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Toshio Heike

Researcher at University of Tokyo

Publications -  32
Citations -  1613

Toshio Heike is an academic researcher from University of Tokyo. The author has contributed to research in topics: T cell & Glycoprotein 130. The author has an hindex of 14, co-authored 32 publications receiving 1573 citations. Previous affiliations of Toshio Heike include Kyoto University.

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STAT3 activation is sufficient to maintain an undifferentiated state of mouse embryonic stem cells

TL;DR: It is strongly suggested that STAT3 activation is required and sufficient to maintain the undifferentiated state of ES cells.
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Activation of T cell-derived lymphokine genes in T cells and fibroblasts: effects of human T cell leukemia virus type I p40x protein and bovine papilloma virus encoded E2 protein.

TL;DR: It is proposed that pX or E2 protein, both in T cells and fibroblasts, activates cellular component(s) in the signal transduction pathway which results in the activation of lymphokine genes in the absence of extracellular stimuli.
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Pyrrolidine dithiocarbamate inhibits intercellular adhesion molecule-1 biosynthesis induced by cytokines in human fibroblasts.

TL;DR: Investigation of the effects of dexamethasone, cyclosporin A, FK506, and pyrrolidine dithiocarbamate on the induction of the ICAM-1 gene by cytokines in fibroblasts suggests that PDTC inhibits ICAM -1 gene expression by inhibiting the association of NF-kappa B (or NF-Kappa B-like) protein with the ICam-1 kappa B site.
Journal Article

Anti-IgM antibody-induced cell death in a human B lymphoma cell line, B104, represents a novel programmed cell death.

TL;DR: B104 cell death was shown to be quite distinct from that of WEHI-231 in cell death kinetics, the mode of cell death, and the response to cyclosporin A, indicating that the death of B104 cells resulting from surface IgM cross-linking represents a hitherto undefined mode of programmed cell death.
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Tool-use learning selectively induces expression of brain-derived neurotrophic factor, its receptor trkB, and neurotrophin 3 in the intraparietal multisensorycortex of monkeys.

TL;DR: Results suggest that brain-derived neurotrophic factor, its receptor trkB, and NT-3 are involved in the reorganization of the somatosensory and visual signals in the anterior bank of the intraparietal sulcus when monkeys are learning the use of the tool.