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Mitsuhiro Fukata

Researcher at Kyushu University

Publications -  57
Citations -  1558

Mitsuhiro Fukata is an academic researcher from Kyushu University. The author has contributed to research in topics: Medicine & Bone marrow. The author has an hindex of 10, co-authored 47 publications receiving 1403 citations.

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Chemotherapy-resistant human AML stem cells home to and engraft within the bone-marrow endosteal region.

TL;DR: A primary human AML xenotransplantation model using newborn nonobese diabetic/severe combined immunodeficient/interleukin (NOD/SCID/IL)2rγnull mice carrying a complete null mutation of the cytokine γc upon the SCID background is developed, demonstrating that LS cells exclusively recapitulate AML and retain self-renewal capacity in vivo.
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CD34+CD38+CD19+ as well as CD34+CD38−CD19+ cells are leukemia-initiating cells with self-renewal capacity in human B-precursor ALL

TL;DR: The identification of CD34+CD38+CD19+ self-renewing B-ALL cells proposes a hierarchy of leukemia-initiating cells (LICs) distinct from that of AML, and provides a powerful tool for directly studying leukemogenesis and for developing therapeutic strategies.
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Characterization and distribution of bone marrow-derived cells in mouse cornea.

TL;DR: Investigation of BM cells and BM-derived hematopoietic stem/progenitor cells from enhanced GFP (eGFP) transgenic mice found that some of these cells are BM- derived antigen-presenting cells such as dendritic cells and macrophages.
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Purified human hematopoietic stem cells contribute to the generation of cardiomyocytes through cell fusion

TL;DR: In this paper, green fluorescent protein (GFP)-labeled BM Lin-ScaI+ hematopoietic progenitors were transplanted into neonatal mice constitutively expressing cyan fluorescence protein (CFP).
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Contribution of Bone Marrow-Derived Hematopoietic Stem/Progenitor Cells to the Generation of Donor-Marker+ Cardiomyocytes In Vivo

TL;DR: The authors' results indicate that HSCs resulted in the generation of cardiomyocytes via myeloid intermediates by fusion-dependent mechanism, which could potentially allow more effective cell-based therapy for cardiac repair.