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1.At anaphase the dicentric chromatid will form a bridge and the acentric a fragment, both of which can be scored.

1.在后期双着绿点将形成一个桥,无着绿点形成一断片,此两者均可记下来。

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2.At this point esch chromosome consist of a pair of chromatids and the two associated chromosomes are termed a tetrad.

2.此时每条由一构成,这两条联合的称为四分

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3.Human Peripheral blood exposed with tritiated water at variousdoses for 54 hr was examined to observe the chromosome and chromatid abe-rrations at metaphases in the first mitosis of lymphocytes.

3.将人外周血在不同剂量的氚水中培养54小时,观察到淋巴细胞第一次有丝分裂中期的型及型畸变。

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生物学基础入门

1.The spindle fibers shorten and the centromere divides, so each chromosome becomes two separate chromatids.

纺锤丝缩短了,着丝粒分裂,所以每个染色体变成两个独立的染色单体。

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生物学基础入门

2.The DNA is exactly replicated, and each chromosome now becomes two identical chromatids joined by the centromere.

DNA 被复制了,每条染色体现在变成了两条由着丝粒连接的同染色单体。

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Osmosis-遗传

3.As a result, a double-stranded break on one of the chromosomes can be repaired by using the sister chromatid.

所以,一条染色体上的双链断裂可利染色单体进行修复

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Osmosis-遗传

4.That donor DNA will act like a sister chromatid as a reference to recreate the lost genetic information.

该供体DNA会像染色单体一样,作为重建遗传信息的参考。

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日常生活医学科普

5.Each daughter cell now has half the number of chromosomes but each chromosome consists of a pair of chromatids.

现在每个子细胞都有一半的染色体,但每个染色体都由一对染色单体组成。

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日常生活医学科普

6.The paired and replicated chromosomes are called bivalents or tetrads, which have two chromosomes and four chromatids, with one chromosome coming from each parent.

配对和复制的染色体被称为二价体(也称为四分体),它们有两条染色体和四个染色单体,每个亲本都有一条染色体。

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日常生活医学科普

7.In prophase 2, we see the disappearance of the nucleoli and the nuclear envelope again as well as the shortening and thickening of the chromatids.

在前期 2,我们看到核膜消失,染色单体变短变厚。

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Osmosis-遗传

8.So now End 1 is placed near a similar nucleotide sequence, called the homologous sequence, because it's found in the same spot on the homologous sister chromatid.

现在End 1位于一段似核苷酸序列附近;这段序列被称为同源序列,位于同源染色单体上的同位点

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Osmosis-遗传

9.Since homology-directed repair uses a sister chromatid as a template, this is a more reliable repair mechanism than non-homologous end joining because there's no loss of nucleotides.

由于同源介导修复是以染色单体为模板,这种修复机制比非同源末端连接更可靠,因为没有核苷酸丢失。

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