Novel molecular basis underlying lethal arrhythmic syndrome due to mutations in cardiac Na/Ca exchanger gene
Novel molecular basis underlying lethal arrhythmic syndrome due to mutations in cardiac Na/Ca exchanger gene
批准号:
18H02808
负责人:
MAKITA Naomasa
金额:
$11.15万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
2018
资助国家:
日本
项目状态:
已结题
起止时间:
2018-04-01 至 2021-03-31
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Mechanisms of Electrical Storm Associated With QT Prolongation: Successful Mapping of Torsades de Pointes in Rabbits
与 QT 延长相关的电风暴机制:成功绘制兔子尖端扭转型室速
DOI:
--
发表时间:
2018
期刊:
影响因子:
--
作者:
[Tsuji Y., Yamazaki M., Niwa R., Tomii N., Arafune T., Honjo H., Dobrev D., Nattel S., Kodama I., Sakuma I., Makita N]
通讯作者:
Makita N
HCN4 Polymorphisms and Tachycardia Induced Cardiomyopathy
HCN4 多态性与心动过速诱发的心肌病
DOI:
--
发表时间:
2018
期刊:
影响因子:
--
作者:
[Nakano Y., Ochi H., Onohara Y., Sairaku A., Tokuyama T., Motoda C., Matsumura H., Tomomori S., Amioka M., Hironobe N., Ohkubo Y., Okamura S., Makita N., Yoshida Y., Chayama K., Kihara Y.]
通讯作者:
Kihara Y.
発症前診断を行ったQT延長症候群の姉妹
症状前诊断患有长 QT 综合征的姐妹
DOI:
--
发表时间:
2019
期刊:
影响因子:
--
作者:
[松下悠紀, 永田弾尺, 小川昌宣, 鹿田佐和子, 石川泰輔, 蒔田直昌]
通讯作者:
蒔田直昌
Novel common genetic predispositions to sudden death in Brugada syndrome distinct from those to diagnostic Brugada-ECG pattern
与诊断性 Brugada-ECG 模式不同的 Brugada 综合征猝死的新常见遗传倾向
DOI:
--
发表时间:
2019
期刊:
影响因子:
--
作者:
[Shinoda M, Saku K, Oga Y, Tohyama T, Nishikawa T, Abe K, Yoshida K, Kuwabara Y, Fujii K, Ishikawa T, Kishi T, Sunagawa K, Tsutsui H., Ishikawa T.]
通讯作者:
Ishikawa T.
Modeling Overlapping Phenotypes of Long-QT and Brugada Syndrome with CACNA1C-E1115K that Alters Ion Selectivity of the Cardiac L-Type Calcium Channel Using Induced Pluripotent Stem Cells
使用 CACNA1C-E1115K 模拟长 QT 和 Brugada 综合征的重叠表型,利用诱导多能干细胞改变心脏 L 型钙通道的离子选择性
DOI:
--
发表时间:
2019
期刊:
影响因子:
--
作者:
[Kashiwa A., Makiyama T., Kohjitani H., Hirose S., Gao J., Kashiwa A., Huang H., Ishikawa T., Ohno S., Chonabayashi K., Suda K., Yoshida Y., Horie M., Makita N., Kimura T.]
通讯作者:
Kimura T.
共 82 条
Novel molecular basis of cardriac conduction disturbance associated with a collagene gene mutation
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批准号:15K15311
-
项目类别:Grant-in-Aid for Challenging Exploratory Research
-
资助金额:$2.33万
-
财政年份:2015
-
负责人:MAKITA Naomasa
-
依托单位:
Elucidation of novel pathophysiology underlysing lethal arrhythmia due to mutations in cardiac ion transporters
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批准号:15H04823
-
项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$11.4万
-
财政年份:2015
-
负责人:MAKITA Naomasa
-
依托单位:
Identification of Novel Genes and Pathogenesis Responsible for Brugada Syndrome Using Whole Exome Sequencing
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批准号:24390199
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$11.48万
-
财政年份:2012
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负责人:MAKITA Naomasa
-
依托单位:
Mutations in cardiac gap junction genes and the pathophysiology underlying progressive cardiac conduction defect.
-
批准号:21590921
-
项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$2.91万
-
财政年份:2009
-
负责人:MAKITA Naomasa
-
依托单位:
Akt phosphorylation and arrhythmogenic modification of the cardiac sodium channel
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批准号:18590757
-
项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.53万
-
财政年份:2006
-
负责人:MAKITA Naomasa
-
依托单位:
Phamacogenomic studies for the genetic basis for lethal arrhythmias
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批准号:15590711
-
项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.24万
-
财政年份:2003
-
负责人:MAKITA Naomasa
-
依托单位:
海外基金