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Takahiro Kunisada

Researcher at Gifu University

Publications -  188
Citations -  12211

Takahiro Kunisada is an academic researcher from Gifu University. The author has contributed to research in topics: Stem cell & Embryonic stem cell. The author has an hindex of 48, co-authored 185 publications receiving 11413 citations. Previous affiliations of Takahiro Kunisada include Kyoto University & St. Marianna University School of Medicine.

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The murine mutation osteopetrosis is in the coding region of the macrophage colony stimulating factor gene

TL;DR: It is shown that op/op fibroblasts are defective in production of functional macrophage colony-stimulating factor (M-CSF), although its messenger RNA (Csfm mRNA) is present at normal levels, and it is concluded that the pathological changes in this mutant result from the absence of M- CSF.
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A more efficient method to generate integration-free human iPS cells

TL;DR: A simple method is reported, using p53 suppression and nontransforming L-Myc, to generate human induced pluripotent stem cells (iPSCs) with episomal plasmid vectors, which may provide iPSCs suitable for autologous and allologous stem-cell therapy in the future.
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Hypoxia promotes expansion of the CD133-positive glioma stem cells through activation of HIF-1alpha.

TL;DR: It is shown that hypoxia (1% oxygen) promotes the self-renewal capacity of CD133-positive human glioma-derived cancer stem cells (CSCs) and the activation of HIF-1α to enhance theSelf-Renewal activity of CD 133-positive cells and to inhibit the induction of CSC differentiation.
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Characterization of CD133+ hepatocellular carcinoma cells as cancer stem/progenitor cells ☆

TL;DR: Investigation of whether CD133(+) cells isolated from human hepatocellular carcinoma cell lines possess cancer stem/progenitor cell-like properties found that among the three cell lines studied, the CD133 antigen was found to be expressed only on the surface of Huh-7 cells.
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Topical drug rescue strategy and skin protection based on the role of Mc1r in UV-induced tanning

TL;DR: It is shown that ultraviolet light potently induces expression of MSH in keratinocytes, but fails to stimulate pigmentation in the absence of functional MC1R in red/blonde-haired Mc1re/e mice, and a clinical strategy for topical small-molecule manipulation of pigmentation is suggested.