Clonal analysis unveils self-renewing lineage-restricted progenitors generated directly from hematopoietic stem cells.
By R. Yamamoto, Yohei Morita, Jun Ooehara, Sanae Hamanaka, M. Onodera, K. Rudolph, H. Ema, H. Nakauchi. Cell, 2013
675 citations recorded by the source corpus.
Subfields: Cell Biology, Hematology, Immunology
View Paper: https://www.semanticscholar.org/paper/912b706c2f013a467c18127ee5918c68ff0e968a
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Citations in the corpus
- Transcriptional Heterogeneity and Lineage Commitment in Myeloid Progenitors. (2015, background): “…and unexplained heterogeneity within hematopoietic compartments calls for new approaches to complement our current models of blood and immune system development (Arinobu et al., 2007; Levine et al., 2015; Murre, 2007; Pronk et al., 2007; Schroeder, 2010; Wilson et al., 2008; Yamamoto et al., 2013).”
- Mapping Transcriptomic Vector Fields of Single Cells (2022, positive): “Notably, we found that the developmental F-LAP for the differentiation of HSC to Meg lineage requires the least time [roughly 31 h, in line with what reported in (Yamamoto et al., 2013)], further corroborating the observation of the early appearance of Meg lineage (Figures 6E and S7D).”
- Human haematopoietic stem cell lineage commitment is a continuous process (2017, neutral): “For instance, unipotent progenitors can derive directly from HSCs without proceeding through oligopotent progenitors 14,15 and lineage commitment was observed in progenitors proposed to be oligopotent 7,10,16 .”