[HTML][HTML] Ras/Raf/MEK/ERK pathway activation in childhood acute lymphoblastic leukemia and its therapeutic targeting

T Knight, JAE Irving - Frontiers in oncology, 2014 - frontiersin.org
Deregulation of the Ras/Raf/MEK/extracellular signal-regulated kinase pathway is a
common event in childhood acute lymphoblastic leukemia and is caused by point mutation …

Ras pathway mutations are prevalent in relapsed childhood acute lymphoblastic leukemia and confer sensitivity to MEK inhibition

J Irving, E Matheson, L Minto, H Blair… - Blood, The Journal …, 2014 - ashpublications.org
For most children who relapse with acute lymphoblastic leukemia (ALL), the prognosis is
poor, and there is a need for novel therapies to improve outcome. We screened samples …

[PDF][PDF] FLT3 Gene involvement in B-cell acute lymphoblastic leukemia (B-ALL)

A Okabe, F Guirales, D Zhao, CA Tirado - J Assoc Genet Technol, 2021 - researchgate.net
The FMS-like tyrosine kinase 3 gene (FLT3) is a receptor tyrosine kinase expressed in early
hematopoietic progenitors that play an important role in hematopoietic development. The …

[HTML][HTML] Genetic mutational analysis of pediatric acute lymphoblastic leukemia from a single center in China using exon sequencing

H Zhang, H Wang, X Qian, S Gao, J Xia, J Liu, Y Cheng… - BMC cancer, 2020 - Springer
Background Acute lymphoblastic leukemia (ALL), the most common childhood malignancy,
is characterized by recurring structural chromosomal alterations and genetic alterations …

[HTML][HTML] The frequency of NPM1 mutations in childhood acute myeloid leukemia

M Braoudaki, C Papathanassiou, K Katsibardi… - Journal of Hematology & …, 2010 - Springer
Background Mutations in the nucleophosmin (NPM1) gene have been solely associated
with childhood acute myeloid leukemia (AML). We evaluated the frequency of NPM1 …

[HTML][HTML] FLT3mutation incidence and timing of origin in a population case series of pediatric leukemia

P Chang, M Kang, A Xiao, J Chang, J Feusner… - BMC cancer, 2010 - Springer
Background Mutations in FLT3 result in activated tyrosine kinase activity, cell growth
stimulation, and a poor prognosis among various subtypes of leukemia. The causes and …

Proteomic analysis of childhood de novo acute myeloid leukemia and myelodysplastic syndrome/AML: correlation to molecular and cytogenetic analyses

M Braoudaki, F Tzortzatou-Stathopoulou… - Amino acids, 2011 - Springer
The aim of this study was to investigate the progression of myelodysplastic syndrome (MDS)
to acute myeloid leukemia (AML) and to provide additional data regarding the proteomic …

[HTML][HTML] FLT3 is implicated in cytarabine transport by human equilibrative nucleoside transporter 1 in pediatric acute leukemia

A Català, M Pastor-Anglada, L Caviedes-Cárdenas… - Oncotarget, 2016 - ncbi.nlm.nih.gov
FLT3 abnormalities are negative prognostic markers in acute leukemia. Infant leukemias are
a subgroup with frequent MLL (KMT2A) rearrangements, FLT3 overexpression and high …

[HTML][HTML] FLT3 internal tandem duplication and D835 mutations in patients with acute lymphoblastic leukemia and its clinical significance

G Elyamany, M Awad, O Alsuhaibani… - … journal of hematology …, 2014 - ncbi.nlm.nih.gov
FLT3 Internal Tandem Duplication and D835 Mutations in Patients with Acute Lymphoblastic
Leukemia and its Clinical Significance - PMC Back to Top Skip to main content NIH NLM Logo …

Sequential monitoring of minimal residual disease in acute lymphoblastic leukemia: 7-year experience in a pediatric hematology/oncology unit

K Katsibardi, MA Moschovi, M Braoudaki… - Leukemia & …, 2010 - Taylor & Francis
We evaluated minimal residual disease (MRD) in 91 children with acute lymphoblastic
leukemia (ALL) by PCR amplification of clonal rearrangements, immunoglobulin (IgH; VDJ …