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These translocation lines were generated from homeologous chromosome pairing, or mis-division and reconstruction of univalent chromosomes.

染色体易位有来源于同祖配对交换,有来源于单价体错分裂或断裂重建。

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Soft tissue sarcomas are a highly heterogeneous and polygenous group of tumor, and characterized by specific chromosome translocations and corresponding fusion genes.

软组织肉瘤是一种起源不同、形态学复杂多样恶性肿瘤,其诊断和鉴别诊断一直是病理学家们挑战之一。

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From the Concept, the formation and the character of supermolecule, the author probes three basic function of supermolecule system: recognition, transformation and translocation.

从超分子概念,组成和特性着手,了超分子体系三大基本功能:识别、催化和输运。

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In this process, protein translocation machineries of the outer and inner membranes, at least three major translocase complexes, are needed to ensure the proper import of precursor proteins.

在此过程中,需线粒体外膜和内膜蛋白质运输机器(至少三种移位酶复合物)来保证前体蛋白质正确运输。

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14) translocation were noted in patients with short stature, and all of these cases were found to have a specific genetic syndrome – maternal uniparental disomy (UPD) of chromosome 14.

14)染色体移位在身材短小病人上发现,这些病例发现都属于一种特殊遗传症候群-第十四母体单亲双染色体。

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With a systematic study on the effects of ionophores and ion channel on the photopotential signals, this paper verified ike nonproton ion translocation in Purple Membrane.

本文通过在介质中加入离子载体或离子通道剂对紫膜光电响应信号进行了系统研究。结果表明:上述光电位信号差异是由紫膜非质子离子迁移引起

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声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。

Osmosis-血液

Mantle cell lymphoma can also result from a chromosomal translocation.

套细胞淋巴色体易位引起。

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Osmosis-血液

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

在易位过程中,两条色体交换了大色体片段。

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Osmosis-血液

Burkitt lymphoma can also result from a chromosomal translocation.

伯基特淋巴色体易位引起。

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Osmosis-遗传

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

最后一个原因能是色体易位,就是两条色体间发生片段交换。

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Osmosis-血液

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

一种已知滤泡性淋巴发生机制,是14号色体和18号色体之间色体易位。

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Osmosis-遗传

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基因易位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,导致这些基因甲基化沉默。

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Osmosis-肌骨

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

尤因肉色体突变有关,特别是22号色体上EWSR1基因和11号色体上FLI1基因之间易位。

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