mendelians造句

• mendelian gene is not a real physical entity but an abstraction or symbol .
  孟德尔式的基因并不是真正的实体，而是抽象概念或者是说明性的符号。
• It is rather disappointing that so few of the features show clear-cut mendelian pedigree patterns .
  颇使人感到失望的是，只有很少的特征能显示出明显的孟德尔系谱类型。
• Chapters 2－5 are devoted to the basic concepts of mendelian and population genetics which are of greatest concern in tree improvement .
  第二到第五章介绍对于改良树木有密切关系的门德尔和群体遗传学的基本概念。
• This information is valuable both as a prelude to linkage analysis, which generally assumes mendelian transmission
  因为性状存在孟德尔遗传是连锁分析的潜在条件。
• If the characteristic is governed by simple mendelian genes, the typical monohybrid and dihybrid ratios become apparent in the f2 generation
  如果其特征取决于单一孟德尔基因，那么典型的单基因杂种和和双基因杂种的遗传比率将在子二代呈现。
• mendelian genetics, genetic mapping techniques, and statistical analysis of large populations and their application to particular studies in behavioral genetics
  孟德尔遗传学，遗传定位技术，和大母群的统计分析及其在行为遗传学中特定研究之应用。
• The segregation proportion of target genes in transgenic tl progeny is 3 : 1 . accordant with the law of mendelian segregation in a single loci . 4
  大白菜转基因植株乃代，经pcr、pcrsouthl检测，后代有分离现象，分离比例趋于3：l，符合盂德尔分离规律。
• Today the subject has four main subdivisions mendelian genetics ( classical genetics ), population genetics, cytogenetics, and molecular or biochemical genetics
  现在，该学科主要包括四大部分?孟德尔遗传学（古典遗传学），种群遗传学，细胞遗传学以及分子或生化遗传学。
• He was blacklisted in the former soviet union and its satellites as the founder of a “ reactionary ” discipline, and mendelian genetics was declared a pseudoscience
  由于他是某个反动学说的创始者，因此前苏联及附庸国都将他列在黑名单上，孟德尔遗传学也被打成伪科学。
• Ninety-four segregating markers were identified, among which 74 ( 78.7 % ) were in agreement with 1 : 1 mendelian ratio, and 20 ( 21.3 % ) were distorted markers
  有94条片段在父本或母本中分离。卡方检验显示74（78.7%）个分离标记符合孟德尔1:1遗传比例，20个为偏分离标记。
• Genetic analysis of progeny from the crosses of wtxcex1-1 and wtxcex1-2 demonstrated that the phenotypes of cex1-2 mutants were inherited as a single recessive mendelian marker
  对wtxcexj和wtxcexl2fz分离群体的遗传分析发现，cexl1和cex12均表现为孟德尔隐性单基因遗传。
• These results indicated that the cloned osg6b " had a constitutive characteristics but not anther specificity, and the transgene was segregated in a mendelian fashion in the tl generation
  研究表明，所克隆的osg6b’不具有花药特异性，而具有组成型表达的特征。第二部分：从大肠杆菌e
• Microsatellite marker has many advantages such as a great quantity, extensive dispersion around the genome, high polyomorphism, mendelian codominant inheritance, rapid and convenient detection
  摘要微卫星标记具有数量多、在基因组中分布广、多态性丰富、呈孟德尔共显性遗性、检测快速方便等特点。
• Excellent tutorials and problem sets for learning biochemistry, cell biology, developmental biology, human biology, molecular biology, mendelian genetics, and immunology from the university of arizona
  为推广生物科技教育,提供了对环境,农业,基因工程,食品生产,保健医疗,生物伦理,学习资源等题目的简单讲解
• Add to that the exceptions of half-bloods, muggle-borns and squibs and the temptation to analyze its hereditability in terms of mendelian genetics becomes almost unbearable ( for some of us anyway )
  除此之外还有混血，麻瓜出身和哑炮，这更使运用孟德尔基因学理论分析遗传的努力变得几乎让人无法忍受（至少对于我们中间的某些人来说）。
• Characters controlled by the dna of extranuclear organelles are not inherited according to mendelian laws and are transmitted only through the female line, since only the female gametes have an appreciable amount of cytoplasm
  由于细胞质大多来自母体所产生的配子，所以由细胞核外的细胞器的dna所控制的遗传性状一般只随母系而遗传，也不符合孟德尔定律。
• It proceeds by testing models of varying degrees of generality, both to determine whether a mendelian locus is likely to exert a large effect on the phenotype of interest and to estimate the magnitude of genetic sources of variation in the trait
  它通过检测一般模型的不同状态，决定是否孟德尔位点对性状发挥大的效应，以及估计性状变异的遗传大小。这一信息有利于进一步所做的连锁分析。
• The researches acquired suggest that manipulating ferritin expression and other soluble components of seed iron in soybeans and possibly other seeds, using mendelian genetic technique and biotechnological approaches, could contribute to a sustainable solution to the global problem of iron deficiency
  已有的研究表明，使用孟德尔遗传方法和生物技术途径提高大豆和其它谷物类种子中铁蛋白的表达和其它可溶性铁成分，将有助于全球性缺铁问题的有效解决。
• Through testing these aflp markers on the hybrids that constructed fe-efficient and fe-inefficient bulk, 18 loci were found maybe linked with fe-efficient trait and exhibited normal mendelian segregation . linkage relationships were established by the inheritance of the markers in the entire analysis population . these markers localized in the same linkage group
  它们在f1分析群体的分离符合1：1的分离比例，通过这18个标记在整个群体的遗传分析建立了连锁关系，并用这18个标记对铁高效性状进行了基因定位，结果表明18个aflp标记位于同一连锁群上。
• In 2001, wilson and his colleagues cloned another two members-human wnk1 gene and wnk4 gene which were located on chromosome 12 and 17, respectively . the two genes are disease-causing genes responsible for a mendelian hypertension . the disease-causing mutations are the large deletions in the first intron in wnk1 gene, causing increased expression in leukocytes
  2001年，wilson等克隆了此家族的另两个成员??人的wnk1和wnk4基因，分别位于12号和17号染色体，这两个基因是一种孟德尔遗传型高血压病的致病基因，致病突变分别是wnk1基因第一内含子的大片段缺失，导致患者白细胞的基因表达量提高5倍左右。