Molecular Basis of Hematological Disease Caused by Inherited or Acquired RUNX1 Mutations
Author:
Funder
Bloodwise
Wellcome Trust
Blood Cancer UK
Leukaemia UK
Medical Research Council
Publisher
Elsevier BV
Subject
Cancer Research,Cell Biology,Genetics,Hematology,Molecular Biology
Reference127 articles.
1. The leukemia-associated AML1 (Runx1)—CBF beta complex functions as a DNA-induced molecular clamp;Bravo;Nat Struct Biol,2001
2. DNA Recognition by the RUNX1 transcription factor is mediated by an allosteric transition in the RUNT domain and by DNA bending;Bartfeld;Structure,2002
3. RUNX: a trilogy of cancer genes;Lund;Cancer Cell,2002
4. The RUNX genes: gain or loss of function in cancer;Blyth;Nat Rev Cancer,2005
5. RUNX1 cooperates with FLT3-ITD to induce leukemia;Behrens;J Exp Med,2017
Cited by 12 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Interface-guided phenotyping of coding variants in the transcription factor RUNX1;Cell Reports;2024-07
2. FLI1 is associated with regulation of DNA methylation and megakaryocytic differentiation in FPDMM caused by a RUNX1 transactivation domain mutation;Scientific Reports;2024-06-18
3. Hereditary predisposition syndromes to myeloid neoplasms: diseases, genes and mechanisms of development;Oncohematology;2024-04-02
4. Pharmacological inhibition of RAS overcomes FLT3 inhibitor resistance in FLT3-ITD+ AML through AP-1 and RUNX1;iScience;2024-04
5. DNA methylation analysis using RUNX1-mutated cells reveals association of FLI1 to familial platelet disorder with associated myeloid malignancies caused by a mutation in the transactivation domain of RUNX1;2024-02-20
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3