原发性血小板增多症
骨髓纤维化
医学
真性红细胞增多症
三重阴性
人口
生物信息学
癌症研究
免疫学
内科学
生物
癌症
骨髓
环境卫生
乳腺癌
作者
Serena Tharakan,John Mascarenhas,Douglas Tremblay
标识
DOI:10.1080/10428194.2023.2277674
摘要
mutated ET. In this review, we summarize the clinical features and prognosis of TN-PMF and -ET as well as diagnostic challenges including identification of non-canonical driver mutations. We also discuss additional molecular drivers to better understand possible pathogenic mechanisms underlying triple negative MPNs. Finally, we highlight current therapeutic approaches as well as novel targets, particularly in the difficult to treat TN-PMF population.
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