influence of trisomy 21 on early neural differentiation
Project/Area Number |
26460275
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
General anatomy (including histology/embryology)
|
Research Institution | Tottori University |
Principal Investigator |
|
Project Period (FY) |
2014-04-01 – 2017-03-31
|
Project Status |
Completed (Fiscal Year 2016)
|
Budget Amount *help |
¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Fiscal Year 2016: ¥780,000 (Direct Cost: ¥600,000、Indirect Cost: ¥180,000)
Fiscal Year 2015: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2014: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
|
Keywords | 遺伝子発現モニター / 人工染色体 / 神経分化誘導 |
Outline of Final Research Achievements |
Chromosomal abnormalities, such as Trisomy for human chromosome 21 (Down syndrome), are thought to be the most common cause of mental retardation. To gain insight into the underlying cellular pathogenesis, we made a new system to monitor differentiation process from forebrain neural precursor cells into interneurons and oligodendrocytes by using a human artificial chromosome vector.
|
Report
(4 results)
Research Products
(3 results)
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[Journal Article] Retargeting of microcell fusion towards recipient cell-oriented transfer of human artificial chromosome2015
Author(s)
Hiratsuka M, Ueda K, Uno N, Uno K, Fukuhara S, Kurosaki H, Takehara S, Osaki M, Kazuki Y, Kurosawa Y, Nakamura T, Katoh M, Oshimura M
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Journal Title
BMC Biotechnol.
Volume: 15
Issue: 1
Pages: 58-58
DOI
Related Report
Peer Reviewed / Open Access / Int'l Joint Research
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