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Updated: Mar 11, 2026

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Establishment of Genome-edited Human Pluripotent Stem Cell Lines: From Targeting to Isolation
Published on: February 2, 2016
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Efficient Genome Editing in Induced Pluripotent Stem Cells with Engineered Nucleases In Vitro
Vittavat Termglinchan1, Timon Seeger1, Caressa Chen1
1Stanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Methods in Molecular Biology (Clifton, N.J.)
|December 3, 2016
Summary
This study introduces an efficient method for precise genome editing in induced pluripotent stem cells (iPSCs) using nucleases and the piggyBac system, improving cardiovascular disease modeling.
Area of Science:
- Cardiovascular disease research
- Stem cell biology
- Genome engineering
Background:
- Induced pluripotent stem cells (iPSCs) are crucial for in vitro cardiovascular disease modeling.
- Engineered nucleases enable precise genome editing but homologous recombination is inefficient.
Purpose of the Study:
- To develop an optimized method for efficient and precise genome editing in pluripotent stem cells.
- To enhance the application of iPSCs technology for cardiovascular disease modeling.
Main Methods:
- Combined site-specific nucleases with the piggyBac transposon system.
- Developed a method for "seamless" genome editing in pluripotent stem cells.
Main Results:
- Achieved high efficiency and fidelity in genome editing.
- Demonstrated an optimized approach for precise genetic modifications in iPSCs.
Conclusions:
- The developed method significantly improves genome engineering efficiency in pluripotent stem cells.
- This advancement facilitates more accurate in vitro modeling of cardiovascular diseases.
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