Web11 jul. 2024 · NPM1 mutations are one of the most common recurrent genetic lesions in AML Occurs in approximately 35% of AML cases overall and 50 - 60% of cases with … WebThe detection of the FLT3-ITD mutation is documented in about 40% of NPM1-mutated AML cases. The deleterious prognostic effects of FLT3-ITD have previously been found to be most clinically relevant when co-occurring with NPM1 mutations, which are characterized by a higher relapse rate and poorer OS [ 35 , 37 , 42 , 43 ].
Synergistic targeting of FLT3 mutations in AML via combined …
Web12 nov. 2024 · Results. Our findings demonstrate myeloid blasts with mutated NPM1 have a characteristic pattern of LAIPs that is present in nearly all cases of AML/MDS‐EB with mutated NPM1 at initial diagnosis and relapse, regardless of morphologic variations, FLT3 ITD status, or karyotype abnormality. The myeloid blasts with mutated NPM1 can be … WebNPM1 mutations may occur in de novo AML cases or can be co-expressed with RUNX1-RUNX1T1 transcripts [37,38]. ... Kern W, Haferlach C, Bacher U, Haferlach T, Schnittger S. Flow cytometric identification of acute myeloid leukemia with limited differentiation and NPM1 type A mutation: a new biologically defined entity. smooth bjj
Standard, 3-Tube, 10-Color Flow Cytometry Panel for Acute …
WebWe investigated whether NPM1m+AML with monocytic or myeloid differentiation have distinct immunophenotype. The study included 160 NPM1m+AMLpatients and 178 AML … Web15 jul. 2024 · Our objective was to design a reliable flow cytometry assay to detect mutated NPM1 in peripheral blood (PB) samples from AML patients, using a polyclonal … Web15 jun. 2024 · These data indicate that mutation-dependent nuclear export of NPM1 leads to nuclear retention and consequent oncogenic functions of the overexpressed lncRNA LONA, thus uncovering a novel NPM1... smooth-billed ani