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Commentary: Peptide-Based Targeting of the L-Type Calcium Channel Corrects the Loss-of-Function Phenotype of Two Novel Mutations of the CACNA1 Gene Associated With Brugada Syndrome

机译：评注：基于肽的L型钙通道的靶向校正与BRUGADA综合征相关的CACNA1基因的两种新突变的功能损失表型

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期刊名称 Frontiers in Physiology
作者
Michelle M. Monasky; Carola Rutigliani; Emanuele Micaglio; Carlo Pappone;
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作者单位

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年(卷),期 2021(-1),-1
年度 2021
页码 -1
总页数 3
原文格式 PDF
正文语种
中图分类人体生理学;
关键词

机译：Brugada综合征;L型钙通道;cacna1c;突变;药物;药物;个性化医学;

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专利

1. Role of mutations in L-type calcium channel genes in Brugada syndrome, early repolarization syndrome, and idiopathic ventricular fibrillation associated with right bundle branch block [J] . WatanabeH., MinaminoT. Circulation journal . 2013,第7期

机译：突变在Brugada综合征，早期复极综合征和特发性室颤与右束支传导阻滞相关的L型钙通道基因中的作用
2. Role of Mutations in L-Type Calcium Channel Genes in Brugada Syndrome, Early Repolarization Syndrome, and Idiopathic Ventricular Fibrillation Associated With Right Bundle Branch Block [J] . Hiroshi Watanabe, Tohru Minamino Circulation journal . 2013,第7期

机译：突变在Brugada综合征，早期复极综合征和特发性室颤与右束支传导阻滞相关的L型钙通道基因中的作用
3. Role of mutations in L-type calcium channel genes in Brugada syndrome, early repolarization syndrome, and idiopathic ventricular fibrillation associated with right bundle branch block [J] . WatanabeH., MinaminoT. Circulation journal . 2013,第7期

机译：突变在Brugada综合征，早期倒钩综合征和右束分支块相关的特发性心室颤动中的作用
4. Search of phenotype related candidate genes using Gene Ontology-based semantic similarity and protein interaction information: Application to Brugada syndrome [C] . Raimon Massanet, Joan-Josep Gallardo-Chacon, Pere Caminal, Annual International Conference of the IEEE Engineering in Medicine and Biology Society . 2009

机译：基于基于基于基于基因属性的语义相似性和蛋白质相互作用信息搜索表型相关候选基因：对Brugada综合征的应用
5. A mutation in cytochrome c oxidase subunit VIa causes defective L-type calcium currents and Leigh syndrome-like phenotypes in Drosophila. [D] . Liu, Wensheng. 2004

机译：细胞色素c氧化酶亚基VIa的突变会导致果蝇的L型钙电流缺陷和Leigh综合征样表型。
6. Peptide-Based Targeting of the L-Type Calcium Channel Corrects the Loss-of-Function Phenotype of Two Novel Mutations of the CACNA1 Gene Associated With Brugada Syndrome [O] . Vittoria Di Mauro, Paola Ceriotti, Francesco Lodola, 2020

机译：L型钙通道的肽的靶向校正与Brugada综合征相关的CACNA1基因的两种新突变的功能丧失表型
7. Commentary: Peptide-Based Targeting of the L-Type Calcium Channel Corrects the Loss-of-Function Phenotype of Two Novel Mutations of the CACNA1 Gene Associated With Brugada Syndrome [O] . Michelle M. Monasky, Carola Rutigliani, Emanuele Micaglio, 2021

机译：评注：基于肽的L型钙通道的靶向校正与BRUGADA综合征相关的CACNA1基因的两种新突变的功能损失表型

Commentary: Peptide-Based Targeting of the L-Type Calcium Channel Corrects the Loss-of-Function Phenotype of Two Novel Mutations of the CACNA1 Gene Associated With Brugada Syndrome

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