• 结果1)枯萎卵妊娠的胎只有囊液,没有胚胎组织。 妊娠囊没有绒毛组织绒毛组织稀疏。

    Results:1) There is no embryonic tissue in gestation sac without or with little villous tissue in anembryonic pregnancy.

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  • 除了研究利用基因调控网络中的小鼠胚胎干细胞优势深入研究必须更加直接地集中于人类干细胞

    Despite the advantages of using mouse es cells in the study of gene regulatory networks, further research must focus more directly on human stem cells.

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  • 胚胎发育早期绒毛滋养层细胞侵袭基因调控机制研究提供了实验基础。

    This study would help us to reveal the mechanism of gene network regulation in EVT invasion in early embryo development.

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  • 目的研究胚胎发育神经视网膜视网膜屏障结构形成作用

    Objective To investigate effects of neural retina on development of the structure of outer blood retinal barrier in embryogenesis.

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  • 基因转染衰老细胞核移植后能支持克隆胚胎早期发育

    The senescent transfected MEF cells as donors of nuclei could support the early development of cloned embryos after nuclear transfer.

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  • 目的探讨胚胎大鼠神经干细胞培养条件基因表达效率

    Objective to explore the culture conditions for the neural stem cells from embryonic rat cortices and to test their efficacy of expressing exogenous gene.

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  • 结果:8胚胎气管壁2 3复层上皮细胞间充构成,上皮细胞的PAS反应阳性

    Result: at 8-week embryo, trachea consists of 2-3 layers of stratified columnar cells and mesenchyme around the cells, the reaction of PAS of epithelium was positive.

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  • 小鼠的造血血管系统起源于胚层胚胎期6.5-7天时在卵黄形成特征性血岛结构发生造血和内皮细胞的分化。

    The hematopoietic and vascular systems of the mouse arise from extraembryonic mesoderm that migrate through primitive streak to the presumptive yolk sac between days 6.5 and 7.0 of gestation.

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  • 而若将金鱼胚胎置入高浓度玻璃溶液中快速浸入液氮,胚胎外溶液实现玻璃态固化

    When fish embryos in high concentration vitrification solutions are directly quenched to LN_2, the extra-embryo solutions can be vitrified.

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  • 我们利用培养胚胎干细胞分化为具有特性细胞再将这些细胞复合维上皮组织

    We derived cell populations with properties of ectodermal and mesenchymal cells in 2D culture and incorporated these divergent cell populations into 3D epithelial tissues.

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  • 我们利用培养胚胎干细胞分化为具有特性细胞再将这些细胞复合维上皮组织

    We derived cell populations with properties of ectodermal and mesenchymal cells in 2D culture and incorporated these divergent cell populations into 3D epithelial tissues.

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