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A single-cell resolution map of mouse hematopoietic stem and progenitor cell differentiation
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Key Points: An expression map of HSPC differentiation from single-cell RNA sequencing of HSPCs provides insights into blood stem cell differentiation. A user-friendly Web resource provides access to single-cell gene expression profiles for the wider research community.
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“But recent state maps from scSeq (9), as well as clonal studies using barcodes (10) and single cell culture (11), suggest that the traditional intermediate cell types are internally heterogeneous in state and fate potential, with HSPCs lying along a continuum of states rather than a stepwise hierarchy.”
From Lineage tracing on transcriptional landscapes links state to fate during differentiation (2020) · cites this paper as [9]
In the citing paper
“When computationally reconstructed, single-cell RNA sequencing (scRNA-seq) profiling of the mammalian hematopoietic system typically produces a largely continuous distribution of cells from the earliest HSCs through the characteristic hematopoietic lineages (Nestorowa et al., 2016; Olsson et al., 2016; Paul et al., 2015; Pellin et al., 2019; Tusi et al., 2018; Weinreb et al., 2020).”
From Unraveling Hematopoiesis through the Lens of Genomics (2020) · cites this paper as Nestorowa et al., 2016
In the citing paper
“As part of the genomics revolution, increasingly accurate deep sequencing and novel methods of cell tracking have revealed hematopoiesis to be more of a continuous and less of a discrete and punctuated process than originally envisioned.”
From Unraveling Hematopoiesis through the Lens of Genomics (2020) · cites this paper as Nestorowa et al., 2016
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Metadata
- Authors
- Nestorowa, S., Hamey, F. K., Pijuan Sala, B., Diamanti, E., Shepherd, M., Laurenti, E., Wilson, N. K., Kent, D. G., & Göttgens, B.
- Affiliations
- Wellcome/MRC Cambridge Stem Cell Institute (GB)
- Department of Haematology and Wellcome Trust-Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Cambridge, United Kingdom
- ORCID
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 2016-08-25
- Volume
- 128
- Issue
- 8
- Pages
- e20-e31
- ISSN
- 0006-4971 (ISSN-L)
- 1528-0020
- PMC
- PMC5305050
- OpenAlex
- W2465917013
- Cited by
- 768
- References
- 55
- Citations by year
- 2026: 46 · 2025: 87 · 2024: 81 · 2023: 89 · 2022: 99 · 2021: 102 · 2020: 104 · 2019: 64 · 2018: 60 · 2017: 31 · 2016: 3
- FWCI
- 27.36
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Blood (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Apollo (University of Cambridge) (acceptedVersion, cc-by)
- Apollo
- Funders
- Wellcome Trust (107630/Z/15/Z, 097922/Z/11/Z)
- Cancer Research UK (12765)
- National Institute for Health and Care Research
- Directorate for Biological Sciences
- Medical Research Council (MR/M008975/1, MC_PC_12009)
- Biotechnology and Biological Sciences Research Council (BB/I00050X/1, 1800757)
- Cambridge Institute for Medical Research, University of Cambridge
- NIHR Cambridge Biomedical Research Centre
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Single-cell and spatial transcriptomics
- Health Sciences › Medicine › Hematology › Hematopoietic Stem Cell Transplantation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene Regulatory Network Analysis
- Keywords
- hematopoietic stem and progenitor cells, single-cell transcriptomics, differentiation trajectories, lymphoid differentiation, erythroid differentiation, cell cycle genes, oxidative phosphorylation, stem cell maintenance, mice
- MeSH terms
- Animals, Cell Cycle, Cell Differentiation, Female, Gene Expression Regulation, Hematopoietic Stem Cells, Mice, Inbred C57BL, Phenotype, RNA, Messenger, Transcription, Genetic, Biomarkers, Gene Expression Profiling, Single-Cell Analysis
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