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Toru Itakura

Researcher at Wakayama Medical University

Publications -  290
Citations -  4892

Toru Itakura is an academic researcher from Wakayama Medical University. The author has contributed to research in topics: Aneurysm & Stenosis. The author has an hindex of 36, co-authored 289 publications receiving 4679 citations.

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Visualization, direct isolation, and transplantation of midbrain dopaminergic neurons

TL;DR: To visualize and isolate live dopamine (DA)-producing neurons in the embryonic ventral mesencephalon and isolate an enriched population of DA neurons from brain tissue, transgenic mice expressing green fluorescent protein (GFP) are generated under the control of the rat tyrosine hydroxylase gene promoter.
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Generation of Dopaminergic Neurons in the Adult Brain from Mesencephalic Precursor Cells Labeled with a nestin-GFP Transgene

TL;DR: These findings indicate that precursor cells harvested from the embryonic ventral mesencephalon can generate dopaminergic neurons able to restore function to the chemically denervated adult striatum.
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Human amniotic epithelial cells produce dopamine and survive after implantation into the striatum of a rat model of Parkinson's disease: a potential source of donor for transplantation therapy.

TL;DR: The results clearly indicate that HAE cells capable of producing DA can survive and function in the brain of a rat model of PD and further studies are needed to develop strategies to enhance the ability of Hae cells to produce DA as well as the graft survival.
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Implantation of human amniotic epithelial cells prevents the degeneration of nigral dopamine neurons in rats with 6-hydroxydopamine lesions

TL;DR: Although the factors that contribute to the currently observed effects remain to be fully determined, implantation of HAE cells could be a viable strategy to counteract the loss of DA neurons in Parkinson's disease.
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EphA4 promotes cell proliferation and migration through a novel EphA4-FGFR1 signaling pathway in the human glioma U251 cell line

TL;DR: The results indicate that EphA4 plays an important role in malignant phenotypes of glioblastoma by enhancing cell proliferation and migration through accelerating a canonical FGFR signaling pathway.