Generation of conditional Acvrl1 knockout mice by CRISPR/Cas9-mediated gene targeting.

Molecular and Cellular Probes(2018)

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摘要
•This study is to generate mutant mice containing the Alk1 gene flanked with LoxP sequences to allow the conditional deletion of Alk1 by the LoxP/Cre system.•CRISPR/Cas9 technique was used to edit Alk1.•CRISPR/Cas9 technique was able to efficiently modify Alk1 and create the target mice.
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关键词
CRISPR/Cas9,Acvrl1,Mouse,Arteriovenous malformation
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