%0 Journal Article %1 schoch2002acute %A Schoch, Claudia %A Kohlmann, Alexander %A Schnittger, Susanne %A Brors, Benedikt %A Dugas, Martin %A Mergenthaler, Susanne %A Kern, Wolfgang %A Hiddemann, Wolfgang %A Eils, Roland %A Haferlach, Torsten %D 2002 %J Proc Natl Acad Sci U S A %K Acute Acute, Analysis; Array Disease; Expression Gene Genetic; Humans; Leukemia, Models, Myeloid, Oligonucleotide Predictive Profiling; Rearrangement; Reproducibility Results Sequence Tests; Value classification/genetics; genetics; of %N 15 %P 10008--10013 %R 10.1073/pnas.142103599 %T Acute myeloid leukemias with reciprocal rearrangements can be distinguished by specific gene expression profiles. %U http://dx.doi.org/10.1073/pnas.142103599 %V 99 %X Acute myeloid leukemia (AML) is a heterogeneous group of genetically defined diseases. Their classification is important with regard to prognosis and treatment. We performed microarray analyses for gene expression profiling on bone marrow samples of 37 patients with newly diagnosed AML. All cases had either of the distinct subtypes AML M2 with t(8;21), AML M3 or M3v with t(15;17), or AML M4eo with inv(16). Diagnosis was established by cytomorphology, cytogenetics, fluorescence in situ hybridization, and reverse transcriptase-PCR in every sample. By using two different strategies for microarray data analyses, this study revealed a unique correlation between AML-specific cytogenetic aberrations and gene expression profiles.

@article{schoch2002acute, __markedentry = {[bbrors:6]}, abstract = {Acute myeloid leukemia (AML) is a heterogeneous group of genetically defined diseases. Their classification is important with regard to prognosis and treatment. We performed microarray analyses for gene expression profiling on bone marrow samples of 37 patients with newly diagnosed AML. All cases had either of the distinct subtypes AML M2 with t(8;21), AML M3 or M3v with t(15;17), or AML M4eo with inv(16). Diagnosis was established by cytomorphology, cytogenetics, fluorescence in situ hybridization, and reverse transcriptase-PCR in every sample. By using two different strategies for microarray data analyses, this study revealed a unique correlation between AML-specific cytogenetic aberrations and gene expression profiles.}, added-at = {2015-04-09T12:36:21.000+0200}, author = {Schoch, Claudia and Kohlmann, Alexander and Schnittger, Susanne and Brors, Benedikt and Dugas, Martin and Mergenthaler, Susanne and Kern, Wolfgang and Hiddemann, Wolfgang and Eils, Roland and Haferlach, Torsten}, biburl = {https://www.bibsonomy.org/bibtex/25f1aac6a0c92ef21408ddb6e14605db5/bbrors}, doi = {10.1073/pnas.142103599}, institution = {Laboratory for Leukemia Diagnostics, Department of Internal Medicine III, University Hospital Grosshadern, Ludwig-Maximilians-University, 81366 Munich, Germany. claudia.schoch@med3.med.uni-muenchen.de}, interhash = {90e7d78d32ed6bbd236411215e925ac8}, intrahash = {5f1aac6a0c92ef21408ddb6e14605db5}, journal = {Proc Natl Acad Sci U S A}, keywords = {Acute Acute, Analysis; Array Disease; Expression Gene Genetic; Humans; Leukemia, Models, Myeloid, Oligonucleotide Predictive Profiling; Rearrangement; Reproducibility Results Sequence Tests; Value classification/genetics; genetics; of}, language = {eng}, medline-pst = {ppublish}, month = Jul, number = 15, owner = {bbrors}, pages = {10008--10013}, pii = {142103599}, pmid = {12105272}, timestamp = {2015-04-09T12:36:21.000+0200}, title = {Acute myeloid leukemias with reciprocal rearrangements can be distinguished by specific gene expression profiles.}, url = {http://dx.doi.org/10.1073/pnas.142103599}, volume = 99, year = 2002 }