为解决遗传性血小板疾病及相关髓系恶性肿瘤（FPDMM）的误诊问题，研究人员对一个有血液系统疾病家族进行研究。重新评估发现 RUNX1 基因外显子 5 - 6 缺失，而非之前认为的 GATA2 缺陷。这一结果有助于准确诊断和疾病监测，意义重大。 在血液疾病的研究领域 ...

Recent structures of the Runx1–CBFβ heterodimer bound to DNA brings to six the number of characterized eukaryotic transcription factor families that use an immunoglobulin (Ig) fold to bind to DNA.

The drugs targeting FLT3 rewire the cell, resulting in the upregulation of other signaling pathway associated genes, which then restored AP-1 and RUNX1 binding. Drugging RAS, which is a key ...