2012 Fiscal Year Final Research Report
遺伝子検査の社会的要請に応じた簡便な遺伝子変異スクリーニング法の開発と普及
| Project/Area Number |
22591122
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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 |
Pediatrics
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| Research Institution | Kanazawa University |
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Principal Investigator |
NIIDA Yo 金沢大学, 子どものこころの発達研究センター, 准教授 (40293344)
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| Project Period (FY) |
2010 – 2012
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| Keywords | 遺伝子診断 / 酵素ミスマッチ法 / MLPA法 |
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| Research Abstract |
In Japan, many clinicians consider DNA diagnosis is one of the clinical laboratory test. However, because of high cost and requirement of special instruments, DNA diagnosis is not come into wide use. In this study, we developed CHIPStechnology as simple, accurate and low cost mutation screening system. We set up CHIPS system to 60 genetic diseases, including 73 genes and demonstrated its utility. We hopespread gene tests by CHIPS among Japanese patients in near feature.
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[Journal Article] Birt-Hogg-Dube症候群の姉弟例2011
Author(s)
中川研, 北楯祥子, 齋藤雅俊, 藤本由貴, 小島好司, 及川卓, 土原一貴, 井口晶晴, 黄寿正, 長内和弘, 栂博久, 新井田要
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Journal Title
臨床放射線
Volume: 56
Pages: 133-137
Peer Reviewed
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