• 目的探讨二硫化染毒小鼠心肌细胞凋亡影响

    Objective to study the effect of carbon disulfide infection of mice myocardial cell apoptosis.

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  • 目的研究病毒性心肌(V MC)小鼠心肌细胞凋亡及其意义。

    Objective to investigate cardiomyocyte apoptosis in viral myocarditis (VMC) mice and its relationship with VMC.

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  • 目的研究急性分离小鼠心肌细胞肿胀激活离子通道通道特征

    AIM: To characterize the single channel properties of swelling-activated chloride channel in freshly isolated mouse cardiac myocytes.

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  • 目的探讨慢性病毒性心肌感染性扩张型心肌小鼠心肌细胞凋亡动态变化

    Purpose to investigate dynamic alteration of apoptosis in myocardium of mice with acute, chronic myocarditis and dilated cardiomyopathy.

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  • 研究表明小鼠研究中,病毒感染心肌细胞使用受体正常心脏跳动所必须的。

    The researchers demonstrated that the receptor which the virus uses to infect heart cells is normally necessary for regular heart beat in mice.

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  • 目的研究小鼠胚胎细胞分化心肌细胞通道、钙通道生理特性

    AIM: To study the electrophysiological characteristics of ion channels of stem cell derived cardiomyocytes (SCDC) of mouse.

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  • 小鼠身上研究表明运动开启遗传计划导致心脏生长心肌细胞分离

    The studies in mice suggest that exercise turns on a genetic program that leads the heart to grow as heart muscle cells divide.

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  • 结论实验组小鼠接种CV B3引起VMC, VMC中存在异常心肌细胞凋亡现象。

    Conclusions VMC can be caused in mice after CVB3 inoculation, abnormal cardiomyocyte apoptosis can be found in VMC.

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  • 结论小鼠大鼠一次性急性力竭运动心肌细胞水肿线粒体损伤

    Conclusion Acute exhaustive exercise can induce myocardial edema and mitochondrial damage in mice and rats.

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  • 方法:连接蛋白43实验小鼠病毒性心肌心肌细胞结蛋白表达免疫测定

    METHODS: The expression of connexin 43 and desmin in cardiac muscle cells of mice with experimental viral myocarditis was determined by immunohistochemistry.

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  • 结论:本法无需添加化学诱导剂,一种简便经济诱导体外培养小鼠es细胞分化心肌细胞方法

    CONCLUSION: a simple and economical method was established to induce mouse es cells cultured in vitro to differentiate into cardiomyocytes without using any chemical reagents.

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  • 结论:本法无需添加化学诱导剂,一种简便经济诱导体外培养小鼠es细胞分化心肌细胞方法

    CONCLUSION: a simple and economical method was established to induce mouse es cells cultured in vitro to differentiate into cardiomyocytes without using any chemical reagents.

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