Wild-Type p53 Overexpression in NPM1-Mutated AML: Potential Implications for Disease Biology and Therapy Response
Human iPSCs-based modeling unveils chromatin remodeling induced by SETBP1 mutation as a potential initiating factor in GATA2 deficiency
LSD1 and GCN5 inhibition facilitates Am80 (tamibarotene)-mediated differentiation therapy in RARA-high non-APL AML
MECOM promotes leukemia progression and inhibits mast cell differentiation through functional competition with GATA2
Rapid increase of C/EBPα p42 induces growth arrest of AML cells by Cop1 deletion in Trib1-expressing AML
Mesenchymal stem cell-derived S100A8 facilitates leukemia stem cell maintenance via TLR4/PI3K/Akt signaling
HDAC7 is a specific therapeutic target in Acute Erythroid Leukemia
Post-transplant cyclophosphamide separates graft-versus host disease and graft versus leukemia effects after HLA- matched stem-cell transplantation for AML
HDZ-740, a Potent FLT3 Inhibitor to Overcome FLT3 Mutations of Acute Myeloid Leukemia
No impact of time from diagnosis to treatment on survival in newly diagnosed AML treated with venetoclax-based regimens