Efficient Gene Disruption in Cultured Primary Human Endothelial Cells by CRISPR/Cas9

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Efficient gene disruption in cultured primary human endothelial cells by CRISPR/Cas9.

RATIONALE The participation of endothelial cells (EC) in many physiological and pathological processes is widely modeled using human EC cultures, but genetic manipulation of these untransformed cells has been technically challenging. Clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 nuclease (Cas9) technology offers a promising new approach. However,...

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NEW METHODS IN CARDIOVASCULAR BIOLOGY Efficient Gene Disruption in Cultured Primary Human Endothelial Cells by CRISPR/Cas9

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Cultured Human Endothelial Cells

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Human endothelial cells (ECs) are widely used to study mechanisms of angiogenesis, inflammation, and endothelial permeability. Targeted gene disruption induced by Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)-CRISPR-Associated Protein 9 (Cas9) nuclease gene editing is potentially an important tool for definitively establishing the functional roles of individual genes in ECs...

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ژورنال

عنوان ژورنال: Circulation Research

سال: 2015

ISSN: 0009-7330,1524-4571

DOI: 10.1161/circresaha.117.306290