Lineage bias in hematopoietic stem cells: more niche or intrinsic factors? [0.03%]
造血干细胞中的系偏向性：更多的栖息位点因素还是内在因素？
Taha Bartu Hayal,Chuanfeng Wu
Taha Bartu Hayal
Not available.
Long-term cardiac morbidity in adolescent and young adult survivors of classical Hodgkin lymphoma: the British Columbia experience [0.03%]
英国不列颠哥伦比亚省经典型霍奇金淋巴瘤年轻幸存者中晚期心脏毒副反应的状况
Kristin C Marr,Terry Tang,Jonathan Simkin et al.
Kristin C Marr et al.
Adolescents and young adults (AYA) with classic Hodgkin lymphoma (cHL) have excellent survival outcomes, however the late effects of treatment, including cardiovascular disease (CVD), can impact long-term disease-free morbidity and mortalit...
Progressive multifocal leukoencephalopathy and BK virus-nephropathy with bispecific antibody therapy in multiple myeloma [0.03%]
多发性骨髓瘤使用双特异性抗体治疗出现进行性多灶性白质脑病及BK病毒肾病
Ariel Siegel,Sidorela Reci,Leah Grossman et al.
Ariel Siegel et al.
Not available.
Talquetamab, a GPRC5D×CD3 bispecific antibody, in Chinese patients with relapsed/refractory multiple myeloma: efficacy and safety from the phase 1/2 MonumenTAL-1 study [0.03%]
GPRC5D×CD3双特异性抗体Talquetamab治疗复发/难治多发性骨髓瘤中国患者的I/II期MonumenTAL-1研究的疗效和安全性
Gang An,Jie Jin,Zhen Cai et al.
Gang An et al.
Not available.
Expanded clinical, genetic, and biological spectrum of filaminopathies with hematological involvement [0.03%]
具有血液系统受累的肌皮尔综合征临床、基因及生物学表型谱系的研究
Charlotte Brillon,Marjorie Poggi,Mathieu Fiore et al.
Charlotte Brillon et al.
Not available.
Adi Sherban,Ofir Wolach
Adi Sherban
Acute leukemia of ambiguous lineage (ALAL) is a rare, high-risk form of acute leukemia. It is characterized by the inability to assign a single lineage of differentiation to the leukemia and can manifest with more than one lineage-defining ...
Response to Comment on: Clinical interrogation of TP53 aberrations and its impact on survival in patients with myeloid neoplasms [0.03%]
对评论的回应：TP53异常的临床检测及其对髓系肿瘤患者生存率的影响
Jayastu Senapati,Naval G Daver
Jayastu Senapati
Not available.
The KLF4-CD46 axis: a novel therapeutic target in transplant-associated thrombotic microangiopathy and beyond [0.03%]
KLF4-CD46轴：移植相关血栓性微血管病及其他疾病的新治疗靶点
Massimo Cugno,Bernhard Lämmle
Massimo Cugno
Not available.
Ex vivo correction of severe coagulation Factor VII deficiency in patient-derived 3D liver organoids [0.03%]
利用患者衍生的3D肝脏类器官体外纠正严重凝血因子FVII缺乏症
Giacomo Roman,Knut H Lauritzen,Sean P Harrison et al.
Giacomo Roman et al.
Coagulation factor (F) VII deficiency is the most frequent among the rare, inherited bleeding disorders and is predominantly caused by missense mutations in the F7 gene. The disease phenotype ranges from asymptomatic cases to extremely seve...
Comment on: Clinical interrogation of TP53 aberrations and its impact on survival in patients with myeloid neoplasms [0.03%]
评论：TP53异常的临床询问及其对髓系肿瘤患者生存的影响
Hamza Sajid
Hamza Sajid
Not available.