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Naoyuki Uchida

Researcher at University of British Columbia

Publications -  8
Citations -  1532

Naoyuki Uchida is an academic researcher from University of British Columbia. The author has contributed to research in topics: Stem cell & Haematopoiesis. The author has an hindex of 8, co-authored 8 publications receiving 1449 citations. Previous affiliations of Naoyuki Uchida include Kyushu University & Fukuoka University.

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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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The hematopoietic stem compartment consists of a limited number of discrete stem cell subsets

TL;DR: The data indicate that the HSC compartment consists of a limited number of distinct HSC subsets, each with predictable behavior, which could provide a basis for the diagnosis of perturbed patterns of HSCs potentially caused by disease or aging.
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Transplantable hematopoietic stem cells in human fetal liver have a CD34+ side population (SP)phenotype

TL;DR: It is shown, for the first time, that SP cells are present in the second-trimester human fetal liver and that early in ontogeny they express CD34, suggesting that the SP phenotype is an important and distinguishing property of human hematopoietic stem cells.
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Different in vivo repopulating activities of purified hematopoietic stem cells before and after being stimulated to divide in vitro with the same kinetics.

TL;DR: Exogenous growth factors can differentially affect the ability of HSCs to execute a self-renewal division within a single cell cycle even when the kinetics of proliferation are the same.
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ABC transporter activities of murine hematopoietic stem cells vary according to their developmental and activation status

TL;DR: The Rhodamine-123 and Hoechst 33342 efflux properties of murine HSCs fluctuate in the same fashion as a number of other HSC markers, suggesting these are regulated by a common control mechanism that operates independently of that regulating the regenerative function of HSCS.