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Yutaka Hanazono

Researcher at Jichi Medical University

Publications -  113
Citations -  2901

Yutaka Hanazono is an academic researcher from Jichi Medical University. The author has contributed to research in topics: Stem cell & Haematopoiesis. The author has an hindex of 28, co-authored 111 publications receiving 2767 citations. Previous affiliations of Yutaka Hanazono include Shiga University of Medical Science & National Institutes of Health.

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Neuroprotective effects of glial cell line-derived neurotrophic factor mediated by an adeno-associated virus vector in a transgenic animal model of amyotrophic lateral sclerosis.

TL;DR: It is shown here that AAV-GDNF leads to substantial and long-lasting expression of transgenic GDNF in a large number of myofibers with its accumulation at the sites of neuromuscular junctions, indicating that A AV-mediated GDNF delivery to the muscle is a promising means of gene therapy for ALS.
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Ex Vivo Expansion of Genetically Marked Rhesus Peripheral Blood Progenitor Cells Results in Diminished Long-Term Repopulating Ability

TL;DR: It was found that the addition of FLT and especially STR during the initial brief transduction period increased engraftment with marked cells into a clinically relevant range, despite lack of evidence for expansion of engrafting cells.
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Delayed delivery of AAV-GDNF prevents nigral neurodegeneration and promotes functional recovery in a rat model of Parkinson's disease

TL;DR: Significant behavioral recovery was observed from 4–20 weeks following AAV-GDNFflag injection, indicating that a delayed delivery of GDNF gene using AAV vector is efficacious even 4 weeks after the onset of progressive degeneration in a rat model of PD.
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Repair of Infarcted Myocardium Mediated by Transplanted Bone Marrow–Derived CD34+ Stem Cells in a Nonhuman Primate Model

TL;DR: The results suggest that the improvement in regional blood flow and cardiac function in cynomolgus monkey acute myocardial infarction is not the result of generation of transplanted cell–derived endothelial cells or cardiomyocytes; and raise the possibility that angiogenic cytokines secreted from transplanted cells potentiateAngiogenic activity of endogenous cells.