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Shigeki Ohta
Researcher at Keio University
Publications - 47
Citations - 2241
Shigeki Ohta is an academic researcher from Keio University. The author has contributed to research in topics: Neural stem cell & Neurosphere. The author has an hindex of 21, co-authored 45 publications receiving 2017 citations. Previous affiliations of Shigeki Ohta include Osaka University & University of Calgary.
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Journal ArticleDOI
Aging results in reduced epidermal growth factor receptor signaling, diminished olfactory neurogenesis, and deficits in fine olfactory discrimination
Eineka Enwere,Tetsuro Shingo,Tetsuro Shingo,Christopher Gregg,Hirokazu Fujikawa,Shigeki Ohta,Samuel Weiss +6 more
TL;DR: Aged mice exhibited no differences from young adult mice in their ability to discriminate between two discrete odors but were significantly poorer at performing discriminations between similar odors, suggesting that the impairment in fine olfactory discrimination with age may result from a reduction in EGF-dependent Olfactory neurogenesis.
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Adrenomedullin Stimulates Two Signal Transduction Pathways, cAMP Accumulation and Ca2+ Mobilization, in Bovine Aortic Endothelial Cells
Yoshiyuki Shimekake,Kiyoshi Nagata,Shigeki Ohta,Yoshikazu Kambayashi,Hiroshi Teraoka,Kazuo Kitamura,Tanenao Eto,Kenji Kangawa,Hisayuki Matsuo +8 more
TL;DR: The results suggest that adrenomedullin elicits the hypotensive effect through at least two mechanisms, a direct action on vascular smooth muscle cells to increase intracellular cAMP and an action on endothelial cells to stimulate nitric oxide release, with both leading to vascular relaxation.
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Generation of Human Melanocytes from Induced Pluripotent Stem Cells
Shigeki Ohta,Yoichi Imaizumi,Yohei Okada,Wado Akamatsu,Reiko Kuwahara,Manabu Ohyama,Masayuki Amagai,Yumi Matsuzaki,Shinya Yamanaka,Hideyuki Okano,Yutaka Kawakami +10 more
TL;DR: This in vitro differentiation system should prove useful for understanding human melanocyte biology and revealing the mechanism of various pigment cell disorders, including melanoma.
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Downregulation of KIF23 suppresses glioma proliferation.
Satoshi Takahashi,Noemi Fusaki,Shigeki Ohta,Yoshihiro Iwahori,Yukihiko Iizuka,Kohei Inagawa,Yutaka Kawakami,Kazunari Yoshida,Masahiro Toda +8 more
TL;DR: Results indicate that downregulation of KIF23 decreases proliferation of glioma cells and that Kif23 may be a novel therapeutic target in malignant gliomas.
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Macrophage migration inhibitory factor (MIF) promotes cell survival and proliferation of neural stem/progenitor cells.
Shigeki Ohta,Aya Misawa,Raita Fukaya,Satoshi Inoue,Yonehiro Kanemura,Hideyuki Okano,Yutaka Kawakami,Masahiro Toda +7 more
TL;DR: Macrophage migration inhibitory factor (MIF) can induce NSPC proliferation and maintenance by multiple signaling pathways acting synergistically, and it may be a potential therapeutic factor, capable of activating NSPCs, for the treatment of degenerative brain disorders.