清脆的
诱导多能干细胞
生物
基因敲除
同源盒
Cas9
突变
基因组编辑
细胞培养
遗传学
转录因子
基因
胚胎干细胞
细胞生物学
癌症研究
计算生物学
作者
Kristin Rädecke,Ambuj Gore,Karin Burau,Magdalena Laugsch,Katrin Köhler,Gudrun Rappold,Sandra Hoffmann
标识
DOI:10.1016/j.scr.2023.103089
摘要
SHOX2 is a homeobox transcription factor associated with atrial fibrillation (AF) and sinus node dysfunction. Here, we generated two homozygous SHOX2 knock-out hiPSC lines from a healthy control line and a corrected AF patient line (disease-specific SHOX2 mutation corrected to WT) using CRISPR/Cas9. These cell lines maintained pluripotency, an ability to differentiate into all three germlayers and a normal karyotype, presenting a valuable tool to investigate the impact of a full SHOX2 knock-out with respect to arrhythmogenic diseases on a cellular level.
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