Daniel T. Starczynowski, Ph.D.

Affiliations: 
2006 Boston University, Boston, MA, United States 
Area:
Molecular Biology
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"Daniel Starczynowski"

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Thomas D. Gilmore grad student 2006 Boston University
 (A mutational and functional analysis of C -terminal sequences of human transcription factor REL: Their role in cellular transformation and transcriptional activation.)
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Publications

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Venkatasubramanian M, Schwartz L, Ramachandra N, et al. (2024) Broad de-regulated U2AF1 splicing is prognostic and augments leukemic transformation via protein arginine methyltransferase activation. Biorxiv : the Preprint Server For Biology
Marion W, Koppe T, Chen CC, et al. (2023) RUNX1 mutations mitigate quiescence to promote transformation of hematopoietic progenitors in Fanconi anemia. Leukemia
Dean ST, Ishikawa C, Zhu X, et al. (2023) Repression of TRIM13 by chromatin assembly factor CHAF1B is critical for AML development. Blood Advances
Bennett JR, Ishikawa C, Agarwal P, et al. (2023) Paralog-specific signaling by IRAK1/4 maintains MyD88-independent functions in MDS/AML. Blood
Barreyro L, Sampson AM, Ishikawa C, et al. (2022) Blocking UBE2N abrogates oncogenic immune signaling in acute myeloid leukemia. Science Translational Medicine. 14: eabb7695
Muto T, Guillamot M, Yeung J, et al. (2022) TRAF6 functions as a tumor suppressor in myeloid malignancies by directly targeting MYC oncogenic activity. Cell Stem Cell
Niederkorn M, Ishikawa C, M Hueneman K, et al. (2021) The deubiquitinase USP15 modulates cellular redox and is a therapeutic target in acute myeloid leukemia. Leukemia
Schieber M, Marinaccio C, Bolanos LC, et al. (2020) FBXO11 is a candidate tumor suppressor in the leukemic transformation of myelodysplastic syndrome. Blood Cancer Journal. 10: 98
Niederkorn M, Agarwal P, Starczynowski DT. (2020) TIFA and TIFAB: FHA-domain proteins involved in inflammation, hematopoiesis, and disease. Experimental Hematology
Muto T, Walker CS, Choi K, et al. (2020) Adaptive response to inflammation contributes to sustained myelopoiesis and confers a competitive advantage in myelodysplastic syndrome HSCs. Nature Immunology
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