Kunstner A, Schwarting J, Witte H, Xing P, Bernard V, Stolting S
Leukemia. 2024; 38(5):1086-1098.
PMID: 38600314
PMC: 11073989.
DOI: 10.1038/s41375-024-02240-8.
Wang X, Liu S, Yu J
Adv Exp Med Biol. 2024; 1442:159-175.
PMID: 38228964
DOI: 10.1007/978-981-99-7471-9_10.
Ahmad M, Hegde M, Wong W, Mohammadhosseini M, Garrett L, Carrascoso A
Blood Adv. 2023; 7(23):7304-7318.
PMID: 37756546
PMC: 10711191.
DOI: 10.1182/bloodadvances.2023010398.
Ernst M, Pronk E, van Dijk C, van Strien P, van Tienhoven T, Wevers M
Hemasphere. 2023; 7(2):e824.
PMID: 36741355
PMC: 9891454.
DOI: 10.1097/HS9.0000000000000824.
Wang C, Tu Z, Cai X, Wang W, Davis A, Nattamai K
Blood Adv. 2023; 7(11):2590-2605.
PMID: 36661340
PMC: 10250926.
DOI: 10.1182/bloodadvances.2022008591.
Regulome analysis in B-acute lymphoblastic leukemia exposes Core Binding Factor addiction as a therapeutic vulnerability.
Wray J, Deltcheva E, Boiers C, Richardson S, Chhetri J, Brown J
Nat Commun. 2022; 13(1):7124.
PMID: 36411286
PMC: 9678885.
DOI: 10.1038/s41467-022-34653-3.
RUNX1-deficient human megakaryocytes demonstrate thrombopoietic and platelet half-life and functional defects.
Lee K, Ahn H, Estevez B, Poncz M
Blood. 2022; 141(3):260-270.
PMID: 36219879
PMC: 9936297.
DOI: 10.1182/blood.2022017561.
Long noncoding RNA promotes erythroid differentiation coordinating with GATA1 and chromatin remodeling.
Zhu J, Ren Y, Han Y, Jin T, Li Y, Ruan X
Blood Sci. 2022; 1(2):161-167.
PMID: 35402806
PMC: 8975080.
DOI: 10.1097/BS9.0000000000000031.
ATP citrate lyase controls hematopoietic stem cell fate and supports bone marrow regeneration.
Umemoto T, Johansson A, Ahmad S, Hashimoto M, Kubota S, Kikuchi K
EMBO J. 2022; 41(8):e109463.
PMID: 35229328
PMC: 9016348.
DOI: 10.15252/embj.2021109463.
MyD88-dependent TLR signaling oppositely regulates hematopoietic progenitor and stem cell formation in the embryo.
Bennett L, Mumau M, Li Y, Speck N
Development. 2022; 149(8).
PMID: 35043940
PMC: 8935211.
DOI: 10.1242/dev.200025.
Insufficiency of FZR1 disturbs HSC quiescence by inhibiting ubiquitin-dependent degradation of RUNX1 in aplastic anemia.
Zhou C, Kuang M, Liu Z, Jia X, Chen Z, Liu Y
Leukemia. 2021; 36(3):834-846.
PMID: 34635784
DOI: 10.1038/s41375-021-01445-5.
Effective therapy for AML with RUNX1 mutation by cotreatment with inhibitors of protein translation and BCL2.
Mill C, Fiskus W, DiNardo C, Birdwell C, Davis J, Kadia T
Blood. 2021; 139(6):907-921.
PMID: 34601571
PMC: 8832475.
DOI: 10.1182/blood.2021013156.
Emerging therapies for inv(16) AML.
Surapally S, Tenen D, Pulikkan J
Blood. 2021; 137(19):2579-2584.
PMID: 33821975
PMC: 8120144.
DOI: 10.1182/blood.2020009933.
RUNX-1 haploinsufficiency causes a marked deficiency of megakaryocyte-biased hematopoietic progenitor cells.
Estevez B, Borst S, Jarocha D, Sudunagunta V, Gonzalez M, Garifallou J
Blood. 2021; 137(19):2662-2675.
PMID: 33569577
PMC: 8120143.
DOI: 10.1182/blood.2020006389.
Different mutant RUNX1 oncoproteins program alternate haematopoietic differentiation trajectories.
Kellaway S, Keane P, Edginton-White B, Regha K, Kennett E, Bonifer C
Life Sci Alliance. 2021; 4(2).
PMID: 33397648
PMC: 7812315.
DOI: 10.26508/lsa.202000864.
Hematopoietic Stem Cell Transcription Factors in Cardiovascular Pathology.
Duddu S, Chakrabarti R, Ghosh A, Shukla P
Front Genet. 2020; 11:588602.
PMID: 33193725
PMC: 7596349.
DOI: 10.3389/fgene.2020.588602.
CHD7 and Runx1 interaction provides a braking mechanism for hematopoietic differentiation.
Hsu J, Huang H, Lee C, Choudhuri A, Wilson N, Abraham B
Proc Natl Acad Sci U S A. 2020; 117(38):23626-23635.
PMID: 32883883
PMC: 7519295.
DOI: 10.1073/pnas.2003228117.
Secondary leukemia in patients with germline transcription factor mutations (RUNX1, GATA2, CEBPA).
Brown A, Hahn C, Scott H
Blood. 2020; 136(1):24-35.
PMID: 32430494
PMC: 7332898.
DOI: 10.1182/blood.2019000937.
Runx1 negatively regulates inflammatory cytokine production by neutrophils in response to Toll-like receptor signaling.
Bellissimo D, Chen C, Zhu Q, Bagga S, Lee C, He B
Blood Adv. 2020; 4(6):1145-1158.
PMID: 32208490
PMC: 7094023.
DOI: 10.1182/bloodadvances.2019000785.
Mutations in the Leukemic Progression of Severe Congenital Neutropenia.
Olofsen P, Touw I
Mol Cells. 2020; 43(2):139-144.
PMID: 32041395
PMC: 7057833.
DOI: 10.14348/molcells.2020.0010.