染色体

Each chromosome consists of two chromatids held together by the centromere.

每个染色体由两个染色单体所组成，它们被一个着丝点联结在一起。

In this procedure, the chromosome 17 centromere is marked with a green florescent signal and HER-2 gene with an orange florescent signal.

在检测过程中，17号染色体的着丝点被绿色的荧光标记，her2被标记为开花状的橙色荧光。

Finally, the authors were able to sequence through the first centromere from a monocot organism. In my opinion, this alone would be worthy of a Nature paper.

另外，作者对第一条单子叶植物染色体的完整着丝粒区域序列进行了测定，在我看来，这个已经可以值得单独作为一篇Nature文章发表了。

It is difficult to find the place of centromere on chromosome precisely. So centromeric index can\'t get an accurate value.

但是由于染色体经Giemasa染色后，着丝点变得不明显了，再加上图像预处理等的影响，着丝点很难准确确定，着丝率的计算也就不会准确。

Following the replication of chromosomes, resultant chromatids remain attached at the centromere.

随着染色体的复制，着丝粒始终连接着形成的两个染色单体。

The paper first has made a comparative reseach on frequency of chromosome chiasma and the length and width of testes follicles of 8 grasshopper species of Caryanda.

同时对卵翅蝗属9种与小蹦蝗属1种蝗虫染色体的总交叉频率与它们精小管各部分长度及宽度等形态进行了比较研究。

In this paper, we analyze the rule of breaking on an X-palindrome between human and chimpanzee for the first time.

在本文中，我们首次通过分析人类和黑猩猩的X染色体上的一条回文序列，来寻找这种对称性破缺的规律。

We analyze for the first time the rules of breaking in an X-palindrome between human and chimpanzee.

首次通过分析人类和黑猩猩的X染色体上的一条回文序列，来寻找这种对称性破缺的规律。

Genetic algorithm is used for the optimal subset searching and the strategy for chromosome coding, the choice of fitness function and the design of genetic operators are discussed.

讨论了遗传算法中染色体的编码方式，适应度函数的选择以及遗传算子的设计方法。

Benign hereditary chorea is an autosomal dominant disorder of early onset characterised by non progressive choreic movements with normal cognitive function occasionally associated with hypothyroidism and respiratory problems.

良性遗传性舞蹈症是一种早发的常染色体显性遗传性疾病，以非进展性的舞蹈样运动为特点，偶尔伴有甲状腺机能减退和呼吸系统疾病，但认知功能正常。

She gently rebuff ed him, but agreed that they could be friends

她婉言拒绝了，但同意作为朋友相处。

If in the penal farm, you were sure to be criticized.

要是在劳改农场，你等着挨绳子吧！