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Cellular origin of prognostic chromosomal aberrations in AML patients

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This work was supported by grants from the Danish Council for Strategic Research (grant numbers 09-065157 BTP, 10-092798 BTP and 133100153 KT-M), the Danish Cancer Society (grant number R72-A4572-13-S2, KT-M), the Novo Nordisk Foundation (grant number 34220, KT-M), the Lundbeck Foundation (grant number 29367, KT-M) and through a center grant from the Novo Nordisk Foundation (The Novo Nordisk Foundation Section for Stem Cell Biology in Human Disease, BTP). This work is based on the joint research activities under the framework of the European Program for Cooperation in Science and Technology (COST, Action BM0801, WG1). LB was supported in part by the Deutsche Forschungsgemeinschaft (Heisenberg-Stipendium BU 1339/3-1) and KT-M is supported by a clinical research fellowship from the Novo Nordisk Foundation (grant number 100191).

Author Contributions

HM-J, JJ, NR, NB, BTP and KT-M conceived and designed the study; NB, LB, MKA and AR provided BM samples; HM-J, JJ, MKA and KT-M collected and assembled the data; HM-J, JJ, NR, FOB, OW, NB, BTP and KT-M analyzed and interpreted the data; KT-M drafted the manuscript. HM-J, JJ, NR, MKA, LB, NB and BTP contributed to the writing of the manuscript.

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Correspondence to K Theilgaard-Mönch.

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The authors declare no conflict of interest.

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Mora-Jensen, H., Jendholm, J., Rapin, N. et al. Cellular origin of prognostic chromosomal aberrations in AML patients. Leukemia 29, 1785–1789 (2015).

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