Differentiation latency and dormancy signatures define fetal liver hematopoietic stem cells at single-cell resolution.
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| Title: | Differentiation latency and dormancy signatures define fetal liver hematopoietic stem cells at single-cell resolution. |
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| Authors: | Ishida T; Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA., Mercoli J; Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA., Heck AM; Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA., Phelps I; Department of Pediatrics, University of Washington, Seattle, WA, USA., Varnum-Finney B; Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA., Dozono S; Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA., Nourigat-McKay C; Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA., Kraskouskas K; Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA., Wellington R; Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA., Waltner O; Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA; Department of Genome Sciences, University of Washington, Seattle, WA, USA., Jackson DL; Department of Genome Sciences, University of Washington, Seattle, WA, USA., Delaney C; Department of Pediatrics, University of Washington, Seattle, WA, USA; Seattle Children's Research Institute, Seattle, WA, USA., Rafii S; Division of Regenerative Medicine, Ansary Stem Cell Institute, Department of Medicine, Weill Cornell Medicine, New York, NY, USA., Bernstein ID; Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA; Department of Pediatrics, University of Washington, Seattle, WA, USA., Aldinger KA; Department of Pediatrics, University of Washington, Seattle, WA, USA; Seattle Children's Research Institute, Seattle, WA, USA; Department of Neurology, University of Washington, Seattle, WA, USA., Trapnell C; Department of Genome Sciences, University of Washington, Seattle, WA, USA., Zhao HG; Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA. Electronic address: hzhao2@fredhutch.org., Hadland B; Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA, USA; Department of Pediatrics, University of Washington, Seattle, WA, USA; Seattle Children's Research Institute, Seattle, WA, USA. Electronic address: bhadland@fredhutch.org. |
| Corporate Authors: | Birth Defects Research Laboratory (BDRL); Department of Pediatrics, University of Washington, Seattle, WA, USA. |
| Source: | Cell reports [Cell Rep] 2025 Oct 28; Vol. 44 (10), pp. 116289. Date of Electronic Publication: 2025 Sep 18. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Cell Press Country of Publication: United States NLM ID: 101573691 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2211-1247 (Electronic) NLM ISO Abbreviation: Cell Rep Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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