原发性血小板增多症
发病机制
表观遗传学
突变
癌症研究
骨髓
生物
医学
遗传学
真性红细胞增多症
免疫学
生物信息学
基因
作者
Dian Zhou,Wei Chen,Kailin Xu
出处
期刊:PubMed
[National Institutes of Health]
日期:2018-02-01
卷期号:26 (1): 287-291
标识
DOI:10.7534/j.issn.1009-2137.2018.01.051
摘要
Essential thrombocythemia(ET) is one of the Ph chromosome-negative myeloproliferative neoplasms. Some studies discovered that the mutation of JAK2 V617F existed in 50%-70% patients with ET. Recently, many significant advances in researches about pathogenesis of ET, such as mutations of JAK2V617F, MPL, CALR and other related mutation; the epigenetic abnomalities in incidence of ET; the changes of bone marrow microenvironment of ET and the regulation of related cytokines were obtained. In this article, the advances of above mentioned aspects of ET are summarized.
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