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PU.1 Expression Defines Distinct Functional Activities in the Phenotypic HSC Compartment of a Murine Inflammatory Stress Model.
Cells. 2022 Feb 15;11(4):680. doi: 10.3390/cells11040680.
Cells. 2022.
PMID: 35203330
Free PMC article.
PU.1 enforces quiescence and limits hematopoietic stem cell expansion during inflammatory stress.
Chavez JS, Rabe JL, Loeffler D, Higa KC, Hernandez G, Mills TS, Ahmed N, Gessner RL, Ke Z, Idler BM, Niño KE, Kim H, Myers JR, Stevens BM, Davizon-Castillo P, Jordan CT, Nakajima H, Ashton J, Welner RS, Schroeder T, DeGregori J, Pietras EM.
Chavez JS, et al. Among authors: nino ke.
J Exp Med. 2021 Jun 7;218(6):e20201169. doi: 10.1084/jem.20201169.
J Exp Med. 2021.
PMID: 33857288
Free PMC article.
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TNF Receptors Choose HSC Fate in Supporting Dnmt3a-Mutant Clonal Hematopoiesis.
Niño KE, Pietras EM.
Niño KE, et al.
Cancer Discov. 2022 Dec 2;12(12):2724-2726. doi: 10.1158/2159-8290.CD-22-1022.
Cancer Discov. 2022.
PMID: 36458433
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PU.1 is required to restrain myelopoiesis during chronic inflammatory stress.
Chavez JS, Rabe JL, Niño KE, Wells HH, Gessner RL, Mills TS, Hernandez G, Pietras EM.
Chavez JS, et al. Among authors: nino ke.
Front Cell Dev Biol. 2023 Jun 26;11:1204160. doi: 10.3389/fcell.2023.1204160. eCollection 2023.
Front Cell Dev Biol. 2023.
PMID: 37497478
Free PMC article.
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