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Haematologica|January 13, 2018
Association of mutations with morphological dysplasia in de novo acute myeloid leukemia without 2016 WHO Classification-defined cytogenetic abnormalitiesOlga K Weinberg, Christopher J Gibson, Traci M Blonquist, et al.
The EMBO Journal|September 16, 2006
Failure to prolyl hydroxylate hypoxia-inducible factor alpha phenocopies VHL inactivation in vivoWilliam Y Kim, Michal Safran, Marshall R M Buckley, et al.
Blood|April 18, 2019
Engineered Bcor mutations lead to acute leukemia of progenitor B-1 lymphocyte origin in a sensitized backgroundMianmian Yin, Yang Jo Chung, R Coleman Lindsley, et al.
Elife|August 2, 2018
Thalidomide promotes degradation of SALL4, a transcription factor implicated in Duane Radial Ray syndromeKatherine A Donovan, Jian An, Radosław P Nowak, et al.
Molecular Cell|December 30, 2008
Small-molecule inhibitors of HIF-2a translation link its 5'UTR iron-responsive element to oxygen sensingMichael Zimmer, Benjamin L Ebert, Christopher Neil, et al.
Cancer Cell|October 16, 2007
FLT3 mutations confer enhanced proliferation and survival properties to multipotent progenitors in a murine model of chronic myelomonocytic leukemiaBenjamin H Lee, Zuzana Tothova, Ross L Levine, et al.
International Journal of Cardiology|May 17, 2024
The clonal hematopoiesis mutation Jak2V617F aggravates endothelial injury and thrombosis in arteries with erosion-like intimasRoberto Molinaro, Rob S Sellar, Amélie Vromman, et al.
British Journal of Haematology|August 8, 2014
L-Leucine improves the anaemia in models of Diamond Blackfan anaemia and the 5q- syndrome in a TP53-independent wayAnupama Narla, Elspeth M Payne, Nirmalee Abayasekara, et al.
Cell Stem Cell|December 4, 2014
Perivascular Gli1+ progenitors are key contributors to injury-induced organ fibrosisRafael Kramann, Rebekka K Schneider, Derek P DiRocco, et al.
Blood|June 10, 2011
Crosstalk between NOTCH and AKT signaling during murine megakaryocyte lineage specificationMelanie G Cornejo, Vinciane Mabialah, Stephen M Sykes, et al.
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