Result The majority of DNA specimens from 12(57%) cases were applicable to be used for the clonality assay of HUMARA gene and the vast majority of DNA specimens were applicable to sequence analysis.
结果57%(12/21)的病例中的大部分样本可以用于克隆性分析,所有病例的大部分样本都可以用于p53基因序列分析。
参考来源 - Ⅱ型子宫内膜癌前期病变的研究Random inactivation of one X-chromosome in somatic cells offers a probability for the clonality analysis. The inactivation pattern can also be used as a parameter to describle the relationship of multiple lesions in a case.
X染色体随机失活类型的分析不但为克隆性分析提供了可能性，而且可以显示同一标本不同病变之间的关系。
参考来源 - 根据X染色体失活类型探讨多发性子宫平滑肌瘤不同结节之间的关系·2,447,543篇论文数据，部分数据来源于NoteExpress
目的通过人雄激素受体(HUMARA)基因位点克隆性分析技术确定掌纤维瘤病是否为肿瘤性增生。
Objective to study the clonality of palmar fibromatosis by molecular genetic analysis of X chromosome inactivation pattern at a polymorphic site of human androgen receptor gene (HUMARA).
克隆与表达弓形虫缓殖子期特异性抗原1（BAG1）的基因，并分析重组抗原的免疫反应性。
Clone and express bradyzoite antigen 1(BAG1) gene of T. gondii, and analyze the immunoreactivity of the recombinant product.
目的 对弓形虫表面抗原SAG4基因进行克隆、表达和免疫反应性分析。
To clone and express surface antigen SAG4 gene of Toxoplasma gondii, and analyze its immunoreactivity.
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