如果我们的一条染色体是由两条灵长类染色体融合而来的话，猜猜它能有点什么？
If one of our chromosomes was formed by the fusion of two primate chromosomes, you know what it would have?
在实际的融合过程中，由两个物种的遗传物质在概念上是可交融的，染色体的一半来自父母一方，一半来自另一方。
In a true hybrid, the genetic material from the two species is mingled at conception, with half the chromosomes coming from one parent and half from the other.
细胞工程主要包括体细胞融合，核移植，细胞器摄取和染色体片段的重组等。
The works mainly comprise the body cells, cell fusion, nuclear transplantation, cell uptake and the reorganization of chromosome segment.
特定的染色体和融合基因可作为白血病的标志物，对白血病的诊断、预后估计、监测治疗和微小残留白血病等方面具有一定的价值。
The specific chromosome and fusion gene are regarded as marker of leukemia, and helpful in leukemia diagnosis, evaluating prognosis, monitoring of treatment and minima residual leukemia.
本研究旨在探讨急性髓系白血病(aml)患者6；9染色体易位与DEK - CAN融合基因表达之间的关系及临床意义。
This study was aimed to explore the relationship of 6; 9 chromosome translocation with DEK-CAN fusion gene expression in patients with acute myeloid leukemia (AML) and its clinical significance.
包括细胞融合技术、细胞器移植、染色体工程和组织培养技术。
Including cell fusion technology, cell transplantation, chromosome engineering and tissue culture.
细胞学观察表明，6一dmap阻止了纺锤体的形成和染色体的移动，导致一个融合的二倍性雄性原核的形成。
According to Cytological observations, 6-dmap disrupted the spindle at mitosis and inhibited chromosome movement, resulting in the formation of one diploid male nucleus.
光钳和微束系统可用来切割染色体，收集染色体片段，融合细胞以及改变细胞和细胞器的行为。
It can be used to microdissect chromosomes, to collect the chromosome segments, to fuse the selected pairs of cells and to change the behavious of cells and organelles.
结论儿童aml进行染色体分析及融合基因的检测，有助于AML诊断及亚型之间的鉴别诊断。
Conclusion Chromosome analysis and detection of fusion genes are helpful in the diagnosis of AML and the differentiation diagnosis of AML subtype.
细胞融合和体细胞染色体加倍是获得杨树多倍体种质的有效途径之一。
Chromosome doubling for somatic cells and somatic hybridization via cell fusion are effective methods to create polyploidy.
应用细胞融合技术和扫描电镜研究了BK(牛肾)细胞早熟凝集染色体(PCC)和诱导PCC的CHO中期染色体的超微结构。
The ultrastructure of prematurely condensed chromosomes (PCC) in BK cells and the CHO metaphase chromosomes (the PCC inducer) were studied with cell fusion technique and SEM.
应用细胞融合技术和扫描电镜研究了BK(牛肾)细胞早熟凝集染色体(PCC)和诱导PCC的CHO中期染色体的超微结构。
The ultrastructure of prematurely condensed chromosomes (PCC) in BK cells and the CHO metaphase chromosomes (the PCC inducer) were studied with cell fusion technique and SEM.
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