Research Projects to Clarify the Molecular Pathogenesis and to Develop Therapeutic or Preventive Strategy for Cardiomyopathy
阐明心肌病分子发病机制并制定治疗或预防策略的研究项目
基本信息
- 批准号:19390208
- 负责人:
- 金额:$ 11.73万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Scientific Research (B)
- 财政年份:2007
- 资助国家:日本
- 起止时间:2007 至 2009
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
In this research, we have identified CARP mutations as the molecular basis of cardiomyopathy. We also found PGM1 as a binding partner of ZASP and revealed that DCM-associated ZASP mutations impaired the binding to PGM1. In addition, PGM1 was found to be localized to Z-disc upon metabolic stress of cardiomyocytes. On the other hand, we reveled that M21 enhanced the phosphorylation of M110. Finally, we demonstrated that calcium sensitizer could prevent the pathological changes in the hearts of a model mice for dilated cardiomyopathy.
在这项研究中,我们确定了 CARP 突变是心肌病的分子基础。我们还发现 PGM1 作为 ZASP 的结合伴侣,并揭示 DCM 相关的 ZASP 突变损害了与 PGM1 的结合。此外,在心肌细胞的代谢应激下,PGM1 被发现定位于 Z 盘。另一方面,我们发现 M21 增强了 M110 的磷酸化。最后,我们证明钙增敏剂可以预防扩张型心肌病模型小鼠心脏的病理变化。
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 novel protein found in the I bands of myofibrils is produced by alternative splicing of the DLST gene
肌原纤维 I 带中发现的一种新蛋白质是通过 DLST 基因的选择性剪接产生的
- DOI:
- 发表时间:2010
- 期刊:
- 影响因子:0
- 作者:Matuda S; Arimura T; Kimura A; Takekura H; Ohta S; Nakano K.
- 通讯作者:Nakano K.
Impaired binding of ZASP/Cypher with phosphoglucomutase 1 is associated with dilated cardiomyopathy
ZASP/Cypher 与磷酸葡萄糖变位酶 1 的结合受损与扩张型心肌病相关
- DOI:
- 发表时间:2009
- 期刊:
- 影响因子:0
- 作者:Arimura T; Inagaki N; Hayashi T; Shichi D; Sato A; Hinohara K; Vatta M; Towbin JA; Chikamori T; Yamashina A; Kimura A.
- 通讯作者:Kimura A.
Replication studies for the association of PSMA6 polymorphism with coronary artery disease in East Asian populations
PSMA6 多态性与东亚人群冠状动脉疾病关联的复制研究
- DOI:
- 发表时间:2009
- 期刊:
- 影响因子:0
- 作者:Hinohara K; Nakajima T; Sasaoka T; Sawabe M; Lee BS; Ban J; Park JE; Izumi T; Kimura A.
- 通讯作者:Kimura A.
ANKRD-the gene encoding cardiac ankyrin repeat protein-is a novel dilated cardiomyopathy gene
ANKRD——编码心脏锚蛋白重复蛋白的基因——是一种新型扩张型心肌病基因
- DOI:
- 发表时间:2009
- 期刊:
- 影响因子:0
- 作者:Moulik M; Vatta M; Witt SH; Alora AM; Murphy RT; McKenna WJ; Boriek A; Oka K; Labeit S; Bowles NE; Arimura T; Kimura A; Towbin JA
- 通讯作者:Towbin JA
Cardiac ankyrin repeat protein gene (ANKRD1) mutations in hypertrophic cardiomyopathy
肥厚型心肌病中的心脏锚蛋白重复蛋白基因 (ANKRD1) 突变
- DOI:
- 发表时间:2009
- 期刊:
- 影响因子:0
- 作者:Arimura T
- 通讯作者:Arimura T
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KIMURA Akinori其他文献
Diversity of ULBP5 in Old-World monkeys (Cercopithecidae) and divergence of the ULBP gene family in primates
旧世界猴(猴科)中 <i>ULBP5</i> 的多样性和灵长类动物中 <i>ULBP</i> 基因家族的分歧
- DOI:
10.2183/pjab.94.029 - 发表时间:
2018 - 期刊:
- 影响因子:0
- 作者:
NARUSE Taeko K.;AKARI Hirofumi;MATANO Tetsuro;KIMURA Akinori - 通讯作者:
KIMURA Akinori
Diversity of ULBP5 in Old-World monkeys (Cercopithecidae) and divergence of the ULBP gene family in primates
旧世界猴(猴科)中 <i>ULBP5</i> 的多样性和灵长类动物中 <i>ULBP</i> 基因家族的分歧
- DOI:
10.2183/pjab.94.029 - 发表时间:
2018 - 期刊:
- 影响因子:0
- 作者:
NARUSE Taeko K.;AKARI Hirofumi;MATANO Tetsuro;KIMURA Akinori - 通讯作者:
KIMURA Akinori
KIMURA Akinori的其他文献
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{{ truncateString('KIMURA Akinori', 18)}}的其他基金
Molecular pathogenesis of heart failure and arrhythmia caused by gene abnormalities
基因异常引起心力衰竭和心律失常的分子发病机制
- 批准号:
16H05296 - 财政年份:2016
- 资助金额:
$ 11.73万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Molecular basis for cardiac muscle diseases caused by functional abnormalities of Z-disc
Z盘功能异常引起的心肌疾病的分子基础
- 批准号:
23659414 - 财政年份:2011
- 资助金额:
$ 11.73万 - 项目类别:
Grant-in-Aid for Challenging Exploratory Research
Development of strategies for handling heart failure based on the molecular pathogenesis of cardiomyopathy
基于心肌病的分子发病机制制定治疗心力衰竭的策略
- 批准号:
22390157 - 财政年份:2010
- 资助金额:
$ 11.73万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
A Parallel Point Generation Using Monte Carlo Methods for Point Based Visualization of Multiple Volume Data
使用蒙特卡罗方法生成并行点以实现多体数据的基于点的可视化
- 批准号:
20700096 - 财政年份:2009
- 资助金额:
$ 11.73万 - 项目类别:
Grant-in-Aid for Young Scientists (B)
Investigation of the molecular mechanisms of cardiac failure focusing on the Z-disc abnormalities
以Z盘异常为中心的心力衰竭分子机制研究
- 批准号:
16390219 - 财政年份:2004
- 资助金额:
$ 11.73万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
相似海外基金
The investigation of genetics and pathophysiological mechanism in hypertrophic cardiomyopathy
肥厚型心肌病的遗传学及病理生理机制研究
- 批准号:
16K09440 - 财政年份:2016
- 资助金额:
$ 11.73万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Genetic analysis and pathological role in ventricular noncompaction associated with fatal arrhythmia
致死性心律失常相关心室致密化不全的遗传分析和病理作用
- 批准号:
15K09685 - 财政年份:2015
- 资助金额:
$ 11.73万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
The investigation of etiology and disease modifier factors in hypertrophic cardiomyopathy
肥厚型心肌病的病因及疾病调节因素调查
- 批准号:
23591049 - 财政年份:2011
- 资助金额:
$ 11.73万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Development of strategies for handling heart failure based on the molecular pathogenesis of cardiomyopathy
基于心肌病的分子发病机制制定治疗心力衰竭的策略
- 批准号:
22390157 - 财政年份:2010
- 资助金额:
$ 11.73万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
The Mutation and Paterns of Subtypes of Troponin-T in Familial Hypertrophic Cardiomyopathy.
家族性肥厚型心肌病肌钙蛋白-T 亚型的突变和模式。
- 批准号:
11670783 - 财政年份:1999
- 资助金额:
$ 11.73万 - 项目类别:
Grant-in-Aid for Scientific Research (C)