an intimate connection? Klaus H. Metzeler UNIVERSITY OF MUNICH In this issue of Blood, Micol et al report the discovery of mutations in the additional sex combs-like 2 (ASXL2) gene in about one-quarter of acute myeloid leukemia (AML) patients carrying the t(8;21) translocation.1 Patients with this chromosomaltranslocation are classified as having “favorable-risk ” disease, but,60 % of them are actually cured by current treatment approaches.2 Activating mutations in the KIT gene occur in approximately one-third of patients with t(8;21) and identify a subgroup with adverse outcomes. However, even among patients with wild-type KIT, the relapse rate exceeds 30%. Expanding our knowledge about cooperating genetic event
Oncogenic activation of tyrosine kinase signaling pathway is recurrent in human leukemia. To gain in...
The reciprocal translocation t(9;22) (q34;q11) that generates the Philadelphia (Ph) chromosome is pr...
In this study we determined the incidence of RAS, KIT, FLT3, and JAK2 mutations in 101 adults patien...
Full list of author information is available at the end of the articleBackground Acute myeloid leuke...
Mutations in codon D816 of the KIT gene represent a recurrent genetic alteration in acute myeloid le...
Chromosomal rearrangements of the human MLL (mixed lineage leukemia) gene are associated with high-r...
Therapy-related myelodysplastic syndrome/acute myeloid leukemia (t-MDS/AML) is an increasingly recog...
Publisher Copyright: © 2021, The Author(s).Acute myeloid leukemia (AML) is a hematological malignanc...
Background and Aim: FLT3 gene is a member of class III receptor Tyrosine Kinase, which is expressed ...
Acute myeloid leukemia (AML), phenotypically and genotypically is a quite heterogeneous disease. Mor...
Full list of author information is available at the end of the articleBackground Acute myeloid leuka...
Mutations in the additional sex comb-like 1 (ASXL1) gene were recently shown in various myeloid mali...
Running title: KIT-D816 mutations in AML1-ETO positive AML are associated with im-paired prognosis *...
Chromosome band 12p13 is known as a recurring site for cytogenetic alteration in a variety of hemato...
In this issue of Blood, Stengel et al advance our knowledge of the genomic landscape of acute lympho...
Oncogenic activation of tyrosine kinase signaling pathway is recurrent in human leukemia. To gain in...
The reciprocal translocation t(9;22) (q34;q11) that generates the Philadelphia (Ph) chromosome is pr...
In this study we determined the incidence of RAS, KIT, FLT3, and JAK2 mutations in 101 adults patien...
Full list of author information is available at the end of the articleBackground Acute myeloid leuke...
Mutations in codon D816 of the KIT gene represent a recurrent genetic alteration in acute myeloid le...
Chromosomal rearrangements of the human MLL (mixed lineage leukemia) gene are associated with high-r...
Therapy-related myelodysplastic syndrome/acute myeloid leukemia (t-MDS/AML) is an increasingly recog...
Publisher Copyright: © 2021, The Author(s).Acute myeloid leukemia (AML) is a hematological malignanc...
Background and Aim: FLT3 gene is a member of class III receptor Tyrosine Kinase, which is expressed ...
Acute myeloid leukemia (AML), phenotypically and genotypically is a quite heterogeneous disease. Mor...
Full list of author information is available at the end of the articleBackground Acute myeloid leuka...
Mutations in the additional sex comb-like 1 (ASXL1) gene were recently shown in various myeloid mali...
Running title: KIT-D816 mutations in AML1-ETO positive AML are associated with im-paired prognosis *...
Chromosome band 12p13 is known as a recurring site for cytogenetic alteration in a variety of hemato...
In this issue of Blood, Stengel et al advance our knowledge of the genomic landscape of acute lympho...
Oncogenic activation of tyrosine kinase signaling pathway is recurrent in human leukemia. To gain in...
The reciprocal translocation t(9;22) (q34;q11) that generates the Philadelphia (Ph) chromosome is pr...
In this study we determined the incidence of RAS, KIT, FLT3, and JAK2 mutations in 101 adults patien...