FLT3 mutations in the activation loop of tyrosine kinase domain are frequently found in infant ALL with MLL rearrangements and pediatric ALL with hyperdiploidy
Author:
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Cited by 183 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. UBTF ‐internal tandem duplication as a novel poor prognostic factor in pediatric acute myeloid leukemia;Genes, Chromosomes and Cancer;2022-12-07
2. Hyperdiploidy: the longest known, most prevalent, and most enigmatic form of acute lymphoblastic leukemia in children;Leukemia;2022-10-20
3. Revealing molecular architecture of FLT3 internal tandem duplication: Development and clinical validation of a web‐based application to generate accurate nomenclature;International Journal of Laboratory Hematology;2022-07-06
4. Genome-wide DNA methylation analysis in pediatric acute myeloid leukemia;Blood Advances;2022-05-27
5. A complex KMT2A::AFF3 fusion resulting from a three-way chromosomal rearrangement in pediatric B lymphoblastic leukemia;Cancer Genetics;2022-04
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