Genetic study for diseases of insufficient development of retinal vessels
| Project/Area Number |
19592047
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Ophthalmology
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| Research Institution | Fukuoka University |
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Principal Investigator |
KONDO Hiroyuki Fukuoka University, 医学部, 准教授 (40268991)
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| Co-Investigator(Kenkyū-buntansha) |
HAYASHI Kenshi 九州大学, 生体防御医学研究所, 学術研究員 (00019671)
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| Project Period (FY) |
2007 – 2009
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| Project Status |
Completed (Fiscal Year 2009)
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| Budget Amount *help |
¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2009: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2008: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2007: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
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| Keywords | 家族性滲出性硝子体網膜症 / 未熟児網膜症 / ノリエ病 / WNTシグナル / 網膜剥離 / 新生血管 / 遺伝子 / 遺伝子診断 / TSPAN12 / Stickler症候群 / PAX3 / 網膜疾患 / SuperTopflash |
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| Research Abstract |
Diseases of insufficient development of retinal vessels are either congenital or acquired diseases that affect vision of infants and children secondary to retinal detachment. The diseases, exemplified by familial exudative vitreoretinopathy and retinopathy of prematurity, are clinically and genetically heterogeneous, and the underlying genetic factors remain to be elucidated. We evaluated the genetic factors by analyzing the patients or using experimental methods to develop a way for future prevention and the treatment.
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Report
(4 results)
Research Products
(51 results)
