Article ; Online: Generation of a human embryonic stem cell line WAe009-A-79 carrying a long QT syndrome mutation in KCNQ1.
2023 Volume 70, Page(s) 103119
Abstract: The voltage-gated potassium channel KvLQT1 encoded by KCNQ1 plays an important role in the repolarization of myocardial action potentials. KCNQ1 mutations can cause Long QT syndrome type 1 (LQT1), which is considered to be the most common causative gene ... ...
Abstract | The voltage-gated potassium channel KvLQT1 encoded by KCNQ1 plays an important role in the repolarization of myocardial action potentials. KCNQ1 mutations can cause Long QT syndrome type 1 (LQT1), which is considered to be the most common causative gene of LQT. In this study, we established a human embryonic stem cell line KCNQ1 |
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MeSH term(s) | Humans ; KCNQ1 Potassium Channel/genetics ; KCNQ1 Potassium Channel/metabolism ; Human Embryonic Stem Cells/metabolism ; Long QT Syndrome/genetics ; Romano-Ward Syndrome/genetics ; Mutation/genetics ; Potassium Channels, Voltage-Gated/genetics ; KCNQ Potassium Channels/genetics |
Chemical Substances | KCNQ1 Potassium Channel ; Potassium Channels, Voltage-Gated ; KCNQ Potassium Channels ; KCNQ1 protein, human |
Language | English |
Publishing date | 2023-05-10 |
Publishing country | England |
Document type | Journal Article ; Research Support, Non-U.S. Gov't |
ZDB-ID | 2393143-7 |
ISSN | 1876-7753 ; 1873-5061 |
ISSN (online) | 1876-7753 |
ISSN | 1873-5061 |
DOI | 10.1016/j.scr.2023.103119 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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