0.01)。
短句来源
     By using phi057,the segeragation ratio of two genotypes,o2o2 and o2O2,detected among 224 individuls of [(CA335×Huangzao4)×CA335] BC 1F 1 population was 1∶1.24,which accorded with Mendelian ratio.
     利用标记phi0 5 7对BC1F1回交群体 [(CA335×黄早四 )×CA335 ]的 2 2 4个单株进行检测 ,两种基因型o2o2和o2O2的分离比为 1∶1 2 4 ,符合孟德尔遗传分离比例。
短句来源
     The test with the marker Phi057 revealed that the segregation ratio of two genotypes, o2o2 and O2o2, in the BCiF, families of (CA335×Huangzao4) ×CA335 with 224 individuals was 1:1.24 as it was expected according to Mendelian segregation.
     利用Phi057标记对BC_1F_1回交群体(CA335×黄早四)×CA335的224个单株进行检测,o2o2和O2o2两种基因型的分离比为1:1.24,符合孟德尔遗传分离比例。
短句来源
     The numbers of loci segregating in Mendelian law were 251(52.1%) and 207(58.6%) for(3∶1) and 1∶1 loci,respectively.
     分离比为1∶1的位点共有353个,占分离位点数的42.3%,符合孟德尔规律的位点207个,占58.6%(占分离位点数的24.8%)。
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  孟德尔定律的
     Development and expansion of Mendelian law
     孟德尔定律的发展与扩充
短句来源
     Genes imprinting means that some genes violate the usual rule of Mendelian inheritance law and their expression is determined by the parents that contributed them.
     基因印迹指的是某些基因呈不遵从孟德尔定律的亲源依赖性单等位基因表达,其另一等位基因不表达或表达极弱,具有这种现象的基因被称为印迹基因。
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  “mendelian”译为未确定词的双语例句
     Objective Congenital fibrosis of the extraocular muscles (CFEOM) is a kind of syndrom following Mendelian inheritance. In our study,eight short tandem repeat(STR) loci including D12S1048, D12S59, D12D331, D12S345 on chromosome 12 and D16S3026, D16S689, D16S3063, D16S3121 on chromosome 16 were chosen as DNA markers for linkage analysis.
     目的 在先天性眼外肌纤维化(congenital fibrosis of the extraocular muscles CFEOM)的CFEOM1和CFEOM3位点,分别选择了位于12号染色体上D12S1048、D12S59、D12D331、D128345和位于16号染色体上的D1683026、D168689、D16S3063、D16S3121共8个STR多态标记进行连锁分析。
短句来源
     The male sterility of MSL GS14-1,GS15-8,GSA-2, SS370 and SS387 inherited in the Mendelian mode of one gene. Some restorer and maintainer lines to these MSL were also found.
     不育系 GS14-1、SS370、GSA-2、GS15-8和 SS387等的不育性遗传与1对相对性状的遗传方式相符,已找到不育系的保持系和恢复系。
短句来源
     Mendelian fashion of hph gene was further confirmed and homozygotes for hph gene were identified in the T2 and T3lines.
     在 T2 、T3世代获得了具 hph基因的纯合体。
短句来源
     The personal identification was studied in Chinese of Han nationality by using six dinucleotide simple tandem repeat polymorphism loci that located in different chromosomes and showed Mendelian codominant inheritances. These six loci are: D1S103,D4S175, D5Sl07,D19S49,D6S89 and D9S58. The results showed;
     为建立二核苷酸简单串联重复顺序(STR)多态位点个体鉴别技术系统,应用6个位于不同染色体呈共显性传递的二核苷酸STE多态位点进行中国汉族人个体鉴别研究,这6个位点是D1S103、D4S175、D5S107、D19S49、D6S89及D9S58。
短句来源
     The separation in F2 between the resistance and sensistive basically according 3:1, while in B1F1 generation is 1:1. The result showed that the inheritance of Bar gene was a single dominant gene and accorded with the law of Mendelian segregationbasically.
     进行自交获得的F2代中抗除草剂植株与感除草剂植株的分离比基本符合3:1的分离比,与安徽品种进行回交得到的B1F1代中,分离比为1:1。 结果表明,抗除草剂转基因小麦杂交与回交后代Bar基因的遗传,符合1对显性基因的分离比例和孟得尔遗传规律。
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  mendelian
Effect of harvesting on the genetic diversity and dynamics of a Mendelian limited population
      
Besides apparent medical importance, the discovery of trinucleotide repeat expansion unraveled a fundamental problem of human genetics: a non-Mendelian type of inheritance called anticipation.
      
The three major fields were molecular cytogenetics and chromosomal disorders, genomics of Mendelian and common diseases, and ethnogenomics of the North Asian population.
      
A genetic model of the non-Mendelian inheritance in the progeny of heterozygous male mice specifically explains sterility of animals carrying the t-complex with complementary lethal genes.
      
Nine marker genes showed deviation from Mendelian monogenic inheritance depending on the cross direction and maternal cytoplasm.
      
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