Hematopoietic Stem Cell Transplantation
Moving in Blood, bioRxiv, Nature Immunology, Stem cell research, medRxiv, Nature Biotechnology, Cell Reports and Cytometry. Part A : the journal of the International Society for Analytical Cytology.
- Moved, week to 22 Oct 2026
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Latest in Hematopoietic Stem Cell Transplantation
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A family with heterozygous RPS19 mutation yielded four iPSC lines representing healthy, silent carrier, and DBA individuals, enabling disease modeling.
- Open access
Fibroblast-derived FGF18 promotes AML progression and immune suppression by activating FGFR3 signaling and forming a feed-forward loop in the bone marrow niche.
- Open access
A Postn+ mesenchymal cell subset is essential for T lymphopoiesis and thymus regeneration, and its transfer enhances T cell production and immune response.
- Open access
- 16 cites
Severe graft-versus-host disease is linked to persistent expansion of alloreactive T cell clones that acquire tissue-resident memory programs during migration to epithelium.
Two human iPSC lines reprogrammed from adult bone marrow MSCs are genomically stable and can differentiate into the three germ layers.
- Open access
Fibro-inflammatory remodeling is a hallmark of clonal hematopoiesis of indeterminate potential, with fibroblasts expanding and acquiring cancer-associated transcriptional states.
- Open access
- 1 cites
IDH3A-driven citrate accumulation controls metabolic fitness and venetoclax resistance in AML stem cells, with knockdown impairing leukemia maintenance.
Translational regulation of Sf1 via a conserved 5' UTR modulates hematopoietic stem cell fate by controlling spliceosome activity and gene splicing.
- Open access
CD4+CD25+FOXP3+ regulatory T cells significantly reduce graft-versus-host disease risk in allogeneic hematopoietic cell transplantation.
IFN-γ-driven inflammation causes long-term bone marrow niche dysfunction after doxorubicin chemotherapy, impairing hematopoietic and skeletal health.
- Open access
- 1 cites
GLS and GEE-GLM modeling approaches reveal significant differences in hematopoietic maturation profiles across disease states, with GEE-GLM highlighting early-stage variations.
- Open access
Epitope editing of KIT combined with BCL11A disruption enables non-genotoxic, in vivo selection of gene-edited HSPCs, enhancing therapeutic potential for blood disorders.
- Open access
P-selectin marks early functional heterogeneity in aging hematopoietic stem cells, with high expression linked to increased DNA damage and myeloid bias in humans and mice.
- Open access
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