4 results match your criteria: "National Research Center for Child Health and Development[Affiliation]"
PLoS One
July 2017
Department of Endocrinology, National Research Center for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo, Japan.
Objective: To investigate the effect of parental personality on birth outcomes.
Design: Prospective cohort study.
Setting: 727 pregnant women and 579 spouses receiving antenatal care at a single-center in rural Tokyo, Japan during 2010-2013.
Leukemia
August 2016
Division of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tokyo, Japan.
Transpl Immunol
November 2007
Department of Research Surgery, National Research Center for Child Health and Development, Japan.
Enhanced green fluorescence protein (EGFP) has been widely applied to gene transduction in cellular and molecular biology as a reporter element. When applied to cell transplantation, it raises fundamental issues concerning cell-associated antigens, in particular, a model of minor histocompatibility antigen(s). Although it is well known that immunological behavior of minor histocompatibility antigens mimic tumor associated antigens (TAA), identified genes coding minor histocompatibility antigens are few and far between.
View Article and Find Full Text PDFTransplant Proc
October 2005
Department of Research Surgery, National Research Center for Child Health and Development, Tokyo, Japan.
Evidence is provided that dendritic cells (DC) generated by either long-term bone marrow cell (BMC) culture with Flt3L and interleukin-6 (IL-6), or after short-term BMC culture with granulocyte macrophage-colony-stimulating factor (GM-CSF) and interleukin-4 (IL-4), contain heterogeneous cell populations of admixed DC and Mphi, regardless of the cytokine source. By employing GM-CSF-independent culture systems with the aid of Flt3/Flk-2 ligand and IL-6 and phenotypic characterization of BMC-derived DC and skin Langerhans cells (LC), revealed similar phenotypes. Furthermore, CD103 (OX62), which is widely used for rat DC separation, was found to be insufficient to enrich DC, due to downregulation of the marker.
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