机译:runx1 runx1患者患有髓细胞增生综合征的患者,降低血液组的红细胞表达抗原
Department of Legal MedicineGunma University Graduate School of MedicineMaebashi Japan;
Department of Legal MedicineGunma University Graduate School of MedicineMaebashi Japan;
Department of Legal MedicineGunma University Graduate School of MedicineMaebashi Japan;
Department of Legal MedicineGunma University Graduate School of MedicineMaebashi Japan;
Department of Legal MedicineGunma University Graduate School of MedicineMaebashi Japan;
Department of Legal MedicineGunma University Graduate School of MedicineMaebashi Japan;
Transfusion ServiceGunma University HospitalMaebashi Japan;
Department of HematologyGunma University Graduate School of MedicineMaebashi Japan;
Department of HematologyUniversity of Occupational and Environmental HealthKitakyushu Japan;
Department of Legal MedicineShimane University School of MedicineIzumo Japan;
Japanese Red Cross Central Blood InstituteTokyo Japan;
Japanese Red Cross Central Blood InstituteTokyo Japan;
Department of Legal MedicineGunma University Graduate School of MedicineMaebashi Japan;
机译:runx1 runx1患者患有髓细胞增生综合征的患者,降低血液组的红细胞表达抗原
机译:在Runx1突变的背景下,急性髓性白血病患者的突变景观或骨髓增生综合征
机译:RunX1和TP53基因中的突变预测患有较低风险的髓细胞增强综合征患者的进展
机译:髓细胞增生综合征患者外周血单核细胞中核苷酸切除修复基因的放射敏感性和表达
机译:使用人类多能干细胞模型探险遗传血小板(Etv6或Runx1)中的遗传血小板减少
机译:先天性血小板减少症患者的两个新的RUNX1突变已演变为高度骨髓增生异常综合征
机译:先天性血小板减少症患者的两个新的RUNX1突变已演变为高度骨髓增生异常综合征