Generation of two homozygous SHOX2 knock-out human induced pluripotent stem cell lines using CRISPR/Cas9
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Developmental Biology,General Medicine
Reference5 articles.
1. Targeted mutation reveals essential functions of the homeodomain transcription factor Shox2 in sinoatrial and pacemaking development;Blaschke;Circulation,2007
2. Functional Characterization of Rare Variants in the SHOX2 Gene Identified in Sinus Node Dysfunction and Atrial Fibrillation;Hoffmann;Front. Genet.,2019
3. Coding and non-coding variants in the SHOX2 gene in patients with early-onset atrial fibrillation;Hoffmann;Basic Res Cardiol.,2016
4. Sinus Node Dysfunction in Atrial Fibrillation: Cause or Effect?;Kezerashvili;J. Atr. Fibrillation,2008
5. Precise Correction of Heterozygous SHOX2 Mutations in hiPSCs Derived from Patients with Atrial Fibrillation via Genome Editing and Sib Selection;Sumer;Stem Cell Reports,2020
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