Genome-wide microsatellite mapping of multi-factorial ocular diseases.
Genome-wide microsatellite mapping of multi-factorial ocular diseases.
批准号:
16209052
负责人:
MIZUKI Nobuhisa
金额:
$30.28万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (A)
财政年份:
2004
资助国家:
日本
项目状态:
已结题
起止时间:
2004 至 2006
中文摘要
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英文摘要
In order to identify susceptibility genes associated with ocular diseases and hypertension, we have performed association study, using 25000 microsatellites(MS) and pooled DNA. The progresses of each disease is as follows.High myopia : 534 samples were collected. After the first, second and third screen, 156 positive markers were passed. As a result of indivisual typing, 26 positive markers were obtained. SNP typings were performing in the surrounding each candidate regionBehcet disease : 427 samples were collected. The first, second and third MS screenings and individual genotyping were finished, and 11 positive markers were obtained. SNP typing are performing in the surrounding each candidate regions.Lattice degeneration : 397 samples were collected. In the first screening, we found significant association for 2851 markers.Hypertension : 508 samples were collected. MS screenings were finished and 135 positive markers were obtained. Individual typing then were performed, and 55 markers were passed. SNP genotyping are performing now.Glaucoma : 192 samples were collected. The first screen using 138 samples was performed and 13.8% positive markers were obtained. The second screen is performing now. Simultaneously, SNP typings using GeneChip are performing.
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Exclusion of the transforming growth factor-β as a candidate gene for high myopia in the Japanese.
排除转化生长因子-β作为日本人高度近视的候选基因。
DOI:
--
发表时间:
2006
期刊:
Jpn J Ophthalmol 51(2)
影响因子:
--
作者:
[Nomura K, Murakami K, Shozu M, Nakama T, Yui N, Inoue M., Hayashi T]
通讯作者:
Hayashi T
HLA検査.基礎からわかるぶどう膜炎
HLA检测。葡萄膜炎的基本认识
DOI:
--
发表时间:
2006
期刊:
影响因子:
--
作者:
[Yoshida K, Kase S, Nakayama K, Nagahama H, Harada T, Ikeda H, Harada C, Imaki J, Ohgami K, Shiratori K, Iliyana B I, Ohno S, Nishi S, Nakayama K I, 佐々木爽]
通讯作者:
佐々木爽
ゲノムワイドなマイクロサテライトによる相関解析を用いたベーチェット病の感受性遺伝子の検索に関する研究、厚生労働科学研究(特定疾患対策研究事業)ベーチェット病に関する研究平成18年度研究報告集 : 9-13
利用全基因组微卫星相关分析寻找白塞病易感基因的研究,厚生劳动省科学研究(特定疾病控制研究项目)白塞病研究2006年研究报告集:9-13
DOI:
--
发表时间:
2007
期刊:
影响因子:
--
作者:
[Nomura K, Murakami K, Shozu M, Shinohara K, Kasai T, Nakama T, Nakamura T, Kawabata R, Yui N, Inoue M., Yoshihara A, 猪子英俊]
通讯作者:
猪子英俊
The study of investigation of susceptibility genes of Behcet disease using Genome-wide microsatellite marker.
利用全基因组微卫星标记调查白塞病易感基因的研究。
DOI:
--
发表时间:
2004
期刊:
The study report of Behcet disease in 2006, The enterprise for the intractable disease, In Japan Ministry of Health
影响因子:
--
作者:
[出村 昌史(金沢大学臓器機能制御学), 生水 真紀夫, 木 啓一, 神崎 晋, 武田 仁勇, Bulun Serdar, Yoshizawa S, Mizuki N]
通讯作者:
Mizuki N
ベーチェット病患者末梢血における細胞傷害性T細胞の活性化レベルの検討、厚生労働科学研究(特定疾患対策研究事業)ベーチェット病に関する研究平成15年度研究報告集 : 34-37
白塞氏病患者外周血中细胞毒性T细胞活化水平的检查,厚生劳动省科学研究(特定疾病控制研究项目)白塞氏病研究2003年研究报告集:34-37
DOI:
--
发表时间:
2004
期刊:
影响因子:
--
作者:
[Harada C, Harada T, Mitamura Y, Quah AH-M, Ohtsuka K, Kotake S, Ohno S, Wada K, Takeuchi S, Tanaka K, 桑名正隆]
通讯作者:
桑名正隆
共 85 条
whole-exome sequencing analysis of uveitis diseases
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批准号:20H03843
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财政年份:2020
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负责人:MIZUKI Nobuhisa
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Whole-exome sequencing in families with late-onset developmental glaucoma
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批准号:26293077
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Analysis of risk factors associated with non-response to infliximab treatment for Behcet's disease
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财政年份:2011
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负责人:MIZUKI Nobuhisa
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依托单位:
Genetic association study of Behcet's disease in multiple ethnic groups
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批准号:22390065
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$11.32万
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财政年份:2010
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负责人:MIZUKI Nobuhisa
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依托单位:
Genome-wide microsatellite mapping of multi-factorial ocular diseases.
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批准号:14370562
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$7.68万
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财政年份:2002
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负责人:MIZUKI Nobuhisa
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依托单位:
海外基金