m chromosome

英 [em ˈkrəʊməsəʊm] 美 [em ˈkroʊməsoʊm]

小染色体

医学



双语例句

  1. Many restraint conditions and the multi-object optimizing model are analyzed and we propose a kind of chromosome design based on N × M two dimension matrix. New genetic operators based on matrix operations are constructed, which are adaptive.
    通过对各种约束条件和多目标优化模型的分析,提出了基于N×M二维矩阵的染色体编码设计,并构造了基于矩阵操作的新的遗传算子,采用了自适应变换等技术。
  2. Chromosome length of metaphase, and prometaphase including the early to late, three stages were 2.19,2.22, 2.32 and 2.29, respectively. It was obvious that the band number per ju chromosome length of different stages had little difference.
    早中期Ⅰ、Ⅱ、Ⅲ和中期染色体组中每单位绝对长度的带数(带/μm)分别为2.19、2.22、2.32和2.29,差异不大。
  3. Analysis of the sterility and chromosome aberration of m_1 plants at meiosis by co~ ( 60)γ-ray irradiation in Rye
    Co~(60)&γ射线对黑麦M1植株染色体畸变的影响及不育性的分析
  4. 8, Z, W chromosome were all metacentrics, No.
    Z、W染色体都为m型;No。
  5. The ApoM gene is located in the major histocompatibility complex Class III region on chromosome 6.The functions of ApoM are to be determined.
    载脂蛋白M位于6号染色体主要组织相容性抗原复合体Ⅲ区。
  6. And Z chromosome were metacentric, and the others were telocentric.
    Z染色体为m型,其余染色体均为t型。
  7. The chromosome markers A, B and M were found in all three kinds of colls. The karyotype differences by G-binding were also observed.
    三种细胞中均可看到A、B和M三种标记染色体,三种细胞的G显带核型也有差异。
  8. Results revealed that the trait of giant-embryo was genetically controlled by a pair of recessive genes, three alleles ( ge~ m, ge, ge~ s) were located on chromosome 7, and several QTLs associated with embryo size had been conducted.
    水稻巨胚受一隐性基因控制,控制稻米巨胚的3个等位基因gem、ge、ges已被定位在水稻第7染色体上,多个与胚大小有关的QTL也被检测。
  9. The results indicated that the size of 28 chromosome of BM was between 1~ 3 μ m with a small fluctuation range, which belongs to miniature chromosomes in the living nature.
    结果表明:中国野蚕28条染色体粗线期大小在1~3μm之间,而且变异范围小,在生物界属于小染色体类。
  10. Objective To set up the technical system of multiplex fluorescence in situ hybridization ( M FISH) and to explore its application in detection of the complex chromosome abnormalities in leukemia.
    目的建立多重荧光原位杂交技术(multiplexfluorescenceinsituhybridization,M-FISH)体系,探讨其在检测白血病复杂核型异常中的应用。
  11. The M 1 and M 2 marker chromosomes are related to No. 1 chromosome.
    其中最为明显的M1和M2标记染色体都与1号染色体有关。
  12. Objective To explore the differences between radiation-induced translocation and dicentric chromosome aberrations detected by multicolor fluorescence in situ hybridization ( M-FISH) method.
    目的探讨用多色荧光原位杂交(MFISH)技术检测的易位和双着丝粒染色体畸变的差异。
  13. The algorithm based on Euclidean similarity measure scatter matrix as the feature evaluation criteria, based on m-dimensional feature as the gene to construct chromosome string, and build the cross/ mutation operator model based on adaptive genetic strategy.
    算法以欧氏相似测度散布矩阵作为特征评价准则,以m维特征为基因构造染色体码串,并采用了基于自适应遗传策略的交叉/变异算子模型。
  14. Chromosome deletion was triggered by Cre/ loxP-mediated inverse sister chromatid recombination in the G2/ M phase of the cell cycle, leading to the generation of daughter cells missing part of or the entire recombinant chromosome.
    在细胞有丝分裂的G2/M期,Cre/loxP介导的反向染色单体重组可以导致染色体删除,分裂后产生的子细胞将丢失全部或者部分的重组染色体。