SSY Lam, AYH Leung - International journal of molecular sciences, 2020 - mdpi.com
Acute myeloid leukaemia (AML) carrying internal tandem duplication (ITD) of Fms-Like Tyrosine kinase 3 (FLT3) gene is associated with high risk of relapse and poor clinical …
A Elshoury, A Przespolewski, J Baron… - Expert Review of …, 2019 - Taylor & Francis
Introduction: Mutations of the FLT3 gene are among most common genetic abnormalities occurring in acute myeloid leukemia (AML) and are associated with dismal prognosis …
F Stölzel, C Steudel, U Oelschlägel, B Mohr, S Koch… - Annals of …, 2010 - Springer
Abstract Treatment of acute myeloid leukemia (AML) remains challenging with many patients harboring unfavorable prognostic parameters such as FLT3 internal tandem …
S Knapper - Expert opinion on investigational drugs, 2011 - Taylor & Francis
Introduction: Activating mutations of the FMS-like tyrosine kinase 3 (FLT3) gene occur at high frequency in acute myeloid leukemia (AML), being detected in> 30% of patients at …
M Levis, D Small - Current pharmaceutical design, 2004 - ingentaconnect.com
Activating mutations of FLT3 (FMS-Like Tyrosine kinase-3) are the most common molecular abnormality in acute myeloid leukemia (AML). Their presence is associated with a worse …
K Spiekermann, RJ Dirschinger… - Blood, The Journal …, 2003 - ashpublications.org
Activating mutations of the protein tyrosine kinase (PTK) FLT3 can be found in approximately 30% of patients with acute myeloid leukemia (AML), thereby representing the most frequent …
MJ Levis - Best Practice & Research Clinical Haematology, 2010 - Elsevier
FLT3 inhibition has been a goal of acute myeloid leukemia (AML) therapy since FLT3 mutations were discovered to have a role in AML. Several FLT3 inhibitors have been …
H Ma, B Nguyen, L Li, S Greenblatt… - Blood, The Journal …, 2014 - ashpublications.org
More than 35% of acute myeloid leukemia (AML) patients harbor a constitutively activating mutation in FMS-like tyrosine kinase-3 (FLT3). The most common type, internal tandem …