X chromosome的例句大全

It indicates the existance of a choice mechanism, by which the pregnant mother keeps extraembryonic tissue ( placenta) to express X chromosome of the same origin in the interface between the tissues of mater-nal and embryo.

胎-母组织介面上的胚外组织只表达与母体同源的X染色体。

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Clearly, the X chromosome Xceeds its feminine responsibilities.

很明显，X染色体不光对雌性起作用。

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AIS, the X-linked recessive genetic disease, is the mutation of androgen receptor gene in the X chromosome and the defect of androgen receptor of the cell membrane, resulting in androgen insensitivity.

AIS属于X连锁隐性遗传病，是位于X染色体上决定雄激素受体的基因发生突变，引起雄激素靶细胞膜上的雄激素受体缺陷，造成对雄激素不敏感。

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Study leader Dr Claude Libert, from Ghent University in Belgium, said: "Statistics show that in humans, as with other mammals, females live longer than males and are more able to fight off shock episodes from sepsis, infection or trauma. We believe this is due to the X chromosome."

来自比利时根特大学的研究领导者克劳德·力博特博士说：“数据表明，在人类和其他哺乳动物中，女性寿命更长，更能抵御因败血症发作引起的休克、感染病和创伤。我们认为这可以归因于X染色体。”

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But that doesn't mean its counterpart, the X chromosome, plays no part. In fact, it has a big role in making sperm.

但是这并不意味着X染色体对男儿身没有影响。X染色体在精子的形成过程中起重要作用。

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[ Results]: 365 samples of the ovarian nurse cell of Anopheles minimus from Yunnan were observed. The chromosomes consist of one telocentric X chromosome, two submetacentric autosomes 2 and two metacentric autosomes 3.The X is the shortest and the 2R is the longest chromosome.

结果：共观察了365张云南微小按蚊卵巢营养细胞多线染色体标本，其染色体由5臂组成，X染色体最短，为端着丝粒；

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A study of the abnormal X chromosome in schizophrenic patients

精神分裂症患者X染色体异常的研究

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One-hundred-forty-four human X chromosome genes had no counterparts in mice.

人类X染色体上有144组基因不同于老鼠。

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Women with the syndrome are missing one or part of their second X chromosome.

患有特纳综合症的女性往往缺失一种或部分第二X染色体。

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Numerical Ranges of Normal Dual Mapping The X chromosome was normal.

正规对偶映象的数值域X染色体无变化。

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Methods Firstly, X chromosome scanning was used to exclude X chromosome.

方法先进行X染色体扫查，排除致病基因位于X染色体的可能；

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Study of fragile X chromosome in the child patients with inherent mental retardation

先天智力低下患儿脆性X染色体分析

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Proceeding of research on X chromosome genetic markers

X染色体遗传标记研究进展

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54.5% of these cases involve the structural rearrangement of X chromosome.

其中6例（54.5%）涉及X染色体结构异常。

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The X chromosome was normal. PCR amplification;

X染色体无变化。普通PCR扩增目的片段；

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The whole X chromosome were dyed light.

X染色体不出现C带阳性区，整个被浅染；

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The abnormality and genetic disorders of X chromosome involved in premature ovarian failure

X染色体异常及其基因缺陷在卵巢早衰发病机制中的研究

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It is nomal in scope. The X chromosome was normal.

属正常范围。X染色体无变化。

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Sometimes there may be abnormalities in the X chromosome in only some cells in the body.

有时可能会有异常的X染色体中，只有一些细胞在人体内。

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A Family of Fragile Site X Chromosome

一个脆性位点X的家庭

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