ETV6: a versatile player in leukemogenesis
SK Bohlander - Seminars in cancer biology, 2005 - Elsevier
Alterations of the ets family transcription factor ETV6 (TEL) and the RUNT domain transcription
factor RUNX1 (AML1) play pivotal roles in the leukemogenesis of various types of …
factor RUNX1 (AML1) play pivotal roles in the leukemogenesis of various types of …
A BCR–JAK2 fusion gene as the result of at(9;22)(p24;q11.2) translocation in a patient with a clinically typical chronic myeloid leukemia
…, B Wörmann, D Haase, SK Bohlander - Genes …, 2005 - Wiley Online Library
Chronic myeloid leukemia (CML) is characterized by the presence of at(9;22)(q34;q11.2),
which leads to the well‐known BCR–ABL1 fusion protein. We describe a patient who was …
which leads to the well‐known BCR–ABL1 fusion protein. We describe a patient who was …
The cell of origin and the leukemia stem cell in acute myeloid leukemia
M Chopra, SK Bohlander - Genes, Chromosomes and Cancer, 2019 - Wiley Online Library
There is experimental and observational evidence that the cells of the leukemic clone in
acute myeloid leukemia (AML) have different phenotypes even though they share the same …
acute myeloid leukemia (AML) have different phenotypes even though they share the same …
Stem cell gene expression programs influence clinical outcome in human leukemia
Xenograft studies indicate that some solid tumors and leukemias are organized as cellular
hierarchies sustained by cancer stem cells (CSCs). Despite the promise of the CSC model, its …
hierarchies sustained by cancer stem cells (CSCs). Despite the promise of the CSC model, its …
Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia.
TR Golub, GF Barker, SK Bohlander… - Proceedings of the …, 1995 - National Acad Sciences
Chromosomal rearrangements involving band 12p13 are found in a wide variety of human
leukemias but are particularly common in childhood acute lymphoblastic leukemia. The …
leukemias but are particularly common in childhood acute lymphoblastic leukemia. The …
MicroRNA expression signatures accurately discriminate acute lymphoblastic leukemia from acute myeloid leukemia
…, Z Qian, J Jin, Y Zhang, SK Bohlander… - Proceedings of the …, 2007 - National Acad Sciences
Acute lymphoblastic leukemia (ALL) is the most common childhood cancer, whereas acute
myeloid leukemia (AML) is the most common acute leukemia in adults. In general, ALL has a …
myeloid leukemia (AML) is the most common acute leukemia in adults. In general, ALL has a …
Distinct microRNA expression profiles in acute myeloid leukemia with common translocations
…, J Jin, Y Zhang, SK Bohlander… - Proceedings of the …, 2008 - National Acad Sciences
MicroRNAs (miRNAs) are postulated to be important regulators in cancers. Here, we report
a genome-wide miRNA expression analysis in 52 acute myeloid leukemia (AML) samples …
a genome-wide miRNA expression analysis in 52 acute myeloid leukemia (AML) samples …
Spectrum and prognostic relevance of driver gene mutations in acute myeloid leukemia
…, M Fiegl, M Subklewe, SK Bohlander… - Blood, The Journal …, 2016 - ashpublications.org
The clinical and prognostic relevance of many recently identified driver gene mutations in
adult acute myeloid leukemia (AML) is poorly defined. We sequenced the coding regions or …
adult acute myeloid leukemia (AML) is poorly defined. We sequenced the coding regions or …
An 86-probe-set gene-expression signature predicts survival in cytogenetically normal acute myeloid leukemia
…, W Hiddemann, SK Bohlander… - Blood, The Journal …, 2008 - ashpublications.org
Patients with cytogenetically normal acute myeloid leukemia (CN-AML) show heterogeneous
treatment outcomes. We used gene-expression profiling to develop a gene signature that …
treatment outcomes. We used gene-expression profiling to develop a gene signature that …
Acute Myeloid Leukemia With Biallelic CEBPA Gene Mutations and Normal Karyotype Represents a Distinct Genetic Entity Associated With a Favorable Clinical …
…, J Braess, W Hiddemann, SK Bohlander… - Journal of clinical …, 2010 - ascopubs.org
Purpose CEBPA mutations are found as either biallelic (biCEBPA) or monoallelic (moCEBPA).
We set out to explore whether the kind of CEBPA mutation is of prognostic relevance in …
We set out to explore whether the kind of CEBPA mutation is of prognostic relevance in …