CACNA1C-E1115K変異ヒトiPS細胞モデルにおけるCav 1.2イオン選択性障害がQT延長症候群・ブルガダ症候群のオーバーラップを引き起こすメカニズムの検討

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CACNA1C-E1115K変異ヒトiPS細胞モデルにおけるCav 1.2イオン選択性障害がQT延長症候群・ブルガダ症候群のオーバーラップを引き起こすメカニズムの検討

Material type: 博士論文

Author: 柏, 麻美

Publisher: Kyoto University

Publication date: 2023-03-23

Material Format: Digital

Capacity, size, etc.: -

Name of awarding university/degree: 京都大学,博士(医学),Doctor of Medical Science

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Material Type: 博士論文
Title: CACNA1C-E1115K変異ヒトiPS細胞モデルにおけるCav 1.2イオン選択性障害がQT延長症候群・ブルガダ症候群のオーバーラップを引き起こすメカニズムの検討
Author/Editor: 柏, 麻美
Author Heading: 柏, 麻美カシワ, アサミ
Publication, Distribution, etc.: Kyoto University
Publication Date: 2023-03-23
Publication Date (W3CDTF): 2023-03-23
Alternative Title: Disrupted Cav1.2 Selectivity Causes Overlapping Long QT and Brugada Syndrome Phenotypes in CACNA1C-E1115K iPS Cell Model
Contributor: 江藤, 浩之
湊谷, 謙司
大鶴, 繁
Degree grantor/type: 京都大学
Date Granted: 2023-03-23
Dissertation Number: 甲第24485号
Degree Type: 博士(医学)
Doctor of Medical Science
Text Language Code: eng
Subject Heading: L-type Ca2+ channel
Induced pluripotent stem cell
Late Na+ channel current
Long QT syndrome
Brugada syndrome
Gene editing
Arrhythmia
NDC: 490
Target Audience: 一般
DOI: 10.14989/doctor.k24485
Access Restrictions: インターネット公開
Rights (production): 学位規則第9条第2項により要約公開
This article was published in Heart Rhythm, S1547-5271(22)02316-5., doi: 10.1016/j.hrthm.2022.08.021., Kashiwa et al., Disrupted CaV1.2 selectivity causes overlapping long QT and Brugada syndrome phenotypes in the CACNA1C-E1115K iPS cell model, Copyright Elsevier (2022).
Is Version Of (DOI): 10.1016/j.hrthm.2022.08.021
http://hdl.handle.net/2433/283604
Data Provider (Database): 国立情報学研究所 : 学術機関リポジトリデータベース（IRDB）（機関リポジトリ）
https://irdb.nii.ac.jp
Original Data Provider (Database): 京都大学 : 京都大学学術情報リポジトリ