目的研究遗传印迹是否与抽动障碍的遗传病因学有关。
Objective To investigate whether genomic imprinting is involved in the etiology of tic disorder.
结论抽动障碍的传递存在亲源特异性表达，抽动障碍病因学中可能存在遗传印迹机制。
Conclusion Parental specific expression exists in the transmission of tic disorder, which gives evidence that genomic imprinting may be involved in the genetic mechanism of tic disorder.
表遗传体系包括DNA甲基化、RNA干涉、基因组印迹和组蛋白密码等多方面。
The system of Epigenetics includes DNA methylation, RNA-interfering, genome imprinting and histone code and so on.
目的建立人血浆因子V（FV）蛋白免疫印迹分析，对遗传性FV缺乏症家系成员血浆FV含量进行分析。
Objective To develope a western blot of human plasma factor V (FV) and conduct immunoblot analyses on riasma FV from a family with hereditary FV deficiency.
目的建立人血浆因子V（FV）蛋白免疫印迹分析，对遗传性FV缺乏症家系成员血浆FV含量进行分析。
Objective To develope a western blot of human plasma factor V (FV) and conduct immunoblot analyses on riasma FV from a family with hereditary FV deficiency.
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