Identification of causative genes for hereditary renal diseases based on inbreeding coefficients
基于近交系数鉴定遗传性肾病致病基因
基本信息
- 批准号:19790725
- 负责人:
- 金额:$ 2.45万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Young Scientists (B)
- 财政年份:2007
- 资助国家:日本
- 起止时间:2007 至 2008
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
スロイド反応性ネフローゼ(SSN)の発症には多因子が関与しているため遺伝学的解析が困難である。本研究では、家族性SSNを対象に遺伝解析を行い、SSNの遺伝要因を解明することを目的とした。本研究で集積した14家系28患児は、家系内で疾患感受性が劣性の遺伝因子で規定されている可能性が高く、マッピング対象として適していると考えられた。そのうちの3家系について既報の候補遺伝子座への連鎖を解析し、いずれも連鎖を除外した。今後は、さらに家系を集積し、全ゲノム領域自己接合体マッピングを試みる予定である。
It is difficult to analyze the multi-factor relationship between the development of SSN and the genetic analysis. The purpose of this study is to analyze the genetic causes of familial SSN. In this study, 28 patients from 14 families were studied. The susceptibility and genetic factors of disease within families were determined. The linkage analysis of candidate loci in three families was carried out, except for the linkage analysis. In the future, the family will be integrated, and the field will be fully integrated.
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
A familial childhood-onset relapsing nephrotic syndrome
- DOI:10.1038/sj.ki.5002110
- 发表时间:2007-05-01
- 期刊:
- 影响因子:19.6
- 作者:Kitamura, A.;Tsukaguchi, H.;Iijima, K.
- 通讯作者:Iijima, K.
Clinical features and mutational survey of NPHS 2 (podocin) in Japanese children with focal segmental glomerulosclerosis who underwent renal transplantation
- DOI:10.1111/j.1399-3046.2007.00752.x
- 发表时间:2008-05-01
- 期刊:
- 影响因子:1.3
- 作者:Furue, Takeki;Hattori, Motoshi;Sakano, Takashi
- 通讯作者:Sakano, Takashi
Notch2 integrates signaling by the transcription factors RBP-J and CREB1 to promote T cell cytotoxicity
- DOI:10.1038/ni.1649
- 发表时间:2008-10-01
- 期刊:
- 影响因子:30.5
- 作者:Maekawa, Yoichi;Minato, Yoshiaki;Yasutomo, Koji
- 通讯作者:Yasutomo, Koji
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KITAMURA Akiko其他文献
KITAMURA Akiko的其他文献
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{{ truncateString('KITAMURA Akiko', 18)}}的其他基金
Media Expressions and Transformation, Body as an Interface Research
媒体表达与转化,身体作为界面研究
- 批准号:
15K12838 - 财政年份:2015
- 资助金额:
$ 2.45万 - 项目类别:
Grant-in-Aid for Challenging Exploratory Research
Clarifying the molecular mechanism of autoinflammation caused by dysfunction of immunoproteasome complexes
阐明免疫蛋白酶体复合物功能障碍引起自身炎症的分子机制
- 批准号:
25461595 - 财政年份:2013
- 资助金额:
$ 2.45万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
The transition of artistic expression in connection with "body" and technology. - A new realm of physical perception and art -
与“身体”和技术相关的艺术表达的转变。
- 批准号:
24652032 - 财政年份:2012
- 资助金额:
$ 2.45万 - 项目类别:
Grant-in-Aid for Challenging Exploratory Research
Dissection of Western Performing Arts: Dialogue for Analysis of the West from an Asian Perspective and the Transition of Performance Art Theories
西方表演艺术剖析:亚洲视角下的西方分析与表演艺术理论变迁的对话
- 批准号:
24320037 - 财政年份:2012
- 资助金额:
$ 2.45万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Identification of a critical gene involved in the pathogenesis of systemic lupus erythematosus by linkage analysis and exome resequencing
通过连锁分析和外显子组重测序鉴定参与系统性红斑狼疮发病机制的关键基因
- 批准号:
23791179 - 财政年份:2011
- 资助金额:
$ 2.45万 - 项目类别:
Grant-in-Aid for Young Scientists (B)
Transition of body expression in Asia~ Exchange between" foreign bodies" that taking a lesson from the past invents
亚洲身体表现的变迁~借鉴过去发明的“异物”之间的交流
- 批准号:
22720059 - 财政年份:2010
- 资助金额:
$ 2.45万 - 项目类别:
Grant-in-Aid for Young Scientists (B)
Genome-wide search for a candidate gene in systemic lupus erythematosus
全基因组搜索系统性红斑狼疮候选基因
- 批准号:
21790991 - 财政年份:2009
- 资助金额:
$ 2.45万 - 项目类别:
Grant-in-Aid for Young Scientists (B)














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