In the translocation, the two chromosomes swap large pieces of chromosome with each other.

在易过程中，两条色体交换了大量的色体片段。

And captive good attending captain ill

善恶易，小人反受大人拜。

Burkitt lymphoma can also result from a chromosomal translocation.

伯基特淋巴瘤也可由色体易。

Finally, there might be a translocation, which is when two chromosomes swap material.

最后一个原因可能是色体易，也就是两条色体间发生片段交换。

One type of change in the cell's DNA that is common in leukemia is known as chromosome translocation.

白血病中常见的一种细胞 DNA 变称为色体易。

Mantle cell lymphoma can also result from a chromosomal translocation.

套细胞淋巴瘤也可由色体易。

One known mechanism for how a follicular lymphoma develops, is a chromosomal translocation between chromosome 14 and chromosome 18.

一种已知的滤泡性淋巴瘤发生机制，是14色体18色体之间的色体易。

Sarah made the film, The Beaver Believers, a documentary about folks trying to save the beaver in part through translocation.

莎拉制作了电影《海狸信徒》一部关于人们试图通过易拯救海狸的纪录片。

The Myc gene stimulates cell growth and metabolism, so the translocation results in increased cell division.

MYC基因刺激细胞生长新陈代谢，因此，易导致细胞分裂加速。

A translocated species could die out from lack of food, for example.

例如，易物种可能会因缺乏食物而灭绝。

Her friends were recovering from the translocation, too.

她的朋友们也从易中恢复过来。

A couple of researchers have recently analyzed reptile translocation and concluded that it can be a very efficient method.

一些研究人员最近分析了爬行动物易， 并得出结论， 这可能是一种非常有效的方法。

Ewing sarcoma is associated with chromosomal mutations, specifically a translocation between the EWSR1 gene on chromosome 22 and FLI1 gene on chromosome 11.

尤因肉瘤与色体突变有关，特别是22色体上的EWSR1基因11色体上的FLI1基因之间的易。

Osteosarcoma is linked to RB1 and TP53 genes mutations, while Ewing sarcoma is thought to arise when there are EWSR1, and FLI1 genes mutation.

骨肉瘤与RB1TP53基因突变有关，尤因肉瘤被认为源于EWSR1FLI1基因的易。

Translocations can disrupt SNRNP and move the small nucleolar RNA genes away from their imprinting center, causing them to get methylated and turned off.

SNRNP基因易会破坏小核内核糖核蛋白（SNRPN），并将核仁小RNA基因移出印记中心，导致这些基因的甲基沉默。

The BCL1 gene encodes the protein cyclin D1, which stimulates cell growth, so once again the translocation results in increased cell division.

BCL1基因编码细胞周期蛋白D1，刺激细胞生长，所以易导致细胞分裂加速。

ALK gene rearrangement ALK gene rearrangements result from inversions or translocations on chromosome 2 and occur in around 4% of patients with NSCLC.

ALK 基因重排 ALK 基因重排是由 2 色体上的倒或易的，大约 4% 的 NSCLC 患者会发生这种情况。

In this case, the BCL1 gene from chromosome 11 ends up next to the immunoglobulin promoter on chromosome 14, which again upregulates its expression.

在这种情况下，11色体上的BCL1基因易至14色体，与14色体上的免疫球蛋白启动子相邻，后者上调了BCL1基因的表达。

As a result, an the BCL2 gene from chromosome 18 is placed after the immunoglobulin heavy chain promoter on chromosome 14, and that results in overexpression of bcl-2.

因此，一个来自18色体的BCL2基因被易到14色体的免疫球蛋白重链启动子后，导致BCL-2过表达。

In this case, the Myc gene is translocated from chromosome 8 where it ends up adjacent to IgH promoter on chromosome 14 and again that upregulates its expression.

在这种情况下，MYC基因从8色体易至14色体，最终与14色体上的IgH启动子相邻，这也上调了它的表达。