Downstream molecular pathways of FLT3 in the pathogenesis of acute myeloid leukemia: biology and therapeutic implications
about
The Potential of Vitamin D-Regulated Intracellular Signaling Pathways as Targets for Myeloid Leukemia TherapyAn overview on the role of FLT3-tyrosine kinase receptor in acute myeloid leukemia: biology and treatmentComparison of safety and toxicity of liposomal doxorubicin vs. conventional anthracyclines: a meta-analysisFISH+CD34+CD38- cells detected in newly diagnosed acute myeloid leukemia patients can predict the clinical outcome.Combined inhibition of GLI and FLT3 signaling leads to effective anti-leukemic effects in human acute myeloid leukemia.Discovery of a Diaminopyrimidine FLT3 Inhibitor Active against Acute Myeloid Leukemia.FLT3 Internal Tandem Duplication and D835 Mutations in Patients with Acute Lymphoblastic Leukemia and its Clinical SignificancemiR-22 has a potent anti-tumour role with therapeutic potential in acute myeloid leukaemiaA Phase II trial of tandutinib (MLN 518) in combination with bevacizumab for patients with recurrent glioblastoma.Blockade of miR-150 maturation by MLL-fusion/MYC/LIN-28 is required for MLL-associated leukemia.SU11652 Inhibits tyrosine kinase activity of FLT3 and growth of MV-4-11 cellsCellular protection using Flt3 and PI3Kα inhibitors demonstrates multiple mechanisms of oxidative glutamate toxicity.Molecular alterations of isocitrate dehydrogenase 1 and 2 (IDH1 and IDH2) metabolic genes and additional genetic mutations in newly diagnosed acute myeloid leukemia patientsDissect: detection and characterization of novel structural alterations in transcribed sequencesGeneration and characterization of a highly effective protein substrate for analysis of FLT3 activityProfiling of somatic mutations in acute myeloid leukemia with FLT3-ITD at diagnosis and relapse.Microenvironmental hypoxia regulates FLT3 expression and biology in AML.A Genome-Wide CRISPR Screen Identifies Genes Critical for Resistance to FLT3 Inhibitor AC220.Silvestrol exhibits significant in vivo and in vitro antileukemic activities and inhibits FLT3 and miR-155 expressions in acute myeloid leukemia.The role of PD-1 and PD-L1 in T-cell immune suppression in patients with hematological malignancies.MUC1-C oncoprotein promotes FLT3 receptor activation in acute myeloid leukemia cellsDistinct signaling programs control human hematopoietic stem cell survival and proliferation.Current findings for recurring mutations in acute myeloid leukemiaNon-receptor protein tyrosine kinases signaling pathways in normal and cancer cells.Targeting FLT3 to treat leukemia.Association of the EGF-TM7 receptor CD97 expression with FLT3-ITD in acute myeloid leukemia.Emerging cell cycle inhibitors for acute myeloid leukemia.Spontaneous Remission in an Older Patient with Relapsed FLT3 ITD Mutant AML.Suppressor of cytokine signaling 6 (SOCS6) negatively regulates Flt3 signal transduction through direct binding to phosphorylated tyrosines 591 and 919 of Flt3.Mutated genes and driver pathways involved in myelodysplastic syndromes—a transcriptome sequencing based approach.Whole-Exome Sequencing of ETV6/RUNX1 in Four Childhood Acute Lymphoblastic Leukaemia CasesFLT3 and FLT3-ITD phosphorylate and inactivate the cyclin-dependent kinase inhibitor p27Kip1 in acute myeloid leukemia.An essential pathway links FLT3-ITD, HCK and CDK6 in acute myeloid leukemiaMiR-424 and miR-155 deregulated expression in cytogenetically normal acute myeloid leukaemia: correlation with NPM1 and FLT3 mutation statusThe antitumor compound triazoloacridinone C-1305 inhibits FLT3 kinase activity and potentiates apoptosis in mutant FLT3-ITD leukemia cells.Internal tandem duplication and tyrosine kinase domain mutations in FLT3 alter the response to daunorubicin in Ba/F3 cells.Eradication of Acute Myeloid Leukemia with FLT3 Ligand-Targeted miR-150 Nanoparticles.Synergistic effect of a novel autophagy inhibitor and Quizartinib enhances cancer cell death.Characterization of children with FLT3-ITD acute myeloid leukemia: a report from the AIEOP AML-2002 study group.MZH29 is a novel potent inhibitor that overcomes drug resistance FLT3 mutations in acute myeloid leukemia.
P2860
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P2860
Downstream molecular pathways of FLT3 in the pathogenesis of acute myeloid leukemia: biology and therapeutic implications
description
2011 nî lūn-bûn
@nan
2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Downstream molecular pathways ...... y and therapeutic implications
@ast
Downstream molecular pathways ...... y and therapeutic implications
@en
Downstream molecular pathways ...... y and therapeutic implications
@nl
type
label
Downstream molecular pathways ...... y and therapeutic implications
@ast
Downstream molecular pathways ...... y and therapeutic implications
@en
Downstream molecular pathways ...... y and therapeutic implications
@nl
prefLabel
Downstream molecular pathways ...... y and therapeutic implications
@ast
Downstream molecular pathways ...... y and therapeutic implications
@en
Downstream molecular pathways ...... y and therapeutic implications
@nl
P2860
P921
P3181
P356
P1476
Downstream molecular pathways ...... y and therapeutic implications
@en
P2093
Shinichiro Takahashi
P2860
P2888
P3181
P356
10.1186/1756-8722-4-13
P407
P5008
P577
2011-04-01T00:00:00Z
P5875
P6179
1005792756