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GAS6 expression identifies high-risk adult AML patients: potential implications for therapyPrognostic gene mutations and distinct gene- and microRNA-expression signatures in acute myeloid leukemia with a sole trisomy 8.Intronic miR-3151 within BAALC drives leukemogenesis by deregulating the TP53 pathway.Expression and prognostic impact of lncRNAs in acute myeloid leukemia.Highly Elevated Serum Hepcidin in Patients with Acute Myeloid Leukemia prior to and after Allogeneic Hematopoietic Cell Transplantation: Does This Protect from Excessive Parenchymal Iron Loading?Heritable polymorphism predisposes to high BAALC expression in acute myeloid leukemiaClinical and pharmacodynamic activity of bortezomib and decitabine in acute myeloid leukemia.miR-3151 interplays with its host gene BAALC and independently affects outcome of patients with cytogenetically normal acute myeloid leukemiaMicroRNA-3151 inactivates TP53 in BRAF-mutated human malignancies.Kinetics of iron removal by phlebotomy in patients with iron overload after allogeneic hematopoietic cell transplantation.inv(16)/t(16;16) acute myeloid leukemia with non-type A CBFB-MYH11 fusions associate with distinct clinical and genetic features and lack KIT mutations.Clinical role of microRNAs in cytogenetically normal acute myeloid leukemia: miR-155 upregulation independently identifies high-risk patientsAntagonistic activities of the immunomodulator and PP2A-activating drug FTY720 (Fingolimod, Gilenya) in Jak2-driven hematologic malignanciesMonoSeq Variant Caller Reveals Novel Mononucleotide Run Indel Mutations in Tumors with Defective DNA Mismatch RepairPreclinical and clinical efficacy of XPO1/CRM1 inhibition by the karyopherin inhibitor KPT-330 in Ph+ leukemias.Persistence of DNMT3A R882 mutations during remission does not adversely affect outcomes of patients with acute myeloid leukaemia.Dissection of the Major Hematopoietic Quantitative Trait Locus in Chromosome 6q23.3 Identifies miR-3662 as a Player in Hematopoiesis and Acute Myeloid Leukemia.Mutational Landscape and Gene Expression Patterns in Adult Acute Myeloid Leukemias with Monosomy 7 as a Sole Abnormality.Epigenetics meets genetics in acute myeloid leukemia: clinical impact of a novel seven-gene scoreTargeting the RAS/MAPK pathway with miR-181a in acute myeloid leukemia.NRAS isoforms differentially affect downstream pathways, cell growth, and cell transformation.Prognostic and biologic significance of long non-coding RNA profiling in younger adults with cytogenetically normal acute myeloid leukemiaStructural characterization of NRAS isoform 5In rare acute myeloid leukemia patients harboring both RUNX1 and NPM1 mutations, RUNX1 mutations are unusual in structure and present in the germline.
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description
onderzoeker
@nl
name
Ann-Kathrin Eisfeld
@ast
Ann-Kathrin Eisfeld
@en
Ann-Kathrin Eisfeld
@es
Ann-Kathrin Eisfeld
@nl
type
label
Ann-Kathrin Eisfeld
@ast
Ann-Kathrin Eisfeld
@en
Ann-Kathrin Eisfeld
@es
Ann-Kathrin Eisfeld
@nl
prefLabel
Ann-Kathrin Eisfeld
@ast
Ann-Kathrin Eisfeld
@en
Ann-Kathrin Eisfeld
@es
Ann-Kathrin Eisfeld
@nl
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P106
P21
P214
P31
P7859
viaf-308743765