RUNX1 gene mutation in primary myelodysplastic syndrome - the mutation can be detected early at diagnosis or acquired during disease progression and is associated with poor outcome
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2007.06811.x/fullpdf
Reference37 articles.
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2. Core-binding factors in haematopoiesis and immune function;De Bruijn;Oncogene,2004
3. SOCS1 methylation in patients with newly diagnosed acute myeloid leukemia;Chen;Genes, Chromosomes and Cancer,2003
4. Acquisition of JAK2, PTPN11, and RAS mutations during disease progression in primary myelodysplastic syndrome;Chen;Leukemia,2006
5. Nucleophosmin mutations in de novo acute myeloid leukemia: the age-dependent incidences and the stability during disease evolution;Chou;Cancer Research,2006
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1. Understanding the Continuum between High-Risk Myelodysplastic Syndrome and Acute Myeloid Leukemia;International Journal of Molecular Sciences;2023-03-06
2. RUNX1 deficiency cooperates with SRSF2 mutation to induce multilineage hematopoietic defects characteristic of MDS;Blood Advances;2022-12-13
3. Higher RUNX1 expression levels are associated with worse overall and leukaemia‐free survival in myelodysplastic syndrome patients;eJHaem;2022-08-19
4. Therapeutic Outcomes and Prognostic Impact of Gene Mutations Including TP53 and SF3B1 in Patients with Del(5q) Myelodysplastic Syndromes (MDS);Clinical Lymphoma Myeloma and Leukemia;2022-07
5. A Novel Prognostic Scoring Model for Myelodysplastic Syndrome Patients With SF3B1 Mutation;Frontiers in Oncology;2022-06-27
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